CN100438907C - Bacterin of tabling gene of E type hepatitis virus - Google Patents

Bacterin of tabling gene of E type hepatitis virus Download PDF

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Publication number
CN100438907C
CN100438907C CNB031168620A CN03116862A CN100438907C CN 100438907 C CN100438907 C CN 100438907C CN B031168620 A CNB031168620 A CN B031168620A CN 03116862 A CN03116862 A CN 03116862A CN 100438907 C CN100438907 C CN 100438907C
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China
Prior art keywords
hepatitis
hev
gene
virus
orf23
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Chinese (zh)
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CN1539504A (en
Inventor
陈勇
洪艳
杨连华
经络
蒋骏航
王怡婷
凌志强
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Zhejiang Academy of Medical Sciences
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Zhejiang Academy of Medical Sciences
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Abstract

The present invention relates to a chimeric gene vaccine preventing hepatitis E virus infection, which belongs to the technical field of a biologic medicine. The chimeric gene vaccine is eukaryotic expression recombinant plasmid containing an open reading frame 2(ORF2) chimeric gene of a hepatitis E virus and an open reading frame 3(ORF3) chimeric gene of the hepatitis E virus. The gene vaccine capable of inducing an organism to generate specific cell immunity and specific humoral immunity is used for preventing viral hepatitis E.

Description

A kind of hepatitis E virus chimeric gene vaccine
Technical field
The present invention relates to the biological medicine technology field, is a kind of chimeric gene vaccine that prevents hepatitis e virus infection.
Background technology
Hepatitis E is the viral hepatitis that is caused by hepatitis E virus (HEV), is the more common infectious disease of developing country, and China is the district occurred frequently, and the crowd infection rate reaches 17.2%, and in rising trend.This disease is popular extensively, and patient's disease symptom is heavy, case fatality rate height (average out to 1%-2% reaches as high as 10%-20%), and the state of an illness is dangerous, and main threat is between twenty and fifty, often causes outburst or popular, brings fear and economic loss to society.1986 to 1988 autonomous region of Xinjiang of China Uygur nationality south, it is popular that maximum up to now HEV once took place, last 20 months, 119280 people that fall ill altogether, 72% is 15～44 years old person between twenty and fifty, total attack rate is 2.96%, case fatality rate 0.59%, the average case fatality rate 13.46% of anemia of pregnant woman, the late pregnancy case fatality rate is up to 20.96%, and popular reason is mainly water source and food pollution.In addition, this disease is also occupied higher ratio in China's acute sporadic viral hepatitis, on average be about 8.6%, and case fatality rate is 2.5%.Along with the use of Hepatitis A Vaccine, the sickness rate of hepatitis A descends year by year significantly, but to have a hepatitis E virus sickness rate of identical fecal-oral transmission approach constantly soaring with hepatitis A virus, and it is very urgent to control this disease.Whole world scientist has carried out painstaking efforts for this reason.
The development effective vaccine is the infectious key of control HEV.Because hepatitis E virus tissue culture difficulty is difficult to develop attenuation or inactivated vaccine.Therefore, the development of gene vaccine and polypeptide vaccine becomes the focus of research.Gene vaccine is a kind of new generation vaccine, has the following advantages: can induce T, bone-marrow-derived lymphocyte to participate in the immunne response of body, and have the characteristic of polypeptide vaccine and synthetic peptide vaccine concurrently; Have the safety of recombinant subunit vaccine and the high efficiency that attenuated live vaccine is induced comprehensive immunne response concurrently; Once inoculation can obtain permanent immunity power; Preparation is simple, and cost is low, and transportation stores convenient, and clinical practice is safe and effective.
It is the key that can the gene vaccine development successful that antigen site is selected.The current research result shows that HEV has 3 opening code-reading frames (ORF), ORF both at home and abroad 1Be positioned at non-structural area, the coding non-structural protein; ORF 2And ORF 3Be positioned at structural area, the former coding structure albumen or nucleocapsid protein contains 7 epitopes, has the antigenicity similar to the HEV particulate antigen, and the latter is between ORF 1And ORF 2Between, contain 4 epitopes.According to above achievement in research, HEV has been carried out big quantity research both at home and abroad, the epitope that proves HEV is mainly at ORF 2And ORF 3In, and carried out ORF 2And ORF 3Expression and antigenicity research.But do not carry out the development of HEV chimeric gene vaccine both at home and abroad as yet.
Summary of the invention
The objective of the invention is to develop a kind of safe, hepatitis E virus (HEV) chimeric gene vaccine (seeing accompanying drawing 1) efficiently, effective measures are provided for the prevention and control hepatitis E is popular.
The present invention is a specimen with hepatitis E patient feces, extracts viral RNA according to a conventional method, with primer 1 and 2, HEV ORF2 gene is carried out the RT-PCR amplification, carries out the RT-PCR amplification with primer 2 and 4 pairs of HEV ORF3 genes.Above-mentioned PCR product is through behind the purification, with behind the BamHI/EcoRI enzyme action ORF2 gene segment being inserted into pET28a +In the plasmid, obtain pET28-ORF2 (seeing accompanying drawing 2), behind the reuse EcoRI/XhoI enzyme action ORF3 genetic fragment is inserted in the pET28-ORF2 plasmid, obtain chimeric recombiant plasmid pET28-ORF23 (seeing accompanying drawing 3).With recombiant plasmid pET28-ORF23 Transformed E .coli BL21 (DE3) bacterial strain, induce with IPTG, with His-purification system purification destination protein, obtain fusion rotein ORF23.This fusion rotein can be used as the preparation that antigen is used for the HEV diagnostic kit, also can be used for preparing the polypeptide vaccine that prevents hepatitis E.
The present invention is a template with chimeric recombiant plasmid pET28-ORF23, carries out pcr amplification with primer T1 and T2.Above-mentioned PCR product with behind the Kpn I/Xba I enzyme action ORF23 gene segment being inserted among the yeast expression recombinant plasmid pPICZ alpha A, obtains chimeric recombinant plasmid pPICZ alpha A-ORF23 (seeing accompanying drawing 4) through behind the purification.Chimeric recombinant plasmid pPICZ alpha A-ORF23, changes in the yeast cells by the plasmid DNA of electrotransfer after with linearisation the plasmid vector linearisation with Sac I, induces with pure methanol, and with His-purification system purification destination protein, acquisition fusion rotein ORF23.This fusion rotein can be used as the preparation that antigen is used for the HEV diagnostic kit, also can be used for preparing the polypeptide vaccine that prevents hepatitis E.
The present invention's BamHI/XhoI double enzymolysis downcuts the HEVORF23 genetic fragment from recombiant plasmid pET28-ORF23, be inserted into pcDNA again 3In the plasmid, obtain recombiant plasmid pcDNA 3-ORF23 (seeing accompanying drawing 5).Recombiant plasmid is as dna gene vaccine Blab/C mice, and immunization route is intramuscular injection, and injected dose is 100ug and 200ug, every 3 the week 1 time, inject altogether 2 times.Get mice serum after the per injection 2 weeks and detect antibody, the T cell proliferative response of mice is detected in last injection back.Found that after 2 immunity, mice all produces the HEV specific antibody, and produce tangible T cell proliferative response.Illustrate that this recombiant plasmid can be used as the HEV chimeric gene vaccine.
Hepatitis E virus (HEV) chimeric gene vaccine, it contains coding HEV opening code-reading frame 2 albumen (ORF2) gene, it can instruct produce HEV protein or with the homologous substantially protein of HEV protein.This nucleotide sequence is called as below HEV ORF2 is shown in:
HEV?ORF2：
CAGCTGTTCT?ACTCTCGTCC?CGTCGTCTCA?GCCAATGGCG?AGCCGACTGT 50
TAAGCTTTAT?ACATCTGTAG?AGAATGCTCA?GCAGGATAAG?GGTATTGCAA 100
TCCCGCATGA?CATCGACCTC?GGGGAGTCTC?GTGTAGTTAT?TCAGGATTAT 150
GACAACCAAC?ATGAGCAGGA?CCGACCGACA?CCTTCCCCAG?CCCCATCGCG 200
CCCTTTTTCT?GTCCTCCGAG?CTAATGATGT?GCTTTGGCTT?TCTTTCACCG 250
CTGCCGAGTA?TGACCAGTCC?ACTTACGGCT?CTTCGACCGG?CCCAGTCTAT 300
GTCTCTGACT?CTGTGACCTT?GGTTAATGTT?GCGACCGGCG?CGCAGGCCGT 350
TGCCCGGTCA?CTCGACTGGA?CCAAGGTCAC?ACTTGATGGT?CGCCCCCTTT 400
CCACCATCCA?GCAGCATTCA?AAGACCTTCT?TTGTCCTGCC?GCTCCGCGGT 450
AAGCTCTCCT?TTTGGGAGGC?AGGTACTACT?AAAGCCGGGT?ACCCTTATAA 500
TTATAACACC?ACTGCTAGTG?ACCAACTGCT?CGTTGAGAAT?GCCGCTGGGC 550
ATCGGGTTGC?TATTTCCACT?TACACCACTA?GCCTGGGTGC?TGGCCCCGTC 600
TCTATTTCCG?CGGTTGCTGT?TTTAGCCCCC?CACTCCGCGC?TAGCATTGCT 650
TGAGGATACC?ATGGACTACC?CTGCCCGCGC?CCATACTTTC?GATGACTTCT 700
GCCCGGAGTG?CCGCCCCCTT?GGCCTCCAGG?GCTGTGCTTT?TCAGTCTACT 750
GTCGCTGAGC?TTCAGCGCCT?TAAGATGAAG?GTGGGTAAAA?CTCGGGAGTT 800
G 801
Hepatitis E virus (HEV) chimeric gene vaccine, it contains coding HEV opening code-reading frame 3 albumen (ORF3) gene, it can instruct produce HEV protein or with the homologous substantially protein of HEV protein.This nucleotide sequence is called as below HEV ORF3 is shown in:
HEV?ORF3：
ATGAATAACA?TGTCTTTTGC?TGCGCCCATG?GGTTCGCGAC?CATGCGCCCT 50
CGGCCTATTT?TGCTGTTGCT?CCTCATGTTT?CTGCCTATGC?TGCCCGCGAC 100
ACCGCCCGGT?CAGCCGTCTG?GCCGCCGTCG?TGGGCGGCGC?AGCGGCGGTT 150
CCGGCGGTGG?TTTCTGGGGT?GACCGGGTTG?ATTCTCAGCC?CTTCGCAATC 200
CCCTATATTC?ATCCAACCAA?CCCCTTCGCC?CCCGATGTCA?CCGCTGCGGC 250
CGGGGCTGGA?CCTCGTGTTC?GCCAACCCGC?CCGACCACTC?GGCTCCGCTT 300
GGCGTGACCA?GGCCCAGCGC?CCCGCCGCTG?CCTCACGTCG?TAGACCTACC 350
ACAGCTGGGG?CCGCGCCGCT?AA 372
Hepatitis E virus (HEV) chimeric gene vaccine, it contains coding HEV ORF2 gene and ORF3 gene simultaneously, and forms a mosaic gene ORF23, it can instruct produce HEV protein or with the homologous substantially protein of HEV protein.This nucleotide sequence is called as below HEV ORF23 is shown in:
HEV?ORF23：
ATGCAGCTGT?TCTACTCTCG?TCCCGTCGTC?TCAGCCAATG?GCGAGCCGAC 50
TGTTAAGCTT?TATACATCTG?TAGAGAATGC?TCAGCAGGAT?AAGGGTATTG 100
CAATCCCGCA?TGACATCGAC?CTCGGGGAGT?CTCGTGTAGT?TATTCAGGAT 150
TATGACAACC?AACATGAGCA?GGACCGACCG?ACACCTTCCC?CAGCCCCATC 200
GCGCCCTTTT?TCTGTCCTCC?GAGCTAATGA?TGTGCTTTGG?CTTTCTTTCA 250
CCGCTGCCGA?GTATGACCAG?TCCACTTACG?GCTCTTCGAC?CGGCCCAGTC 300
TATGTCTCTG?ACTCTGTGAC?CTTGGTTAAT?GTTGCGACCG?GCGCGCAGGC 350
CGTTGCCCGG?TCACTCGACT?GGACCAAGGT?CACACTTGAT?GGTCGCCCCC 400
TTTCCACCAT?CCAGCAGCAT?TCAAAGACCT?TCTTTGTCCT?GCCGCTCCGC 450
GGTAAGCTCT?CCTTTTGGGA?GGCAGGTACT?ACTAAAGCCG?GGTACCCTTA 500
TAATTATAAC?ACCACTGCTA?GTGACCAACT?GCTCGTTGAG?AATGCCGCTG 550
GGCATCGGGT?TGCTATTTCC?ACTTACACCA?CTAGCCTGGG?TGCTGGCCCC 600
GTCTCTATTT?CCGCGGTTGC?TGTTTTAGCC?CCCCACTCCG?CGCTAGCATT 650
GCTTGAGGAT?ACCATGGACT?ACCCTGCCCG?CGCCCATACT?TTCGATGACT 700
TCTGCCCGGA?GTGCCGCCCC?CTTGGCCTCC?AGGGCTGTGC?TTTTCAGTCT 750
ACTGTCGCTG?AGCTTCAGCG?CCTTAAGATG?AAGGTGGGTA?AAACTCGGGA 800
GTTGAATTCG?GGTGGAATGA?ATAACATGTC?TTTTGCTGCG?CCCATGGGTT 850
CGCGACCATG?CGCCCTCGGC?CTATTTTGCT?GTTGCTCCTC?ATGTTTCTGC 900
CTATGCTGCC?CGCGACACCG?CCCGGTCAGC?CGTCTGGCCG?CCGTCGTGGG 950
CGGCGCAGCG?GCGGTTCCGG?CGGTGGTTTC?TGGGGTGACC?GGGTTGATTC 1000
TCAGCCCTTC?GCAATCCCCT?ATATTCATCC?AACCAACCCC?TTCGCCCCCG 1050
ATGTCACCGC?TGCGGCCGGG?GCTGGACCTC?GTGTTCGCCA?ACCCGCCCGA 1100
CCACTCGGCT?CCGCTTGGCG?TGACCAGGCC?CAGCGCCCCG?CCGCTGCCTC 1150
ACGTCGTAGA?CCTACCACAG?CTGGGGCCGC?GCCGCTAA 1188
Hepatitis E virus (HEV) chimeric gene vaccine, it is that mosaic gene ORF23 is inserted in the eukaryon expression plasmid, constitutes recombiant plasmid, recombiant plasmid can be used as a kind of chimeric gene vaccine that prevents hepatitis e virus infection.
Hepatitis E virus mosaic gene ORF23, it can be inserted in all kinds of expression vectors, constitutes recombinant expression, and can give expression to HEV ORF2 and ORF3 fusion rotein, and this fusion rotein can be used for preparing the polypeptide vaccine that prevents hepatitis E.
A kind of brand-new vaccine that gene vaccine gets up as developed recently not only can bring out body and produce protection antibody, the more important thing is the cellular immunization that can induce at virus.Studies show that the mechanism of gene vaccine inducing cell immunity is that it has simulated viral natural infection process.After plasmid DNA (gene vaccine) was absorbed by the myocyte, synthetic protein was degraded to the peptide section that contains epitope, enters endoplasmic reticulum and combines with MHC I quasi-molecule, is transported to cell membrane again, activates the CD8 that is subjected to the restriction of MHC I quasi-molecule +CTL.Merocrine secretion is gone into the antigen of blood, induces humoral immunization, or is captured by antigen presenting cells such as dendritic cell, combines through processing and with MHC II quasi-molecule, activates CD4 +The Th cell, secretion of gamma-IFN, cytokines such as IL-2 participate in immunoregulation effect.The mankind that appear as of gene vaccine conquer viral disease etc. and have brought hope, have very wide application prospect.
Description of drawings
Fig. 1 is the structural representation of hepatitis E virus chimeric gene vaccine of the present invention.
Fig. 2 is the structure flow chart that contains the recombiant plasmid pET28-ORF2 of hepatitis E virus ORF2 gene.
Fig. 3 is the structure flow chart that contains the recombiant plasmid pET28-ORF23 of hepatitis E virus ORF2 gene and ORF3 gene.
Fig. 4 is the structure flow chart that contains the yeast expression recombinant plasmid pPICZ alpha A-ORF23 of hepatitis E virus ORF2 gene and ORF3 gene.
Fig. 5 is the chimeric gene vaccine pcDNA that contains hepatitis E virus ORF2 gene and ORF3 gene 3The structure flow chart of-ORF23.
The specific embodiment
Embodiment 1: the structure that contains the prokaryotic expression plasmid of HEV ORF23 mosaic gene
With hepatitis E patient feces is specimen, extracts viral RNA according to a conventional method, with primer 1 and 2, HEV ORF2 gene is carried out the RT-PCR amplification, carries out the RT-PCR amplification with primer 2 and 4 pairs of HEV ORF3 genes.Reverse transcription reaction (RT) condition is: 42 ℃ 1 hour; The PCR condition is: 94 ℃ 1 minute, 52 ℃ 1 minute, 72 ℃ 2 minutes, totally 35 circulations.Above-mentioned PCR product is through behind the purification, with behind the BamHI/EcoRI enzyme action ORF2 gene segment being inserted into pET28a +In the plasmid, obtain pET28-ORF2 (seeing accompanying drawing 2), behind the reuse EcoRI/XhoI enzyme action ORF3 genetic fragment is inserted in the pET28-ORF2 plasmid, obtain chimeric recombiant plasmid pET28-ORF23 (seeing accompanying drawing 3).
Primer 1:5 ' GTC GGA TCC ATG CAG CTG TTC TAC TCC CGT 3 '
Primer 2: 5 ' GTC GAA TTC AAC TCC CGA GTT TTA CC 3 '
Primer 3:5 ' GGC TGG AAT TCG GGT GGA ATG AAT AAC ATG 3 '
Primer 4:5 ' GTG GCT CGA GTT AGC GGC GCG GCC CCA GCT GT 3 '
The expression of chimeric protein ORF23 and purification: with recombinant expression pET28-ORF23 Transformed E .coliBL21 (DE3) bacterial strain, the picking monoclonal is cultured to A for 37 ℃ with the LB of 50ug/ml kanamycin 600Reach about 0.8, induce inductive condition with the IPTG of 0.5mM: 32 ℃, 4 hours.Centrifugal collection thalline, (0.5M NaCl, 20mM Tris-HCl PH7.9) suspend, and the Ultrasonic Pulverization thalline with His-purification system purification destination protein, obtains fusion rotein ORF23 with buffer.Fusion rotein is through ELISA, and evaluations such as Western-blot are the HEV specific antigen.Fusion rotein ORF23 can be used as the preparation that antigen is used for the HEV diagnostic kit, also can be used for preventing the preparation of the polypeptide vaccine of hepatitis E.
Embodiment 2: the yeast expression construction of recombinant plasmid that contains HEV ORF23 mosaic gene
With chimeric recombiant plasmid pET28-ORF23 is template, carries out pcr amplification with primer T1 and T2.The PCR condition is: 94 ℃ 1 minute, 52 ℃ 1 minute, 72 ℃ 2 minutes, 33 circulations.Above-mentioned PCR product with behind the Kpn I/Xba I enzyme action ORF23 gene segment being inserted among the yeast expression recombinant plasmid pPICZ alpha A, obtains chimeric recombinant plasmid pPICZ alpha A-ORF23 (seeing accompanying drawing 4) through behind the purification.
Primer T1:5 ' GAC TGG GTA CCC AGC TGT TCT ACT CTC GT 3 '
Primer T2:5 ' GTA CTC TAG ACA GCG GCG CGG TCC CAG C 3 '
The expression of chimeric protein ORF23 and purification: with chimeric recombinant plasmid pPICZ alpha A-ORF23 with Sac I with linearization of plasmid vector, change in the yeast cells by the plasmid DNA of electrotransfer after linearisation.Electricity changes the back cell and cultivates, screens up to obtaining single bacterium colony with the YPDS flat board that contains 100ug/ml Zeocin.Dull and stereotyped and the dull and stereotyped mensuration table of the MMH shape of reuse MDH.Institute is obtained the wild type bacterium colony, use the MGYH culture medium, 28-30 ℃, the 250-300rpm shaken cultivation is up to A 600=2-6, centrifugal collecting cell, and with MMH culture medium re-suspended cell, induce with pure methanol to final concentration 0.5%.Centrifugal collection thalline, with buffer (50mM sodium phosphate, PH7.4,1mM PMSF, 1mM EDTA, 5% glycerol) suspends, with His-purification system purification destination protein, obtain fusion rotein ORF23, fusion rotein is through ELISA, evaluations such as Western-blot are the HEV specific antigen.Fusion rotein ORF23 can be used as the preparation that antigen is used for the HEV diagnostic kit, also can be used for preventing the preparation of the polypeptide vaccine of hepatitis E.
Embodiment 3: the structure of chimeric gene vaccine and immune mouse experiment
Use the BamHI/XhoI double enzymolysis, from recombiant plasmid pet28-ORF23, downcut HEV ORF23 genetic fragment, be inserted into pcDNA again 3In the plasmid, obtain recombiant plasmid pcDNA 3-ORF23 (seeing accompanying drawing 1, accompanying drawing 5).Recombiant plasmid is as chimeric gene vaccine immunity Blab/C mice, and immunization route is intramuscular injection, and injected dose is 100ug and 200ug, every 3 weeks 1 time, injects altogether 2 times.Get mice serum after the per injection 2 weeks and detect antibody, the T cell proliferative response of mice is detected in last injection back.Found that after 2 immunity, mice all produces the HEV specific antibody, and produce tangible T cell proliferative response.Illustrate that recombiant plasmid can be used as the HEV chimeric gene vaccine.
＜110〉Zhejiang Academy of Medical Sciences
＜120〉a kind of hepatitis E virus chimeric gene vaccine
＜130〉hepatitis E patent
<160>9
<170>PatentIn?version?3.1
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<211>1188
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<213>Hepatitis?E?virus
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atgcagctgt?tctactctcg?tcccgtcgtc?tcagccaatg?gcgagccgac?tgttaagctt 60
tatacatctg?tagagaatgc?tcagcaggat?aagggtattg?caatcccgca?tgacatcgac 120
ctcggggagt?ctcgtgtagt?tattcaggat?tatgacaacc?aacatgagca?ggaccgaccg 180
acaccttccc?cagccccatc?gcgccctttt?tctgtcctcc?gagctaatga?tgtgctttgg 240
ctttctttca?ccgctgccga?gtatgaccag?tccacttacg?gctcttcgac?cggcccagtc 300
tatgtctctg?actctgtgac?cttggttaat?gttgcgaccg?gcgcgcaggc?cgttgcccgg 360
tcactcgact?ggaccaaggt?cacacttgat?ggtcgccccc?tttccaccat?ccagcagcat 420
tcaaagacct?tctttgtcct?gccgctccgc?ggtaagctct?ccttttggga?ggcaggtact 480
actaaagccg?ggtaccctta?taattataac?accactgcta?gtgaccaact?gctcgttgag 540
aatgccgctg?ggcatcgggt?tgctatttcc?acttacacca?ctagcctggg?tgctggcccc 600
gtctctattt?ccgcggttgc?tgttttagcc?ccccactccg?cgctagcatt?gcttgaggat 660
accatggact?accctgcccg?cgcccatact?ttcgatgact?tctgcccgga?gtgccgcccc 720
cttggcctcc?agggctgtgc?ttttcagtct?actgtcgctg?agcttcagcg?ccttaagatg 780
aaggtgggta?aaactcggga?gttgaattcg?ggtggaatga?ataacatgtc?ttttgctgcg 840
cccatgggtt?cgcgaccatg?cgccctcggc?ctattttgct?gttgctcctc?atgtttctgc 900
ctatgctgcc?cgcgacaccg?cccggtcagc?cgtctggccg?ccgtcgtggg?cggcgcagcg 960
gcggttccgg?cggtggtttc?tggggtgacc?gggttgattc?tcagcccttc?gcaatcccct 1020
atattcatcc?aaccaacccc?ttcgcccccg?atgtcaccgc?tgcggccggg?gctggacctc 1080
gtgttcgcca?acccgcccga?ccactcggct?ccgcttggcg?tgaccaggcc?cagcgccccg 1140
ccgctgcctc?acgtcgtaga?cctaccacag?ctggggccgc?gccgctaa 1188
<210>2
<211>801
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<213>Hepatitis?E?virus
<220>
<221>gene
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cagctgttct?actctcgtcc?cgtcgtctca?gccaatggcg?agccgactgt?taagctttat 60
acatctgtag?agaatgctca?gcaggataag?ggtattgcaa?tcccgcatga?catcgacctc 120
ggggagtctc?gtgtagttat?tcaggattat?gacaaccaac?atgagcagga?ccgaccgaca 180
ccttccccag?ccccatcgcg?ccctttttct?gtcctccgag?ctaatgatgt?gctttggctt 240
tctttcaccg?ctgccgagta?tgaccagtcc?acttacggct?cttcgaccgg?cccagtctat 300
gtctctgact?ctgtgacctt?ggttaatgtt?gcgaccggcg?cgcaggccgt?tgcccggtca 360
ctcgactgga?ccaaggtcac?acttgatggt?cgcccccttt?ccaccatcca?gcagcattca 420
aagaccttct?ttgtcctgcc?gctccgcggt?aagctctcct?tttgggaggc?aggtactact 480
aaagccgggt?acccttataa?ttataacacc?actgctagtg?accaactgct?cgttgagaat 540
gccgctgggc?atcgggttgc?tatttccact?tacaccacta?gcctgggtgc?tggccccgtc 600
tctatttccg?cggttgctgt?tttagccccc?cactccgcgc?tagcattgct?tgaggatacc 660
atggactacc?ctgcccgcgc?ccatactttc?gatgacttct?gcccggagtg?ccgccccctt 720
ggcctccagg?gctgtgcttt?tcagtctact?gtcgctgagc?ttcagcgcct?taagatgaag 780
gtgggtaaaa?ctcgggagtt?g 801
<210>3
<211>372
<212>DNA
<213>Hepatitis?E?virus
<220>
<221>gene
<222>(1)..(372)
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atgaataaca?tgtcttttgc?tgcgcccatg?ggttcgcgac?catgcgccct?cggcctattt 60
tgctgttgct?cctcatgttt?ctgcctatgc?tgcccgcgac?accgcccggt?cagccgtctg 120
gccgccgtcg?tgggcggcgc?agcggcggtt?ccggcggtgg?tttctggggt?gaccgggttg 180
attctcagcc?cttcgcaatc?ccctatattc?atccaaccaa?ccccttcgcc?cccgatgtca 240
ccgctgcggc?cggggctgga?cctcgtgttc?gccaacccgc?ccgaccactc?ggctccgctt 300
ggcgtgacca?ggcccagcgc?cccgccgctg?cctcacgtcg?tagacctacc?acagctgggg 360
ccgcgccgct?aa 372
<210>4
<211>30
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<221>primer
<222>(1)..(30)
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<222>(1)..(26)
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gtcgaattca?actcccgagt?tttacc 26
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<221>primer
<222>(1)..(32)
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<222>(1)..(28)
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Claims (1)

1, a kind of hepatitis E virus chimeric gene vaccine is characterized in that:
(i) it is that HEV ORF23 is inserted into plasmid pcDNA 3In the recombiant plasmid pcDNA that obtains 3-ORF23, its plasmid map are the plasmid maps shown in the accompanying drawing 1, and
(ii) HEV ORF23 sequence is as follows:
ATGCAGCTGT?TCTACTCTCG?TCCCGTCGTC?TCAGCCAATG?GCGAGCCGAC?50
TGTTAAGCTT?TATACATCTG?TAGAGAATGC?TCAGCAGGAT?AAGGGTATTG?100
CAATCCCGCA?TGACATCGAC?CTCGGGGAGT?CTCGTGTAGT?TATTCAGGAT?150
TATGACAACC?AACATGAGCA?GGACCGACCG?ACACCTTCCC?CAGCCCCATC?200
GCGCCCTTTT?TCTGTCCTCC?GAGCTAATGA?TGTGCTTTGG?CTTTCTTTCA?250
CCGCTGCCGA?GTATGACCAG?TCCACTTACG?GCTCTTCGAC?CGGCCCAGTC?300
TATGTCTCTG?ACTCTGTGAC?CTTGGTTAAT?GTTGCGACCG?GCGCGCAGGC?350
CGTTGCCCGG?TCACTCGACT?GGACCAAGGT?CACACTTGAT?GGTCGCCCCC?400
TTTCCACCAT?CCAGCAGCAT?TCAAAGACCT?TCTTTGTCCT?GCCGCTCCGC?450
GGTAAGCTCT?CCTTTTGGGA?GGCAGGTACT?ACTAAAGCCG?GGTACCCTTA?500
TAATTATAAC?ACCACTGCTA?GTGACCAACT?GCTCGTTGAG?AATGCCGCTG?550
GGCATCGGGT?TGCTATTTCC?ACTTACACCA?CTAGCCTGGG?TGCTGGCCCC?600
GTCTCTATTT?CCGCGGTTGC?TGTTTTAGCC?CCCCACTCCG?CGCTAGCATT?650
GCTTGAGGAT?ACCATGGACT?ACCCTGCCCG?CGCCCATACT?TTCGATGACT?700
TCTGCCCGGA?GTGCCGCCCC?CTTGGCCTCC?AGGGCTGTGC?TTTTCAGTCT?750
ACTGTCGCTG?AGCTTCAGCG?CCTTAAGATG?AAGGTGGGTA?AAACTCGGGA?800
GTTGAATTCG?GGTGGAATGA?ATAACATGTC?TTTTGCTGCG?CCCATGGGTT 850
CGCGACCATG?CGCCCTCGGC?CTATTTTGCT?GTTGCTCCTC?ATGTTTCTGC 900
CTATGCTGCC?CGCGACACCG?CCCGGTCAGC?CGTCTGGCCG?CCGTCGTGGG 950
CGGCGCAGCG?GCGGTTCCGG?CGGTGGTTTC?TGGGGTGACC?GGGTTGATTC 1000
TCAGCCCTTC?GCAATCCCCT?ATATTCATCC?AACCAACCCC?TTCGCCCCCG 1050
ATGTCACCGC?TGCGGCCGGG?GCTGGACCTC?GTGTTCGCCA?ACCCGCCCGA 1100
CCACTCGGCT?CCGCTTGGCG?TGACCAGGCC?CAGCGCCCCG?CCGCTGCCTC 1150
ACGTCGTAGA?CCTACCACAG?CTGGGGCCGC?GCCGCTAA 1188。
CNB031168620A 2003-05-09 2003-05-09 Bacterin of tabling gene of E type hepatitis virus Expired - Fee Related CN100438907C (en)

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