CN1229358A - 从合成的rna转录物制备双rna病毒的方法 - Google Patents
从合成的rna转录物制备双rna病毒的方法 Download PDFInfo
- Publication number
- CN1229358A CN1229358A CN97197688A CN97197688A CN1229358A CN 1229358 A CN1229358 A CN 1229358A CN 97197688 A CN97197688 A CN 97197688A CN 97197688 A CN97197688 A CN 97197688A CN 1229358 A CN1229358 A CN 1229358A
- Authority
- CN
- China
- Prior art keywords
- leu
- ala
- pro
- gly
- ser
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000000034 method Methods 0.000 title claims description 24
- 108091032973 (ribonucleotides)n+m Proteins 0.000 claims abstract description 82
- 241000702626 Infectious bursal disease virus Species 0.000 claims abstract description 78
- 241000700605 Viruses Species 0.000 claims abstract description 77
- 239000002299 complementary DNA Substances 0.000 claims abstract description 53
- 238000001890 transfection Methods 0.000 claims abstract description 38
- 239000013612 plasmid Substances 0.000 claims abstract description 30
- 208000015181 infectious disease Diseases 0.000 claims abstract description 26
- 238000013518 transcription Methods 0.000 claims abstract description 24
- 230000035897 transcription Effects 0.000 claims abstract description 24
- 230000002458 infectious effect Effects 0.000 claims abstract description 20
- 210000004027 cell Anatomy 0.000 claims description 64
- 210000003292 kidney cell Anatomy 0.000 claims description 33
- 241000282552 Chlorocebus aethiops Species 0.000 claims description 31
- 229960005486 vaccine Drugs 0.000 claims description 23
- 241000287828 Gallus gallus Species 0.000 claims description 14
- 101710081079 Minor spike protein H Proteins 0.000 claims description 11
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 11
- 230000002779 inactivation Effects 0.000 claims description 11
- 101710118046 RNA-directed RNA polymerase Proteins 0.000 claims description 10
- 201000010099 disease Diseases 0.000 claims description 10
- 239000001963 growth medium Substances 0.000 claims description 9
- 238000002360 preparation method Methods 0.000 claims description 7
- 231100000331 toxic Toxicity 0.000 claims description 6
- 230000002588 toxic effect Effects 0.000 claims description 6
- 238000000746 purification Methods 0.000 claims description 5
- 239000002775 capsule Substances 0.000 claims description 3
- 210000003837 chick embryo Anatomy 0.000 claims description 3
- 101710136297 Protein VP2 Proteins 0.000 claims description 2
- 101800003658 Protein VP4 Proteins 0.000 claims description 2
- 210000002950 fibroblast Anatomy 0.000 claims description 2
- 101710121537 mRNA (guanine-N(7))-methyltransferase Proteins 0.000 claims description 2
- 210000001161 mammalian embryo Anatomy 0.000 claims description 2
- 230000009467 reduction Effects 0.000 claims description 2
- 241000271566 Aves Species 0.000 claims 3
- 101710136295 Protein VP5 Proteins 0.000 claims 1
- 238000002741 site-directed mutagenesis Methods 0.000 claims 1
- 108020004414 DNA Proteins 0.000 abstract description 30
- 102000040650 (ribonucleotides)n+m Human genes 0.000 abstract description 29
- 101710137500 T7 RNA polymerase Proteins 0.000 abstract description 9
- 241001493065 dsRNA viruses Species 0.000 abstract description 9
- 238000013461 design Methods 0.000 abstract description 7
- 238000000338 in vitro Methods 0.000 abstract description 7
- 108091026890 Coding region Proteins 0.000 abstract description 3
- 230000006648 viral gene expression Effects 0.000 abstract description 3
- 229940031551 inactivated vaccine Drugs 0.000 abstract 1
- 230000008506 pathogenesis Effects 0.000 abstract 1
- 210000003501 vero cell Anatomy 0.000 abstract 1
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 description 527
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 414
- KZSNJWFQEVHDMF-UHFFFAOYSA-N Valine Chemical compound CC(C)C(N)C(O)=O KZSNJWFQEVHDMF-UHFFFAOYSA-N 0.000 description 377
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 description 370
- AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical compound C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 description 356
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 306
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 304
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 285
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 260
- AGPKZVBTJJNPAG-WHFBIAKZSA-N L-isoleucine Chemical compound CC[C@H](C)[C@H](N)C(O)=O AGPKZVBTJJNPAG-WHFBIAKZSA-N 0.000 description 233
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 191
- ZDXPYRJPNDTMRX-VKHMYHEASA-N L-glutamine Chemical compound OC(=O)[C@@H](N)CCC(N)=O ZDXPYRJPNDTMRX-VKHMYHEASA-N 0.000 description 180
- 102000039446 nucleic acids Human genes 0.000 description 35
- 108020004707 nucleic acids Proteins 0.000 description 35
- 150000007523 nucleic acids Chemical class 0.000 description 35
- 102220369447 c.1352G>A Human genes 0.000 description 26
- 102220369446 c.1274G>A Human genes 0.000 description 19
- 102220369445 c.668T>C Human genes 0.000 description 18
- 102220023257 rs387907546 Human genes 0.000 description 18
- 102220023256 rs387907547 Human genes 0.000 description 17
- 102220023258 rs387907548 Human genes 0.000 description 17
- 108090000623 proteins and genes Proteins 0.000 description 16
- 239000000203 mixture Substances 0.000 description 14
- 239000000047 product Substances 0.000 description 14
- 235000018102 proteins Nutrition 0.000 description 14
- 102000004169 proteins and genes Human genes 0.000 description 14
- 238000011160 research Methods 0.000 description 13
- 239000006228 supernatant Substances 0.000 description 13
- 239000002773 nucleotide Substances 0.000 description 12
- 125000003729 nucleotide group Chemical group 0.000 description 12
- 230000003612 virological effect Effects 0.000 description 11
- 102000004190 Enzymes Human genes 0.000 description 10
- 108090000790 Enzymes Proteins 0.000 description 10
- 229940024606 amino acid Drugs 0.000 description 10
- 235000001014 amino acid Nutrition 0.000 description 10
- 150000001413 amino acids Chemical class 0.000 description 10
- 230000009182 swimming Effects 0.000 description 10
- 230000003321 amplification Effects 0.000 description 9
- 238000003199 nucleic acid amplification method Methods 0.000 description 9
- 101710132601 Capsid protein Proteins 0.000 description 8
- 101710197658 Capsid protein VP1 Proteins 0.000 description 8
- 102000004163 DNA-directed RNA polymerases Human genes 0.000 description 8
- 108090000626 DNA-directed RNA polymerases Proteins 0.000 description 8
- 101710108545 Viral protein 1 Proteins 0.000 description 8
- 238000010166 immunofluorescence Methods 0.000 description 8
- 244000144977 poultry Species 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- 241000702263 Reovirus sp. Species 0.000 description 7
- 238000010839 reverse transcription Methods 0.000 description 7
- 108010076039 Polyproteins Proteins 0.000 description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 238000011084 recovery Methods 0.000 description 5
- 108091092562 ribozyme Proteins 0.000 description 5
- 239000002356 single layer Substances 0.000 description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- 241001465754 Metazoa Species 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- 101000702488 Rattus norvegicus High affinity cationic amino acid transporter 1 Proteins 0.000 description 4
- 230000000890 antigenic effect Effects 0.000 description 4
- 108010040443 aspartyl-aspartic acid Proteins 0.000 description 4
- 239000012752 auxiliary agent Substances 0.000 description 4
- 238000005520 cutting process Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 230000014509 gene expression Effects 0.000 description 4
- 238000002347 injection Methods 0.000 description 4
- 239000007924 injection Substances 0.000 description 4
- 238000011081 inoculation Methods 0.000 description 4
- 238000001638 lipofection Methods 0.000 description 4
- 230000001717 pathogenic effect Effects 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 238000003757 reverse transcription PCR Methods 0.000 description 4
- 210000002966 serum Anatomy 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 239000003381 stabilizer Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- 102000016911 Deoxyribonucleases Human genes 0.000 description 3
- 108010053770 Deoxyribonucleases Proteins 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- 241000710921 Infectious pancreatic necrosis virus Species 0.000 description 3
- 108091028043 Nucleic acid sequence Proteins 0.000 description 3
- 241000283973 Oryctolagus cuniculus Species 0.000 description 3
- BELBBZDIHDAJOR-UHFFFAOYSA-N Phenolsulfonephthalein Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2S(=O)(=O)O1 BELBBZDIHDAJOR-UHFFFAOYSA-N 0.000 description 3
- 102000006382 Ribonucleases Human genes 0.000 description 3
- 108010083644 Ribonucleases Proteins 0.000 description 3
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 3
- 101710172711 Structural protein Proteins 0.000 description 3
- 239000000427 antigen Substances 0.000 description 3
- 108091007433 antigens Proteins 0.000 description 3
- 102000036639 antigens Human genes 0.000 description 3
- 238000003556 assay Methods 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000029087 digestion Effects 0.000 description 3
- 239000003085 diluting agent Substances 0.000 description 3
- LOKCTEFSRHRXRJ-UHFFFAOYSA-I dipotassium trisodium dihydrogen phosphate hydrogen phosphate dichloride Chemical compound P(=O)(O)(O)[O-].[K+].P(=O)(O)([O-])[O-].[Na+].[Na+].[Cl-].[K+].[Cl-].[Na+] LOKCTEFSRHRXRJ-UHFFFAOYSA-I 0.000 description 3
- 238000004043 dyeing Methods 0.000 description 3
- 238000012869 ethanol precipitation Methods 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- 229960003444 immunosuppressant agent Drugs 0.000 description 3
- 230000001861 immunosuppressant effect Effects 0.000 description 3
- 239000003018 immunosuppressive agent Substances 0.000 description 3
- 238000009413 insulation Methods 0.000 description 3
- 238000002372 labelling Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 230000007246 mechanism Effects 0.000 description 3
- 230000007170 pathology Effects 0.000 description 3
- 229960003531 phenolsulfonphthalein Drugs 0.000 description 3
- 239000002953 phosphate buffered saline Substances 0.000 description 3
- 239000002243 precursor Substances 0.000 description 3
- 230000001681 protective effect Effects 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 229940083542 sodium Drugs 0.000 description 3
- 235000015424 sodium Nutrition 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000010257 thawing Methods 0.000 description 3
- 210000002845 virion Anatomy 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- YBJHBAHKTGYVGT-ZKWXMUAHSA-N (+)-Biotin Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)O)SC[C@@H]21 YBJHBAHKTGYVGT-ZKWXMUAHSA-N 0.000 description 2
- ZKHQWZAMYRWXGA-KQYNXXCUSA-N Adenosine triphosphate Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O ZKHQWZAMYRWXGA-KQYNXXCUSA-N 0.000 description 2
- DXQIQUIQYAGRCC-CIUDSAMLSA-N Arg-Asp-Gln Chemical compound C(C[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CCC(=O)N)C(=O)O)N)CN=C(N)N DXQIQUIQYAGRCC-CIUDSAMLSA-N 0.000 description 2
- ADPACBMPYWJJCE-FXQIFTODSA-N Arg-Ser-Asp Chemical compound [H]N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(O)=O)C(O)=O ADPACBMPYWJJCE-FXQIFTODSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- NZWDWXSWUQCNMG-GARJFASQSA-N Asp-Lys-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CCCCN)NC(=O)[C@H](CC(=O)O)N)C(=O)O NZWDWXSWUQCNMG-GARJFASQSA-N 0.000 description 2
- 108010014303 DNA-directed DNA polymerase Proteins 0.000 description 2
- 102000016928 DNA-directed DNA polymerase Human genes 0.000 description 2
- 241000991587 Enterovirus C Species 0.000 description 2
- FFVXLVGUJBCKRX-UKJIMTQDSA-N Gln-Ile-Val Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](C(C)C)C(=O)O)NC(=O)[C@H](CCC(=O)N)N FFVXLVGUJBCKRX-UKJIMTQDSA-N 0.000 description 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
- OWSWUWDMSNXTNE-GMOBBJLQSA-N Ile-Pro-Asp Chemical compound CC[C@H](C)[C@@H](C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(=O)O)C(=O)O)N OWSWUWDMSNXTNE-GMOBBJLQSA-N 0.000 description 2
- 241000711450 Infectious bronchitis virus Species 0.000 description 2
- KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical compound CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 description 2
- GNRPTBRHRRZCMA-RWMBFGLXSA-N Leu-Met-Pro Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CCSC)C(=O)N1CCC[C@@H]1C(=O)O)N GNRPTBRHRRZCMA-RWMBFGLXSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- MJVAVZPDRWSRRC-UHFFFAOYSA-N Menadione Chemical compound C1=CC=C2C(=O)C(C)=CC(=O)C2=C1 MJVAVZPDRWSRRC-UHFFFAOYSA-N 0.000 description 2
- RIIFMEBFDDXGCV-VEVYYDQMSA-N Met-Thr-Asn Chemical compound CSCC[C@H](N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@H](C(O)=O)CC(N)=O RIIFMEBFDDXGCV-VEVYYDQMSA-N 0.000 description 2
- LBSWWNKMVPAXOI-GUBZILKMSA-N Met-Val-Ser Chemical compound CSCC[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CO)C(O)=O LBSWWNKMVPAXOI-GUBZILKMSA-N 0.000 description 2
- KZNQNBZMBZJQJO-UHFFFAOYSA-N N-glycyl-L-proline Natural products NCC(=O)N1CCCC1C(O)=O KZNQNBZMBZJQJO-UHFFFAOYSA-N 0.000 description 2
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 description 2
- 108091092724 Noncoding DNA Proteins 0.000 description 2
- 108091034117 Oligonucleotide Proteins 0.000 description 2
- 108700026244 Open Reading Frames Proteins 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- XQLBWXHVZVBNJM-FXQIFTODSA-N Pro-Ala-Ser Chemical compound OC[C@@H](C(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H]1CCCN1 XQLBWXHVZVBNJM-FXQIFTODSA-N 0.000 description 2
- MHBSUKYVBZVQRW-HJWJTTGWSA-N Pro-Phe-Ile Chemical compound [H]N1CCC[C@H]1C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H]([C@@H](C)CC)C(O)=O MHBSUKYVBZVQRW-HJWJTTGWSA-N 0.000 description 2
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 2
- 241000711798 Rabies lyssavirus Species 0.000 description 2
- AUNGANRZJHBGPY-SCRDCRAPSA-N Riboflavin Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-SCRDCRAPSA-N 0.000 description 2
- 241000702670 Rotavirus Species 0.000 description 2
- KNZQGAUEYZJUSQ-ZLUOBGJFSA-N Ser-Asp-Ala Chemical compound C[C@@H](C(=O)O)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CO)N KNZQGAUEYZJUSQ-ZLUOBGJFSA-N 0.000 description 2
- SYCFMSYTIFXWAJ-DCAQKATOSA-N Ser-Val-His Chemical compound CC(C)[C@@H](C(=O)N[C@@H](CC1=CN=CN1)C(=O)O)NC(=O)[C@H](CO)N SYCFMSYTIFXWAJ-DCAQKATOSA-N 0.000 description 2
- YLXAMFZYJTZXFH-OLHMAJIHSA-N Thr-Asn-Asp Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC(=O)N)C(=O)N[C@@H](CC(=O)O)C(=O)O)N)O YLXAMFZYJTZXFH-OLHMAJIHSA-N 0.000 description 2
- NLJKZUGAIIRWJN-LKXGYXEUSA-N Thr-Asp-Cys Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CS)C(=O)O)N)O NLJKZUGAIIRWJN-LKXGYXEUSA-N 0.000 description 2
- KBLYJPQSNGTDIU-LOKLDPHHSA-N Thr-Glu-Pro Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CCC(=O)O)C(=O)N1CCC[C@@H]1C(=O)O)N)O KBLYJPQSNGTDIU-LOKLDPHHSA-N 0.000 description 2
- UQCNIMDPYICBTR-KYNKHSRBSA-N Thr-Thr-Gly Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H]([C@@H](C)O)C(=O)NCC(O)=O UQCNIMDPYICBTR-KYNKHSRBSA-N 0.000 description 2
- 108010001244 Tli polymerase Proteins 0.000 description 2
- ISAKRJDGNUQOIC-UHFFFAOYSA-N Uracil Chemical compound O=C1C=CNC(=O)N1 ISAKRJDGNUQOIC-UHFFFAOYSA-N 0.000 description 2
- 239000011543 agarose gel Substances 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 238000009395 breeding Methods 0.000 description 2
- 230000001488 breeding effect Effects 0.000 description 2
- 210000001669 bursa of fabricius Anatomy 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 238000005352 clarification Methods 0.000 description 2
- 238000010367 cloning Methods 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- OVBPIULPVIDEAO-LBPRGKRZSA-N folic acid Chemical compound C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-LBPRGKRZSA-N 0.000 description 2
- 239000012634 fragment Substances 0.000 description 2
- 230000008014 freezing Effects 0.000 description 2
- 238000007710 freezing Methods 0.000 description 2
- 230000012010 growth Effects 0.000 description 2
- DKAGJZJALZXOOV-UHFFFAOYSA-N hydrate;hydrochloride Chemical compound O.Cl DKAGJZJALZXOOV-UHFFFAOYSA-N 0.000 description 2
- FDGQSTZJBFJUBT-UHFFFAOYSA-N hypoxanthine Chemical compound O=C1NC=NC2=C1NC=N2 FDGQSTZJBFJUBT-UHFFFAOYSA-N 0.000 description 2
- 230000036039 immunity Effects 0.000 description 2
- 238000011534 incubation Methods 0.000 description 2
- 230000001939 inductive effect Effects 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 230000003472 neutralizing effect Effects 0.000 description 2
- 238000012856 packing Methods 0.000 description 2
- 230000035479 physiological effects, processes and functions Effects 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 108010031719 prolyl-serine Proteins 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- DAEPDZWVDSPTHF-UHFFFAOYSA-M sodium pyruvate Chemical compound [Na+].CC(=O)C([O-])=O DAEPDZWVDSPTHF-UHFFFAOYSA-M 0.000 description 2
- ATHGHQPFGPMSJY-UHFFFAOYSA-N spermidine Chemical compound NCCCCNCCCN ATHGHQPFGPMSJY-UHFFFAOYSA-N 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 description 2
- 208000024891 symptom Diseases 0.000 description 2
- 230000002194 synthesizing effect Effects 0.000 description 2
- 210000001541 thymus gland Anatomy 0.000 description 2
- 238000013519 translation Methods 0.000 description 2
- 241000712461 unidentified influenza virus Species 0.000 description 2
- 230000001018 virulence Effects 0.000 description 2
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 1
- JKMHFZQWWAIEOD-UHFFFAOYSA-N 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid Chemical compound OCC[NH+]1CCN(CCS([O-])(=O)=O)CC1 JKMHFZQWWAIEOD-UHFFFAOYSA-N 0.000 description 1
- PWKSKIMOESPYIA-UHFFFAOYSA-N 2-acetamido-3-sulfanylpropanoic acid Chemical compound CC(=O)NC(CS)C(O)=O PWKSKIMOESPYIA-UHFFFAOYSA-N 0.000 description 1
- QKNYBSVHEMOAJP-UHFFFAOYSA-N 2-amino-2-(hydroxymethyl)propane-1,3-diol;hydron;chloride Chemical compound Cl.OCC(N)(CO)CO QKNYBSVHEMOAJP-UHFFFAOYSA-N 0.000 description 1
- IBAOFQIOOBQLHE-UHFFFAOYSA-N 2-amino-3,9-dihydropurin-9-ium-6-one;chloride Chemical compound Cl.N1C(N)=NC(=O)C2=C1N=CN2 IBAOFQIOOBQLHE-UHFFFAOYSA-N 0.000 description 1
- QDGAVODICPCDMU-UHFFFAOYSA-N 2-amino-3-[3-[bis(2-chloroethyl)amino]phenyl]propanoic acid Chemical compound OC(=O)C(N)CC1=CC=CC(N(CCCl)CCCl)=C1 QDGAVODICPCDMU-UHFFFAOYSA-N 0.000 description 1
- KWTQSFXGGICVPE-UHFFFAOYSA-N 2-amino-5-(diaminomethylideneamino)pentanoic acid;hydron;chloride Chemical compound Cl.OC(=O)C(N)CCCN=C(N)N KWTQSFXGGICVPE-UHFFFAOYSA-N 0.000 description 1
- ASJSAQIRZKANQN-CRCLSJGQSA-N 2-deoxy-D-ribose Chemical compound OC[C@@H](O)[C@@H](O)CC=O ASJSAQIRZKANQN-CRCLSJGQSA-N 0.000 description 1
- KVYRCBOUKXJXDK-UHFFFAOYSA-N 3,4-dimethylphenazine-1,2-diamine hydrochloride Chemical compound Cl.C1=CC=CC2=NC3=C(C)C(C)=C(N)C(N)=C3N=C21 KVYRCBOUKXJXDK-UHFFFAOYSA-N 0.000 description 1
- XJZYXTWSMDRIJE-UHFFFAOYSA-N 3,7-dihydropurin-6-one;sodium Chemical compound [Na].O=C1N=CNC2=C1NC=N2 XJZYXTWSMDRIJE-UHFFFAOYSA-N 0.000 description 1
- MKPCNMXYTMQZBE-UHFFFAOYSA-N 7h-purin-6-amine;sulfuric acid;dihydrate Chemical compound O.O.OS(O)(=O)=O.NC1=NC=NC2=C1NC=N2.NC1=NC=NC2=C1NC=N2 MKPCNMXYTMQZBE-UHFFFAOYSA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- TTXMOJWKNRJWQJ-FXQIFTODSA-N Ala-Arg-Ser Chemical compound OC[C@@H](C(O)=O)NC(=O)[C@@H](NC(=O)[C@@H](N)C)CCCN=C(N)N TTXMOJWKNRJWQJ-FXQIFTODSA-N 0.000 description 1
- WMYJZJRILUVVRG-WDSKDSINSA-N Ala-Gly-Gln Chemical compound C[C@H](N)C(=O)NCC(=O)N[C@H](C(O)=O)CCC(N)=O WMYJZJRILUVVRG-WDSKDSINSA-N 0.000 description 1
- 102100027211 Albumin Human genes 0.000 description 1
- 108010088751 Albumins Proteins 0.000 description 1
- 229930183010 Amphotericin Natural products 0.000 description 1
- QGGFZZLFKABGNL-UHFFFAOYSA-N Amphotericin A Natural products OC1C(N)C(O)C(C)OC1OC1C=CC=CC=CC=CCCC=CC=CC(C)C(O)C(C)C(C)OC(=O)CC(O)CC(O)CCC(O)C(O)CC(O)CC(O)(CC(O)C2C(O)=O)OC2C1 QGGFZZLFKABGNL-UHFFFAOYSA-N 0.000 description 1
- 241000272525 Anas platyrhynchos Species 0.000 description 1
- XMKXONRMGJXCJV-LAEOZQHASA-N Asp-Val-Glu Chemical compound OC(=O)C[C@H](N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(O)=O)C(O)=O XMKXONRMGJXCJV-LAEOZQHASA-N 0.000 description 1
- 241000700663 Avipoxvirus Species 0.000 description 1
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 241000283707 Capra Species 0.000 description 1
- UDMBCSSLTHHNCD-UHFFFAOYSA-N Coenzym Q(11) Natural products C1=NC=2C(N)=NC=NC=2N1C1OC(COP(O)(O)=O)C(O)C1O UDMBCSSLTHHNCD-UHFFFAOYSA-N 0.000 description 1
- 108091035707 Consensus sequence Proteins 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- AUNGANRZJHBGPY-UHFFFAOYSA-N D-Lyxoflavin Natural products OCC(O)C(O)C(O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- CKLJMWTZIZZHCS-UHFFFAOYSA-N D-OH-Asp Natural products OC(=O)C(N)CC(O)=O CKLJMWTZIZZHCS-UHFFFAOYSA-N 0.000 description 1
- QNAYBMKLOCPYGJ-UHFFFAOYSA-N D-alpha-Ala Natural products CC([NH3+])C([O-])=O QNAYBMKLOCPYGJ-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- HMFHBZSHGGEWLO-SOOFDHNKSA-N D-ribofuranose Chemical compound OC[C@H]1OC(O)[C@H](O)[C@@H]1O HMFHBZSHGGEWLO-SOOFDHNKSA-N 0.000 description 1
- 238000001712 DNA sequencing Methods 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 241000255601 Drosophila melanogaster Species 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000588724 Escherichia coli Species 0.000 description 1
- 241000712469 Fowl plague virus Species 0.000 description 1
- 241000701047 Gallid alphaherpesvirus 2 Species 0.000 description 1
- YRHZWVKUFWCEPW-GLLZPBPUSA-N Gln-Thr-Gln Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)O)NC(=O)[C@H](CCC(=O)N)N)O YRHZWVKUFWCEPW-GLLZPBPUSA-N 0.000 description 1
- MWMJCGBSIORNCD-AVGNSLFASA-N Glu-Leu-Leu Chemical compound [H]N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(O)=O MWMJCGBSIORNCD-AVGNSLFASA-N 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- 239000007995 HEPES buffer Substances 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- PFOUFRJYHWZJKW-NKIYYHGXSA-N His-Thr-Gln Chemical compound C[C@H]([C@@H](C(=O)N[C@@H](CCC(=O)N)C(=O)O)NC(=O)[C@H](CC1=CN=CN1)N)O PFOUFRJYHWZJKW-NKIYYHGXSA-N 0.000 description 1
- PMMYEEVYMWASQN-DMTCNVIQSA-N Hydroxyproline Chemical compound O[C@H]1CN[C@H](C(O)=O)C1 PMMYEEVYMWASQN-DMTCNVIQSA-N 0.000 description 1
- UGQMRVRMYYASKQ-UHFFFAOYSA-N Hypoxanthine nucleoside Natural products OC1C(O)C(CO)OC1N1C(NC=NC2=O)=C2N=C1 UGQMRVRMYYASKQ-UHFFFAOYSA-N 0.000 description 1
- GLYJPWIRLBAIJH-UHFFFAOYSA-N Ile-Lys-Pro Natural products CCC(C)C(N)C(=O)NC(CCCCN)C(=O)N1CCCC1C(O)=O GLYJPWIRLBAIJH-UHFFFAOYSA-N 0.000 description 1
- OTSVBELRDMSPKY-PCBIJLKTSA-N Ile-Phe-Asn Chemical compound CC[C@H](C)[C@@H](C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CC(=O)N)C(=O)O)N OTSVBELRDMSPKY-PCBIJLKTSA-N 0.000 description 1
- 206010061598 Immunodeficiency Diseases 0.000 description 1
- 208000029462 Immunodeficiency disease Diseases 0.000 description 1
- 208000002979 Influenza in Birds Diseases 0.000 description 1
- 108090000723 Insulin-Like Growth Factor I Proteins 0.000 description 1
- 102100034343 Integrase Human genes 0.000 description 1
- 101710203526 Integrase Proteins 0.000 description 1
- QNAYBMKLOCPYGJ-UWTATZPHSA-N L-Alanine Natural products C[C@@H](N)C(O)=O QNAYBMKLOCPYGJ-UWTATZPHSA-N 0.000 description 1
- CKLJMWTZIZZHCS-UWTATZPHSA-N L-Aspartic acid Natural products OC(=O)[C@H](N)CC(O)=O CKLJMWTZIZZHCS-UWTATZPHSA-N 0.000 description 1
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-Histidine Natural products OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 description 1
- FFEARJCKVFRZRR-UHFFFAOYSA-N L-Methionine Natural products CSCCC(N)C(O)=O FFEARJCKVFRZRR-UHFFFAOYSA-N 0.000 description 1
- ONIBWKKTOPOVIA-BYPYZUCNSA-N L-Proline Chemical compound OC(=O)[C@@H]1CCCN1 ONIBWKKTOPOVIA-BYPYZUCNSA-N 0.000 description 1
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 1
- IFQSXNOEEPCSLW-DKWTVANSSA-N L-cysteine hydrochloride Chemical compound Cl.SC[C@H](N)C(O)=O IFQSXNOEEPCSLW-DKWTVANSSA-N 0.000 description 1
- 229930182844 L-isoleucine Natural products 0.000 description 1
- 239000004395 L-leucine Substances 0.000 description 1
- 235000019454 L-leucine Nutrition 0.000 description 1
- BVHLGVCQOALMSV-JEDNCBNOSA-N L-lysine hydrochloride Chemical compound Cl.NCCCC[C@H](N)C(O)=O BVHLGVCQOALMSV-JEDNCBNOSA-N 0.000 description 1
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 description 1
- 229930195722 L-methionine Natural products 0.000 description 1
- 229930182821 L-proline Natural products 0.000 description 1
- ZYLJULGXQDNXDK-GUBZILKMSA-N Leu-Gln-Asp Chemical compound [H]N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CC(O)=O)C(O)=O ZYLJULGXQDNXDK-GUBZILKMSA-N 0.000 description 1
- WXZOHBVPVKABQN-DCAQKATOSA-N Leu-Met-Asp Chemical compound CC(C)C[C@@H](C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(=O)O)C(=O)O)N WXZOHBVPVKABQN-DCAQKATOSA-N 0.000 description 1
- LOGFVTREOLYCPF-RHYQMDGZSA-N Lys-Pro-Thr Chemical compound C[C@@H](O)[C@@H](C(O)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CCCCN LOGFVTREOLYCPF-RHYQMDGZSA-N 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- 240000000233 Melia azedarach Species 0.000 description 1
- RDLSEGZJMYGFNS-FXQIFTODSA-N Met-Ser-Asp Chemical compound [H]N[C@@H](CCSC)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(O)=O)C(O)=O RDLSEGZJMYGFNS-FXQIFTODSA-N 0.000 description 1
- OVBPIULPVIDEAO-UHFFFAOYSA-N N-Pteroyl-L-glutaminsaeure Natural products C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)NC(CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-UHFFFAOYSA-N 0.000 description 1
- 101710163270 Nuclease Proteins 0.000 description 1
- 241000237502 Ostreidae Species 0.000 description 1
- 238000012408 PCR amplification Methods 0.000 description 1
- 229930182555 Penicillin Natural products 0.000 description 1
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 description 1
- 108091005804 Peptidases Proteins 0.000 description 1
- HGNGAMWHGGANAU-WHOFXGATSA-N Phe-Gly-Ile Chemical compound CC[C@H](C)[C@@H](C(O)=O)NC(=O)CNC(=O)[C@@H](N)CC1=CC=CC=C1 HGNGAMWHGGANAU-WHOFXGATSA-N 0.000 description 1
- 241000702656 Phytoreovirus Species 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004365 Protease Substances 0.000 description 1
- 108010076504 Protein Sorting Signals Proteins 0.000 description 1
- 241001068263 Replication competent viruses Species 0.000 description 1
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 1
- 101710141795 Ribonuclease inhibitor Proteins 0.000 description 1
- 229940122208 Ribonuclease inhibitor Drugs 0.000 description 1
- 102100037968 Ribonuclease inhibitor Human genes 0.000 description 1
- PYMYPHUHKUWMLA-LMVFSUKVSA-N Ribose Natural products OC[C@@H](O)[C@@H](O)[C@@H](O)C=O PYMYPHUHKUWMLA-LMVFSUKVSA-N 0.000 description 1
- 238000012300 Sequence Analysis Methods 0.000 description 1
- DKKGAAJTDKHWOD-BIIVOSGPSA-N Ser-Asn-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CC(=O)N)NC(=O)[C@H](CO)N)C(=O)O DKKGAAJTDKHWOD-BIIVOSGPSA-N 0.000 description 1
- MLSQXWSRHURDMF-GARJFASQSA-N Ser-His-Pro Chemical compound C1C[C@@H](N(C1)C(=O)[C@H](CC2=CN=CN2)NC(=O)[C@H](CO)N)C(=O)O MLSQXWSRHURDMF-GARJFASQSA-N 0.000 description 1
- WNDUPCKKKGSKIQ-CIUDSAMLSA-N Ser-Pro-Gln Chemical compound OC[C@H](N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(N)=O)C(O)=O WNDUPCKKKGSKIQ-CIUDSAMLSA-N 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 102000013275 Somatomedins Human genes 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 241001130226 Tellina virus Species 0.000 description 1
- FQPDRTDDEZXCEC-SVSWQMSJSA-N Thr-Ile-Ser Chemical compound [H]N[C@@H]([C@@H](C)O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(O)=O FQPDRTDDEZXCEC-SVSWQMSJSA-N 0.000 description 1
- 239000004473 Threonine Substances 0.000 description 1
- 208000036142 Viral infection Diseases 0.000 description 1
- FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 description 1
- MECHNRXZTMCUDQ-UHFFFAOYSA-N Vitamin D2 Natural products C1CCC2(C)C(C(C)C=CC(C)C(C)C)CCC2C1=CC=C1CC(O)CCC1=C MECHNRXZTMCUDQ-UHFFFAOYSA-N 0.000 description 1
- FHHZHGZBHYYWTG-INFSMZHSSA-N [(2r,3s,4r,5r)-5-(2-amino-7-methyl-6-oxo-3h-purin-9-ium-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl [[[(2r,3s,4r,5r)-5-(2-amino-6-oxo-3h-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl] phosphate Chemical compound N1C(N)=NC(=O)C2=C1[N+]([C@H]1[C@@H]([C@H](O)[C@@H](COP([O-])(=O)OP(O)(=O)OP(O)(=O)OC[C@@H]3[C@H]([C@@H](O)[C@@H](O3)N3C4=C(C(N=C(N)N4)=O)N=C3)O)O1)O)=CN2C FHHZHGZBHYYWTG-INFSMZHSSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- UDMBCSSLTHHNCD-KQYNXXCUSA-N adenosine 5'-monophosphate Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O UDMBCSSLTHHNCD-KQYNXXCUSA-N 0.000 description 1
- 229950006790 adenosine phosphate Drugs 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 229960003767 alanine Drugs 0.000 description 1
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 1
- HMFHBZSHGGEWLO-UHFFFAOYSA-N alpha-D-Furanose-Ribose Natural products OCC1OC(O)C(O)C1O HMFHBZSHGGEWLO-UHFFFAOYSA-N 0.000 description 1
- KOSRFJWDECSPRO-UHFFFAOYSA-N alpha-L-glutamyl-L-glutamic acid Natural products OC(=O)CCC(N)C(=O)NC(CCC(O)=O)C(O)=O KOSRFJWDECSPRO-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 229910021502 aluminium hydroxide Inorganic materials 0.000 description 1
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 229960004050 aminobenzoic acid Drugs 0.000 description 1
- 229940009444 amphotericin Drugs 0.000 description 1
- APKFDSVGJQXUKY-INPOYWNPSA-N amphotericin B Chemical compound O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/C=C/C=C/C=C/[C@H](C)[C@@H](O)[C@@H](C)[C@H](C)OC(=O)C[C@H](O)C[C@H](O)CC[C@@H](O)[C@H](O)C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 APKFDSVGJQXUKY-INPOYWNPSA-N 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 230000000692 anti-sense effect Effects 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 238000009455 aseptic packaging Methods 0.000 description 1
- 229960005261 aspartic acid Drugs 0.000 description 1
- 210000003719 b-lymphocyte Anatomy 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- VEZXCJBBBCKRPI-UHFFFAOYSA-N beta-propiolactone Chemical compound O=C1CCO1 VEZXCJBBBCKRPI-UHFFFAOYSA-N 0.000 description 1
- 229960002685 biotin Drugs 0.000 description 1
- 235000020958 biotin Nutrition 0.000 description 1
- 239000011616 biotin Substances 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- FAPWYRCQGJNNSJ-UBKPKTQASA-L calcium D-pantothenic acid Chemical compound [Ca+2].OCC(C)(C)[C@@H](O)C(=O)NCCC([O-])=O.OCC(C)(C)[C@@H](O)C(=O)NCCC([O-])=O FAPWYRCQGJNNSJ-UBKPKTQASA-L 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 238000004113 cell culture Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000001311 chemical methods and process Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 229960001231 choline Drugs 0.000 description 1
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 238000012761 co-transfection Methods 0.000 description 1
- 210000001072 colon Anatomy 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 231100000433 cytotoxic Toxicity 0.000 description 1
- 230000001472 cytotoxic effect Effects 0.000 description 1
- 230000034994 death Effects 0.000 description 1
- 239000003398 denaturant Substances 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- FFYPMLJYZAEMQB-UHFFFAOYSA-N diethyl pyrocarbonate Chemical compound CCOC(=O)OC(=O)OCC FFYPMLJYZAEMQB-UHFFFAOYSA-N 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 231100000676 disease causative agent Toxicity 0.000 description 1
- 230000035622 drinking Effects 0.000 description 1
- 239000003651 drinking water Substances 0.000 description 1
- 235000020188 drinking water Nutrition 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000001647 drug administration Methods 0.000 description 1
- 239000003937 drug carrier Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 238000001976 enzyme digestion Methods 0.000 description 1
- 229960002061 ergocalciferol Drugs 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000009313 farming Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- GNBHRKFJIUUOQI-UHFFFAOYSA-N fluorescein Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 GNBHRKFJIUUOQI-UHFFFAOYSA-N 0.000 description 1
- 238000000799 fluorescence microscopy Methods 0.000 description 1
- 229960000304 folic acid Drugs 0.000 description 1
- 235000019152 folic acid Nutrition 0.000 description 1
- 239000011724 folic acid Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 229960002989 glutamic acid Drugs 0.000 description 1
- 108010055341 glutamyl-glutamic acid Proteins 0.000 description 1
- RWSXRVCMGQZWBV-WDSKDSINSA-N glutathione Chemical compound OC(=O)[C@@H](N)CCC(=O)N[C@@H](CS)C(=O)NCC(O)=O RWSXRVCMGQZWBV-WDSKDSINSA-N 0.000 description 1
- 235000003969 glutathione Nutrition 0.000 description 1
- 229960003180 glutathione Drugs 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 230000012447 hatching Effects 0.000 description 1
- 229960002885 histidine Drugs 0.000 description 1
- 230000007813 immunodeficiency Effects 0.000 description 1
- 230000001524 infective effect Effects 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- CDAISMWEOUEBRE-GPIVLXJGSA-N inositol Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](O)[C@@H]1O CDAISMWEOUEBRE-GPIVLXJGSA-N 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 238000007918 intramuscular administration Methods 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 229960000310 isoleucine Drugs 0.000 description 1
- 229960003136 leucine Drugs 0.000 description 1
- 230000033001 locomotion Effects 0.000 description 1
- 210000002751 lymph Anatomy 0.000 description 1
- 239000006166 lysate Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 229910001463 metal phosphate Inorganic materials 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 229960004452 methionine Drugs 0.000 description 1
- 230000035772 mutation Effects 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229960003512 nicotinic acid Drugs 0.000 description 1
- 235000001968 nicotinic acid Nutrition 0.000 description 1
- 239000011664 nicotinic acid Substances 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- -1 oleoyl oxygen Chemical compound 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 235000020636 oyster Nutrition 0.000 description 1
- 229940049954 penicillin Drugs 0.000 description 1
- 235000020030 perry Nutrition 0.000 description 1
- 238000000053 physical method Methods 0.000 description 1
- 239000010773 plant oil Substances 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920001184 polypeptide Polymers 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 229960002429 proline Drugs 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- ZUFQODAHGAHPFQ-UHFFFAOYSA-N pyridoxine hydrochloride Chemical compound Cl.CC1=NC=C(CO)C(CO)=C1O ZUFQODAHGAHPFQ-UHFFFAOYSA-N 0.000 description 1
- 229960004172 pyridoxine hydrochloride Drugs 0.000 description 1
- 235000019171 pyridoxine hydrochloride Nutrition 0.000 description 1
- 239000011764 pyridoxine hydrochloride Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 230000008521 reorganization Effects 0.000 description 1
- 230000010076 replication Effects 0.000 description 1
- 108091008146 restriction endonucleases Proteins 0.000 description 1
- 210000001995 reticulocyte Anatomy 0.000 description 1
- 229960002477 riboflavin Drugs 0.000 description 1
- 235000019192 riboflavin Nutrition 0.000 description 1
- 239000002151 riboflavin Substances 0.000 description 1
- 239000003161 ribonuclease inhibitor Substances 0.000 description 1
- 102220004457 rs11567847 Human genes 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 229960001153 serine Drugs 0.000 description 1
- 238000004088 simulation Methods 0.000 description 1
- IFGCUJZIWBUILZ-UHFFFAOYSA-N sodium 2-[[2-[[hydroxy-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyphosphoryl]amino]-4-methylpentanoyl]amino]-3-(1H-indol-3-yl)propanoic acid Chemical compound [Na+].C=1NC2=CC=CC=C2C=1CC(C(O)=O)NC(=O)C(CC(C)C)NP(O)(=O)OC1OC(C)C(O)C(O)C1O IFGCUJZIWBUILZ-UHFFFAOYSA-N 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- BBMHARZCALWXSL-UHFFFAOYSA-M sodium dihydrogenphosphate monohydrate Chemical compound O.[Na+].OP(O)([O-])=O BBMHARZCALWXSL-UHFFFAOYSA-M 0.000 description 1
- 229940054269 sodium pyruvate Drugs 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- HKDXLLDCXWUUKY-UHFFFAOYSA-M sodium;7h-purin-3-ide-2,6-dione Chemical compound [Na+].O=C1NC(=O)NC2=C1[N-]C=N2 HKDXLLDCXWUUKY-UHFFFAOYSA-M 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 235000010356 sorbitol Nutrition 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 229940063673 spermidine Drugs 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- DPJRMOMPQZCRJU-UHFFFAOYSA-M thiamine hydrochloride Chemical compound Cl.[Cl-].CC1=C(CCO)SC=[N+]1CC1=CN=C(C)N=C1N DPJRMOMPQZCRJU-UHFFFAOYSA-M 0.000 description 1
- 229960000344 thiamine hydrochloride Drugs 0.000 description 1
- 235000019190 thiamine hydrochloride Nutrition 0.000 description 1
- 239000011747 thiamine hydrochloride Substances 0.000 description 1
- 229960002898 threonine Drugs 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- FGMPLJWBKKVCDB-UHFFFAOYSA-N trans-L-hydroxy-proline Natural products ON1CCCC1C(O)=O FGMPLJWBKKVCDB-UHFFFAOYSA-N 0.000 description 1
- 230000002103 transcriptional effect Effects 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 229960004441 tyrosine Drugs 0.000 description 1
- 241000701161 unidentified adenovirus Species 0.000 description 1
- 241000701447 unidentified baculovirus Species 0.000 description 1
- 241001529453 unidentified herpesvirus Species 0.000 description 1
- 229940035893 uracil Drugs 0.000 description 1
- 229960004295 valine Drugs 0.000 description 1
- 230000009385 viral infection Effects 0.000 description 1
- 235000019155 vitamin A Nutrition 0.000 description 1
- 239000011719 vitamin A Substances 0.000 description 1
- MECHNRXZTMCUDQ-RKHKHRCZSA-N vitamin D2 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)/C=C/[C@H](C)C(C)C)=C\C=C1\C[C@@H](O)CCC1=C MECHNRXZTMCUDQ-RKHKHRCZSA-N 0.000 description 1
- 235000001892 vitamin D2 Nutrition 0.000 description 1
- 239000011653 vitamin D2 Substances 0.000 description 1
- 235000012711 vitamin K3 Nutrition 0.000 description 1
- 239000011652 vitamin K3 Substances 0.000 description 1
- 229940045997 vitamin a Drugs 0.000 description 1
- 229940041603 vitamin k 3 Drugs 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1
Images
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/12—Viral antigens
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N7/00—Viruses; Bacteriophages; Compositions thereof; Preparation or purification thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/51—Medicinal preparations containing antigens or antibodies comprising whole cells, viruses or DNA/RNA
- A61K2039/525—Virus
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2720/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA dsRNA viruses
- C12N2720/00011—Details
- C12N2720/10011—Birnaviridae
- C12N2720/10051—Methods of production or purification of viral material
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S424/00—Drug, bio-affecting and body treating compositions
- Y10S424/816—Viral vaccine for avian species, e.g. poultry or other birds
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S424/00—Drug, bio-affecting and body treating compositions
- Y10S424/826—Bacterial vaccine for avian species, e.g. poultry or other birds
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Virology (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Genetics & Genomics (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Microbiology (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Immunology (AREA)
- Biomedical Technology (AREA)
- Oncology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Communicable Diseases (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Mycology (AREA)
- Epidemiology (AREA)
- Molecular Biology (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
利用起源于克隆的DNA的合成转录物已经开发了制备活的双RNA病毒如感染性的囊病病毒(IBDV),一种双RNA病毒家族的形成区段的双链(ds)RNA病毒的系统。构建了独立的全长cDNA克隆,它们分别含有IBDV的RNAA和B区段的整个编码和非编码区。利用T7RNA聚合酶对线性化质粒体外转录产生两个区段的合成RNA。利用合并的两区段的正意义转录物转染非洲绿猴肾细胞,在早至转染后36小时产生感染性病毒。dsRNA病毒的反遗传系统的开发将大大简化病毒基因表达的调节和病理的研究和产生新的活和失活疫苗的设计。
Description
发明背景
感染性囊病病毒(IBDV),一个双RNA病毒家族的成员,是小鸡中高免疫抑制疾病的成因剂(Kibenge,F.S.B.等人,病毒遗传杂志,69,1757-1775(1988))。感染性囊病(IBD)或传染性粘液囊病的特征是破坏法氏囊中的淋巴滤泡。在3-6周龄的完全敏感的鸡群中,该临床疾病引起严重的免疫抑制,导致由于妨碍生长,饲料的效率降低和死亡等引起的损失。小于3周龄的敏感鸡群没有显示该疾病外在的临床症状,但具有明显的感染特征,囊受到损害。
与该疾病的症状相关的病毒称为感染性囊病病毒(IBDV)。IBDV是对国家和世界家禽业有主要经济重要性影响的致病原。它通过破坏法氏囊中的产生抗体的B细胞的前体,在小鸡中引起严重的免疫缺陷。免疫抑制引起对其它疾病的敏感性增加,并干扰抗新城鸡瘟病、马立克氏病和感染性支气管炎病毒的有效接种。
已知的IBDV血清型有两种。血清型I病毒是鸡的致病原,而血清型II病毒感染鸡和火鸡。火鸡的感染的临床意义目前还是未知。
IBDV属于称为双RNA病毒的病毒组类,该组类包括其它双区段RNA病毒,如感染性胰坏死病毒(鱼),tellina病毒和蚝病毒(双壳类软体动物)和果蝇X病毒(果蝇)。这些病毒都含有高分子量(MW)的双链RNA基因组。
IBDV病毒粒子的外壳由几个结构蛋白质组成。已经报道了9个之多的结构蛋白质,但有证据表明它们中的一些可能有前体—产物的关系(Kibenge,F.S.B.等人,病毒遗传杂志,69,1757-1775(1988))。病毒蛋白质(VP)的命名和分子量表示如下。病毒蛋白 分子量
VP1 90千道尔顿
VP2 41千道尔顿
VP3 32千道尔顿
VP4 28千道尔顿
VP5 17千道尔顿
鉴定了IBDV的基因组中双链RNA的两区段。IBDV基因组由在核苷酸碱基对2827(区段B)到3261(区段A)之间变化的双链(ds)RNA的两个区段组成(Mundt,E.等人,病毒学,209,10-18(1995))。较大的区段A编码聚蛋白,这种蛋白质通过自我蛋白水解形成成熟的病毒蛋白质VP2、VP3和VP4(Hudson,P.J.等人,核酸研究,14,5001-5012(1986))。VP2和VP3是病毒粒子的主要结构蛋白。VP2是IBDV的主要的宿主保护性免疫原,含有导致诱导中和抗体的抗原区(Azad,等人,病毒学,161,145-152(1987))。在聚蛋白基因前面和与之部分重迭的第二个开放读码框架(ORF),编码存在于IBDV感染的细胞中的功能未知的蛋白质(VP5)(Mundt,E.等人,病毒遗传杂志,76,437-443(1995))。较小的区段B编码VP1,VP1是具有聚合酶和加帽酶活性的90千道尔顿多功能蛋白质(Spies,U.等人,病毒研究,8,127-140(1987);Spies,U.,等人,病毒遗传杂志,71,977-981(1990))。
已经证明VP2蛋白质是IBDV的主要的宿主保护性免疫原,含有导致诱导中和抗体的抗原区。已经证明含有中和位点的区域是高度构型依赖的。已经有人认为VP3蛋白质是特异于基团的抗原,因为抗来自血清型I和II病毒的抗原的单克隆抗体能够识别该抗原。VP4蛋白质似乎是病毒编码的蛋白酶,参与加工VP2、VP3和VP4蛋白质的前体聚蛋白的加工。
虽然已经公开了各种IBDV毒株的基因组区段A和B的核苷酸序列,只是在最近才确定了两区段的完全的5’和3’非编码序列。IBDV区段A和B的5’非编码区含有32个核苷酸的共有序列,而两区段的3’非编码末端序列是不相关的,但在相同血清型的IBDV毒株中是保守的(Mundt,E.等人,病毒学,209,10-18(1995))。正如在其它含有dsRNA的病毒如哺乳动物和植物呼肠病毒和轮状病毒中所证明的,这些末端可能含有在包装和调节IBDV基因表达中很重要的序列(Anzola,等人,Proc.Natl.Acad.Sci.USA,84,8301-8305(1987);Zou,S.等人,病毒学,186,377-388(1992);Gorziglia,M.I.,等人,Proc.Natl.Acad.Sci.USA,89,5784-5788(1992))。
在最近几年,利用依赖DNA的RNA聚合酶产生的转录物已经从克隆的cDNA产生出许多感染性动物RNA病毒(Boyer,J.C.,等人,病毒学,198,415-426(1994))。例如,脊髓灰质炎病毒,正链RNA病毒,流感病毒,区段化的负链RNA病毒,狂犬病毒,非区段化的负链RNA病毒;所有这些是从它们各自的基因组的克隆cDNA得到的(van derWerf,S.等人,Proc.Natl.Acad.Sci.USA,83,2330-2334(1986),Enaml,M.等人,Proc.Natl.Acad.Sci.USA,87,3802-3805(1990);Schnell,M.J.等人,EMBO杂志,13,4195-4205(1994))。对于呼肠病毒,发现当与来自不同血清型的辅助病毒互补时,用SSRNA、dsRNA和体外翻译的呼肠病毒产物联合转染细胞产生感染性呼肠病毒(Roner,M.R.,等人,病毒学,179,845-852(1990))。但是,至今,没有报道只来自合成RNA的区段化的dsRNA基因组感染性病毒。
发明概要
本发明涉及感染性囊病病毒(IBDV),它与小鸡的传染性粘液囊病相关。更具体地说,本发明涉及利用起源于克隆的cDNA的合成转录物制备感染性囊病病毒(IBDV)的系统。本发明将有助于病毒基因表达的调节和病理的研究和设计产生新的活和失活的疫苗。本发明的详细说明
在开发IBDV的反遗传系统的尝试中,分别构建了三个含有血清型I毒株D78或血清型II毒株23/82的区段A和血清型I毒株P2的区段B的独立的全长cDNA克隆。利用T7 RNA聚合酶通过线性质粒的体外转录反应产生区段A和B的合成的RNA。通过转染非洲绿猴肾细胞评估未用DNase或RNase处理或已处理的这些区段的转录物的感染性病毒的生产。
本发明人已经证明源于相应于区段化的dsRNA动物病毒的整个基因组的克隆DNA的合成转录物能够产生复制病毒。在利用起源于含有dsRNA基因组的病毒(IBDV)的克隆cDNA的合成的正意义RNA转染细胞后回收感染性病毒,完成了产生RNA病毒的反感染系统的探索。许多研究者已经从克隆的cDNA产生动物感染性RNA病毒(Boyer,J.C.,等人,病毒学,198,415-426(1994))。Van der Werf等人是第一个利用T7 RNA聚合酶在克隆的cDNA模板上产生的合成RNA生产脊髓灰质炎病毒,一种正链RNA病毒(van der Werf,S.,等人,Proc.Natl.Acad.Sci.USA,83,2330-2334(1986))。后来,从它们各自的基因组的克隆cDNA,Enami等人获得了流感病毒,一种区段化的负链RNA病毒(Enami,M.等人,Proc.Natl.Acad.Sci.USA,87,3802-3805(1990));和Schnell等人制得了狂犬病毒,一种非区段化的负链RNA病毒(Schnell,M.J.等人,EMBO杂志,13,4195-4205(1994))。通过合成的ssRNA、dsRNA、体外翻译的呼肠病毒产物转染细胞,Roner等人开发了区段化的dsRNA呼肠病毒的感染性系统,并与不同血清型的辅助病毒互补(Roner,M.R.等人,病毒学,179,845-852(1990))。通过噬菌斑测试,将得到的病毒与辅助病毒区别开来。但是,在这一系统中,使用辅助病毒是必要的。相反,现在叙述的IBDV反遗传系统不需要辅助病毒或其它病毒蛋白。利用两区段的正意义RNA转染细胞足以产生感染性病毒(IBDV)。在区段A的3’末端分别转录的另外一个或四个核苷酸的结局没有确定。但是,这并不阻止病毒dsRNA的复制。不同的研究者观察到正链RNA病毒有同样的效果(Boyer,J.C.,等人,病毒学,198,415-426(1994))。
用两个区段的正意义RNA转染同一细胞对于成功地恢复IBDV是必要的。通过细胞的翻译机制将两个区段的转染RNA翻译。假定区段A的聚蛋白加工成VP2、VP3和VP4蛋白质,它们形成病毒的外壳。白区段B翻译出蛋白质VP1可能起依赖于RNA的RNA聚合酶的作用,从两个区段的合成正链转录负链,反应产物形成dsRNA。最近,Dobos报道了感染性胰坏死病毒(IPNV),双RNA病毒家族中的一个原型病毒,通过依赖于病毒粒子RNA的RNA聚合酶在体外的转录是由VP1引导的,然后通过不对称、半保守、链替代机制进行加工,在病毒基因组的复制过程中只合成正链(Dobos,P.,病毒学,208,10-25(1995))。本发明系统显示负链的合成在正链的合成之前。得到的转录负链RNA是否用作为正链转录的模板仍然是进一步研究的主题。
为了证明转染细胞的上清液中含有的感染性IBDV确实起源于合成的转录物,生产了含有血清型II毒株的区段A和血清型I毒株的区段B的人工嵌合体。序列分析证实了这一基因组联合。该结果同样表明Mundt和Muller描述的终端序列基元可能导致病毒基因组的复制,分类和包装(Mundt,E.等人,病毒学,209,10-18(1995))。血清型特异性终端序列的存在显然不阻止在血清型I区段B的依赖RNA的RNA聚合酶VP1的作用下,适当复制血清型II A区段。产生重组病毒的能力将大大帮助分析血清型特异的和血清型共同的终端序列的准确功能。
感染性IBDV的回收证实只有两区段的正链RNA才足以启动dsRNA的复制。所以,该结果与呼肠病毒和轮状病毒复制的一般特征一致,其中正链RNA的作用是作为合成子代负链的模板以便产生dsRNA(Schonberg,M.,等人,Proc.Natl Acad.Sci.USA,Patton,J.T.,病毒研究,6,217-233(1986);Chen,D.,等人,病毒学杂志,68,7030-7039(1994))。但是,Spies等人和Dobos建议的半保守、链替代机制不能排除在外(Spies,U.等人,病毒研究,8,127-140(1987);Dobos,P.,病毒学,208,10-25(1995))。IBDV反遗传系统的开发将大大简化将来基因表达和病理的研究,和辅助产生新的活和失活IBDV疫苗的设计。
如本申请书所用,如用于核酸的术语“合成的”指这是人制造的核酸,与天然存在的核酸不同。对于制造方法,该术语的含义没有限制,可以是化学或生物的,只要制造方法包括人的干预即可。
术语“cDNA”是指含有区段A和B和区段A和B的5’和3’非编码区的任何cDNA。
术语“感染性”如用于病毒,表明病毒具有再生能力。该病毒可以是致病原或非致病原,并且仍然是感染性的。
本发明提供了利用合成RNA转录物产生感染性囊病病毒的系统。这一系统可以用于病毒基因表达的调节和病理的研究和产生新的活和失活IBDV疫苗的设计。
本发明提供含有至少一个拷贝的本发明的cDNA的重组载体。重组载体也可以含有其它必需序列,如本领域已知的表达控制序列、标记、扩增基因、信号序列、启动子和诸如此类。为了这一目的的有用载体是质粒,病毒如杆状病毒、疱疹病毒(HVT)和痘病毒,例如,家禽痘病毒和诸如此类。
本文还提供了利用本发明的重组载体转化的宿主细胞或利用本发明的合成RNA转染的宿主细胞。宿主细胞可以是原核或真核宿主细胞。适当的例子有大肠杆菌、昆虫细胞系如Sf-9、鸡胚成纤维细胞(CEF)、鸡胚肾细胞(CEK)、非洲绿猴肾细胞Vero和诸如此类。
同样是本发明的一部分的是含有家禽保护量的重组产生的病毒或病毒一部分的IBDV家禽疫苗,其中病毒是失活或经修饰的,以致它不再具有毒力。
通过化学或物理方法可以失活病毒。例如用酶、甲醛、β-丙酸内酯、环乙亚胺、或其衍生物、有机溶剂(如卤代烃)和/或去垢剂处理病毒可以达到化学失活。如果需要,在病毒已经失活后,可以中和失活的物质。通过将病毒进行如UV光照射、X-放射、或γ辐射可以进行物理失活。
通过已知方法包括在生产感染性病毒之前或之后进行连续传代、缺失核酸序列和位点特异诱变,可以将病毒减毒以产生保留足够的抗原性但毒力减弱的病毒。
用于家禽接种的生理可接受载体是本领域已知的,不需要在本文进一步叙述。除了对家禽是生理可接受的,该载体必须不干扰疫苗引发的免疫应答和/或不干扰它的多肽产物的表达。
其它添加剂如助剂和稳定剂等也可以本领域已知的量包含在疫苗中。优选地,助剂如氢氧化铝、磷酸铝、植物和动物油和诸如此类可以足以增强对IBDV的免疫应答的量与疫苗一起给药。加入疫苗的助剂的量将根据助剂的特性而变化,通常范围在IBDV重量的约0.1到约100倍,优选地为IBDV重量的约1到约10倍。
本发明的疫苗也可以含有各种稳定剂。任何适当的稳定剂都可以利用,包括碳水化合物如山梨醇、甘露醇、淀粉、蔗糖、糊精或葡萄糖;蛋白质如白蛋白或酪蛋白;和缓冲液如碱性金属磷酸盐和诸如此类。当通过冷冻制备干燥疫苗制剂时稳定剂是特别有利的。
疫苗可以通过任何适当的已知接种家禽的方法给药,包括经鼻的、眼的、通过注射、在饮用中、在饲料中、通过接触等诸如此类。优选地,将疫苗通过大量给药技术给药,如将疫苗放入饮用水中,或通过喷洒动物所处的环境。当通过注射给药时,优选地将疫苗经皮给药。如本文所用的非肠道给药指通过静脉内、皮下、肌肉内或腹膜内注射给药。
将本发明的疫苗在孵化之前或之后对家禽给药以便在任何时候防止IBD。优选地,疫苗是在出生的时间之前,和动物约6周龄之后给药。家禽定义包括,但不限于鸡、公鸡、母鸡、焙烤小鸡、繁殖的鸡、生蛋的鸡、火鸡和鸭。
疫苗可以在无菌包装中以单位形式或以其它量提供。优选地,将它冷冻储藏,在低于-20℃,更优选地,在低于-70℃储藏。在使用之前解冻,然后可以立即再冷冻。对于家禽给药,可以将重组生产的病毒悬浮于载体中,量为104到107pfu/毫升,更优选地,在载体如盐溶液中为105到106pfu/毫升。失活的疫苗可以含有悬浮于载体中的104到107pfu/毫升的抗原等价物。如本领域已知,其它载体也可以利用。药学可接受载体的例子是稀释剂和本领域已知的惰性药学载体。优选地,载体或稀释剂是与大量给药技术给药疫苗相容的。但是,载体或稀释剂也可以与其它给药方法如注射、滴眼、滴鼻等诸如此类相容。
本发明也可以用于产生与IBDV物质联合的疫苗。IBDV物质可以与新城鸡瘟病病毒感染性支气管炎病毒、呼肠病毒、腺病毒和/或马立克氏病毒的抗原物质联合。
本发明前面的实施方案将进一步在下面的实施例中阐述。但是,本发明不限于这些实施例。对本领域技术人员而言,不离开本发明的范围的变化将是显然的。
附图的简要描述
图1是用于合成含有T7 RNA聚合酶的IBDV正意义ssRNA的cDNA构建体的图解说明。构建体pUC19FLAD78含有IBDV毒株D78的区段A的cDNA,重组质粒pUC18FLA23含有IBDV毒株23/82的区段A的全长cDNA。IBDV的区段A编码聚蛋白质(VP2-VP4-VP3)和最近鉴定的VP5蛋白质。质粒pUC18FLBP2含有毒株P2的区段B的cDNA,它编码依赖于RNA的RNA聚合酶(VP1)。病毒特异性序列下面划线,T7启动子序列是斜体。鉴定了限制位点并用黑体表示。用垂直的箭头表示线性质粒的切割位点。用水平箭头表示转录方向。
图2显示用于转染非洲绿猴肾细胞株细胞的转录反应产物的琼脂糖凝胶分析。在体外利用T7 RNA聚合酶和线性质粒pUC19FLAD78转录的合成RNA(泳道2,4和6),含有IBDV毒株D78的区段A的cDNA;pUC18FLBP2(泳道1,3和5)含有毒株P2的区段B的cDNA。在转录后,反应混合物利用DNase(泳道1和2),RNase(泳道3和4)处理或仍然未处理(泳道5和6)。在1%的琼脂糖凝胶上分析2微升反应产物。将HindIII/EcoR I消化的λDNA用作分子量标记(泳道M)。
图3显示了来自嵌合体IBDV毒株23A/P2B的区段A和B的克隆的RT-PCR片断的核苷酸序列(黑体)分别与血清型II毒株23/82和血清型I毒株P2的区段A和B的已知序列的比较。相同的核苷酸以冒号表示。
图4显示了pUC18FLA23的DNA序列。
图5显示了pUC19FLAD78的DNA序列。
图6显示了pUC18FLBP2的DNA序列。
实施例
病毒和细胞 将两个IBDV血清型I毒株(来自德国的减毒P2毒株和疫苗毒株D78(intervet international))和一个血清型II毒株(apathogenic23/82毒株)在鸡胚细胞(CEC)中繁殖并纯化(Mundt,E.等人,病毒学,209,10-18(1995);Vakharia,V.N.等人,病毒研究,31,265-273(1994))。在用5%胎牛血清(FCS)补充的M199培养基中生长非洲绿猴肾细胞并用于转染实验。在非洲绿猴肾细胞中进行进一步繁殖恢复的病毒和免疫荧光研究(Mundt,E.等人,病毒遗传杂志,76,437-443(1995))。对于噬菌斑测试,制备和使用了第二代CEC的单层(Muller,H.,等人,病毒研究,4,297-309(1986))。
构建IBDV基因组的全长cDNA克隆 单独制备了全长IBDV区段A和B的cDNA克隆。利用标准克隆程序和各种方法制备了含有毒株D78的RNA区段A的整个编码区的cDNA克隆(Vakharia,V.N.,等人,病毒研究,31,265-273(1994))。将D78末端序列与最近公开的其它IBDV毒株的末端序列比较(Mundt,E.等人,病毒学,209,10-18(1995)),观察到D78 cDNA克隆在5’和3’末端分别缺乏保守的起始的17和最后10个核苷酸。所以,为了构建区段A的全长cDNA的克隆,合成了两个引物对(A5’-D78,A5-IPD78和A3’-IPD78),并用于PCR扩增(表1)。根据供应商的方案(新英格兰生物实验室),利用“Deep Vent聚合酶”(高保真,耐热DNA聚合酶)扩增该DNA区段。将扩增的片断克隆到pCRII载体(Invitrogen公司)的EcoR I位点,以便分别得到质粒pCRD78A5’和pCRD78A3’。利用EcoR I和Sal I消化各个质粒,将得到的片断连接到EcoR I消化的pUC19上以便得到质粒pUC19FLAD78(SEQ ID NO:27和29),该质粒含有编码所有结构蛋白(VP2,VP4和VP3,SEQ ID NO:30)以及非结构VP5蛋白(SEQ ID NO:28)的区段A的全长cDNA拷贝(图1)。
将两个引物对(A5’-23,A5IP23和A3’-23,A3-IP23;参见表1)用于毒株23/82的病毒基因组dsRNA的逆转录(RT),该逆转录利用了“SuperScript RT II”(RNA指导的DNA聚合酶,其RNase H的活性减弱,GIBCO/BRL)。通过酚/氯仿提取和乙醇沉淀纯化RT反应产物。为了得到引物对A5’-23、A5-IP23,和A3’-23、A3-IP23,分别连接的两个cDNA片断,通过PCR,利用“Deep Vent聚合酶”扩增RT反应产物。根据供应商的方案进行RT和PCR。将得到的PCR片断末端平齐化,并连接进入Sma I切割的pUC18载体以便得到pUC23A5’和pUC23A3’。将质粒pUC23A3’中含有的区段A的3’末端连接进入Hind III-BstB I切割的质粒pUC23A5’以便建立毒株23/82的区段A的全长cDNA。将得到的质粒命名为pUC18FLA23(SEQ ID NO:31和33)(图1),它编码结构蛋白VP2、VP3和VP4(SEQ ID NO:32)和非结构蛋白质VP5(SEQ ID NO:34)。
为了得到P2毒株的区段B的cDNA克隆,根据公开的序列设计两个引物对(B5’-P2,B5-IPP2和B3’-P2,B3-IPP2),用于RT-PCR扩增(参见表1)。利用基因组dsRNA作为模板,根据供应商的方案合成和扩增cDNA片断(Perkin-Elmer Cetus)。将扩增的片断末端平齐化,连接进入Sma I切割的pBS载体(Stratagene)以便得到克隆pBSP2B5’和pBSP2B3’。为了构建区段B的全长克隆,首先在pUC18载体的EcoRI和Pst I位点之间亚克隆质粒pBSP2B5’的5’末端片断以便得到pUCP2B5’。然后,将质粒pBSP2B3’的3’末端片断插入在质粒pUCP2B5’的唯一的Bgl II和Pst I位点以便得到全长的质粒pUC18FLBP2(SEQ ID NO:25),该质粒编码VP1蛋白质(SEQ IDNO:26)(图1)。利用“序列酶”DNA测序系统(美国生化)可以对质粒pUC18FLBP2、pUC18FLA23和pUC19FLAD78完全测序,利用“DNASIS”(Pharmacia)或“PC/Gene”(Intelligenetics)软件分析序列数据。利用T7 RNA聚合酶(Promega)体外转录和体外翻译偶联网织红细胞裂解液系统以测试全长构建体的完整性。
合成RNA的转录和转染 分别利用BsrG I、Nsi I和Pst I酶消化质粒pUC19FLAD78、pUC18FLA23和pUC18FLBP2,并用作T7 RNA聚合酶(Promega)体外翻译的模板。简要地说,将限制酶切割测试调节到0.5%SDS,并与蛋白酶K(0.5毫克/毫升)在37℃,温育1小时。在乙醇沉淀后,回收线性DNA模板(约3微克),并分别加入转录反应混合物(50微升),转录混合物含有40毫摩尔浓度Tris-HCl(pH7.9)、10毫摩尔浓度的NaCl、6毫摩尔浓度的MgCl2、2毫摩尔浓度的亚精胺、各0.5毫摩尔浓度的ATP、CTP和UTP、0.1毫摩尔浓度GTP、0.25毫摩尔浓度的帽子类似物[m7G(5’)PPP(5’)G]、120单位“RNasin”(核糖核酸酶抑制剂)和150单位T7 RNA聚合酶(Promega),在37℃温育1小时。通过酚/氯仿提取和乙醇沉淀纯化合成的RNA转录物。作为对照,利用DNase或RNase(Promega)在纯化步骤之前处理转录产物。
在60毫米培养皿中将非洲绿猴肾细胞株系生长至80%汇合,并且用磷酸缓冲盐水(PBS)洗涤一次。将3毫升的“OPTI-MEM I”(该培养基是含有HEPES缓冲液、碳酸氢钠、次黄嘌呤、胸腺嘧啶、丙酮酸钠、L-谷氨酰胺、微量元素、生长因子和酚红的还原血清培养基;从GIBCO/BRL获得)加入到该单层,在二氧化碳培养箱,于37℃将细胞培养1小时。同时,将0.15毫升的“OPTI-MEM I”与1.25微克的“脂质转染”试剂(N-(1-(2,3-二油酰氧)丙基)-N,N,N-三甲基铵氯和二油酰磷脂酰乙醇胺,GIBCO/BRL)-起在室温下的聚苯乙烯试管中保温45分钟。将悬浮于0.15毫升的焦碳酸二乙酯处理的水中的合成的RNA转录物的两个区段加入到OPTI-MEM脂质转染剂混合物,缓慢混合,置于冰上保温5分钟。在从60毫米的培养皿的单层去除“OPTI-MEM”并且用新鲜的1.5毫升的“OPTI-MEM”替代之后,将含有核酸的混合物逐滴加入到非洲绿猴肾细胞株系细胞并且缓慢涡动。在37℃保温2小时之后,用含有5%FCS(没有浸洗细胞)的M199培养基(氯化钙(无水)、9水硝酸铁、氯化钾、硫酸镁(无水)、氯化钠、一水磷酸二氢钠、碳酸氢钠、L-丙氨酸、L-盐酸精氨酸、L-天冬氨酸、一水盐酸L-半胱氨酸、2盐酸L-半胱氨酸、L-谷氨酸、L-谷氨酰胺、甘氨酸、一水盐酸L-组氨酸、L-羟基脯氨酸、L-异亮氨酸、L-亮氨酸、盐酸L-赖氨酸、L-甲硫氨酸、L-苯丙氨酸、L-脯氨酸、L-丝氨酸、L-苏氨酸、L-色氨酸、2水L-酪氨酸2钠、L-缬氨酸、α维生素E磷酸2钠、抗坏血酸、生物素、维生素D2、D-泛酸钙、绿化胆碱、叶酸、I-肌醇、3水二甲萘醌亚硫酸氢钠、烟酸、烟酰胺、对—氨基苯甲酸、盐酸吡哆醇、核黄素、盐酸硫胺素、乙酸维生素A、硫酸腺嘌呤、腺苷酸、ATP、Na2、胆固醇、2-脱氧-D-核糖、D-葡萄糖、谷胱甘肽、盐酸鸟嘌呤、次黄嘌呤钠、酚红钠、核糖、乙酸钠(无水)、胸腺嘧啶、吐温80、尿嘧啶和黄嘌呤钠;从Mediatech公司获得)替换混合物,以所需的时间间隔进一步在37℃将细胞保温。产生的IBDV的鉴定
用从由pUC18FLA23和pUC18FLP2B转录物转染的非洲绿猴肾细胞系细胞过滤(0.2微米)得的上清液感染CEC。感染后16小时,分离整个细胞的核酸(Mundt,E.等人,病毒学,209,10-18(1995))。根据公开的序列设计引物,将RT-PCR片段扩增,克隆和测序(Mundt,E.等人,病毒学,209,10-18(1995))。通过利用“DNASIS”软件分析序列数据。免疫荧光测定
用从感染的非洲绿猴肾细胞系细胞获得的上清液(在冰冻和冻融之后)感染在盖玻片上生长到80%汇合的非洲绿猴肾细胞系细胞,在37℃保温2天。然后洗涤细胞,用丙酮固定并且多克隆兔抗-IBDV血清处理,洗涤之后将细胞用荧光素标记的山羊抗兔抗体(Kirkegaard&Perry实验室)处理并用荧光显微镜检查。噬菌斑测试
在60毫米培养皿中生长的次代CEC的单层用来自于转染的非洲绿猴肾细胞系细胞的上清液接种。在感染1小时之后,用PBS将细胞洗涤一次和用含有10%磷酸胰蛋白胨肉汤、2%FCS、0.112%碳酸氢钠、103单位的青霉素、103微克/毫升的链霉素、0.25微克/毫升的两性霉素、0.005%中性红、0.0015%酚红的0.8%纯净琼脂(Difco)覆盖。将细胞在37℃保温2-3天直到能够观察到噬菌斑并且计数(Muller,H.等人,病毒研究,4,297-309(1986))。IBDV基因组的全长cDNA克隆的构建
为了研制用于dsRNA病毒IBDV的反遗传系统,构建两个独立的cDNA克隆,它们含有毒株D78的区段A和毒株P2的区段B(附图1)。各个质粒或者编码结构蛋白质的前体(VP2,VP4,VP3)和VP5或仅编码VP1蛋白质(依赖于RNA的RNA聚合酶)。用Pst I消化质粒pUC18FLBP2并且由T7 RNA聚合酶体外转录以产生含有正确的5’-和3’-末端的RNA。基于用BsrG I消化和转录,质粒pUC19FLAD78产生含有正确的5’-末端但是在3’末端具有另外的4个核苷酸的RNA。在兔网状细胞系统中将上述质粒的转录和转译偶合产生蛋白质产物,该产物是经正确地加工过的并且在SDS-聚丙烯酰胺凝胶和自动自显影分离之后与标记物IBDV蛋白质一起共迁移(数据未显示)。感染性病毒的转录,转染和繁殖
利用线性化的全长cDNA质粒作为模板,用T7 RNA聚合酶体外分别合成IBDV区段A和B的正意义转录物(参见附图2)。虽然在中性凝胶上对于区段B(泳道1和5)观察到两个种类的RNA转录物,在变性凝胶上分离这些样品仅产生一个特异于转录物的谱带(数据未显示)。为了显示两个区段的正意义RNA转录物需要制备感染性病毒,用不同的核酸酶保温转录混合物,如附图2所示。在用DNA酶(泳道1+2)、RNA酶(泳道3+4)处理转录产物之后或没有处理(泳道5+6)之后回收的合成的RNA用于转染非洲绿猴肾细胞株系细胞。作为模拟对照,仅使用脂质转染试剂,在转染之后5天,仅在用未处理的或DNA酶处理的转录产物转染的非洲绿猴肾细胞系细胞中观察到细胞毒性作用(CPE),但是在用RNA酶处理的转录混合物或模拟物转染的对照没有观察到。另外,当仅用区段A或B的RNA转染非洲绿猴肾细胞系细胞时(数据没有显示),没有检测到CPE。这些结果证实在用IBDV的两个区段的正意义ssRNA转染非洲绿猴肾细胞系细胞之后确保IBDV的复制。为了验证导致非洲绿猴肾细胞系细胞中CPE的因子的确是IBDV,将转染的非洲绿猴肾细胞系细胞冷冻—冻融,并且通过离心使上清液澄清,并且用于感染CEC或非洲绿猴肾细胞系细胞。用来自未处理或DNA酶处理的转录混合物感染的非洲绿猴肾细胞系细胞的上清液感染CEC,在接种一天后即表现出CPE(表2)。但是,用来自于RNA酶处理的转录混合物、未处理的区段A或B转录混合物感染的非洲绿猴肾细胞系细胞,和模拟物转染的非洲绿猴肾细胞系细胞的上清液感染CEC,甚至在5天之后也没有检测到CPE。类似地当用类似于上面描述的上清液感染盖玻片上的非洲绿猴肾细胞系细胞并且在免疫荧光染色之后2天检查,仅来自于未处理的或DNA酶处理的转录混合物转染的非洲绿猴肾细胞系细胞的上清液获得阳性免疫荧光信号(表2)。转染病毒的回收
为了测定感染性病毒的回收的时间点,用区段A和B结合的RNA转录物转染非洲绿猴肾细胞系细胞。在转染之后4、8、16、24、36和48小时时,通过感染状态和噬菌斑测试检查上清液中转染性病毒的存在,如表3所示。我们的结果表明,可以早至转染之后36小时回收病毒。病毒效价是2.3×102pfu/毫升,表明在晚于转染之后48小时获得的样品中效价有所下降。嵌合病毒的制备
为了证明IBDV的两个区段的正意义ssRNA足于恢复成感染性病毒,制备嵌合IBDV。通过Nsi I消化将含有血清型II毒株的区段A的全长序列的质粒pUC18FLA23线性化,利用T7 RNA聚合酶体外合成ssRNA。ssRNA转录物限定了正确的5’末端但是在3’末端含有一个额外的残基(附图1)。用血清型II毒株23/82的区段A的ssRNA和血清型I毒株P2的区段B的ssRNA转染非洲绿猴肾细胞系细胞。转染5天之后,当CPE显示时,澄清上清液(在冷冻—冻融之后)并且用于感染CEC。在CEC中第二次传代之后,通过RT-PCR分析病毒的基因组RNA并且对PCR产物进行测序。将区段A的引物设计为特异于仅扩增来自于血清型II毒株的区段A的序列。对于区段B的引物与两种血清型的序列均结合。克隆该扩增的片段并且测序。获得的区段A的序列显示与血清型II毒株23/82的已知区段A序列良好地匹配,而区段B序列显示与出版的血清型I毒株的区段B序列则完全同源(附图3)。
表1 用于构建IBDV基因组区段A和B的全长cDNA克隆的寡聚核苷酸
核苷酸序列 方向 名称 核苷酸编号
TAATACGACTCACTATA GGATACGATCGGTCTGACCCCGGGGGAGTCA | (+) | A5′-D78 | 1-31 |
AGAGAATTCTAATACGACTCACTATA GGATACGATCGGTCTGAC | (+) | A5′-23 | 1-48 |
TGTAC AGGGGACCC GCGAACGGATCCAATT | (-) | A3′-D78 | 3237-3261 |
CGGCGAATTCATGCAT AGGGGACCCGCGAACGGATC | (-) | A3′-23 | 3242-3261 |
CGTCGACTACGGGATTCTGG | (-) | A5-IPD78 | 1711-1730 |
CAGAGGCAGTACTCCGTCTG | (-) | A5-IP23 | 1971-1990 |
AGTCGACGGG ATTCTTGCTT | (+) | A3-IPD78 | 1723-1742 |
GAAGGTGTGCGAGAGGAC | (+) | A3-IP23 | 1883-1900 |
AGAGAATTCTAATACGACTCACTATA GGATACGATGGGTCTGAC | (+) | B5′-P2 | 1-18 |
CGATCTGCTGCA GGGGGCCCCCGCAGGCGAAGG | (-) | B3′-P2 | 2807-2827 |
CTTGAGACTCTTGTTCTCTACTCC | (-) | B5-IPP2 | 1915-1938 |
ATACAGCAAAGATCTCGGG | (+) | B3-IPP2 | 1839-1857 |
用于克隆的寡聚核苷酸引物的组成和定位。用斜体字标记T7启动子序列,底下划线的为病毒特异性序列,用黑体字标记限制性位点。用有意义(+)和反义(-)显示了引物中的病毒特异性序列的定向。引物结合的位置(核苷酸编号)是根据出版的P2毒株(2)序列确定的。
表2 从区段A和B的合成的RNA制备感染性IBDV
转染的物质 CPE 免疫荧光测定
ssRNA A+B,DNA酶处理的 | + | + |
ssRNA A+B,RNA酶处理的 | - | - |
ssRNA A+B,未处理的 | + | + |
ssRNA A,未处理的 | - | - |
ssRNA B,未处理的 | - | - |
仅脂质转染剂 | - | - |
用来自于转录反应的区段A和B的合成的RNA转染非洲绿猴肾细胞系细胞,所述RNA未用或已用DNA酶或RNA酶处理。在5天之后,收集上清液,通过离心澄清,分析病毒的存在。根据接种1-2天之后胞毒作用(CPE)的出现在CEC中测定所回收病毒的感染性。用兔抗—IBDV血清,通过对感染的非洲绿猴肾细胞系细胞的免疫荧光染色测定回收的病毒的特异性。
表3 转染后不同的时间回收的病毒转染后的时间(小时) CPE 免疫荧光测定 pfu/毫升
4 | - | - | 0 |
8 | - | - | 0 |
16 | - | - | 0 |
24 | - | - | 0 |
36 | + | + | 2.3×102 |
48 | + | + | 6.0×101 |
如描述的,用区段A和B的合成的RNA转染非洲绿猴肾细胞系细胞。在CEC中通过CPE和在非洲绿猴肾细胞系细胞中进行免疫荧光染色测定来分别检测回收的病毒的感染性和特异性。在用来自于转染的非洲绿猴肾细胞系细胞的上清液接种细胞之后,将次代CEC的单层用于噬菌斑测试。计算病毒的近似效价,以每升的噬菌斑形成单位表示(pfu/毫升)。
序列表(1)总的资料:(i)申请人:VAKHARIA,Vikram N.;MUNDT,Egbert(ii)发明创造名称:从合成的RNA转录物制备双RNA病毒的方法(iii)序列数目:34(iv)通信地址:
(A)联系人:NIKAIDO,MARMELSTEIN,MURRAY & ORAM LLP
(B)街道:655,15大街,N.W.,Suite 330-G Street Lobby
(C)城市:华盛顿
(D)州:DC
(E)国家:美国
(F)邮编:20005-5701(v)计算机可读方式:
(A)媒介类型:软盘
(B)计算机:IBM PC兼容机
(C)操作系统:PC-DOS/MS-DOS
(D)软件程序:PatentIn Release #1.0,版本#1.30(vi)当前申请数据:
(A)申请号:US
(B)申请日期:
(C)分类:(viii)代理人/代理信息:
(A)姓名:KITTS,MonicaC.
(B)登记号:36,105
(C)案卷/卷宗号:P8172-6002(ix)通讯信息:
(A)电话:202/638-5000
(B)传真:202/638-4810(2)SEQ ID NO:1的信息:(i)序列特征:
(A)长度:46个碱基对
(B)类型:核酸
(C)链型:双链
(D)拓扑结构:环状(ii)分子类型:cDNA(xi)SEQ ID NO:1的序列描述GAATTCGGCT TTAATACGAC TCACTATAGG ATACGATCGG TCTGAC 46(2)SEQ ID NO:2的信息:(i)序列特征:
(A)长度:41个碱基对
(B)类型:核酸
(C)链型:双链
(D)拓扑结构:环状(ii)分子类型:cDNA(xi)SEQ ID NO:2的序列描述AATTGGATCC GTTCGCGGGT CCCCTGTACA AAGCCGAATT C 41(2)SEQ ID NO:3的信息:(i)序列特征:
(A)长度:36个碱基对
(B)类型:核酸
(C)链型:双链
(D)拓扑结构:环状(ii)分子类型:cDNA(xi)SEQ ID NO:3的序列描述CGGCGAATTC ATGCATAGGG GACCCGCGAA CGGATC 36(2)SEQ ID NO:4的信息:(i)序列特征:
(A)长度:44个碱基对
(B)类型:核酸
(C)链型:双链
(D)拓扑结构:环状(ii)分子类型:cDNA(xi)SEQ ID NO:4的序列描述GTCAGACCGA TCGTATCCTA TAGTGAGTCG TATTAGAATT CTCT 44(2)SEQ ID NO:5的信息:
(i)序列特征:
(A)长度:33个碱基对
(B)类型:核酸
(C)链型:双链
(D)拓扑结构:环状
(ii)分子类型:cDNA
(xi)SEQ ID NO:5的序列描述
TTGCATGCCT GCAGGGGGCC CCCGCAGGCG AAG 33
(2)SEQ ID NO:6:的信息:
(i)序列特征:
(A)长度:31个碱基对
(B)类型:核酸
(C)链型:双链
(D)拓扑结构:环状
(ii)分子类型:cDNA
(xi)SEQ ID NO:6的序列描述
TCGTATCCTA TAGTGAGTCG TATTAGAATT C 31
(2)SEQ ID NO:7的信息:
(i)序列特征:
(A)长度:120个碱基对
(B)类型:核酸
(C)链型:单链
(D)拓扑结构:线形
(ii)分子类型:DNA
(xi)SEQ ID NO:7的序列描述GGAAGCCTGA GTGAGTTGAC TGACTACAGC TACAACGGGC TGATGTCAGC CACTGCGAAC 60ATCAACGACA AGATCGGGAA CGTTCTAGTT GGAGAAGGGG TGACTGTTCT CAGTCTACCG 120
(2)SEQ ID NO:8的信息:
(i)序列特征:
(A)长度:120个碱基对
(B)类型:核酸
(C)链型:单链
(D)拓扑结构:线形
(ii)分子类型:DNA
(xi)SEQ ID NO:8的序列描述GGAAGCCTGA GTGAGTTGAC TGACTACAGC TACAACGGGC TGATGTCAGC CACTGCGAAC 60ATCAACGACA AGATCGGGAA CGTTCTAGTT GGAGAAGGGG TGACTGTTCT CAGTCTACC 119
(2)SEQ ID NO:9的信息:
(i)序列特征:
(A)长度:120个碱基对
(B)类型:核酸
(C)链型:单链
(D)拓扑结构:线形
(ii)分子类型:DNA
(xi)SEQ ID NO:9的序列描述GGAAGCCTGA GTGAACTGAC AGATGTTAGC TACAATGGGT TGATGTCTGC AACAGCCAAC 60ATCAACGACA AAATTGGGAA CGTCCTAGTA GGGGAAGGGG TCACCGTCCT CAGCTTACCC 120
(2)SEQ ID NO:10的信息:
(i)序列特征:
(A)长度:120个碱基对
(B)类型:核酸
(C)链型:单链
(D)拓扑结构:线形
(ii)分子类型:DNA
(xi)SEQ ID NO:10的序列描述TTTTCAATAG TCCACAGGCG CGAACGAAGA TCTCAGCAGC GTTCGGCATA AAGCCTACTG 60CTGGACAAGA CGTGGAAGAA CTCTTGATCC CCAAAGTCTG GGTGCCACCT GAGGATCCGC 120
(2)SEQ ID NO:11的信息:
(i)序列特征:
(A)长度:120个碱基对
(B)类型:核酸
(C)链型:单链
(D)拓扑结构:线形
(ii)分子类型:DNA
(xi)SEQ ID NO:11的序列描述TTTTCAACAG TCCACAGGCG CGAAGCACGA TCTCAGCAGC GTTCGGCATA AAGCCTACTG 60CTGGACAAGA CGTGGAAGAA CTCTTGATCC CTAAAGTTTG GGTGCCACCT GAGGATCCGC 120
(2)SEQ ID NO:12的信息:
(i)序列特征:
(A)长度:120个碱基对
(B)类型:核酸
(C)链型:单链
(D)拓扑结构:线形
(ii)分子类型:DNA
(xi)SEQ ID NO:12的序列描述TTTTCAACAG TCCACAGGCG CGAAGCACGA TCTCAGCAGC GTTCGGCATA AAGCCTACTG 60CTGGACAAGA CGTGGAAGAA CTCTTGATCC CTAAAGTTTG GGTGCCACCT GAGGATCCGC 120
(2)SEQ ID NO:13的信息:
(i)序列特征:
(A)长度:48个碱基对
(B)类型:核酸
(C)链型:单链
(D)拓扑结构:线形
(ii)分子类型:DNA
(xi)SEQ ID NO:13的序列描述TAATACGACT CACTATAGGA TACGATCGGT CTGACCCCGG GGGAGTCA 48
(2)SEQ ID NO:14的信息:
(i)序列特征:
(A)长度:44个碱基对
(B)类型:核酸
(C)链型:单链
(D)拓扑结构:线形
(ii)分子类型:DNA
(xi)SEQ ID NO:14的序列描述AGAGAATTCT AATACGACTC ACTATAGGAT ACGATCGGTC TGAC 44
(2)SEQ ID NO:15的信息:
(i)序列特征:
(A)长度:30个碱基对
(B)类型:核酸
(C)链型:单链
(D)拓扑结构:线形
(ii)分子类型:DNA
(xi)SEQ ID NO:15的序列描述TGTACAGGGG ACCCGCGAAC GGATCCAATT 30
(2)SEQ ID NO:16的信息:
(i)序列特征:
(A)长度:36个碱基对
(B)类型:核酸
(C)链型:单链
(D)拓扑结构:线形
(ii)分子类型:DNA
(xi)SEQ ID NO:16的序列描述CGGCGAATTC ATGCATAGGG GACCCGCGAA CGGATC 36
(2)SEQ ID NO:17的信息:
(i)序列特征:
(A)长度:20个碱基对
(B)类型:核酸
(C)链型:单链
(D)拓扑结构:线形
(ii)分子类型:DNA
(xi)SEQ ID NO:17的序列描述CGTCGACTAC GGGATTCTGG 20
(2)SEQ ID NO:18的信息:
(i)序列特征:
(A)长度:20个碱基对
(B)类型:核酸
(C)链型:单链
(D)拓扑结构:线形
(ii)分子类型:DNA
(xi)SEQ ID NO:18的序列描述CAGAGGCAGT ACTCCGTCTG 20
(2)SEQ ID NO:19的信息:
(i)序列特征:
(A)长度:20个碱基对
(B)类型:核酸
(C)链型:单链
(D)拓扑结构:线形
(ii)分子类型:DNA
(xi)SEQ ID NO:19的序列描述AGTCGACGGG ATTCTTGCTT 20
(2)SEQ ID NO:20的信息:
(i)序列特征:
(A)长度:18个碱基对
(B)类型:核酸
(C)链型:单链
(D)拓扑结构:线形
(ii)分子类型:DNA
(xi)SEQ ID NO:20的序列描述GAAGGTGTGC GAGAGGAC 18
(2)SEQ ID NO:21的信息:
(i)序列特征:
(A)长度:44个碱基对
(B)类型:核酸
(C)链型:单链
(D)拓扑结构:线形
(ii)分子类型:DNA
(xi)SEQ ID NO:21的序列描述AGAGAATTCT AATACGACTC ACTATAGGAT ACGATGGGTC TGAC 44
(2)SEQ ID NO:22的信息:
(i)序列特征:
(A)长度:33个碱基对
(B)类型:核酸
(C)链型:单链
(D)拓扑结构:线形
(ii)分子类型:DNA
(xi)SEQ ID NO:22的序列描述CGATCTGCTG CAGGGGGCCC CCGCAGGCGA AGG 33
(2)SEQ ID NO:23的信息:
(i)序列特征:
(A)长度:24个碱基对
(B)类型:核酸
(C)链型:单链
(D)拓扑结构:线形
(ii)分子类型:DNA
(xi)SEQ ID NO:23的序列描述CTTGAGACTC TTGTTCTCTA CTCC 24
(2)SEQ ID NO:24的信息:
(i)序列特征:
(A)长度:19个碱基对
(B)类型:核酸
(C)链型:单链
(D)拓扑结构:线形
(ii)分子类型:DNA
(xi)SEQ ID NO:24的序列描述ATACAGCAAA GATCTCGGG 19
(2)SEQ ID NO:25的信息:
(i)序列特征:
(A)长度:2827个碱基对
(B)类型:核酸
(C)链型:单链
(D)拓扑结构:环形
(ii)分子类型:cDNA
(ix)特征:
(A)名称/KEY:CDS
(B)位置:112..2745
(xi)SEQ ID NO:25的序列描述GGATACGATG GGTCTGACCC TCTGGGAGTC ACGAATTAAC GTGGCTACTA GGGGCGATAC 60CCGCCGCTGG CCGCCACGTT AGTGGCTCCT CTTCTTGATG ATTCTGCCAC C ATG AGT 117
Met Ser
1GAC ATT TTC AAC AGT CCA CAG GCG CGA AGC ACG ATC TCA GCA GCG TTC 165Asp Ile Phe Asn Ser Pro Gln Ala Arg Ser Thr Ile Ser Ala Ala Phe
5 10 15GGC ATA AAG CCT ACT GCT GGA CAA GAC GTG GAA GAA CTC TTG ATC CCT 213Gly Ile Lys Pro Thr Ala Gly Gln Asp Val Glu Glu Leu Leu Ile Pro
20 25 30AAA GTT TGG GTG CCA CCT GAG GAT CCG CTT GCC AGC CCT AGT CGA CTG 261Lys Val Trp Val Pro Pro Glu Asp Pro Leu Ala Ser Pro Ser Arg Leu35 40 45 50GCA AAG TTC CTC AGA GAG AAC GGC TAC AAA GTT TTG CAG CCA CGG TCT 309Ala Lys Phe Leu Arg Glu Asn Gly Tyr Lys Val Leu Gln Pro Arg Ser
55 60 65CTG CCC GAG AAT GAG GAG TAT GAG ACC GAC CAA ATA CTC CCA GAC TTA 357Leu Pro Glu Asn Glu Glu Tyr Glu Thr Asp Gln Ile Leu Pro Asp Leu
70 75 80GCA TGG ATG CGA CAG ATA GAA GGG GCT GTT TTA AAA CCC ACT CTA TCT 405Ala Trp Met Arg Gln Ile Glu Gly Ala Val Leu Lys Pro Thr Leu Ser
85 90 95CTC CCT ATT GGA GAT CAG GAG TAC TTC CCA AAG TAC TAC CCA ACA CAT 453Leu Pro Ile Gly Asp Gln Glu Tyr Phe Pro Lys Tyr Tyr Pro Thr His
100 105 110CGC CCT AGC AAG GAG AAG CCC AAT GCG TAC CCG CCA GAC ATC GCA CTA 501Arg Pro Ser Lys Glu Lys Pro Asn Ala Tyr Pro Pro Asp Ile Ala Leu115 120 125 130CTC AAG CAG ATG ATT TAC CTG TTT CTC CAG GTT CCA GAG GCC AAC GAG 549Leu Lys Gln Met Ile Tyr Leu Phe Leu Gln Val Pro Glu Ala Asn Glu
135 140 145GGC CTA AAG GAT GAA GTA ACC CTC TTG ACC CAA AAC ATA AGG GAC AAG 597Gly Leu Lys Asp Glu Val Thr Leu Leu Thr Gln Asn Ile Arg Asp Lys
150 155 160GCC TAT GGA AGT GGG ACC TAC ATG GGA CAA GCA AAT CGA CTT GTG GCC 645Ala Tyr Gly Ser Gly Thr Tyr Met Gly Gln Ala Asn Arg Leu Val Ala
165 170 175ATG AAG GAG GTC GCC ACT GGA AGA AAC CCA AAC AAG GAT CCT CTA AAG 693Met Lys Glu Val Ala Thr Gly Arg Asn Pro Asn Lys Asp Pro Leu Lys
180 185 190CTT GGG TAC ACT TTT GAG AGC ATC GCG CAG CTA CTT GAC ATC ACA CTA 741Leu Gly Tyr Thr Phe Glu Ser Ile Ala Gln Leu Leu Asp Ile Thr Leu195 200 205 210CCG GTA GGC CCA CCC GGT GAG GAT GAC AAG CCC TGG GTG CCA CTC ACA 789Pro Val Gly Pro Pro Gly Glu Asp Asp Lys Pro Trp Val Pro Leu Thr
215 220 225AGA GTG CCG TCA CGG ATG TTG GTG CTG ACG GGA GAC GTA GAT GGC GAC 837Arg Val Pro Ser Arg Met Leu Val Leu Thr Gly Asp Val Asp Gly Asp
230 235 240TTT GAG GTT GAA GAT TAC CTT CCC AAA ATC AAC CTC AAG TCA TCA AGT 885Phe Glu Val Glu Asp Tyr Leu Pro Lys Ile Asn Leu Lys Ser Ser Ser
245 250 255GGA CTA CCA TAT GTA GGT CGC ACC AAA GGA GAG ACA ATT GGC GAG ATG 933Gly Leu Pro Tyr Val Gly Arg Thr Lys Gly Glu Thr Ile Gly Glu Met
260 265 270ATA GCT ATC TCA AAC CAG TTT CTC AGA GAG CTA TCA ACA CTG TTG AAG 981Ile Ala Ile Ser Asn Gln Phe Leu Arg Glu Leu Ser Thr Leu Leu Lys275 280 285 290CAA GGT GCA GGG ACA AAG GGG TCA AAC AAG AAG AAG CTA CTC AGC ATG 1029Gln Gly Ala Gly Thr Lys Gly Ser Asn Lys Lys Lys Leu Leu Ser Met
295 300 305TTA AGT GAC TAT TGG TAC TTA TCA TGC GGG CTT TTG TTT CCA AAG GCT 1077Leu Ser Asp Tyr Trp Tyr Leu Ser Cys Gly Leu Leu Phe Pro Lys Ala
310 315 320GAA AGG TAC GAC AAA AGT ACA TGG CTC ACC AAG ACC CGG AAC ATA TGG 1125Glu Arg Tyr Asp Lys Ser Thr Trp Leu Thr Lys Thr Arg Asn Ile Trp
325 330 335TCA GCT CCA TCC CCA ACA CAC CTC ATG ATC TCT ATG ATC ACC TGG CCC 1173Ser Ala Pro Ser Pro Thr His Leu Met Ile Ser Met Ile Thr Trp Pro
340 345 350GTG ATG TCC AAC AGC CCA AAT AAC GTG TTG AAC ATT GAA GGG TGT CCA 1221Val Met Ser Asn Ser Pro Asn Asn Val Leu Asn Ile Glu Gly Cys Pro355 360 365 370TCA CTC TAC AAA TTC AAC CCG TTC AGA GGA GGG TTG AAC AGG ATC GTC 1269Ser Leu Tyr Lys Phe Asn Pro Phe Arg Gly Gly Leu Asn Arg Ile Val
375 380 385GAG TGG ATA TTG GCC CCG GAA GAA CCC AAG GCT CTT GTA TAT GCG GAC 1317Glu Trp Ile Leu Ala Pro Glu Glu Pro Lys Ala Leu Val Tyr Ala Asp
390 395 400AAC ATA TAC ATT GTC CAC TCA AAC ACG TGG TAC TCA ATT GAC CTA GAG 1365Asn Ile Tyr Ile Val His Ser Asn Thr Trp Tyr Ser Ile Asp Leu Glu
405 410 415AAG GGT GAG GCA AAC TGC ACT CGC CAA CAC ATG CAA GCC GCA ATG TAC 1413Lys Gly Glu Ala Asn Cys Thr Arg Gln His Met Gln Ala Ala Met Tyr
420 425 430TAC ATA CTC ACC AGA GGG TGG TCA GAC AAC GGC GAC CCA ATG TTC AAT 1461Tyr Ile Leu Thr Arg Gly Trp Ser Asp Asn Gly Asp Pro Met Phe Asn435 440 445 450CAA ACA TGG GCC ACC TTT GCC ATG AAC ATT GCC CCT GCT CTA GTG GTG 1509Gln Thr Trp Ala Thr Phe Ala Met Asn Ile Ala Pro Ala Leu Val Val
455 460 465GAC TCA TCG TGC CTG ATA ATG AAC CTG CAA ATT AAG ACC TAT GGT CAA 1557Asp Ser Ser Cys Leu Ile Met Asn Leu Gln Ile Lys Thr Tyr Gly Gln
470 475 480GGC AGC GGG AAT GCA GCC ACG TTC ATC AAC AAC CAC CTC TTG AGC ACA 1605Gly Ser Gly Asn Ala Ala Thr Phe Ile Asn Asn His Leu Leu Ser Thr
485 490 495CTA GTG CTT GAC CAG TGG AAC CTG ATG AGA CAG CCC AGA CCA GAC AGC 1653Leu Val Leu Asp Gln Trp Asn Leu Met Arg Gln Pro Arg Pro Asp Ser
500 505 510GAG GAG TTC AAA TCA ATT GAG GAC AAG CTA GGT ATC AAC TTT AAG ATT 1701Glu Glu Phe Lys Ser Ile Glu Asp Lys Leu Gly Ile Asn Phe Lys Ile515 520 525 530GAG AGG TCC ATT GAT GAT ATC AGG GGC AAG CTG AGA CAG CTT GTC CTC 1749Glu Arg Ser Ile Asp Asp Ile Arg Gly Lys Leu Arg Gln Leu Val Leu
535 540 545CTT GCA CAA CCA GGG TAC CTG AGT GGG GGG GTT GAA CCA GAA CAA TCC 1797Leu Ala Gln Pro Gly Tyr Leu Ser Gly Gly Val Glu Pro Glu Gln Ser
550 555 560AGC CCA ACT GTT GAG CTT GAC CTA CTA GGG TGG TCA GCT ACA TAC AGC 1845Ser Pro Thr Val Glu Leu Asp Leu Leu Gly Trp Ser Ala Thr Tyr Ser
565 570 575AAA GAT CTC GGG ATC TAT GTG CCG GTG CTT GAC AAG GAA CGC CTA TTT 1893Lys Asp Leu Gly Ile Tyr Val Pro Val Leu Asp Lys Glu Arg Leu Phe
580 585 590TGT TCT GCT GCG TAT CCC AAG GGA GTA GAG AAC AAG AGT CTC AAG TCC 1941Cys Ser Ala Ala Tyr Pro Lys Gly Val Glu Asn Lys Ser Leu Lys Ser595 600 605 610AAA GTC GGG ATC GAG CAG GCA TAC AAG GTA GTC AGG TAT GAG GCG TTG 1989Lys Val Gly Ile Glu Gln Ala Tyr Lys Val Val Arg Tyr Glu Ala Leu
615 620 625AGG TTG GTA GGT GGT TGG AAC TAC CCA CTC CTG AAC AAA GCC TGC AAG 2037Arg Leu Val Gly Gly Trp Asn Tyr Pro Leu Leu Asn Lys Ala Cys Lys
630 635 640AAT AAC GCA GGC GCC GCT CGG CGG CAT CTG GAG GCC AAG GGG TTC CCA 2085Asn Asn Ala Gly Ala Ala Arg Arg His Leu Glu Ala Lys Gly Phe Pro
645 650 655CTC GAC GAG TTC CTA GCC GAG TGG TCT GAG CTG TCA GAG TTC GGT GAG 2133Leu Asp Glu Phe Leu Ala Glu Trp Ser Glu Leu Ser Glu Phe Gly Glu
660 665 670GCC TTC GAA GGC TTC AAT ATC AAG CTG ACC GTA ACA TCT GAG AGC CTA 2181Ala Phe Glu Gly Phe Asn Ile Lys Leu Thr Val Thr Ser Glu Ser Leu675 680 685 690GCC GAA CTG AAC AAG CCA GTA CCC CCC AAG CCC CCA AAT GTC AAC AGA 2229Ala Glu Leu Asn Lys Pro Val Pro Pro Lys Pro Pro Asn Val Asn Arg
695 700 705CCA GTC AAC ACT GGG GGA CTC AAG GCA GTC AGC AAC GCC CTC AAG ACC 2277Pro Val Asn Thr Gly Gly Leu Lys Ala Val Ser Asn Ala Leu Lys Thr
710 715 720GGT CGG TAC AGG AAC GAA GCC GGA CTG AGT GGT CTC GTC CTT CTA GCC 2325Gly Arg Tyr Arg Asn Glu Ala Gly Leu Ser Gly Leu Val Leu Leu Ala
725 730 735ACA GCA AGA AGC CGT CTG CAA GAT GCA GTT AAG GCC AAG GCA GAA GCC 2373Thr Ala Arg Ser Arg Leu Gln Asp Ala Val Lys Ala Lys Ala Glu Ala
740 745 750GAG AAA CTC CAC AAG TCC AAG CCA GAC GAC CCC GAT GCA GAC TGG TTC 2421Glu Lys Leu His Lys Ser Lys Pro Asp Asp Pro Asp Ala Asp Trp Phe755 760 765 770GAA AGA TCA GAA ACT CTG TCA GAC CTT CTG GAG AAA GCC GAC ATC GCC 2469Glu Arg Ser Glu Thr Leu Ser Asp Leu Leu Glu Lys Ala Asp Ile Ala
775 780 785AGC AAG GTC GCC CAC TCA GCA CTC GTG GAA ACA AGC GAC GCC CTT GAA 2517Ser Lys Val Ala His Ser Ala Leu Val Glu Thr Ser Asp Ala Leu Glu
790 795 800GCA GTT CAG TCG ACT TCC GTG TAC ACC CCC AAG TAC CCA GAA GTC AAG 2565Ala Val Gln Ser Thr Ser Val Tyr Thr Pro Lys Tyr Pro Glu Val Lys
805 810 815AAC CCA CAG ACC GCC TCC AAC CCC GTT GTT GGG CTC CAC CTG CCC GCC 2613Asn Pro Gln Thr Ala Ser Asn Pro Val Val Gly Leu His Leu Pro Ala
820 825 830AAG AGA GCC ACC GGT GTC CAG GCC GCT CTT CTC GGA GCA GGA ACG AGC 2661Lys Arg Ala Thr Gly Val Gln Ala Ala Leu Leu Gly Ala Gly Thr Ser835 840 845 850AGA CCA ATG GGG ATG GAG GCC CCA ACA CGG TCC AAG AAC GCC GTG AAA 2709Arg Pro Met Gly Met Glu Ala Pro Thr Arg Ser Lys Asn Ala Val Lys
855 860 865ATG GCC AAA CGG CGG CAA CGC CAA AAG GAG AGC CGC TAACAGCCAT 2755Met Ala Lys Arg Arg Gln Arg Gln Lys Glu Ser Arg
870 875GATGGGAACC ACTCAAGAAG AGGACACTAA TCCCAGACCC CGTATCCCCG GCCTTCGCCT 2815GCGGGGGCCC CC 2827
(2)SEQ ID NO:26的信息:
(i)序列特征:
(A)长度:878个氨基酸
(B)类型:氨基酸
(D)拓扑结构:线形
(ii)分子类型:蛋白质
(xi)SEQ ID NO:26的序列描述Met Ser Asp Ile Phe Asn Ser Pro Gln Ala Arg Ser Thr Ile Ser Ala1 5 10 15Ala Phe Gly Ile Lys Pro Thr Ala Gly Gln Asp Val Glu Glu Leu Leu
20 25 30Ile Pro Lys Val Trp Val Pro Pro Glu Asp Pro Leu Ala Ser Pro Ser
35 40 45Arg Leu Ala Lys Phe Leu Arg Glu Asn Gly Tyr Lys Val Leu Gln Pro
50 55 60Arg Ser Leu Pro Glu Asn Glu Glu Tyr Glu Thr Asp Gln Ile Leu Pro65 70 75 80Asp Leu Ala Trp Met Arg Gln Ile Glu Gly Ala Val Leu Lys Pro Thr
85 90 95Leu Ser Leu Pro Ile Gly Asp Gln Glu Tyr Phe Pro Lys Tyr Tyr Pro
100 105 110Thr His Arg Pro Ser Lys Glu Lys Pro Asn Ala Tyr Pro Pro Asp Ile
115 120 125Ala Leu Leu Lys Gln Met Ile Tyr Leu Phe Leu Gln Val Pro Glu Ala
130 135 140Asn Glu Gly Leu Lys Asp Glu Val Thr Leu Leu Thr Gln Asn Ile Arg145 150 155 160Asp Lys Ala Tyr Gly Ser Gly Thr Tyr Met Gly Gln Ala Asn Arg Leu
165 170 175Val Ala Met Lys Glu Val Ala Thr Gly Arg Asn Pro Asn Lys Asp Pro
180 185 190Leu Lys Leu Gly Tyr Thr Phe Glu Ser Ile Ala Gln Leu Leu Asp Ile
195 200 205Thr Leu Pro Val Gly Pro Pro Gly Glu Asp Asp Lys Pro Trp Val Pro
210 215 220Leu Thr Arg Val Pro Ser Arg Met Leu Val Leu Thr Gly Asp Val Asp225 230 235 240Gly Asp Phe Glu Val Glu Asp Tyr Leu Pro Lys Ile Asn Leu Lys Ser
245 250 255Ser Ser Gly Leu Pro Tyr Val Gly Arg Thr Lys Gly Glu Thr Ile Gly
260 265 270Glu Met Ile Ala Ile Ser Asn Gln Phe Leu Arg Glu Leu Ser Thr Leu
275 280 285Leu Lys Gln Gly Ala Gly Thr Lys Gly Ser Asn Lys Lys Lys Leu Leu
290 295 300Ser Met Leu Ser Asp Tyr Trp Tyr Leu Ser Cys Gly Leu Leu Phe Pro305 310 315 320Lys Ala Glu Arg Tyr Asp Lys Ser Thr Trp Leu Thr Lys Thr Arg Asn
325 330 335Ile Trp Ser Ala Pro Ser Pro Thr His Leu Met Ile Ser Met Ile Thr
340 345 350Trp Pro Val Met Ser Asn Ser Pro Asn Asn Val Leu Asn Ile Glu Gly
355 360 365Cys Pro Ser Leu Tyr Lys Phe Asn Pro Phe Arg Gly Gly Leu Asn Arg
370 375 380Ile Val Glu Trp Ile Leu Ala Pro Glu Glu Pro Lys Ala Leu Val Tyr385 390 395 400Ala Asp Asn Ile Tyr Ile Val His Ser Asn Thr Trp Tyr Ser Ile Asp
405 410 415Leu Glu Lys Gly Glu Ala Asn Cys Thr Arg Gln His Met Gln Ala Ala
420 425 430Met Tyr Tyr Ile Leu Thr Arg Gly Trp Ser Asp Asn Gly Asp Pro Met
435 440 445Phe Asn Gln Thr Trp Ala Thr Phe Ala Met Asn Ile Ala Pro Ala Leu
450 455 460Val Val Asp Ser Ser Cys Leu Ile Met Asn Leu Gln Ile Lys Thr Tyr465 470 475 480Gly Gln Gly Ser Gly Asn Ala Ala Thr Phe Ile Asn Asn His Leu Leu
485 490 495Ser Thr Leu Val Leu Asp Gln Trp Asn Leu Met Arg Gln Pro Arg Pro
500 505 510Asp Ser Glu Glu Phe Lys Ser Ile Glu Asp Lys Leu Gly Ile Asn Phe
515 520 525Lys Ile Glu Arg Ser Ile Asp Asp Ile Arg Gly Lys Leu Arg Gln Leu
530 535 540Val Leu Leu Ala Gln Pro Gly Tyr Leu Ser Gly Gly Val Glu Pro Glu545 550 555 560Gln Ser Ser Pro Thr Val Glu Leu Asp Leu Leu Gly Trp Ser Ala Thr
565 570 575Tyr Ser Lys Asp Leu Gly Ile Tyr Val Pro Val Leu Asp Lys Glu Arg
580 585 590Leu Phe Cys Ser Ala Ala Tyr Pro Lys Gly Val Glu Asn Lys Ser Leu
595 600 605Lys Ser Lys Val Gly Ile Glu Gln Ala Tyr Lys Val Val Arg Tyr Glu
610 615 620Ala Leu Arg Leu Val Gly Gly Trp Asn Tyr Pro Leu Leu Asn Lys Ala625 630 635 640Cys Lys Asn Asn Ala Gly Ala Ala Arg Arg His Leu Glu Ala Lys Gly
645 650 655Phe Pro Leu Asp Glu Phe Leu Ala Glu Trp Ser Glu Leu Ser Glu Phe
660 665 670Gly Glu Ala Phe Glu Gly Phe Asn Ile Lys Leu Thr Val Thr Ser Glu
675 680 685Ser Leu Ala Glu Leu Asn Lys Pro Val Pro Pro Lys Pro Pro Asn Val
690 695 700Asn Arg Pro Val Asn Thr Gly Gly Leu Lys Ala Val Ser Asn Ala Leu705 710 715 720Lys Thr Gly Arg Tyr Arg Asn Glu Ala Gly Leu Ser Gly Leu Val Leu
725 730 735Leu Ala Thr Ala Arg ser Arg Leu Gln Asp Ala Val Lys Ala Lys Ala
740 745 750Glu Ala Glu Lys Leu His Lys Ser Lys Pro Asp Asp Pro Asp Ala Asp
755 760 765Trp Phe Glu Arg Ser Glu Thr Leu Ser Asp Leu Leu Glu Lys Ala Asp
770 775 780Ile Ala Ser Lys Val Ala His Ser Ala Leu Val Glu Thr Ser Asp Ala785 790 795 800Leu Glu Ala Val Gln Ser Thr Ser Val Tyr Thr Pro Lys Tyr Pro Glu
805 810 815Val Lys Asn Pro Gln Thr Ala Ser Asn Pro Val Val Gly Leu His Leu
820 825 830Pro Ala Lys Arg Ala Thr Gly Val Gln Ala Ala Leu Leu Gly Ala Gly
835 840 845Thr Ser Arg Pro Met Gly Met Glu Ala Pro Thr Arg Ser Lys Asn Ala
850 855 860Val Lys Met Ala Lys Arg Arg Gln Arg Gln Lys Glu Ser Arg865 870 875
(2)SEQ ID NO:27的信息:
(i)序列特征:
(A)长度:3261个碱基对
(B)类型:核酸
(C)链型:单链
(D)拓扑结构:环形
(ii)分子类型:cDNA
(ix)特征
(A)名称/KEY:CDS
(B)位置:97..531
(xi)SEQ ID NO:27的序列描述GGATACGATC GGTCTGACCC CGGGGGAGTC ACCCGGGGAC AGGCCGTCAA GGCCTTGTTC 60CAGGATGGGA CTCCTCCTTC TACAACGCTA TCATTG ATG GTT AGT AGA GAT CAG 114
Met Val Ser Arg Asp Gln
880ACA AAC GAT CGC AGC GAT GAC AAA CCT GCA AGA TCA AAC CCA ACA GAT 162Thr Asn Asp Arg Ser Asp Asp Lys Pro Ala Arg Ser Asn Pro Thr Asp885 890 895 900TGT TCC GTT CAT ACG GAG CCT TCT GAT GCC AAC AAC CGG ACC GGC GTC 210Cys Ser Val His Thr Glu Pro Ser Asp Ala Asn Asn Arg Thr Gly Val
905 910 915CAT TCC GGA CGA CAC CCT GGA GAA GCA CAC TCT CAG GTC AGA GAC CTC 258His Ser Gly Arg His Pro Gly Glu Ala His Ser Gln Val Arg Asp Leu
920 925 930GAC CTA CAA TTT GAC TGT GGG GGA CAC AGG GTC AGG GCT AAT TGT CTT 306Asp Leu Gln Phe Asp Cys Gly Gly His Arg Val Arg Ala Asn Cys Leu
935 940 945TTT CCC TGG ATT CCC TGG CTC AAT TGT GGG TGC TCA CTA CAC ACT GCA 354Phe Pro Trp Ile Pro Trp Leu Asn Cys Gly Cys Ser Leu His Thr Ala
950 955 960GGG CAA TGG GAA CTA CAA GTT CGA TCA GAT GCT CCT GAC TGC CCA GAA 402Gly Gln Trp Glu Leu Gln Val Arg Ser Asp Ala Pro Asp Cys Pro Glu965 970 975 980CCT ACC GGC CAG TTA CAA CTA CTG CAG GCT AGT GAG TCG GAG TCT CAC 450Pro Thr Gly Gln Leu Gln Leu Leu Gln Ala Ser Glu Ser Glu Ser His
985 990 995AGT GAG GTC AAG CAC ACT TCC TGG TGG CGT TTA TGC ACT AAA CGG CAC 498Ser Glu Val Lys His Thr Ser Trp Trp Arg Leu Cys Thr Lys Arg His
1000 1005 1010CAT AAA CGC CGT GAC CTT CCAAGG AAG CCT GAG TGAACTGACA GATGTTAGCT 551His Lys Arg Arg Asp Leu Pro Arg Lys Pro Glu
1015 1020ACAATGGGTT GATGTCTGCA ACAGCCAACA TCAACGACAA AATTGGGAAC GTCCTAGTAG 611GGGAAGGGGT CACCGTCCTC AGCTTACCCA CATCATATGA TCTTGGGTAT GTGAGGCTTG 671GTGACCCCAT TCCCGCAATA GGGCTTGACC CAAAAATGGT AGCCACATGT GACAGCAGTG 731ACAGGCCCAG AGTCTACACC ATAACTGCAG CCGATGATTA CCAATTCTCA TCACAGTACC 791AACCAGGTGG GGTAACAATC ACACTGTTCT CAGCCAACAT TGATGCCATC ACAAGCCTCA 851GCGTTGGGGG AGAGCTCGTG TTTCAAACAA GCGTCCACGG CCTTGTACTG GGCGCCACCA 911TCTACCTCAT AGGCTTTGAT GGGACAACGG TAATCACCAG GGCTGTGGCC GCAAACAATG 971GGCTGACGAC CGGCACCGAC AACCTTATGC CATTCAATCT TGTGATTCCA ACAAACGAGA 1031TAACCCAGCC AATCACATCC ATCAAACTGG AGATAGTGAC CTCCAAAAGT GGTGGTCAGG 1091CAGGGGATCA GATGTCATGG TCGGCAAGAG GGAGCCTAGC AGTGACGATC CATGGTGGCA 1151ACTATCCAGG GGCCCTCCGT CCCGTCACGC TAGTGGCCTA CGAAAGAGTG GCAACAGGAT 1211CCGTCGTTAC GGTCGCTGGG GTGAGCAACT TCGAGCTGAT CCCAAATCCT GAACTAGCAA 1271AGAACCTGGT TACAGAATAC GGCCGATTTG ACCCAGGAGC CATGAACTAC ACAAAATTGA 1331TACTGAGTGA GAGGGACCGT CTTGGCATCA AGACCGTCTG GCCAACAAGG GAGTACACTG 1391ACTTTCGTGA ATACTTCATG GAGGTGGCCG ACCTCAACTC TCCCCTGAAG ATTGCAGGAG 1451CATTCGGCTT CAAAGACATA ATCCGGGCCA TAAGGAGGAT AGCTGTGCCG GTGGTCTCCA 1511CATTGTTCCC ACCTGCCGCT CCCCTAGCCC ATGCAATTGG GGAAGGTGTA GACTACCTGC 1571TGGGCGATGA GGCACAGGCT GCTTCAGGAA CTGCTCGAGC CGCGTCAGGA AAAGCAAGAG 1631CTGCCTCAGG CCGCATAAGG CAGCTGACTC TCGCCGCCGA CAAGGGGTAC GAGGTAGTCG 1691CGAATCTATT CCAGGTGCCC CAGAATCCCG TAGTCGACGG GATTCTTGCT TCACCTGGGG 1751TACTCCGCGG TGCACACAAC CTCGACTGCG TGTTAAGAGA GGGTGCCACG CTATTCCCTG 1811TGGTTATTAC GACAGTGGAA GACGCCATGA CACCCAAAGC ATTGAACAGC AAAATGTTTG 1871CTGTCATTGA AGGCGTGCGA GAAGACCTCC AACCTCCATC TCAAAGAGGA TCCTTCATAC 1931GAACTCTCTC TGGACACAGA GTCTATGGAT ATGCTCCAGA TGGGGTACTT CCACTGGAGA 1991CTGGGAGAGA CTACACCGTT GTCCCAATAG ATGATGTCTG GGACGACAGC ATTATGCTGT 2051CCAAAGATCC CATACCTCCT ATTGTGGGAA ACAGTGGAAA TCTAGCCATA GCTTACATGG 2111ATGTGTTTCG ACCCAAAGTC CCAATCCATG TGGCTATGAC GGGAGCCCTC AATGCTTGTG 2171GCGAGATTGA GAAAGTAAGC TTTAGAAGCA CCAAGCTCGC CACTGCACAC CGACTTGGCC 2231TTAGGTTGGC TGGTCCCGGA GCATTCGATG TAAACACCGG GCCCAACTGG GCAACGTTCA 2291TCAAACGTTT CCCTCACAAT CCACGCGACT GGGACAGGCT CCCCTACCTC AACCTACCAT 2351ACCTTCCACC CAATGCAGGA CGCCAGTACC ACCTTGCCAT GGCTGCATCA GAGTTCAAAG 2411AGACCCCCGA ACTCGAGAGT GCCGTCAGAG CAATGGAAGC AGCAGCCAAC GTGGACCCAC 2471TATTCCAATC TGCACTCAGT GTGTTCATGT GGCTGGAAGA GAATGGGATT GTGACTGACA 2531TGGCCAACTT CGCACTCAGC GACCCGAACG CCCATCGGAT GCGAAATTTT CTTGCAAACG 2591CACCACAAGC AGGCAGCAAG TCGCAAAGGG CCAAGTACGG GACAGCAGGC TACGGAGTGG 2651AGGCTCGGGG CCCCACACCA GAGGAAGCAC AGAGGGAAAA AGACACACGG ATCTCAAAGA 2711AGATGGAGAC CATGGGCATC TACTTTGCAA CACCAGAATG GGTAGCACTC AATGGGCACC 2771GAGGGCCAAG CCCCGGCCAG CTAAAGTACT GGCAGAACAC ACGAGAAATA CCGGACCCAA 2831ACGAGGACTA TCTAGACTAC GTGCATGCAG AGAAGAGCCG GTTGGCATCA GAAGAACAAA 2891TCCTAAGGGC AGCTACGTCG ATCTACGGGG CTCCAGGACA GGCAGAGCCA CCCCAAGCTT 2951TCATAGACGA AGTTGCCAAA GTCTATGAAA TCAACCATGG ACGTGGCCCA AACCAAGAAC 3011AGATGAAAGA TCTGCTCTTG ACTGCGATGG AGATGAAGCA TCGCAATCCC AGGCGGGCTC 3071TACCAAAGCC CAAGCCAAAA CCCAATGCTC CAACACAGAG ACCCCCTGGT CGGCTGGGCC 3131GCTGGATCAG GACCGTCTCT GATGAGGACC TTGAGTGAGG CTCCTGGGAG TCTCCCGACA 3191CCACCCGCGC AGGTGTGGAC ACCAATTCGG CCTTACAACA TCCCAAATTG GATCCGTTCG 3251CGGGTCCCCT 3261
(2)SEQ ID NO:28的信息:
(i)序列特征:
(A)长度:145氨基酸
(B)类型:氨基酸
(D)拓扑结构:线形
(ii)分子类型:蛋白质
(xi)SEQ ID NO:28的序列描述Met Val Ser Arg Asp Gln Thr Asn Asp Arg Ser Asp Asp Lys Pro Ala1 5 10 15Arg Ser Asn Pro Thr Asp Cys Ser Val His Thr Glu Pro Ser Asp Ala
20 25 30Asn Asn Arg Thr Gly Val His Ser Gly Arg His Pro Gly Glu Ala His
35 40 45Ser Gln Val Arg Asp Leu Asp Leu Gin Phe Asp Cys Gly Gly His Arg
50 55 60Val Arg Ala Asn Cys Leu Phe Pro Trp Ile Pro Trp Leu Asn Cys Gly65 70 75 80Cys Ser Leu His Thr Ala Gly Gln Trp Glu Leu Gln Val Arg Ser Asp
85 90 95Ala Pro Asp Cys Pro Glu Pro Thr Gly Gln Leu Gln Leu Leu Gln Ala
100 105 110Ser Glu Ser Glu Ser His Ser Glu Val Lys His Thr Ser Trp Trp Arg
115 120 125Leu Cys Thr Lys Arg His His Lys Arg Arg Asp Leu Pro Arg Lys Pro
130 135 140Glu145
(2)SEQ ID NO:29的信息:
(i)序列特征:
(A)长度:3261个碱基对
(B)类型:核酸
(C)链型:单链
(D)拓扑结构:环形
(ii)分子类型:cDNA
(ix)特征:
(A)名称/KEY:CDS
(B)位置:131..3166
(xi)SEQ ID NO:29的序列描述GGATACGATC GGTCTGACCC CGGGGGAGTC ACCCGGGGAC AGGCCGTCAA GGCCTTGTTC 60CAGGATGGGA CTCCTCCTTC TACAACGCTA TCATTGATGG TTAGTAGAGA TCAGACAAAC 120GATCGCAGCG ATG ACA AAC CTG CAA GAT CAA ACC CAA CAG ATT GTT CCG 169
Met Thr Asn Leu Gln Asp Gln Thr Gln Gln Ile Val Pro
150 155TTC ATA CGG AGC CTT CTG ATG CCA ACA ACC GGA CCG GCG TCC ATT CCG 217Phe Ile Arg Ser Leu Leu Met Pro Thr Thr Gly Pro Ala Ser Ile Pro
160 165 170GAC GAC ACC CTG GAG AAG CAC ACT CTC AGG TCA GAG ACC TCG ACC TAC 265Asp Asp Thr Leu Glu Lys His Thr Leu Arg Ser Glu Thr Ser Thr Tyr175 180 185 190AAT TTG ACT GTG GGG GAC ACA GGG TCA GGG CTA ATT GTC TTT TTC CCT 313Asn Leu Thr Val Gly Asp Thr Gly Ser Gly Leu Ile Val Phe Phe Pro
195 200 205GGA TTC CCT GGC TCA ATT GTG GGT GCT CAC TAC ACA CTG CAG GGC AAT 361Gly Phe Pro Gly Ser Ile Val Gly Ala His Tyr Thr Leu Gln Gly Asn
210 215 220GGG AAC TAC AAG TTC GAT CAG ATG CTC CTG ACT GCC CAG AAC CTA CCG 409Gly Asn Tyr Lys Phe Asp Gln Met Leu Leu Thr Ala Gln Asn Leu Pro
225 230 235GCC AGT TAC AAC TAC TGC AGG CTA GTG AGT CGG AGT CTC ACA GTG AGG 457Ala Ser Tyr Asn Tyr Cys Arg Leu Val Ser Arg Ser Leu Thr Val Arg
240 245 250TCA AGC ACA CTT CCT GGT GGC GTT TAT GCA CTA AAC GGC ACC ATA AAC 505Ser Ser Thr Leu Pro Gly Gly Val Tyr Ala Leu Asn Gly Thr Ile Asn255 260 265 270GCC GTG ACC TTC CAA GGA AGC CTG AGT GAA CTG ACA GAT GTT AGC TAC 553Ala Val Thr Phe Gln Gly Ser Leu Ser Glu Leu Thr Asp Val Ser Tyr
275 280 285AAT GGG TTG ATG TCT GCA ACA GCC AAC ATC AAC GAC AAA ATT GGG AAC 601Asn Gly Leu Met Ser Ala Thr Ala Asn Ile Asn Asp Lys Ile Gly Asn
290 295 300GTC CTA GTA GGG GAA GGG GTC ACC GTC CTC AGC TTA CCC ACA TCA TAT 649Val Leu Val Gly Glu Gly Val Thr Val Leu Ser Leu Pro Thr Ser Tyr
305 310 315GAT CTT GGG TAT GTG AGG CTT GGT GAC CCC ATT CCC GCA ATA GGG CTT 697Asp Leu Gly Tyr Val Arg Leu Gly Asp Pro Ile Pro Ala Ile Gly Leu
320 325 330GAC CCA AAA ATG GTA GCC ACA TGT GAC AGC AGT GAC AGG CCC AGA GTC 745Asp Pro Lys Met Val Ala Thr Cys Asp Ser Ser Asp Arg Pro Arg Val335 340 345 350TAC ACC ATA ACT GCA GCC GAT GAT TAC CAA TTC TCA TCA CAG TAC CAA 793Tyr Thr Ile Thr Ala Ala Asp Asp Tyr Gln Phe Ser Ser Gln Tyr Gln
355 360 365CCA GGT GGG GTA ACA ATC ACA CTG TTC TCA GCC AAC ATT GAT GCC ATC 841Pro Gly Gly Val Thr Ile Thr Leu Phe Ser Ala Asn Ile Asp Ala Ile
370 375 380ACA AGC CTC AGC GTT GGG GGA GAG CTC GTG TTT CAA ACA AGC GTC CAC 889Thr Ser Leu Ser Val Gly Gly Glu Leu Val Phe Gln Thr Ser Val His
385 390 395GGC CTT GTA CTG GGC GCC ACC ATC TAC CTC ATA GGC TTT GAT GGG ACA 937Gly Leu Val Leu Gly Ala Thr Ile Tyr Leu Ile Gly Phe Asp Gly Thr
400 405 410ACG GTA ATC ACC AGG GCT GTG GCC GCA AAC AAT GGG CTG ACG ACC GGC 985Thr Val Ile Thr Arg Ala Val Ala Ala Asn Asn Gly Leu Thr Thr Gly415 420 425 430ACC GAC AAC CTT ATG CCA TTC AAT CTT GTG ATT CCA ACA AAC GAG ATA 1033Thr Asp Asn Leu Met Pro Phe Asn Leu Val Ile Pro Thr Asn Glu Ile
435 440 445ACC CAG CCA ATC ACA TCC ATC AAA CTG GAG ATA GTG ACC TCC AAA AGT 1081Thr Gln Pro Ile Thr Ser Ile Lys Leu Glu Ile Val Thr Ser Lys Ser
450 455 460GGT GGT CAG GCA GGG GAT CAG ATG TCA TGG TCG GCA AGA GGG AGC CTA 1129Gly Gly Gln Ala Gly Asp Gln Met Ser Trp Ser Ala Arg Gly Ser Leu
465 470 475GCA GTG ACG ATC CAT GGT GGC AAC TAT CCA GGG GCC CTC CGT CCC GTC 1177Ala Val Thr Ile His Gly Gly Asn Tyr Pro Gly Ala Leu Arg Pro Val
480 485 490ACG CTA GTG GCC TAC GAA AGA GTG GCA ACA GGA TCC GTC GTT ACG GTC 1225Thr Leu Val Ala Tyr Glu Arg Val Ala Thr Gly Ser Val Val Thr Val495 500 505 510GCT GGG GTG AGC AAC TTC GAG CTG ATC CCA AAT CCT GAA CTA GCA AAG 1273Ala Gly Val Ser Asn Phe Glu Leu Ile Pro Asn Pro Glu Leu Ala Lys
515 520 525AAC CTG GTT ACA GAA TAC GGC CGA TTT GAC CCA GGA GCC ATG AAC TAC 1321Asn Leu Val Thr Glu Tyr Gly Arg Phe Asp Pro Gly Ala Met Asn Tyr
530 535 540ACA AAA TTG ATA CTG AGT GAG AGG GAC CGT CTT GGC ATC AAG ACC GTC 1369Thr Lys Leu Ile Leu Ser Glu Arg Asp Arg Leu Gly Ile Lys Thr Val
545 550 555TGG CCA ACA AGG GAG TAC ACT GAC TTT CGT GAA TAC TTC ATG GAG GTG 1417Trp Pro Thr Arg Glu Tyr Thr Asp Phe Arg Glu Tyr Phe Met Glu Val
560 565 570GCC GAC CTC AAC TCT CCC CTG AAG ATT GCA GGA GCA TTC GGC TTC AAA 1465Ala Asp Leu Asn Ser Pro Leu Lys Ile Ala Gly Ala Phe Gly Phe Lys575 580 585 590GAC ATA ATC CGG GCC ATA AGG AGG ATA GCT GTG CCG GTG GTC TCC ACA 1513Asp Ile Ile Arg Ala Ile Arg Arg Ile Ala Val Pro Val Val Ser Thr
595 600 605TTG TTC CCA CCT GCC GCT CCC CTA GCC CAT GCA ATT GGG GAA GGT GTA 1561Leu Phe Pro Pro Ala Ala Pro Leu Ala His Ala Ile Gly Glu Gly Val
610 615 620GAC TAC CTG CTG GGC GAT GAG GCA CAG GCT GCT TCA GGA ACT GCT CGA 1609Asp Tyr Leu Leu Gly Asp Glu Ala Gln Ala Ala Ser Gly Thr Ala Arg
625 630 635GCC GCG TCA GGA AAA GCA AGA GCT GCC TCA GGC CGC ATA AGG CAG CTG 1657Ala Ala Ser Gly Lys Ala Arg Ala Ala Ser Gly Arg Ile Arg Gln Leu
640 645 650ACT CTC GCC GCC GAC AAG GGG TAC GAG GTA GTC GCG AAT CTA TTC CAG 1705Thr Leu Ala Ala Asp Lys Gly Tyr Glu Val Val Ala Asn Leu Phe Gln655 660 665 670GTG CCC CAG AAT CCC GTA GTC GAC GGG ATT CTT GCT TCA CCT GGG GTA 1753Val Pro Gln Asn Pro Val Val Asp Gly Ile Leu Ala Ser Pro Gly Val
675 680 685CTC CGC GGT GCA CAC AAC CTC GAC TGC GTG TTA AGA GAG GGT GCC ACG 1801Leu Arg Gly Ala His Asn Leu Asp Cys Val Leu Arg Glu Gly Ala Thr
690 695 700CTA TTC CCT GTG GTT ATT ACG ACA GTG GAA GAC GCC ATG ACA CCC AAA 1849Leu Phe Pro Val Val Ile Thr Thr Val Glu Asp Ala Met Thr Pro Lys
705 710 715GCA TTG AAC AGC AAA ATG TTT GCT GTC ATT GAA GGC GTG CGA GAA GAC 1897Ala Leu Asn Ser Lys Met Phe Ala Val Ile Glu Gly Val Arg Glu Asp
720 725 730CTC CAA CCT CCA TCT CAA AGA GGA TCC TTC ATA CGA ACT CTC TCT GGA 1945Leu Gln Pro Pro Ser Gln Arg Gly Ser Phe Ile Arg Thr Leu Ser Gly735 740 745 750CAC AGA GTC TAT GGA TAT GCT CCA GAT GGG GTA CTT CCA CTG GAG ACT 1993His Arg Val Tyr Gly Tyr Ala Pro Asp Gly Val Leu Pro Leu Glu Thr
755 760 765GGG AGA GAC TAC ACC GTT GTC CCA ATA GAT GAT GTC TGG GAC GAC AGC 2041Gly Arg Asp Tyr Thr Val Val Pro Ile Asp Asp Val Trp Asp Asp Ser
770 775 780ATT ATG CTG TCC AAA GAT CCC ATA CCT CCT ATT GTG GGA AAC AGT GGA 2089Ile Met Leu Ser Lys Asp Pro Ile Pro Pro Ile Val Gly Asn Ser Gly
785 790 795AAT CTA GCC ATA GCT TAC ATG GAT GTG TTT CGA CCC AAA GTC CCA ATC 2137Asn Leu Ala Ile Ala Tyr Met Asp Val Phe Arg Pro Lys Val Pro Ile
800 805 810CAT GTG GCT ATG ACG GGA GCC CTC AAT GCT TGT GGC GAG ATT GAG AAA 2185His Val Ala Met Thr Gly Ala Leu Asn Ala Cys Gly Glu Ile Glu Lys815 820 825 830GTA AGC TTT AGA AGC ACC AAG CTC GCC ACT GCA CAC CGA CTT GGC CTT 2233Val Ser Phe Arg Ser Thr Lys Leu Ala Thr Ala His Arg Leu Gly Leu
835 840 845AGG TTG GCT GGT CCC GGA GCA TTC GAT GTA AAC ACC GGG CCC AAC TGG 2281Arg Leu Ala Gly Pro Gly Ala Phe Asp Val Asn Thr Gly Pro Asn Trp
850 855 860GCA ACG TTC ATC AAA CGT TTC CCT CAC AAT CCA CGC GAC TGG GAC AGG 2329Ala Thr Phe Ile Lys Arg Phe Pro His Asn Pro Arg Asp Trp Asp Arg
865 870 875CTC CCC TAC CTC AAC CTA CCA TAC CTT CCA CCC AAT GCA GGA CGC CAG 2377Leu Pro Tyr Leu Asn Leu Pro Tyr Leu Pro Pro Asn Ala Gly Arg Gln
880 885 890TAC CAC CTT GCC ATG GCT GCA TCA GAG TTC AAA GAG ACC CCC GAA CTC 2425Tyr His Leu Ala Met Ala Ala Ser Glu Phe Lys Glu Thr Pro Glu Leu895 900 905 910GAG AGT GCC GTC AGA GCA ATG GAA GCA GCA GCC AAC GTG GAC CCA CTA 2473Glu Ser Ala Val Arg Ala Met Glu Ala Ala Ala Asn Val Asp Pro Leu
915 920 925TTC CAA TCT GCA CTC AGT GTG TTC ATG TGG CTG GAA GAG AAT GGG ATT 2521Phe Gln Ser Ala Leu Ser Val Phe Met Trp Leu Glu Glu Asn Gly Ile
930 935 940GTG ACT GAC ATG GCC AAC TTC GCA CTC AGC GAC CCG AAC GCC CAT CGG 2569Val Thr Asp Met Ala Asn Phe Ala Leu Ser Asp Pro Asn Ala His Arg
945 950 955ATG CGA AAT TTT CTT GCA AAC GCA CCA CAA GCA GGC AGC AAG TCG CAA 2617Met Arg Asn Phe Leu Ala Asn Ala Pro Gln Ala Gly Ser Lys Ser Gln
960 965 970AGG GCC AAG TAC GGG ACA GCA GGC TAC GGA GTG GAG GCT CGG GGC CCC 2665Arg Ala Lys Tyr Gly Thr Ala Gly Tyr Gly Val Glu Ala Arg Gly Pro975 980 985 990ACA CCA GAG GAA GCA CAG AGG GAA AAA GAC ACA CGG ATC TCA AAG AAG 2713Thr Pro Glu Glu Ala Gln Arg Glu Lys Asp Thr Arg Ile Ser Lys Lys
995 1000 1005ATG GAG ACC ATG GGC ATC TAC TTT GCA ACA CCA GAA TGG GTA GCA CTC 2761Met Glu Thr Met Gly Ile Tyr Phe Ala Thr Pro Glu Trp Val Ala Leu
1010 1015 1020AAT GGG CAC CGA GGG CCA AGC CCC GGC CAG CTA AAG TAC TGG CAG AAC 2809Asn Gly His Arg Gly Pro Ser Pro Gly Gln Leu Lys Tyr Trp Gln Asn
1025 1030 1035ACA CGA GAA ATA CCG GAC CCA AAC GAG GAC TAT CTA GAC TAC GTG CAT 2857Thr Arg Glu Ile Pro Asp Pro Asn Glu Asp Tyr Leu Asp Tyr Val His
1040 1045 1050GCA GAG AAG AGC CGG TTG GCA TCA GAA GAA CAA ATC CTA AGG GCA GCT 2905Ala Glu Lys Ser Arg Leu Ala Ser Glu Glu Gln Ile Leu Arg Ala Ala1055 1060 1065 1070ACG TCG ATC TAC GGG GCT CCA GGA CAG GCA GAG CCA CCC CAA GCT TTC 2953Thr Ser Ile Tyr Gly Ala Pro Gly Gln Ala Glu Pro Pro Gln Ala Phe
1075 1080 1085ATA GAC GAA GTT GCC AAA GTC TAT GAA ATC AAC CAT GGA CGT GGC CCA 3001Ile Asp Glu Val Ala Lys Val Tyr Glu Ile Asn His Gly Arg Gly Pro
1090 1095 1100AAC CAA GAA CAG ATG AAA GAT CTG CTC TTG ACT GCG ATG GAG ATG AAG 3049Asn Gln Glu Gln Met Lys Asp Leu Leu Leu Thr Ala Met Glu Met Lys
1105 1110 1115CAT CGC AAT CCC AGG CGG GCT CTA CCA AAG CCC AAG CCA AAA CCC AAT 3097His Arg Asn Pro Arg Arg Ala Leu Pro Lys Pro Lys Pro Lys pro Asn
1120 1125 1130GCT CCA ACA CAG AGA CCC CCT GGT CGG CTG GGC CGC TGG ATC AGG ACC 3145Ala Pro Thr Gln Arg Pro Pro Gly Arg Leu Gly Arg Trp Ile Arg Thr1135 1140 1145 1150GTC TCT GAT GAG GAC CTT GAG TGAGGCTCCT GGGAGTCTCC CGACACCACC 3196Val Ser Asp Glu Asp Leu Glu
1155CGCGCAGGTG TGGACACCAA TTCGGCCTTA CAACATCCCA AATTGGATCC GTTCGCGGGT 3256CCCCT 3261
(2)SEQ ID NO:30的信息:
(i)序列特征:
(A)长度:1012个氨基酸
(B)类型:氨基酸
(D)拓扑结构:线形
(ii)分子类型:蛋白质
(xi)SEQ ID NO:30的序列描述Met Thr Asn Leu Gln Asp Gln Thr Gln Gln Ile Val Pro Phe Ile Arg1 5 10 15Ser Leu Leu Met Pro Thr Thr Gly Pro Ala Ser Ile Pro Asp Asp Thr
20 25 30Leu Glu Lys His Thr Leu Arg Ser Glu Thr Ser Thr Tyr Asn Leu Thr
35 40 45Val Gly Asp Thr Gly Ser Gly Leu Ile Val Phe Phe Pro Gly Phe Pro
50 55 60Gly Ser Ile Val Gly Ala His Tyr Thr Leu Gln Gly Asn Gly Asn Tyr65 70 75 80Lys Phe Asp Gln Met Leu Leu Thr Ala Gln Asn Leu Pro Ala Ser Tyr
85 90 95Asn Tyr Cys Arg Leu Val Ser Arg Ser Leu Thr Val Arg Ser Ser Thr
100 105 110Leu Pro Gly Gly Val Tyr Ala Leu Asn Gly Thr Ile Asn Ala Val Thr
115 120 125Phe Gln Gly Ser Leu Ser Glu Leu Thr Asp Val Ser Tyr Asn Gly Leu
130 135 140Met Ser Ala Thr Ala Asn Ile Asn Asp Lys Ile Gly Asn Val Leu Val145 150 155 160Gly Glu Gly Val Thr Val Leu Ser Leu Pro Thr Ser Tyr Asp Leu Gly
165 170 175Tyr Val Arg Leu Gly Asp Pro Ile Pro Ala Ile Gly Leu Asp Pro Lys
180 185 190Met Val Ala Thr Cys Asp Ser Ser Asp Arg Pro Arg Val Tyr Thr Ile
195 200 205Thr Ala Ala Asp Asp Tyr Gln Phe Ser Ser Gln Tyr Gln Pro Gly Gly
210 215 220Val Thr Ile Thr Leu Phe Ser Ala Asn Ile Asp Ala Ile Thr Ser Leu225 230 235 240Ser Val Gly Gly Glu Leu Val Phe Gln Thr Ser Val His Gly Leu Val
245 250 255Leu Gly Ala Thr Ile Tyr Leu Ile Gly Phe Asp Gly Thr Thr Val Ile
260 265 270Thr Arg Ala Val Ala Ala Asn Asn Gly Leu Thr Thr Gly Thr Asp Asn
275 280 285Leu Met Pro Phe Asn Leu Val Ile Pro Thr Asn Glu Ile Thr Gln Pro
290 295 300Ile Thr Ser Ile Lys Leu Glu Ile Val Thr Ser Lys Ser Gly Gly Gln305 310 315 320Ala Gly Asp Gln Met Ser Trp Ser Ala Arg Gly Ser Leu Ala Val Thr
325 330 335Ile His Gly Gly Asn Tyr Pro Gly Ala Leu Arg Pro Val Thr Leu Val
340 345 350Ala Tyr Glu Arg Val Ala Thr Gly Ser Val Val Thr Val Ala Gly Val
355 360 365Ser Asn Phe Glu Leu Ile Pro Asn Pro Glu Leu Ala Lys Asn Leu Val
370 375 380Thr Glu Tyr Gly Arg Phe Asp Pro Gly Ala Met Asn Tyr Thr Lys Leu385 390 395 400Ile Leu Ser Glu Arg Asp Arg Leu Gly Ile Lys Thr Val Trp Pro Thr
405 410 415Arg Glu Tyr Thr Asp Phe Arg Glu Tyr Phe Met Glu Val Ala Asp Leu
420 425 430Asn Ser Pro Leu Lys Ile Ala Gly Ala Phe Gly Phe Lys Asp Ile Ile
435 440 445Arg Ala Ile Arg Arg Ile Ala Val Pro Val Val Ser Thr Leu Phe Pro
450 455 460Pro Ala Ala Pro Leu Ala His Ala Ile Gly Glu Gly Val Asp Tyr Leu465 470 475 480Leu Gly Asp Glu Ala Gln Ala Ala Ser Gly Thr Ala Arg Ala Ala Ser
485 490 495Gly Lys Ala Arg Ala Ala Ser Gly Arg Ile Arg Gln Leu Thr Leu Ala
500 505 510Ala Asp Lys Gly Tyr Glu Val Val Ala Asn Leu Phe Gln Val Pro Gln
515 520 525Asn Pro Val Val Asp Gly Ile Leu Ala Ser Pro Gly Val Leu Arg Gly
530 535 540Ala His Asn Leu Asp Cys Val Leu Arg Glu Gly Ala Thr Leu Phe Pro545 550 555 560Val Val Ile Thr Thr Val Glu Asp Ala Met Thr Pro Lys Ala Leu Asn
565 570 575Ser Lys Met Phe Ala Val Ile Glu Gly Val Arg Glu Asp Leu Gln Pro
580 585 590Pro Ser Gln Arg Gly Ser Phe Ile Arg Thr Leu Ser Gly His Arg Val
595 600 605Tyr Gly Tyr Ala Pro Asp Gly Val Leu Pro Leu Glu Thr Gly Arg Asp
610 615 620Tyr Thr Val Val Pro Ile Asp Asp Val Trp Asp Asp Ser Ile Met Leu625 630 635 640Ser Lys Asp Pro Ile Pro Pro Ile Val Gly Asn Ser Gly Asn Leu Ala
645 650 655Ile Ala Tyr Met Asp Val Phe Arg Pro Lys Val Pro Ile His Val Ala
660 665 670Met Thr Gly Ala Leu Asn Ala Cys Gly Glu Ile Glu Lys Val Ser Phe
675 680 685Arg Ser Thr Lys Leu Ala Thr Ala His Arg Leu Gly Leu Arg Leu Ala
690 695 700Gly Pro Gly Ala Phe Asp Val Asn Thr Gly Pro Asn Trp Ala Thr Phe705 710 715 720Ile Lys Arg Phe Pro His Asn Pro Arg Asp Trp Asp Arg Leu Pro Tyr
725 730 735Leu Asn Leu Pro Tyr Leu Pro Pro Asn Ala Gly Arg Gln Tyr His Leu
740 745 750Ala Met Ala Ala Ser Glu Phe Lys Glu Thr Pro Glu Leu Glu Ser Ala
755 760 765Val Arg Ala Met Glu Ala Ala Ala Asn Val Asp Pro Leu Phe Gln Ser
770 775 780Ala Leu Ser Val Phe Met Trp Leu Glu Glu Asn Gly Ile Val Thr Asp785 790 795 800Met Ala Asn Phe Ala Leu Ser Asp Pro Asn Ala His Arg Met Arg Asn
805 810 815Phe Leu Ala Asn Ala Pro Gln Ala Gly Ser Lys Ser Gln Arg Ala Lys
820 825 830Tyr Gly Thr Ala Gly Tyr Gly Val Glu Ala Arg Gly Pro Thr Pro Glu
835 840 845Glu Ala Gln Arg Glu Lys Asp Thr Arg Ile Ser Lys Lys Met Glu Thr
850 855 860Met Gly Ile Tyr Phe Ala Thr Pro Glu Trp Val Ala Leu Asn Gly His865 870 875 880Arg Gly Pro Ser Pro Gly Gln Leu Lys Tyr Trp Gln Asn Thr Arg Glu
885 890 895Ile Pro Asp Pro Asn Glu Asp Tyr Leu Asp Tyr Val His Ala Glu Lys
900 905 910Ser Arg Leu Ala Ser Glu Glu Gln Ile Leu Arg Ala Ala Thr Ser Ile
915 920 925Tyr Gly Ala Pro Gly Gln Ala Glu Pro Pro Gln Ala Phe Ile Asp Glu
930 935 940Val Ala Lys Val Tyr Glu Ile Asn His Gly Arg Gly Pro Asn Gln Glu945 950 955 960Gln Met Lys Asp Leu Leu Leu Thr Ala Met Glu Met Lys His Arg Asn
965 970 975Pro Arg Arg Ala Leu Pro Lys Pro Lys Pro Lys Pro Asn Ala Pro Thr
980 985 990Gln Arg Pro Pro Gly Arg Leu Gly Arg Trp Ile Arg Thr Val Ser Asp
995 1000 1005Glu Asp Leu Glu
1010
(2)SEQ ID NO:31的信息:
(i)序列特征:
(A)长度:3264个碱基对
(B)类型:核酸
(C)链型:单链
(D)拓扑结构:环形
(ii)分子类型:cDNA
(ix)特征:
(A)名称/KEY:CDS
(B)位置:97..531
(xi)SEQ ID NO:31的序列描述GGATACGATC GGTCTGACCC CGGGGGAGTC ACCCGGGGAC AGGCCATCAC TGCCTTGTTC 60CTGGTTGGAA CTCCTCTTTC TGCTGTACTA TCGTTG ATG GTG AGT AGA GAT CAG 114
Met Val Ser Arg Asp Gln
1015ACA AAC GAT CGC AGC GAT GAC AAA CCT GAT GGA TCA CAC CCA ACA GAT 162Thr Asn Asp Arg Ser Asp Asp Lys Pro Asp Gly Ser His Pro Thr Asp
1020 1025 1030TGT TCC GTT CAT ACG GAG CCT TCT GAT GCC AAC GAC CGG ACC GGC GTC 210Cys Ser Val His Thr Glu Pro Ser Asp Ala Asn Asp Arg Thr Gly Val1035 1040 1045 1050CAT TCC GGA CGA CAC CCT GGA GAA GCA CAC ACT CAG GTC CGA AAC CTC 258His Ser Gly Arg His Pro Gly Glu Ala His Thr Gln Val Arg Asn Leu
1055 1060 1065GAC TTA CAA CTT GAC TGT AGG GGA TAC AGG GTC AGG ACT AAT TGT CTT 306Asp Leu Gln Leu Asp Cys Arg Gly Tyr Arg Val Arg Thr Asn Cys Leu
1070 1075 1080TTT CCC TGG ATT CCC TGG TTC AGT TGT AGG TGC TCA CTA CAC ACT GCA 354Phe Pro Trp Ile Pro Trp Phe Ser Cys Arg Cys Ser Leu His Thr Ala
1085 1090 1095GAG CAG TGG GAA CTA CCA ATT CGA CCA GAT GCT CCT GAC AGC GCA GAA 402Glu Gln Trp Glu Leu Pro Ile Arg Pro Asp Ala Pro Asp Ser Ala Glu
1100 1105 1110CCT GCC TGC CAG CTA CAA CTA CTG CAG GCT AGT GAG CAG GAG TCT AAC 450Pro Ala Cys Gln Leu Gln Leu Leu Gln Ala Ser Glu Gln Glu Ser Asn1115 1120 1125 1130CGT ACG GTC AAG CAC ACT CCC TGG TGG CGT TTA TGC ACT AAA CGG AAC 498Arg Thr Val Lys His Thr Pro Trp Trp Arg Leu Cys Thr Lys Arg Asn
1135 1140 1145CAT AAA CGC AGT GAC CTT CCA CGG AAG CCT GAG TGAGTTGACT GACTACAGCT 551His Lys Arg Ser Asp Leu Pro Arg Lys Pro Glu
1150 1155ACAACGGGCT GATGTCAGCC ACTGCGAACA TCAACGACAA GATCGGGAAC GTTCTAGTTG 611GAGAAGGGGT GACTGTTCTC AGTCTACCGA CTTCATATGA CCTTAGTTAT GTGAGACTCG 671GTGACCCCAT CCCCGCAGCA GGACTCGACC CGAAGTTGAT GGCCACGTGC GACAGTAGTG 731ACAGACCCAG AGTCTACACC ATAACAGCTG CAGATGAATA CCAATTCTCG TCACAACTCA 791TCCCGAGTGG CGTGAAGACC ACACTGTTCT CCGCCAACAT CGATGCTCTC ACCAGCTTCA 851GCGTTGGTGG TGAGCTTGTC TTCAGCCAAG TAACGATCCA AAGCATTGAA GTGGACGTCA 911CCATTCACTT CATTGGGTTT GACGGGACAG ACGTAGCAGT CAAGGCAGTT GCAACAGACT 971TTGGGCTGAC AACTGGGACA AACAACCTTG TGCCATTCAA CCTGGTGGTC CCAACAAATG 1031AGATCACCCA GCCCATCACT TCCATGAAAC TAGAGGTTGT GACCTACAAG ATTGGCGGCA 1091CCGCTGGTGA CCCAATATCA TGGACAGTGA GTGGTACACT AGCTGTGACG GTGCACGGAG 1151GCAACTACCC TGGGGCTCTC CGTCCTGTCA CCCTGGTGGC CTATGAACGA GTGGCTGCAG 1211GATCTGTTGT CACAGTTGCA GGGGTGAGCA ACTTCGAGCT AATCCCCAAC CCTGAGCTTG 1271CAAAGAACCT AGTTACAGAG TATGGCCGCT TTGACCCCGG AGCAATGAAC TACACCAAAC 1331TAATACTGAG TGAGAGAGAT CGTCTAGGCA TCAAGACAGT CTGGCCCACC AGGGAGTACA 1391CCGATTTCAG GGAGTACTTC ATGGAGGTTG CAGATCTCAA CTCACCCCTA AAGATTGCAG 1451GAGCATTTGG CTTTAAGGAC ATAATCCGAG CCATTCGGAA GATTGCGGTG CCAGTGGTAT 1511CCACACTCTT CCCTCCAGCT GCACCCCTAG CACATGCAAT CGGAGAAGGT GTAGACTACC 1571TCCTGGGCGA CGAGGCCCAA GCAGCCTCAG GGACAGCTCG AGCCGCGTCA GGAAAAGCTA 1631GAGCTGCCTC AGGACGAATA AGGCAGCTAA CTCTCGCAGC TGACAAGGGG TGCGAGGTAG 1691TCGCCAACAT GTTCCAGGTG CCCCAGAATC CCATTGTTGA TGGCATTCTG GCATCCCCAG 1751GAATCCTGCG TGGCGCACAC AACCTCGACT GCGTGCTATG GGAGGGAGCC ACTCTTTTCC 1811CTGTTGTCAT TACGACACTC GAGGATGAGC TGACCCCCAA GGCACTGAAC AGCAAAATGT 1871TTGCTGTCAT TGAAGGTGTG CGAGAGGACC TCCAGCCTCC ATCCCAACGG GGATCCTTCA 1931TTCGAACTCT CTCTGGCCAT AGAGTCTATG GCTATGCCCC AGACGGAGTA CTGCCTCTGG 1991AGACCGGGAG AGACTACACC GTTGTCCCAA TTGATGATGT GTGGGACGAT AGCATAATGC 2051TGTCGCAGGA CCCCATACCT CCAATCATAG GGAACAGCGG CAACCTAGCC ATAGCATACA 2111TGGATGTCTT CAGGCCCAAG GTCCCCATCC ACGTGGCTAT GACAGGGGCC CTCAATGCCC 2171GCGGTGAGAT CGAGAGTGTT ACGTTCCGCA GCACCAAACT CGCCACAGCC CACCGACTTG 2231GCATGAAGTT AGCTGGTCCT GGAGCCTATG ACATTAATAC AGGACCTAAC TGGGCAACGT 2291TCGTCAAACG TTTCCCTCAC AATCCCCGAG ACTGGGACAG GTTGCCCTAC CTCAACCTTC 2351CTTATCTCCC ACCAACAGCA GGACGTCAGT TCCATCTAGC CCTGGCTGCC TCCGAGTTCA 2411AAGAGACCCC AGAACTCGAA GACGCTGTGC GCGCAATGGA TGCCGCTGCA AATGCCGACC 2471CATTGTTCCG CTCAGCTCTC CAGGTCTTCA TGTGGTTGGA AGAAAACGGG ATTGTGACCG 2531ACATGGCTAA CTTCGCCCTC AGCGACCCAA ACGCGCATAG GATGAAAAAC TTCCTAGCAA 2591ACGCACCCCA GGCTGGAAGC AAGTCGCAGA GGGCCAAGTA TGGCACGGCA GGCTACGGAG 2651TGGAGGCTCG AGGCCCCACA CCAGAAGAGG CACAGAGGGA AAAAGACACA CGGATCTCCA 2711AGAAGATGGA AACAATGGGC ATCTACTTCG CGACACCGGA ATGGGTGGCT CTCAACGGGC 2771ACCGAGGCCC AAGCCCCGGC CAACTCAAGT ACTGGCAAAA CACAAGAGAA ATACCAGAGC 2831CCAATGAGGA CTACCCAGAC TATGTGCACG CGGAGAAGAG CCGGTTGGCG TCAGAAGAAC 2891AGATCCTACG GGCAGCCACG TCGATCTACG GGGCTCCAGG ACAGGCTGAA CCACCCCAGG 2951CCTTCATAGA CGAGGTCGCC AGGGTCTATG AAATCAACCA TGGGCGTGGT CCAAACCAGG 3011AGCAGATGAA GGACCIGCIC CTGACTGCGA TGGAGATGAA GCATCGCAAT CCCAGGCGGG 3071CTCCACCAAA GCCAAAGCCA AAACCCAATG CTCCATCACA GAGACCCCCT GGACGGCTGG 3131GCCGCTGGAT CAGGACGGTC TCCGACGAGG ACTTGGAGTG AGGCTCCTGG GAGTCTCCCG 3191ACACTACCCG CGCAGGTGTG GACACCAATT CGGCCTTCTA CCATCCCAAA TTGGATCCGT 3251TCGCGGGTCC CCT 3264
(2)SEQ ID NO:32:的信息:
(i)序列特征:
(A)长度:145个氨基酸
(B)类型:氨基酸
(D)拓扑学:线形
(ii)分子类型:蛋白质
(xi)SEQ ID NO:32的序列描述Met Val Ser Arg Asp Gln Thr Asn Asp Arg Ser Asp Asp Lys Pro Asp1 5 10 15Gly Ser His Pro Thr Asp Cys Ser Val His Thr Glu Pro Ser Asp Ala
20 25 30Asn Asp Arg Thr Gly Val His Ser Gly Arg His Pro Gly Glu Ala His
35 40 45Thr Gln Val Arg Asn Leu Asp Leu Gln Leu Asp Cys Arg Gly Tyr Arg
50 55 60Val Arg Thr Asn Cys Leu Phe Pro Trp Ile Pro Trp Phe Ser Cys Arg65 70 75 80Cys Ser Leu His Thr Ala Glu Gln Trp Glu Leu Pro Ile Arg Pro Asp
85 90 95Ala Pro Asp Ser Ala Glu Pro Ala Cys Gln Leu Gln Leu Leu Gln Ala
100 105 110Ser Glu Gln Glu Ser Asn Arg Thr Val Lys His Thr Pro Trp Trp Arg
115 120 125Leu Cys Thr Lys Arg Asn His Lys Arg Ser Asp Leu Pro Arg Lys Pro
130 135 140Glu145(2)SEQ ID NO:33的信息:(i)序列特征:
(A)长度:3264个碱基对
(B)类型:核酸
(C)链型:单链
(D)拓扑结构:环形(ii)分子类型:cDNA(ix)特征:
(A)名称/KEY:CDS
(B)位置:131..3169(xi)SEQ ID NO:33的序列描述GGATACGATC GGTCTGACCC CGGGGGAGTC ACCCGGGGAC AGGCCATCAC TGCCTTGTTC 60CTGGTTGGAA CTCCTCTTTC TGCTGTACTA TCGTTGATGG TGAGTAGAGA TCAGACAAAC 120GATCGCAGCG ATG ACA AAC CTG ATG GAT CAC ACC CAA CAG ATT GTT CCG 169
Met Thr Asn Leu Met Asp His Thr Gln Gln Ile Val Pro
150 155TTC ATA CGG AGC CTT CTG ATG CCA ACG ACC GGA CCG GCG TCC ATT CCG 217Phe Ile Arg Ser Leu Leu Met Pro Thr Thr Gly Pro Ala Ser Ile Pro
160 165 170GAC GAC ACC CTG GAG AAG CAC ACA CTC AGG TCC GAA ACC TCG ACT TAC 265Asp Asp Thr Leu Glu Lys His Thr Leu Arg Ser Glu Thr Ser Thr Tyr175 180 185 190AAC TTG ACT GTA GGG GAT ACA GGG TCA GGA CTA ATT GTC TTT TTC CCT 313Asn Leu Thr Val Gly Asp Thr Gly Ser Gly Leu Ile Val Phe Phe Pro
195 200 205GGA TTC CCT GGT TCA GTT GTA GGT GCT CAC TAC ACA CTG CAG AGC AGT 361Gly Phe Pro Gly Ser Val Val Gly Ala His Tyr Thr Leu Gln Ser Ser
210 215 220GGG AAC TAC CAA TTC GAC CAG ATG CTC CTG ACA GCG CAG AAC CTG CCT 409Gly Asn Tyr Gln Phe Asp Gln Met Leu Leu Thr Ala Gln Asn Leu Pro
225 230 235GCC AGC TAC AAC TAC TGC AGG CTA GTG AGC AGG AGT CTA ACC GTA CGG 457Ala Ser Tyr Asn Tyr Cys Arg Leu Val Ser Arg Ser Leu Thr Val Arg
240 245 250TCA AGC ACA CTC CCT GGT GGC GTT TAT GCA CTA AAC GGA ACC ATA AAC 505Ser Ser Thr Leu Pro Gly Gly Val Tyr Ala Leu Asn Gly Thr Ile Asn255 260 265 270GCA GTG ACC TTC CAC GGA AGC CTG AGT GAG TTG ACT GAC TAC AGC TAC 553Ala Val Thr Phe His Gly Ser Leu Ser Glu Leu Thr Asp Tyr Ser Tyr
275 280 285AAC GGG CTG ATG TCA GCC ACT GCG AAC ATC AAC GAC AAG ATC GGG AAC 601Asn Gly Leu Met Ser Ala Thr Ala Asn Ile Asn Asp Lys Ile Gly Asn
290 295 300GTT CTA GTT GGA GAA GGG GTG ACT GTT CTC AGT CTA CCG ACT TCA TAT 649Val Leu Val Gly Glu Gly Val Thr Val Leu Ser Leu Pro Thr Ser Tyr
305 310 315GAC CTT AGT TAT GTG AGA CTC GGT GAC CCC ATC CCC GCA GCA CGA CTC 697Asp Leu Ser Tyr Val Arg Leu Gly Asp Pro Ile Pro Ala Ala Gly Leu
320 325 330GAC CCG AAG TTG ATG GCC ACG TGC GAC AGT AGT GAC AGA CCC AGA GTC 745Asp Pro Lys Leu Met Ala Thr Cys Asp Ser Ser Asp Arg Pro Arg Val335 340 345 350TAC ACC ATA ACA GCT GCA GAT GAA TAC CAA TTC TCG TCA CAA CTC ATC 793Tyr Thr Ile Thr Ala Ala Asp Glu Tyr Gln Phe Ser Ser Gln Leu Ile
355 360 365CCG AGT GGC GTG AAG ACC ACA CTG TTC TCC GCC AAC ATC GAT GCT CTC 841Pro Ser Gly Val Lys Thr Thr Leu Phe Sar Ala Asn Ile Asp Ala Leu
370 375 380ACC AGC TTC AGC GTT GGT GGT GAG CTT GTC TTC AGC CAA GTA ACG ATC 889Thr Ser Phe Ser Val Gly Gly Glu Leu Val Phe Ser Gln Val Thr Ile
385 390 395CAA AGC ATT GAA GTG GAC GTC ACC ATT CAC TTC ATT GGG TTT GAC GGG 937Gln Ser Ile Glu Val Asp Val Thr Ile His Phe Ile Gly Phe Asp Gly
400 405 410ACA GAC GTA GCA GTC AAG GCA GTT GCA ACA GAC TTT GGG CTG ACA ACT 985Thr Asp Val Ala Val Lys Ala Val Ala Thr Asp Phe Gly Leu Thr Thr415 420 425 430GGG ACA AAC AAC CTT GTG CCA TTC AAC CTG GTG GTC CCA ACA AAT GAG 1033Gly Thr Asn Asn Leu Val Pro Phe Asn Leu Val Val Pro Thr Asn Glu
435 440 445ATC ACC CAG CCC ATC ACT TCC ATG AAA CTA GAG GTT GTG ACC TAC AAG 1081Ile Thr Gln Pro Ile Thr Ser Met Lys Leu Glu Val Val Thr Tyr Lys
450 455 460ATT GGC GGC ACC GCT GGT GAC CCA ATA TCA TGG ACA GTG AGT GGT ACA 1129Ile Gly Gly Thr Ala Gly Asp Pro Ile Ser Trp Thr Val Ser Gly Thr
465 470 475CTA GCT GTG ACG GTG CAC GGA GGC AAC TAC CCT GGG GCT CTC CGT CCT 1177Leu Ala Val Thr Val His Gly Gly Asn Tyr Pro Gly Ala Leu Arg Pro
480 485 490GTC ACC CTG GTG GCC TAT GAA CGA GTG GCT GCA GGA TCT GTT GTC ACA 1225Val Thr Leu Val Ala Tyr Glu Arg Val Ala Ala Gly Ser Val Val Thr495 500 505 510GTT GCA GGG GTG AGC AAC TTC GAG CTA ATC CCC AAC CCT GAG CTT GCA 1273Val Ala Gly Val Ser Asn Phe Glu Leu Ile Pro Asn Pro Glu Leu Ala
515 520 525AAG AAC CTA GTT ACA GAG TAT GGC CGC TTT GAC CCC GGA GCA ATG AAC 1321Lys Asn Leu Val Thr Glu Tyr Gly Arg Phe Asp Pro Gly Ala Met Asn
530 535 540TAC ACC AAA CTA ATA CTG AGT GAG AGA GAT CGT CTA GGC ATC AAG ACA 1369Tyr Thr Lys Leu Ile Leu Ser Glu Arg Asp Arg Leu Gly Ile Lys Thr
545 550 555GTC TGG CCC ACC AGG GAG TAC ACC GAT TTC AGG GAG TAC TTC ATG GAG 1417Val Trp Pro Thr Arg Glu Tyr Thr Asp Phe Arg Glu Tyr Phe Met Glu
560 565 570GTT GCA GAT CTC AAC TCA CCC CTA AAG ATT GCA GGA GCA TTT GGC TTT 1465Val Ala Asp Leu Asn Ser Pro Leu Lys Ile Ala Gly Ala Phe Gly Phe575 580 585 590AAG GAC ATA ATC CGA GCC ATT CGG AAG ATT GCG GTG CCA GTG GTA TCC 1513Lys Asp Ile Ile Arg Ala Ile Arg Lys Ile Ala Val Pro Val Val Ser
595 600 605ACA CTC TTC CCT CCA GCT GCA CCC CTA GCA CAT GCA ATC GGA GAA GGT 1561Thr Leu Phe Pro Pro Ala Ala Pro Leu Ala His Ala Ile Gly Glu Gly
610 615 620GTA GAC TAC CTC CTG GGC GAC GAG GCC CAA GCA GCC TCA GGG ACA GCT 1609Val Asp Tyr Leu Leu Gly Asp Glu Ala Gln Ala Ala Ser Gly Thr Ala
625 630 635CGA GCC GCG TCA GGA AAA GCT AGA GCT GCC TCA GGA CGA ATA AGG CAG 1657Arg Ala Ala Ser Gly Lys Ala Arg Ala Ala Ser Gly Arg Ile Arg Gln
640 645 650CTA ACT CTC GCA GCT GAC AAG GGG TGC GAG GTA GTC GCC AAC ATG TTC 1705Leu Thr Leu Ala Ala Asp Lys Gly Cys Glu Val Val Ala Asn Met Phe655 660 665 670CAG GTG CCC CAG AAT CCC ATT GTT GAT GGC ATT CTG GCA TCC CCA GGA 1753Gln Val Pro Gln Asn Pro Ile Val Asp Gly Ile Leu Ala Ser Pro Gly
675 680 685ATC CTG CGT GGC GCA CAC AAC CTC GAC TGC GTG CTA TGG GAG GGA GCC 1801Ile Leu Arg Gly Ala His Asn Leu Asp Cys Val Leu Trp Glu Gly Ala
690 695 700ACT CTT TTC CCT GTT GTC ATT ACG ACA CTC GAG GAT GAG CTG ACC CCC 1849Thr Leu Phe Pro Val Val Ile Thr Thr Leu Glu Asp Glu Leu Thr Pro
705 710 715AAG GCA CTG AAC AGC AAA ATG TTT GCT GTC ATT GAA GGT GTG CGA GAG 1897Lys Ala Leu Asn Ser Lys Met Phe Ala Val Ile Glu Gly Val Arg Glu
720 725 730GAC CTC CAG CCT CCA TCC CAA CGG GGA TCC TTC ATT CGA ACT CTC TCT 1945Asp Leu Gln Pro Pro Ser Gln Arg Gly Ser Phe Ile Arg Thr Leu Ser735 740 745 750GGC CAT AGA GTC TAT GGC TAT GCC CCA GAC GGA GTA CTG CCT CTG GAG 1993Gly His Arg Val Tyr Gly Tyr Ala Pro Asp Gly Val Leu Pro Leu Glu
755 760 765ACC GGG AGA GAC TAC ACC GTT GTC CCA ATT GAT GAT GTG TGG GAC GAT 2041Thr Gly Arg Asp Tyr Thr Val Val Pro Ile Asp Asp Val Trp Asp Asp
770 775 780AGC ATA ATG CTG TCG CAG GAC CCC ATA CCT CCA ATC ATA GGG AAC AGC 2089Ser Ile Met Leu Ser Gln Asp Pro Ile Pro Pro Ile Ile Gly Asn Ser
785 790 795GGC AAC CTA GCC ATA GCA TAC ATG GAT GTC TTC AGG CCC AAG GTC CCC 2137Gly Asn Leu Ala Ile Ala Tyr Met Asp Val Phe Arg Pro Lys Val Pro
800 805 810ATC CAC GTG GCT ATG ACA GGG GCC CTC AAT GCC CGC GGT GAG ATC GAG 2185Ile His Val Ala Met Thr Gly Ala Leu Asn Ala Arg Gly Glu Ile Glu815 820 825 830AGT GTT ACG TTC CGC AGC ACC AAA CTC GCC ACA GCC CAC CGA CTT GGC 2233Ser Val Thr Phe Arg Ser Thr Lys Leu Ala Thr Ala His Arg Leu Gly
835 840 845ATG AAG TTA GCT GGT CCT GGA GCC TAT GAC ATT AAT ACA GGA CCT AAC 2281Met Lys Leu Ala Gly Pro Gly Ala Tyr Asp Ile Asn Thr Gly Pro Asn
850 855 860TGG GCA ACG TTC GTC AAA CGT TTC CCT CAC AAT CCC CGA GAC TGG GAC 2329Trp Ala Thr Phe Val Lys Arg Phe Pro His Asn Pro Arg Asp Trp Asp
865 870 875AGG TTG CCC TAC CTC AAC CTT CCT TAT CTC CCA CCA ACA GCA GGA CGT 2377Arg Leu Pro Tyr Leu Asn Leu Pro Tyr Leu Pro Pro Thr Ala Gly Arg
880 885 890CAG TTC CAT CTA GCC CTG GCT GCC TCC GAG TTC AAA GAG ACC CCA GAA 2425Gln Phe His Leu Ala Leu Ala Ala Ser Glu Phe Lys Glu Thr Pro Glu895 900 905 910CTC GAA GAC GCT GTG CGC GCA ATG GAT GCC GCT GCA AAT GCC GAC CCA 2473Leu Glu Asp Ala Val Arg Ala Met Asp Ala Ala Ala Asn Ala Asp Pro
915 920 925TTG TTC CGC TCA GCT CTC CAG GTC TTC ATG TGG TTG GAA GAA AAC GGG 2521Leu Phe Arg Ser Ala Leu Gln Val Phe Met Trp Leu Glu Glu Asn Gly
930 935 940ATT GTG ACC GAC ATG GCT AAC TTC GCC CTC AGC GAC CCA AAC GCG CAT 2569Ile Val Thr Asp Met Ala Asn Phe Ala Leu Ser Asp Pro Asn Ala His
945 950 955AGG ATG AAA AAC TTC CTA GCA AAC GCA CCC CAG GCT GGA AGC AAG TCG 2617Arg Met Lys Asn Phe Leu Ala Asn Ala Pro Gln Ala Gly Ser Lys Ser
960 965 970CAG AGG GCC AAG TAT GGC ACG GCA GGC TAC GGA GTG GAG GCT CGA GGC 2665Gln Arg Ala Lys Tyr Gly Thr Ala Gly Tyr Gly Val Glu Ala Arg Gly975 980 985 990CCC ACA CCA GAA GAG GCA CAG AGG GAA AAA GAC ACA CGG ATC TCC AAG 2713Pro Thr Pro Glu Glu Ala Gln Arg Glu Lys Asp Thr Arg Ile Ser Lys
995 1000 1005AAG ATG GAA ACA ATG GGC ATC TAC TTC GCG ACA CCG GAA TGG GTG GCT 2761Lys Met Glu Thr Met Gly Ile Tyr Phe Ala Thr Pro Glu Trp Val Ala
1010 1015 1020CTC AAC GGG CAC CGA GGC CCA AGC CCC GGC CAA CTC AAG TAC TGG CAA 2809Leu Asn Gly His Arg Gly Pro Ser Pro Gly Gln Leu Lys Tyr Trp Gln
1025 1030 1035AAC ACA AGA GAA ATA CCA GAG CCC AAT GAG GAC TAC CCA GAC TAT GTG 2857Asn Thr Arg Glu Ile Pro Glu Pro Asn Glu Asp Tyr Pro Asp Tyr Val
1040 1045 1050CAC GCG GAG AAG AGC CGG TTG GCG TCA GAA GAA CAG ATC CTA CGG GCA 2905His Ala Glu Lys Ser Arg Leu Ala Ser Glu Glu Gln Ile Leu Arg Ala1055 1060 1065 1070GCC ACG TCG ATC TAC GGG GCT CCA GGA CAG GCT GAA CCA CCC CAG GCC 2953Ala Thr Ser Ile Tyr Gly Ala Pro Gly Gln Ala Glu Pro Pro Gln Ala
1075 1080 1085TTC ATA GAC GAG GTC GCC AGG GTC TAT GAA ATC AAC CAT GGG CGT GGT 3001Phe Ile Asp Glu Val Ala Arg Val Tyr Glu Ile Asn His Gly Arg Gly
1090 1095 1100CCA AAC CAG GAG CAG ATG AAG GAC CTG CTC CTG ACT GCG ATG GAG ATG 3049Pro Asn Gln Glu Gln Met Lys Asp Leu Leu Leu Thr Ala Met Glu Met
1105 1110 1115AAG CAT CGC AAT CCC AGG CGG GCT CCA CCA AAG CCA AAG CCA AAA CCC 3097Lys His Arg Asn Pro Arg Arg Ala Pro Pro Lys Pro Lys Pro Lys Pro
1120 1125 1130AAT GCT CCA TCA CAG AGA CCC CCT GGA CGG CTG GGC CGC TGG ATC AGG 3145Asn Ala Pro Ser Gln Arg Pro Pro Gly Arg Leu Gly Arg Trp Ile Arg1135 1140 1145 1150ACG GTC TCC GAC GAG GAC TTG GAG TGAGGCTCCT GGGAGTCTCC CGACACTACC 3199Thr Val Ser Asp Glu Asp Leu Glu
1155CGCGCAGGTG TGGACACCAA TTCGGCCTTC TACCATCCCA AATTGGATCC GTTCGCGGGT 3259CCCCT 3264(2)SEQ ID NO:34的信息:(i)序列特征:
(A)长度:1013个氨基酸
(B)类型:氨基酸
(D)拓扑结构:线形(ii)分子类型:蛋白质(xi)SEQ ID NO:34的序列描述Met Thr Asn Leu Met Asp His Thr Gln Gln Ile Val Pro Phe Ile Arg1 5 10 15Ser Leu Leu Met Pro Thr Thr Gly Pro Ala Ser Ile Pro Asp Asp Thr
20 25 30Leu Glu Lys His Thr Leu Arg Ser Glu Thr Ser Thr Tyr Asn Leu Thr
35 40 45Val Gly Asp Thr Gly Ser Gly Leu Ile Val Phe Phe Pro Gly Phe Pro
50 55 60Gly Ser Val Val Gly Ala His Tyr Thr Leu Gln Ser Ser Gly Asn Tyr65 70 75 80Gln Phe Asp Gln Met Leu Leu Thr Ala Gln Asn Leu Pro Ala Ser Tyr
85 90 95Asn Tyr Cys Arg Leu Val Ser Arg Ser Leu Thr Val Arg Ser Ser Thr
100 105 110Leu Pro Gly Gly Val Tyr Ala Leu Asn Gly Thr Ile Asn Ala Val Thr
115 120 125Phe His Gly Ser Leu Ser Glu Leu Thr Asp Tyr Ser Tyr Asn Gly Leu
130 135 140Met Ser Ala Thr Ala Asn Ile Asn Asp Lys Ile Gly Asn Val Leu Val145 150 155 160Gly Glu Gly Val Thr Val Leu Ser Leu Pro Thr Ser Tyr Asp Leu Ser
165 170 175Tyr Val Arg Leu Gly Asp Pro Ile Pro Ala Ala Gly Leu Asp Pro Lys
180 185 190Leu Met Ala Thr Cys Asp Ser Ser Asp Arg Pro Arg Val Tyr Thr Ile
195 200 205Thr Ala Ala Asp Glu Tyr Gln Phe Ser Ser Gln Leu Ile Pro Ser Gly
210 215 220Val Lys Thr Thr Leu Phe Ser Ala Asn Ile Asp Ala Leu Thr Ser Phe225 230 235 240Ser Val Gly Gly Glu Leu Val Phe Ser Gln Val Thr Ile Gln Ser Ile
245 250 255Glu Val Asp Val Thr Ile His Phe Ile Gly Phe Asp Gly Thr Asp Val
260 265 270Ala Val Lys Ala Val Ala Thr Asp Phe Gly Leu Thr Thr Gly Thr Asn
275 280 285Asn Leu Val Pro Phe Asn Leu Val Val Pro Thr Asn Glu Ile Thr Gln
290 295 300Pro Ile Thr Ser Met Lys Leu Glu Val Val Thr Tyr Lys Ile Gly Gly305 310 315 320Thr Ala Gly Asp Pro Ile Ser Trp Thr Val Ser Gly Thr Leu Ala Val
325 330 335Thr Val His Gly Gly Asn Tyr Pro Gly Ala Leu Arg Pro Val Thr Leu
340 345 350Val Ala Tyr Glu Arg Val Ala Ala Gly Ser Val Val Thr Val Ala Gly
355 360 365Val Ser Asn Phe Glu Leu Ile Pro Asn Pro Glu Leu Ala Lys Asn Leu
370 375 380Val Thr Glu Tyr Gly Arg Phe Asp Pro Gly Ala Met Asn Tyr Thr Lys385 390 395 400Leu Ile Leu Ser Glu Arg Asp Arg Leu Gly Ile Lys Thr Val Trp Pro
405 410 415Thr Arg Glu Tyr Thr Asp Phe Arg Glu Tyr Phe Met Glu Val Ala Asp
420 425 430Leu Asn Ser Pro Leu Lys Ile Ala Gly Ala Phe Gly Phe Lys Asp Ile
435 440 445Ile Arg Ala Ile Arg Lys Ile Ala Val Pro Val Val Ser Thr Leu Phe
450 455 460Pro Pro Ala Ala Pro Leu Ala His Ala Ile Gly Glu Gly Val Asp Tyr465 470 475 480Leu Leu Gly Asp Glu Ala Gln Ala Ala Ser Gly Thr Ala Arg Ala Ala
485 490 495Ser Gly Lys Ala Arg Ala Ala Ser Gly Arg Ile Arg Gln Leu Thr Leu
500 505 510Ala Ala Asp Lys Gly Cys Glu Val Val Ala Asn Met Phe Gln Val Pro
515 520 525Gln Asn Pro Ile Val Asp Gly Ile Leu Ala Ser Pro Gly Ile Leu Arg
530 535 540Gly Ala His Asn Leu Asp Cys Val Leu Trp Glu Gly Ala Thr Leu Phe545 550 555 560Pro Val Val Ile Thr Thr Leu Glu Asp Glu Leu Thr Pro Lys Ala Leu
565 570 575Asn Ser Lys Met Phe Ala Val Ile Glu Gly Val Arg Glu Asp Leu Gln
580 585 590Pro Pro Ser Gln Arg Gly Ser Phe Ile Arg Thr Leu Ser Gly His Arg
595 600 605Val Tyr Gly Tyr Ala Pro Asp Gly Val Leu Pro Leu Glu Thr Gly Arg
610 615 620Asp Tyr Thr Val Val Pro Ile Asp Asp Val Trp Asp Asp Ser Ile Met625 630 635 640Leu Ser Gln Asp Pro Ile Pro Pro Ile Ile Gly Asn Ser Gly Asn Leu
645 650 655Ala Ile Ala Tyr Met Asp Val Phe Arg Pro Lys Val Pro Ile His Val
660 665 670Ala Met Thr Gly Ala Leu Asn Ala Arg Gly Glu Ile Glu Ser Val Thr
675 680 685Phe Arg Ser Thr Lys Leu Ala Thr Ala His Arg Leu Gly Met Lys Leu
690 695 700Ala Gly Pro Gly Ala Tyr Asp Ile Asn Thr Gly Pro Asn Trp Ala Thr705 710 715 720Phe Val Lys Arg Phe Pro His Asn Pro Arg Asp Trp Asp Arg Leu Pro
725 730 735Tyr Leu Asn Leu Pro Tyr Leu Pro Pro Thr Ala Gly Arg Gln Phe His
740 745 750Leu Ala Leu Ala Ala Ser Glu Phe Lys Glu Thr Pro Glu Leu Glu Asp
755 760 765Ala Val Arg Ala Met Asp Ala Ala Ala Asn Ala Asp Pro Leu Phe Arg
770 775 780Ser Ala Leu Gln Val Phe Met Trp Leu Glu Glu Asn Gly Ile Val Thr785 790 795 800Asp Met Ala Asn Phe Ala Leu Ser Asp Pro Asn Ala His Arg Met Lys
805 810 815Asn Phe Leu Ala Asn Ala Pro Gln Ala Gly Ser Lys Ser Gln Arg Ala
820 825 830Lys Tyr Gly Thr Ala Gly Tyr Gly Val Glu Ala Arg Gly Pro Thr Pro
835 840 845Glu Glu Ala Gln Arg Glu Lys Asp Thr Arg Ile Ser Lys Lys Met Glu
850 855 860Thr Met Gly Ile Tyr Phe Ala Thr Pro Glu Trp Val Ala Leu Asn Gly865 870 875 880His Arg Gly Pro Ser Pro Gly Gln Leu Lys Tyr Trp Gln Asn Thr Arg
885 890 895Glu Ile Pro Glu Pro Asn Glu Asp Tyr Pro Asp Tyr Val His Ala Glu
900 905 910Lys Ser Arg Leu Ala Ser Glu Glu Gln Ile Leu Arg Ala Ala Thr Ser
915 920 925Ile Tyr Gly Ala Pro Gly Gln Ala Glu Pro Pro Gln Ala Phe Ile Asp
930 935 940Glu Val Ala Arg Val Tyr Glu Ile Asn His Gly Arg Gly Pro Asn Gln945 950 955 960Glu Gln Met Lys Asp Leu Leu Leu Thr Ala Met Glu Met Lys His Arg
965 970 975Asn Pro Arg Arg Ala Pro Pro Lys Pro Lys Pro Lys Pro Asn Ala Pro
980 985 990Ser Gln Arg Pro Pro Gly Arg Leu Gly Arg Trp Ile Arg Thr Val Ser
995 1000 1005Asp Glu Asp Leu Glu
1010
Claims (20)
1.用于制备活的双RNA病毒的方法,包括下列步骤:
制备含有感染性囊病病毒基因组区段A和B的cDNA,
将所述的cDNA转录以产生合成的RNA转录物,
用所述的合成的RNA转录物转染宿主细胞,
在培养基中培养所述的宿主细胞,和从所述的培养基中分离活的感染性囊病病毒。
2.根据权利要求1所述的方法,其中所述的双RNA病毒是感染性囊病病毒。
3.根据权利要求1所述的方法,其中所述的宿主细胞是非洲绿猴肾细胞系细胞。
4.根据权利要求1所述的方法,其中所述的cDNA的区段A和B是独立制备的。
5.根据权利要求4所述的方法,其中所述的区段A存在于质粒pUC19FLAD78或pUC18FLA23上。
6.根据权利要求4所述的方法,其中所述的区段B存在于质粒pUC18FLBP2上。
7.活的感染性囊病病毒,其中所述的病毒是通过一种方法制备的,该方法包括步骤:
制备含有感染性囊病病毒基因组区段A和B的cDNA,
将所述的cDNA转录以产生合成的RNA转录物,
用所述的合成的RNA转录物转染宿主细胞,
在培养基中培养所述的宿主细胞,和
从所述的培养基中分离活的感染性囊病病毒。
8.编码感染性囊病病毒的蛋白质VP1、VP2、VP3、VP4和VP5的合成的RNA。
9.用权利要求8所述的合成的RNA转染的宿主细胞。
10.含有感染性囊病病毒基因组的至少一部分的cDNA,所述的一部分选自由感染性囊病病毒区段A、区段B和区段A和B组成的组,其中所述的cDNA包括所述片段的5’和3’末端。
11.包含权利要求10所述的cDNA的重组载体。
12.根据权利要求11所述的载体,其中所述的载体是质粒。
13.根据权利要求12所述的载体,其中所述的质粒选自由pUC19FLAD78,pUC18FLA23和pUC19FLBP2组成的组。
14.用权利要求11所述的载体转化的宿主细胞。
15.包含权利要求7所述的感染性囊病病毒的疫苗,其中所述的感染性囊病病毒在给药之前是失活的或减毒的。
16.制备活的感染性囊病病毒疫苗的方法,该方法包括如下步骤:
制备含有感染性囊病病毒基因组区段A和B的全长cDNA,
将所述的cDNA转录以产生合成的RNA转录物,
纯化所述的合成的RNA转录物,
用所述的纯化的RNA转录物转染宿主细胞,
在培养基中培养所述的宿主细胞,
从所述的培养基中分离活的感染性囊病病毒,
将所述活的感染性囊病病减毒以产生具有降低的毒性的病毒,和
将所述活的感染性囊病病毒与药物学可接受载体结合以产生活的感染性囊病病毒疫苗。
17.根据权利要求16所述的方法,其中所述的活的感染性囊病病毒通过连续的传代或位点特异性诱变来减毒的。
18.根据权利要求1所述的方法,其中所述的宿主细胞是家禽细胞。
19.根据权利要求18所述的方法,其中所述的家禽细胞是鸡、火鸡或鹌鹑细胞。
20.根据权利要求19的方法,其中所述的家禽细胞是鸡胚成纤维细胞或鸡胚肾细胞。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/708,541 | 1996-09-05 | ||
US08/708,541 US5871744A (en) | 1996-09-05 | 1996-09-05 | Method for generating birnavirus from synthetic RNA transcripts |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1229358A true CN1229358A (zh) | 1999-09-22 |
CN1168500C CN1168500C (zh) | 2004-09-29 |
Family
ID=24846203
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB971976880A Expired - Fee Related CN1168500C (zh) | 1996-09-05 | 1997-07-31 | 从合成的rna转录物制备双rna病毒的方法 |
Country Status (18)
Country | Link |
---|---|
US (1) | US5871744A (zh) |
EP (2) | EP0959901A4 (zh) |
JP (1) | JP4670025B2 (zh) |
KR (1) | KR100475427B1 (zh) |
CN (1) | CN1168500C (zh) |
AT (1) | ATE460178T1 (zh) |
AU (1) | AU741055B2 (zh) |
BR (1) | BR9712012B1 (zh) |
CA (1) | CA2264488C (zh) |
CZ (1) | CZ299417B6 (zh) |
DE (1) | DE69739805D1 (zh) |
ES (1) | ES2342325T3 (zh) |
HU (1) | HUP9904365A3 (zh) |
IL (2) | IL128804A0 (zh) |
NO (1) | NO991074L (zh) |
NZ (1) | NZ334667A (zh) |
PL (1) | PL190220B1 (zh) |
WO (1) | WO1998009646A1 (zh) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101016547B (zh) * | 2007-01-25 | 2010-07-28 | 浙江大学 | 海洋双rna病毒mabv重组蛋白的制备方法与应用 |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6596280B1 (en) * | 1997-07-31 | 2003-07-22 | University Of Maryland Biotechnology Institute | Method for generating birnavirus from synthetic RNA transcripts |
WO1999050419A2 (en) * | 1998-03-31 | 1999-10-07 | University Of Maryland Biotechnology Institute | A method for generating nonpathogenic, infectious pancreatic necrosis virus (ipnv) from synthetic rna transcripts |
WO2000012677A2 (en) * | 1998-09-01 | 2000-03-09 | The University Of Hong Kong | Generation of recombinant infectious bursal disease viruses by reverse genetics technology and the use of the recombinant viruses as attenuated vaccines |
HUP9802974A1 (hu) * | 1998-12-19 | 2000-09-28 | Mezőgazdasági Biotechnológiai Kutatóközpont | Fertőző bursitis elleni DNS-vakcina |
US6492148B1 (en) * | 1999-03-05 | 2002-12-10 | Akzo Nobel Nv | Genetically engineered cell culture adapted infectious bursal disease virus (IBDV) mutants |
US6468984B1 (en) | 1999-06-08 | 2002-10-22 | Innovo Biotechnologies Ltd. | DNA vaccine for protecting an avian against infectious bursal disease virus |
EP1069187A1 (en) * | 1999-07-14 | 2001-01-17 | Stichting Dienst Landbouwkundig Onderzoek | Mosaic Infectious Bursal Disease Virus vaccines |
US7431930B2 (en) * | 2002-03-01 | 2008-10-07 | Intervet International B.V. | Infectious bursal disease virus (IBDV) mutant expressing virus neutralising epitopes specific for classic-and variant IBDV strains |
ES2217967B1 (es) * | 2003-03-31 | 2006-01-01 | Consejo Sup. Investig. Cientificas | Procedimiento de produccion de particulas virales vacias (vlps) del virus inductor de la bursitis infecciosa (ibdv), composiciones necesarias para su puesta a punto y su uso en la elaboracion de vacunas frente al ibdv. |
ES2307346B1 (es) * | 2004-01-21 | 2009-11-13 | Consejo Sup. Investig. Cientificas | Capsidas vacias (vlps(-vp4)) del virus causante de la enfermedad de la bursitis infecciosa (ibdv), su procedimiento de obtencion y aplicaciones. |
ES2307345B1 (es) * | 2004-01-21 | 2009-11-13 | Consejo Sup. Investig. Cientificas | Capsidas vacias quimericas del virus causante de la enfermedad de la bursitis infecciosa (ibdv), su procedimiento de obtencion y aplicaciones. |
US7244432B2 (en) * | 2004-12-08 | 2007-07-17 | University Of Maryland Biotechnology Institute | Infectious bursal disease virus (IBDV) variant from Georgia |
ES2310062B1 (es) * | 2005-07-15 | 2009-11-13 | Bionostra, S.L. | Particulas pseudovirales vacias quimericas derivadas del virus causante de la enfermedad de la bursitis infecciosa (ibdv), procedimiento de obtencion y aplicaciones. |
KR100757541B1 (ko) * | 2005-11-08 | 2007-09-10 | 엘지전자 주식회사 | 플라즈마 디스플레이 장치 및 그의 화상 처리방법 |
WO2008068661A1 (en) * | 2006-12-01 | 2008-06-12 | Hepc Biotechnológiai Kutató És Fejleszto Kft. | Compositions and methods for the treatment of viral hepatitis |
EP2407534A1 (en) | 2010-07-14 | 2012-01-18 | Neo Virnatech, S.L. | Methods and reagents for obtaining transcriptionally active virus-like particles and recombinant virions |
CN109321583B (zh) * | 2018-09-29 | 2023-08-15 | 福建省农业科学院畜牧兽医研究所 | 一种构建番鸭呼肠孤病毒反向遗传系统的方法 |
AU2020329166A1 (en) | 2019-08-09 | 2022-03-03 | Nutcracker Therapeutics, Inc. | Microfluidic apparatus and methods of use thereof |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4530831A (en) * | 1982-11-02 | 1985-07-23 | Akzo N.V. | Infectious Bursal Disease vaccine |
CA1334941C (en) * | 1985-05-30 | 1995-03-28 | Ahmed Azad Azad | Cloning and expression of a host-protective immunogens of ibdv |
AU602875B2 (en) * | 1985-12-18 | 1990-11-01 | British Technology Group Limited | Newcastle disease virus gene clones |
US5192539A (en) * | 1988-07-21 | 1993-03-09 | Akzo N.V. | Infectious bursal disease virus production in continuous cell lines |
US5518724A (en) * | 1988-08-02 | 1996-05-21 | University Of Maryland | Infectious bursal disease virus |
NZ235474A (en) * | 1989-10-18 | 1992-12-23 | Univ Maryland | Virus capable of inducing infectious bursal disease; assay and vaccine |
JPH05501064A (ja) * | 1990-05-04 | 1993-03-04 | ユニバーシティ オブ メリーランド アット カレッジ パーク | Ibdvタンパク質に関連する特異的dna配列並びにベクター、宿主およびワクチン |
EP0597016A4 (en) * | 1991-07-26 | 1996-04-24 | Virogenetics Corp | Infectious bursal disease virus recombinant poxvirus vaccine. |
US5788970A (en) * | 1994-03-29 | 1998-08-04 | The University Of Maryland College Park | Chimeric infectious bursal disease virus CDNA clones, expression products and vaccines based thereon |
-
1996
- 1996-09-05 US US08/708,541 patent/US5871744A/en not_active Expired - Lifetime
-
1997
- 1997-07-31 JP JP51264398A patent/JP4670025B2/ja not_active Expired - Fee Related
- 1997-07-31 NZ NZ334667A patent/NZ334667A/xx not_active IP Right Cessation
- 1997-07-31 BR BRPI9712012-0A patent/BR9712012B1/pt not_active IP Right Cessation
- 1997-07-31 AT AT07012332T patent/ATE460178T1/de not_active IP Right Cessation
- 1997-07-31 EP EP19970936185 patent/EP0959901A4/en not_active Withdrawn
- 1997-07-31 AU AU38918/97A patent/AU741055B2/en not_active Ceased
- 1997-07-31 DE DE69739805T patent/DE69739805D1/de not_active Expired - Lifetime
- 1997-07-31 CN CNB971976880A patent/CN1168500C/zh not_active Expired - Fee Related
- 1997-07-31 CA CA002264488A patent/CA2264488C/en not_active Expired - Fee Related
- 1997-07-31 EP EP07012332A patent/EP1930026B1/en not_active Expired - Lifetime
- 1997-07-31 ES ES07012332T patent/ES2342325T3/es not_active Expired - Lifetime
- 1997-07-31 KR KR10-1999-7001899A patent/KR100475427B1/ko not_active IP Right Cessation
- 1997-07-31 CZ CZ0074299A patent/CZ299417B6/cs not_active IP Right Cessation
- 1997-07-31 PL PL97332184A patent/PL190220B1/pl not_active IP Right Cessation
- 1997-07-31 IL IL12880497A patent/IL128804A0/xx active IP Right Grant
- 1997-07-31 HU HU9904365A patent/HUP9904365A3/hu unknown
- 1997-07-31 WO PCT/US1997/012955 patent/WO1998009646A1/en not_active Application Discontinuation
-
1999
- 1999-03-03 IL IL128804A patent/IL128804A/en not_active IP Right Cessation
- 1999-03-04 NO NO19991074A patent/NO991074L/no not_active Application Discontinuation
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101016547B (zh) * | 2007-01-25 | 2010-07-28 | 浙江大学 | 海洋双rna病毒mabv重组蛋白的制备方法与应用 |
Also Published As
Publication number | Publication date |
---|---|
CN1168500C (zh) | 2004-09-29 |
IL128804A0 (en) | 2000-01-31 |
NO991074L (no) | 1999-04-29 |
NZ334667A (en) | 2000-09-29 |
IL128804A (en) | 2006-08-01 |
ATE460178T1 (de) | 2010-03-15 |
BR9712012B1 (pt) | 2009-08-11 |
HUP9904365A2 (hu) | 2000-04-28 |
JP4670025B2 (ja) | 2011-04-13 |
KR100475427B1 (ko) | 2005-03-10 |
CA2264488C (en) | 2009-04-07 |
JP2001501082A (ja) | 2001-01-30 |
WO1998009646A1 (en) | 1998-03-12 |
US5871744A (en) | 1999-02-16 |
CA2264488A1 (en) | 1998-03-12 |
EP0959901A4 (en) | 2002-11-04 |
DE69739805D1 (de) | 2010-04-22 |
KR20010029487A (ko) | 2001-04-06 |
PL332184A1 (en) | 1999-08-30 |
NO991074D0 (no) | 1999-03-04 |
BR9712012A (pt) | 2000-01-18 |
EP1930026A1 (en) | 2008-06-11 |
CZ74299A3 (cs) | 1999-08-11 |
EP1930026B1 (en) | 2010-03-10 |
AU741055B2 (en) | 2001-11-22 |
PL190220B1 (pl) | 2005-11-30 |
AU3891897A (en) | 1998-03-26 |
HUP9904365A3 (en) | 2001-06-28 |
EP0959901A1 (en) | 1999-12-01 |
CZ299417B6 (cs) | 2008-07-16 |
ES2342325T3 (es) | 2010-07-05 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN1168500C (zh) | 从合成的rna转录物制备双rna病毒的方法 | |
CN1087175C (zh) | 能够产生抗猪呼吸和生殖系统疾病致病性病毒的免疫应答的疫苗 | |
CN1298738C (zh) | 修饰的麻疹病毒v蛋白 | |
CN1155707C (zh) | 鼠疫疫苗 | |
CN1240833C (zh) | 新型腈水合酶 | |
CN1147769A (zh) | 含有副流感病毒的、用于预防猪呼吸和生殖疾病的疫苗 | |
CN1620500A (zh) | 包含功能性缺失的基因组的冠状病毒样颗粒 | |
CN1055501C (zh) | 重组禽痘病毒,培养被上述病毒感染的细胞以及从上述病毒得到的家禽疫苗 | |
CN1761759A (zh) | Hpv31l1在酵母中的优化表达 | |
CN1191357C (zh) | 口服的免疫原性细菌肠毒素在转基因植物中的表达 | |
CN1813062A (zh) | 噬菌体溶菌素 | |
CN1515669A (zh) | 由氧化葡糖杆菌t-100得到的l-山梨酮脱氢酶 | |
CN100335131C (zh) | 重组火鸡疱疹病毒及其应用 | |
CN1455816A (zh) | 从cDNA中挽救犬热病病毒 | |
CN88100373A (zh) | 阿凡曼菌素及其培养菌的生产方法 | |
CN1990869A (zh) | 鸡传染性法氏囊病病毒VP2 cDNA、其表达载体、所表达的重组蛋白及应用 | |
CN1073155C (zh) | 2-酮-l-古洛糖酸的生产方法 | |
CN1173203A (zh) | 纯化的乳头状瘤病毒蛋白 | |
CN1170935C (zh) | 虾青素合成酶 | |
CN1373807A (zh) | 镶嵌传染性腔上囊病病毒疫苗 | |
CN1160454C (zh) | 用于抗日本脑炎病毒感染的灭活疫苗的增强免疫原及其生产方法 | |
CN1198918C (zh) | 减毒的活胸膜肺炎放线杆菌 | |
CN1228450C (zh) | 抗原制剂 | |
CN1313605C (zh) | 一种禽流感病毒基因重配株d3/f-r2/6及其构建方法 | |
CN1247230A (zh) | 醋酸杆菌的木糖醇脱氢酶及其基因 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
REG | Reference to a national code |
Ref country code: HK Ref legal event code: GR Ref document number: 1049665 Country of ref document: HK |
|
C17 | Cessation of patent right | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20040929 Termination date: 20120731 |