CN105018489A - Kit for recognizing Brucella wild strain and vaccine strains A19 and S2 - Google Patents

Kit for recognizing Brucella wild strain and vaccine strains A19 and S2 Download PDF

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CN105018489A
CN105018489A CN201510483012.9A CN201510483012A CN105018489A CN 105018489 A CN105018489 A CN 105018489A CN 201510483012 A CN201510483012 A CN 201510483012A CN 105018489 A CN105018489 A CN 105018489A
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brucella
vaccine strain
seq
strain
sample
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CN105018489B (en
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何洪彬
赵贵民
王洪梅
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DAIRY CATTLE RESEARCH CENTER OF SHANDONG ACADEMY OF AGRICULTURAL SCIENCES
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DAIRY CATTLE RESEARCH CENTER OF SHANDONG ACADEMY OF AGRICULTURAL SCIENCES
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Abstract

The invention relates to a kit for recognizing a Brucella wild strain and vaccine strains A19 and S2. The kit comprises a special primer pair SEQ ID No.1 and SEQ ID No.2 for recognizing the Brucella vaccine strain A19 and a special primer pair SEQ ID No.3 and SEQ ID No.4 for recognizing the Brucella vaccine strain S2. The kit is used for conducting further sequencing analysis on a PCR amplification product after the Brucella and other conventional bacterial strains are distributed on a PCR amplification-electrophoresis detection area, and the Brucella A19 and S2 vaccine strains in a clinic sample can be rapidly and effectively recognized and diagnosed according to the sequencing result.

Description

Differentiate the test kit of brucella street strain and vaccine strain A19 and S2
Technical field
The invention belongs to biological technical field, be specifically related to a kind of test kit differentiating brucella street strain and vaccine strain A19 and S2.
Background technology
Brucellosis (Brucellosis) suffers from transmissible disease altogether by the bacterial a kind of people and animals (beast) be distributed widely in all over the world of Brucella, and it not only affects sound development but also the harm humans public health health of livestock industry.Defend the national Epidemic Situation of Notifiable Infectious Diseases data of planning commission's announcement according to country, it is 57222 that Chinese people in 2014 infects brucellosis number, and sickness rate increased 31.48% than 2013.The contagium that people infects brucellosis is mainly derived from the animal of infection and contaminated livestock product, and therefore, controlling and eliminate animal brucellosis, is the basic guarantee preventing human infection's cloth Lu Shi disease.
Current vaccine immunity is still one of major measure controlling animal brucellosis.The brucella vaccine strain that present mainly uses is ox kind S19 strain and RB51 strain and sheep kind Rev.1 strain, and these vaccine strain China not yet introduce at present and use.Vaccine strain mainly B. abortus A19 vaccine strain and the pig kind brucella S2 vaccine strain that China uses, also once used sheep kind M5-90 vaccine strain, in the past because virulence problem does not temporarily re-use now.The use of A19 and S2 vaccine strain provides important leverage for the prevention and control of China's fauna brucellosis, but also there is the gordian technique bottleneck problem cannot differentiating vaccine strain and wild virus infection strain.Although competitive ELISA (cELISA) and fluorescence polarization experiment (FPT) are with the advantage of its high-throughput and operating aspect, the serology infected at brucella attenuated vaccine and wild strain differentiates certain application, but concerning the serum sample of Unknown Background, single detects still can not definitely differentiate vaccine immunity or wild virus infection.From etiology aspect differential diagnosis brucella street strain nucleic acid, accurately can judge whether animal body carries disease germs, the quarantine for cloth brucellosis animals showing positive is eliminated and is provided support.Therefore, utilize molecular biology method, according to vaccine strain and other brucella strain genome difference base sequences, by pcr amplification and PCR primer sequencing, effectively can realize the molecular identificalion of vaccine strain and street strain, be applied to clinical discriminating, technical guarantee can be provided for the discriminating of China A19 and S2 vaccine strain.
Summary of the invention
Contriver is by genome sequence comparison, find with other Brucella bacterial genomes DNA sequence dnas unlike, A19 vaccine strain is in genome 22840 site, i.e. 344 site of SEQ ID No.5, lack 7 nucleotide sequences, this site postorder is classified as AGATTTCAGA, and other brucella sequences are AGATTTCAGATTTCAGA, because be the tumor-necrosis factor glycoproteins of AGATTTC herein, so there will be two kinds of sequence deletion phenomenons (AGATTTC or TTTCAGA) when sequence alignment.At this deletion segment upstream and downstream place design primer, by sequencing after pcr amplification, the difference of sequence alignment and order-checking peak figure just specificity can differentiate B. abortus A19 vaccine strain.We find that pig kind brucella S2 vaccine strain is in genome 246967 site equally, compared with other Brucella bacterial genomes, S2 vaccine strain is in this site, namely 369 site of SEQ ID No.6 lack 25 nucleotide sequences (TCCCTCATAAATGGCTTTCTTCATA), according to this deletion sequence, design of amplification primers of the present invention, by whether there is overlapping peak in sequence alignment and peak figure just itself and other brucella street strain or vaccine strain can be differentiated, be more than propose technical basis of the present invention.
The object of this invention is to provide a kind of test kit and the using method thereof of differentiating brucella street strain and vaccine strain A19 and S2, this test kit can differentiate brucella A19 and S2 vaccine strain in clinical sample specifically.
For realizing the object of the invention, adopt following technical scheme:
Differentiate the test kit of brucella street strain and vaccine strain A19 and S2, this PCR kit is made up of PCR reaction solution, archaeal dna polymerase, positive quality control standard substance and negative quality control standard product;
Described PCR reaction solution comprises to be identified and the primer pair of check order A19 vaccine strain and S2 vaccine strain specific nucleotide sequences, wherein differentiate that the upstream primer sequence of A19 vaccine strain is as shown in SEQ ID No.1, downstream primer sequence is as shown in SEQ ID No.2, differentiate that the upstream primer sequence of S2 vaccine strain is as shown in SEQ ID No.3, downstream primer sequence is as shown in SEQ ID No.4.As follows respectively:
SEQ ID No.1:5'-TTCACCGTCATCGGATAATAGGTGCCA-3'
SEQ ID No.2:5'-GGCGGGCTGCATTCTTTACTCTGC-3'
SEQ ID No.3:5'-CCTGCTGAGCGATGACCACCA-3'
SEQ ID No.4:5'-CCGCCAGAACATGCGATTTGA-3'
Described positive quality control standard substance comprise B. abortus A19 vaccine strain positive quality control standard substance and pig kind brucella S2 vaccine strain positive quality control standard substance;
The pEASY-T3 recombinant plasmid that described B. abortus A19 vaccine strain positive quality control standard substance are made up of the nucleotide fragments containing 562 bases forms, and the pEASY-T3 recombinant plasmid that described pig kind brucella S2 vaccine strain positive quality control standard substance are made up of the nucleotide fragments containing 539 bases forms.
The described sequence containing the nucleotide fragments of 562 bases is as shown in SEQ ID No.5:
SEQ ID No.5:
5'-TTCACCGTCATCGGATAATAGGTGCCACCCTTTACCGTCGCATCATTGCAGACGATCATGCATTCGCGGCCCGATACGCGCCCGATGCCGGTGATGAAGCCAGCGGCGGGCGCTGCCCCGCCATACATGCCATGCGCTGCCGTCAGCCCCAGTTCCAGAAAGGGGGAACCCGGATCGAGCAATTGCGCCACGCGCTCACGGGGCAGAAGTTTTCCGCGCGAAACATGGCGGTCGCGCGCTTTCTCGCCGCCGCCGTCAATGGCAATGCGCGAGGCTTCCGCCACCACGTCGATTGCCGCCAGCATGGCCTTGCGGTTGGCCTCGAAGCTTGCGCTGCGCGTCGAGATTTCAGAACCGGCATCAACGGGTCTCCTGAAAGAGTTCCCGTCCGATCAGCATACGCCGGATTTCCGACGTGCCCGCGCCGATTTCATAAAGCTTGGCATCGCGCAAAAGGCGGCCCGTCGGATAATCGTTGATATAGCCGTTGCCGCCGAGAGACTGGATCGCCTGCAAGGCCATCTGCGTGGCATTTTCCGCAGAGTAAAGAATGCAGCCCGCC-3'
The described sequence containing the nucleotide fragments of 539 bases is as SEQ ID No.6:
SEQ ID No.6:
5'-CCTGCTGAGCGATGACCACCACCGAGCCGCGGTCGAACACGGCAAGCTGATTGGCCTGTTTGGAACGGTCGGCAAGCTCGCGCATGAAGGGCGTGGCGAAGGAGGCAAGCCTGCGCACCGGCGCATGGAGTTGCGCAAGCCCGAACAGCTTCAGCGTCAGTGAATAACGGTCGCCATCGAGTTTGGTGACATAGCCGCGCTTCACCAGCCGGTCCAGCATCCGGTAAAATTCGTTGGGGCTGCGGTCGAGATGCTTGGCGATCTCGGCCTGTGTCAGCCCGCCATCCACACTCGCCAGCAATTCCAATATGTCCAGCCCCTTGTCCAGCGCGGGCGCGCGATAGCGATCGTCAGTTTCCAAGGTCGGCTACGAACAGCGTAAAGGGTGAAAGGAATAACCACCCGCAAATCGCCTTGACCATGTTTGAATAATATGTTTGCATATAAATGGAAGCCCCACAATCGGGGAACGTGGACGGGGGAGCGTCCGCTAATAAGGAGGAGACGAATGCAGGATTTCAAATCGCATGTTCTGGCGG-3'
Described PCR reaction solution also comprises containing dNTPs, Mg 2+, distilled water PCR damping fluid.
The described nucleotide fragments containing 562 bases clones to obtain from B. abortus A19 vaccine strain, and the described nucleotide fragments containing 539 bases clones to obtain from pig kind brucella S2 vaccine strain.
Described negative quality control standard product are aseptic double-distilled water (ddH 2o).
Invention further provides the using method of the PCR kit differentiating brucella street strain and vaccine strain A19 and S2, condition and the step of the method are as follows:
(1) genomic dna of sample to be tested is extracted;
Described sample to be detected is blood, milk sample, tissue samples, aerosol sample etc.
(2) with the sample genomic dna extracted for template, sample DNA, positive quality control standard substance and negative quality control standard product are joined respectively in the PCR reaction tubes of the 50 μ L systems containing PCR reaction solution and archaeal dna polymerase, increase according to the PCR reaction conditions after optimizing, concrete reaction conditions is: 94 DEG C of 3min, 94 DEG C of 30sec, 60 DEG C of 30sec, 72 DEG C of 30sec, 35 circulations, 72 DEG C of 10min;
Described PCR reaction solution is by identifying the primer pair of brucella A19 vaccine strain and S2 vaccine strain and containing dNTPs, Mg 2+, distilled water PCR damping fluid composition;
Described primer pair is respectively SEQ ID No.1, SEQ ID No.2 and SEQ ID No.3, SEQ ID No.4, respectively called after A19-F, A19-R and S2-F, S2-R, and sequence is as follows:
Forward primer A19-F:5'-TTCACCGTCATCGGATAATAGGTGCCA-3'
Reverse primer A19-R:5'-GGCGGGCTGCATTCTTTACTCTGC-3'
Forward primer S2-F:5'-CCTGCTGAGCGATGACCACCA-3'
Reverse primer S2-R:5'-CCGCCAGAACATGCGATTTGA-3'
Described PCR reaction system is 50 μ L, specifically comprises following component:
(3) 50 μ L PCR primer are got, detect with 1.5% agarose gel electrophoresis, observe and differentiate that B. abortus A19 strain primer pair amplifies goes out 562bp and size is corresponding with it band, differentiate that pig kind brucella S2 vaccine strain primer pair amplifies goes out 539bp and size is corresponding with it band; Those skilled in the art should know, when agarose gel electrophoresis detects, show the band corresponding with object stripe size, mean pcr amplification product size close, because of sample source or target kind difference, PCR primer size has less difference, but display band is corresponding, and the such as band differed within the scope of 30bp/20bp all shows size correspondence.
(4) if above-mentioned PCR detected result and object band are not inconsistent, then pattern of descriptive parts is that brucella is negative, if PCR test strip size is correct, then cuts glue to positive band and reclaims purifying, and then carry out sequencing.
(5) result judges:
A19 vaccine strain identification result judges, use the 562bp of A19-F primer pair purifying or size is corresponding with it product to check order, if sequencing result peak figure is simple spike, mate completely with after SEQ ID No.5 comparison, then this sample is A19 vaccine strain; If sequencing result peak figure is simple spike, have more 7 nucleotide sequences (AGATTTC or TTTCAGA) with after SEQ ID No.5 comparison in the 344th site, then this sample is other brucella street strain or the vaccine strains except A19 vaccine strain; If sequencing result and SEQ ID No.5 comparison, in the sequence the 354th of peak figure, namely occur cover peak after AGATTTCAGA, then this sample is A19 vaccine strain and other brucella strains mixing.
S2 vaccine strain identification result judges, use the 539bp of S2-F primer pair purifying and size is corresponding with it product to check order, if sequencing result peak figure is simple spike, mate completely with after SEQ ID No.6 comparison, then this sample is S2 vaccine strain; If sequencing result peak figure is simple spike, have more 25 nucleotide sequences (TCCCTCATAAATGGCTTTCTTCATA) with after SEQ ID No.6 comparison in the 369th site, then this sample is other brucella street strain or the vaccine strains except S2 vaccine strain; If sequencing result and SEQ ID No.5 comparison, occur cover peak behind peak graphic sequence the 369th site, then this sample is S2 vaccine strain and other brucella strains mixing.
It should be understood by those skilled in the art that above-mentioned discrimination method, its direct object is strain identification kind, and non-acquisition medical diagnosis on disease result.
The present invention achieves following effect:
(1) for the discriminating of China A19 and S2 vaccine strain provides new technique means;
(2) primer pair of the present invention has higher specificity, by amplification-electrophoresis detection, effectively can distinguish brucella and other Conventional bacteria bacterial strains;
(3) other brucella street strains and vaccine strain are made a distinction, have high accuracy rate by discrimination method of the present invention effectively.
Accompanying drawing explanation
Fig. 1 A19 vaccine strain deletion segment place upstream and downstream sequence pcr amplification, +: template is the pcr amplification product 562bp – of A19 vaccine strain positive quality control standard substance: template is negative quality control standard product, 1-5: template is respectively the pcr amplification product 562bp of B. abortus vaccine strain A19 strain, pig kind brucella vaccine strain S2 strain, brucella melitensis vaccine strain M5-90 strain, Br.ovis 63/290 strain, dog brucella RM6/66 pnca gene group DNA; 6-10: template is respectively Escherichia coli O 157: H7, Yersinia enterocolitica O:9, Salmonellas, streptococcus aureus, cow mycobacteria genomic dna.
Fig. 2 S2 vaccine strain deletion segment place upstream and downstream sequence pcr amplification, +: template is the pcr amplification product 539bp – of S2 vaccine strain positive quality control standard substance: template is negative quality control standard product, 1-5: template is respectively the pcr amplification product 539bp of pig kind brucella vaccine strain S2 strain, B. abortus vaccine strain A19 strain, brucella melitensis vaccine strain M5-90 strain, Br.ovis 63/290 strain, dog brucella RM6/66 pnca gene group DNA; 6-10: template is respectively Escherichia coli O 157: H7, Yersinia enterocolitica O:9, Salmonellas, streptococcus aureus, cow mycobacteria genomic dna.
Fig. 3 A19 vaccine strain deletion segment place sequencing peak figure, A: order-checking peak figure is simple spike, and mate completely with after SEQID No.5 comparison, detection template is A19 vaccine strain.B: order-checking peak figure is simple spike, and have more 7 nucleotide sequences (AGATTTC or TTTCAGA) with after SEQ ID No.5 comparison in 344 site, detection template is other brucella street strain or vaccine strains except A19 vaccine strain.Behind sequence the 354th site, namely there is cover peak in C: sequencing result and SEQ ID No.5 comparison, peak figure, detection template is A19 vaccine strain and the mixing of other brucella strains after AGATTTCAGA sequence.
Fig. 4 S2 vaccine strain deletion segment place sequencing peak figure, A: order-checking peak figure is simple spike, and mate completely with after SEQ ID No.6 comparison, detection template is S2 vaccine strain.B: order-checking peak figure is simple spike, and have more 25 nucleotide sequences (TCCCTCATAAATGGCTTTCTTCATA) at 369 places with after SEQ ID No.6 comparison, detection template is other brucella street strain or vaccine strains except S2 vaccine strain.C: sequencing result and SEQ ID No.6 comparison, peak figure in sequence site 369 after there is cover peak, detection template is S2 vaccine strain and the mixing of other brucella strains.
Embodiment
Following embodiment is used for further illustrating the present invention, but is not used for limiting the scope of the invention.
Following examples all conveniently test conditions and method are carried out, or according to the test conditions that manufacturer advises.
1. test materials
B. abortus vaccine strain A19 strain (B.abortus A19), pig kind brucella vaccine strain S2 strain (B.suis S2), brucella melitensis vaccine strain M5-90 strain (B.melitensis M5-90), Br.ovis 63/290 strain (B.ovis 63/290), dog brucella RM6/66 strain (B.canis RM6/66), Escherichia coli O 157: H7, Yersinia enterocolitica O:9, Salmonellas, streptococcus aureus (CMCC25623), cow mycobacteria (M.bovis ATCC 19210), be diagnosed as the blood of the brucella positive clinically, milk sample, the DNA samples such as aborted fetus tissue and aerosol are preserved by Cow Research Center, Shandong Academy of Agricultural Sciences's disease research room.
Archaeal dna polymerase (TaKaRa LA Taq) is purchased from precious biotechnology (Dalian) company limited, agarose is purchased from Beijing Quanshijin Biotechnology Co., Ltd, Fast DNA extraction test kit, DNA of bacteria extract test kit, sepharose recovery test kit etc. all purchased from TIANGEN Biotech (Beijing) Co., Ltd., and other biochemical reagents are import packing or domestic analytical pure.PCR primer is synthesized by Sangon Biotech (Shanghai) Co., Ltd., and determined dna sequence is completed by Shandong Academy of Agricultural Sciences center of checking order.
2. laboratory apparatus
Grads PCR instrument (TaKaRa TP-600), electrophoresis apparatus (Beijing Liuyi Instrument Factory DYY-6C type), Alpha human-like gel imaging system red (ProteinSimple company of the U.S.), DNA sequencer (ABI3730XL DNA Analyzer).
Embodiment one, differentiate the using method of the PCR kit of brucella street strain and vaccine strain A19 and S2
(1) genomic dna of sample to be tested is extracted: use Fast DNA extraction test kit to carry out the extraction of genomic dna to blood to be detected, milk sample, tissue samples, aerosol equal samples.
(2) with the sample genomic dna extracted for template, use A19-F respectively, A19-R and S2-F, S2-R primer pair carries out pcr amplification, simultaneously using positive quality control standard substance and negative quality control standard product as positive and negative control, successively each component of 50 μ L reaction systems is added in PCR reaction tubes, be respectively 10 × PCR Buffer:5.0 μ L, dNTP Mixture (2.5mM): 8.0 μ L, the forward primer of 10 μMs: 2.0 μ L, the reverse primer of 10 μMs: 2.0 μ L, sample to be tested DNA:5.0 μ L, archaeal dna polymerase: 0.5 μ L, finally add 27.5 μ L distilled water (ddH 2o) 50 μ L are supplied.The expanding effect of PCR directly has influence on specificity and the susceptibility of detected result, therefore needs to be optimized the correlation parameter in PCR reaction conditions, comprises the concentration of primer, Mg 2+concentration, annealing temperature, annealing time, cycle index and extension time etc.The optimization of PCR reaction conditions adopts prior art, and the PCR reaction conditions after final optimization pass is: primer concentration is 0.4 μm of oL/L, Mg 2+concentration is 0.2mmoL/L, PCR reaction conditions: 94 DEG C of 3min, 94 DEG C of 30sec, 60 DEG C of 30sec, 72 DEG C of 30sec, 35 circulations, 72 DEG C of 10min.Pcr amplification is carried out with the reaction conditions that above-mentioned optimization is good.
(3) after reaction terminates, get 50 μ L PCR primer, carry out electrophoresis (120V25min) with 1.5% sepharose to detect, observe and differentiate that B. abortus A19 strain primer pair amplifies goes out the band of 562bp, differentiate that pig kind brucella S2 vaccine strain amplifies the band of 539bp.
(4) if above-mentioned PCR detected result and object band are not inconsistent, then pattern of descriptive parts is that brucella is negative, if PCR test strip size is correct, then cuts glue to positive band and reclaims purifying, then carry out sequencing by DNA sequencer.
(5) result judges:
A19 vaccine strain identification result judges, use the 562bp product of A19-F primer pair purifying to check order, if sequencing result peak figure is simple spike, mate completely with after SEQ ID No.5 comparison, then this sample is A19 vaccine strain; If sequencing result peak figure is simple spike, have more 7 nucleotide sequences (AGATTTC or TTTCAGA) with after SEQ ID No.5 comparison in the 344th site, then this sample is other brucella street strain or the vaccine strains except A19 vaccine strain; If sequencing result and SEQ ID No.5 comparison, in the sequence the 354th of peak figure, namely occur cover peak after AGATTTCAGA, then this sample is A19 vaccine strain and other brucella strains mixing.
S2 vaccine strain identification result judges, use the 539bp product of S2-F primer pair purifying to check order, if sequencing result peak figure is simple spike, mate completely with after SEQ ID No.6 comparison, then this sample is S2 vaccine strain; If sequencing result peak figure is simple spike, have more 25 nucleotide sequences (TCCCTCATAAATGGCTTTCTTCATA) with after SEQ ID No.6 comparison in the 369th site, then this sample is other brucella street strain or the vaccine strains except S2 vaccine strain; If sequencing result and SEQ ID No.6 comparison, occur cover peak behind peak graphic sequence the 369th site, then this sample is S2 vaccine strain and other brucella strains mixing.
The assembling of embodiment two, PCR kit
(1) PCR reaction solution is prepared:
1. 2 are designed respectively to the primer identifying Brucella abortus A19 vaccine strain and pig kind brucella S2 vaccine strain: be SEQ ID No.1, SEQ ID No.2 and SEQ ID No.3, SEQ ID No.4, called after A19-F, A19-R and S2-F, S2-R, sequence is as follows:
A19-F:5'-TTCACCGTCATCGGATAATAGGTGCCA-3'
A19-R:5'-GGCGGGCTGCATTCTTTACTCTGC-3'
S2-F:5'-CCTGCTGAGCGATGACCACCA-3'
S2-R:5'-CCGCCAGAACATGCGATTTGA-3'
2. the preparation of PCR reaction solution: PCR reaction solution is by the primer of B. abortus A19 vaccine strain or pig kind brucella S2 vaccine strain with containing dNTPs, Mg 2+, distilled water (ddH 2o) PCR damping fluid composition, the cumulative volume of PCR reaction solution is 44.5 μ L, and the amount of every bar primer is 2 μ L (primer concentration is 10 μm of oL/L), containing dNTPs, Mg 2+, distilled water (ddH 2the total amount of PCR buffer reagent O) is 40.5 μ L, wherein distilled water (ddH 2o) be 27.5 μ L.
(2) preparation of positive quality control standard substance:
1. the extraction of template DNA: respectively test kit is extracted to the bacterium liquid application DNA of bacteria of B. abortus vaccine strain A19 and pig kind brucella vaccine strain S2 and extract DNA.
2. pcr amplification: with the DNA extracted for template, according to PCR reaction system: DNA profiling 5 μ L, archaeal dna polymerase 0.5 μ L, PCR reaction solution 44.5 μ L, PCR reaction conditions is: 94 DEG C of 3min, 94 DEG C of 30sec, 60 DEG C of 30sec, 72 DEG C of 30sec, 35 circulations, 72 DEG C of 10min, object that PCR instrument increases fragment, the agarose gel electrophoresis (120V 25min) with 1.5% identifies PCR object product.
3. the structure of recombinant plasmid and the foundation of positive quality control standard substance: PCR primer is carried out gel-purified recovery, then connects pEASY-T3 carrier, transforms, and after extracting plasmid, double digestion is identified, is checked order by positive recombinant plasmid, and carries out sequence alignment.The recombinant plasmid that sequence is correct is the positive quality control standard substance of acquisition.
Said positive quality control standard substance comprise B. abortus A19 vaccine strain positive quality control standard substance and pig kind brucella S2 vaccine strain positive quality control standard substance.
Said B. abortus A19 vaccine strain positive quality control standard substance are formed by containing the recombinant plasmid after the nucleotide fragments of 562 bases is connected to pEASY-T3 carrier, and said pig kind brucella S2 vaccine strain positive quality control standard substance are made up of the recombinant plasmid after the nucleotide fragments containing 539 bases is connected to pEASY-T3 carrier.
(3) negative quality control standard product: negative quality control standard product are aseptic double-distilled water, volume is 5 μ L.
Embodiment three, brucella vaccine strain identification reagent box specific test
Adopt PCR kit of the present invention respectively to B. abortus A19, pig kind brucella S2, brucella melitensis M5-90, Br.ovis 63/290 strain, dog brucella RM6/66 strain, Escherichia coli O 157: H7, Yersinia enterocolitica O:9, Salmonellas, streptococcus aureus, cow mycobacteria genomic dna increase, and establish the positive and negative control, the specificity of checking PCR reaction, PCR reaction conditions is: 94 DEG C of 5min, 94 DEG C of 30sec, 60 DEG C of 30sec, 72 DEG C of 30sec, 35 circulations, 72 DEG C of 10min.Purifying and the order-checking of PCR primer is carried out again after reaction terminates.
B. abortus A19 vaccine strain differentiates specific outcome as shown in Figure 1, in agarose gel electrophoresis result :+be positive quality control standard substance, 1-5: be respectively B. abortus A19, pig kind brucella S2, brucella melitensis M5-90, Br.ovis 63/290 strain, dog brucella RM6/66 strain all amplifies band , Er –, 6-10 of 562bp: be respectively negative quality control standard product, Escherichia coli O 157: H7, Yersinia enterocolitica O:9, Salmonellas, streptococcus aureus and cow mycobacteria all without band.After sequencing, sequence and peak figure comparison result are as shown in Figure 3, and only have A19 vaccine strain 344 to locate the disappearance (Fig. 3-A) of existence 7 nucleotide sequences (AGATTTC), other brucella strains and vaccine strain result are shown in Fig. 3-B.
Pig kind brucella S2 vaccine strain differentiates specific outcome as shown in Figure 2, in agarose gel electrophoresis result :+be positive quality control standard substance, 1-5: be respectively pig kind brucella S2, B. abortus A19, brucella melitensis M5-90, Br.ovis 63/290 strain, dog brucella RM6/66 strain all amplifies band , Er –, 6-10 of 539bp: be respectively negative quality control standard product, Escherichia coli O 157: H7, Yersinia enterocolitica O:9, Salmonellas, streptococcus aureus and cow mycobacteria all without band.After sequencing, sequence and peak figure comparison result are as shown in Figure 4, S2 vaccine strain is only had to there is disappearance (Fig. 4 of 25 nucleotide sequences (TCCCTCATAAATGGCTTTCTTCATA) in 369 site, A), other brucella strains and vaccine strain result are shown in Fig. 4-B.
The discriminating of embodiment four, brucella positive clinical sample vaccine strain
Respectively to the brucella positive sample (through pcr amplification sequence verification) that this laboratory is preserved, comprise 2 parts of blood samples, the cowshed aerosol sample of 2 parts of milk samples, 2 parts of aborted fetus tissue samples and 2 parts of different dairy cow farms carries out the discriminating of vaccine strain, result is as shown in the table.

Claims (10)

1. one kind for differentiating the primer sets of brucella wild mushroom and vaccine strain A19 and S2, it is characterized in that, comprise: for differentiating primer SEQ ID No.1 and the SEQ ID No.2 of brucella vaccine strain A19, for differentiating primer SEQ ID No.3 and the SEQ ID No.4 of brucella vaccine strain S2.
2. primer sets according to claim 1 for the preparation of differentiate and/detect the application of brucellar test kit, chip.
3. comprise the test kit of primer sets according to claim 1.
4. test kit according to claim 3, is characterized in that, also comprises: PCR reaction solution, archaeal dna polymerase, positive quality control standard substance and negative quality control standard product.
5. test kit according to claim 4, is characterized in that, described positive quality control standard substance comprise B. abortus A19 vaccine strain positive quality control standard substance and pig kind brucella S2 vaccine strain positive quality control standard substance.
6. test kit according to claim 5, it is characterized in that, the recombinant plasmid that described B. abortus A19 vaccine strain positive quality control standard substance are made up of nucleotide fragments shown in SEQ ID NO.5 and pEASY-T3 forms, and the recombinant plasmid that described pig kind brucella S2 vaccine strain positive quality control standard substance are made up of nucleotide fragments shown in SEQ ID NO.6 and pEASY-T3 forms.
7. for differentiating a brucellar method, it is characterized in that, comprising the steps:
(1) genomic dna of sample to be tested is extracted;
(2) with the sample genomic dna extracted for template, carry out pcr amplification, the primer adopted is the primer SEQ ID No.1 and the SEQ ID No.2 that differentiate brucella vaccine strain A19, and the primer SEQ ID No.3 of/discriminating brucella vaccine strain S2 and SEQ ID No.4;
(3) PCR primer is got, detect with agarose gel electrophoresis, observe and whether occur the 562bp that B. abortus vaccine strain A19 primer pair amplifies goes out and the band that size is corresponding with it, and/539bp that pig kind brucella vaccine strain S2 amplifies and size is corresponding with it band;
(4) if above-mentioned PCR detected result and object band are not inconsistent, then pattern of descriptive parts is that brucella is negative, and object band conforms to, be then brucella.
8. differentiate a method of brucella street strain and vaccine strain A19 and S2, it is characterized in that,
(1) genomic dna of sample to be tested is extracted
(2) with the sample genomic dna extracted for template, carry out pcr amplification, the primer adopted is primer sets according to claim 1;
(3) PCR primer is got, detect with agarose gel electrophoresis, observe and whether occur the 562bp that B. abortus vaccine strain A19 primer pair amplifies goes out and the band that size is corresponding with it, and the 539bp that amplifies of pig kind brucella vaccine strain S2 and size is corresponding with it band;
(4) if above-mentioned PCR detected result and object band are not inconsistent, then pattern of descriptive parts is that brucella is negative, if PCR test strip size is correct, then cuts glue to positive band and reclaims purifying, and then carry out sequencing;
(5) result judges: A19 vaccine strain identification result judges, check order to using the 562bp of SEQ ID NO:1 and SEQ IDNO:2 primer pair purifying or size is corresponding with it product, if sequencing result peak figure is simple spike, mate completely with after SEQ ID No.5 comparison, then this sample is A19 vaccine strain; If sequencing result peak figure is simple spike, have more 7 nucleotide sequences with after SEQ ID No.5 comparison in the 344th site, then this sample is other brucella street strain or the vaccine strains except A19 vaccine strain; If sequencing result and SEQ ID No.5 comparison, after the sequence the 354th of peak figure, namely after AGATTTCAGA, occur cover peak, then this sample is A19 vaccine strain and other brucella strains mixing;
S2 vaccine strain identification result judges, check order to using the 539bp of SEQ ID NO:3 and SEQ ID NO:4 primer pair purifying and size is corresponding with it product, if sequencing result peak figure is simple spike, mate completely with after SEQID No.6 comparison, then this sample is S2 vaccine strain; If sequencing result peak figure is simple spike, have more 25 nucleotide sequences with after SEQ ID No.6 comparison in the 369th site, then this sample is other brucella street strain or the vaccine strains except S2 vaccine strain; If sequencing result and SEQ ID No.6 comparison, occur cover peak behind peak graphic sequence the 369th site, then this sample is S2 vaccine strain and other brucella strains mixing.
9. method described in claim 7 or 8, is characterized in that, described sample to be tested is blood, milk sample, tissue samples, aerosol sample.
10. method described in claim 7 or 8, is characterized in that, pcr amplification condition is: 94 DEG C of 3min, 94 DEG C of 30sec, 60 DEG C of 30sec, 72 DEG C of 30sec, 35 circulations, 72 DEG C of 10min.
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CN109055589A (en) * 2018-10-08 2018-12-21 石河子大学 A kind of LAMP method identifies brucella epidemic strain and S2 plants of primer, kit and its application
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