CN1676613A - Quantitative PCR detecting kit and method for detecting vibrio parahaemolyticus thereof - Google Patents
Quantitative PCR detecting kit and method for detecting vibrio parahaemolyticus thereof Download PDFInfo
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- CN1676613A CN1676613A CNA200410077367XA CN200410077367A CN1676613A CN 1676613 A CN1676613 A CN 1676613A CN A200410077367X A CNA200410077367X A CN A200410077367XA CN 200410077367 A CN200410077367 A CN 200410077367A CN 1676613 A CN1676613 A CN 1676613A
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Abstract
This invention relates to a fluorescence quantitative PCR reagent box and a method testing vibro parahaemolyticus. The reagent box is composed of PCR reacting agent tube, the tube of sample treatment, the tube of positive comparison, the tube of negative comparison, the tube of standard product, the tube of Taq DNA polyose and the tube of dehydronium. The testing procedures are: first collect and treat the pending tested sample, then implement molecular quantitative PCR test, according the CT values of positive and negative sample comparisons and the CT of tested samples to judge whether the sample is positive or negative, then record the fluorescence value and CT value of each sample, and get the standard curve from the computer to calculate the copy's number of vibro parahaemolyticus of each sample. This invention has sealed-loop operation, avoids the fake positive, and the reaction and hybridization is synchronous, and the testing time is short.
Description
Affiliated technical field
The present invention relates to the composition of the measurement of microorganism, the method that specifically relates to a kind of PCR kit for fluorescence quantitative and be used to detect Vibrio parahemolyticus.
Technical background
(Vibrio parahaemolyticus VP) is a kind of halophilism bacterium to Vibrio parahemolyticus, belongs to vibrionaceae (Vibrio) Vibrio, easily causes food poisoning.The heat-resisting Mutation of Thermostable Direct Hemolysin (TDH) that Vibrio parahaemolyticus produces is important virulence factor, and specific gene tdh is the main factor that Vibrio parahaemolyticus causes food poisoning.
At present, China's Vibrio parahemolyticus conventional sense method has Kahagawa phenomenon (Kanagawa phenomenon, technology such as KP) test, biochemical identification, serological reaction, nucleic acid hybridization, but these tests or method need be cultivated through increasing bacterium, exist complex operation, required time long (about 4 days) etc. not enough.
Along with the development of microbial genome, a kind of quantitative PCR technique has appearred again in recent years, and this technology is a kind of outer-gene amplification technique.Those skilled in the art know that according to the specific gene tdh sequence of Vibrio parahaemolyticus, the design primer is that the PCR that can carry out Vibrio parahaemolyticus detects.But directly use conventional PCR detection kit to detect Vibrio parahemolyticus, remain in following insoluble technical problem: 1, do not contain molecular beacon probe in the reaction tubes of Chang Gui PCR detection kit, must " operation of uncapping " the PCR product be shifted, carrying out agarose electrophoresis or Southern shifts experiment such as hybridization the PCR product is identified, pollute easily, cause false positive, and expend time in (4～5 hours), health ministry has limited it and has used clinically; 2, Chang Gui PCR detection kit does not contain standard substance, can not carry out detection by quantitative to Vibrio parahemolyticus.
Summary of the invention
Technical problem to be solved by this invention is an improvement PCR detection kit, for use in detecting Vibrio parahemolyticus.
The technical solution that the present invention addresses the above problem is:
A kind of quantitative PCR detection kit is characterized in that this test kit is made up of following test tube:
(1) PCR reaction tubes: inner reaction tube liquid is made by following parts by volume component: 4～6 parts of 10 * Buffer damping fluids, 25mM MgCl
22～4 parts of solution, 4～8 parts of 1.25mMdNTP solution, sequence are that 50 0.2～1.0 part of μ M upstream primer, the sequence of 5 '-TGGCTGACATCCTACATGAC-3 ' is that 50 0.2～1.0 part of μ M downstream primer, the sequence of 5 '-TCTTCACCAACAAAGTTAGC-3 ' is 50 0.2～1.0 part of μ M ring molecule beacon probe, 25～30 parts of the deionized waters of 5 '-FAM-CGAGCGGCTATAAGCACGGTCATTCTGCTGGCTCG-DABCYL-3 ';
(2) sample treatment solution pipe: treatment solution is made by following parts by volume component in the pipe: 200～250 parts of 8～12 parts of 0.5mol/LEDTA (PH8.0), 1%SDS200～300 part, 5～8 parts of 20mg/ml Proteinase Ks and distilled water;
(3) positive control pipe: reagent is the reorganization positive plasmid DNA of following insertion sequence in the pipe:
GGTCAATGTA GAGGTCTCTG ACTTTTGGAC AAACCGTAAT GTAAAAAGAA AACCGTACAA
AGATGTTTAT GGTCAATCAG TATTCACAAC GTCAGGTACT AAATGGCTGA CATCCTACAT
GACTGTGAAC ATTAATGATA AAGACTATAC AATGGCAGCG GTGTCTGGCT ATAAGCACGG
TCATTCTGCT GTGTTCGTAA AATCAGATCA AGTACAGCTT CAACATTCCT ATGATTCTGT
AGCTAACTTT GTTGGTGAAG ATGAAGATTC TATTCCAAGT AAAATGTATT TGGATGAAAC
TCCAGAATAT TTTGTTAATG TAGAAGCATA TGAGAGTGGT AGTGG
(4) negative control pipe: reagent is the negative plasmid DNA of reorganization in the pipe;
(5) standard QC: reagent is respectively 10 in the pipe
7, 10
6, 10
5Each one of the reorganization positive plasmid DNA of copy/ml;
(6) polysaccharase pipe: reagent is 5U/ μ l Taq archaeal dna polymerase pipe in the pipe;
(7) deionization water pipe: reagent is deionized water in the pipe;
Above-mentioned quantitative PCR detection kit is used to detect the method for Vibrio parahemolyticus, is made up of following steps in regular turn:
(1) collection of sample to be tested and processing: get the broth culture 50 μ l of 15 kinds of bacteriums such as comprising Vibrio parahemolyticus, salmonella, intestinal bacteria in the laboratory, as sample.Or clinical (scene) will be correlated with sea-food 20 gram or add basic protein peptone incubated overnight after homogenate, with PBS by 1: 1 weight ratio mixing, 800rpm, centrifugal 1 minute, got supernatant 1200rpm centrifugal 5 minutes, abandon supernatant, suspend with 200 μ l PBS liquid, as sample.
After pending liquid thaws fully, get 50 μ l and add in the 0.5ml centrifuge tube, add sample to be tested 50 μ l again, mixing was placed 10 minutes for 37 ℃, and 100 ℃ were boiled 10 minutes then, centrifugal 10 seconds of 12 000rpm, and supernatant liquor is as amplification template.This template can be preserved a week for 2～8 ℃, can preserve one month for-18 ℃.Negative control and positive control need not to handle, and directly get machine amplification on the 5 μ l.
(2) application of sample: get archaeal dna polymerase 0.5 μ l earlier and add (centrifugal 10 seconds of effective preceding 10 000rpm of need of archaeal dna polymerase and reaction solution) in the reaction solution pipe, each the 5 μ l of sample supernatant liquor, negative control, positive control and standard substance (needing mixing before adding) that get then after the processing add respectively in the reaction solution pipe, and 10 000rpm went up the machine amplification in centrifugal 10 seconds behind the mixing.
(3) pcr amplification and real-time fluorescence detect: amplification program is 94 ℃ of pre-sex change 3 minutes, cycling condition be 94 ℃ 30 seconds, 55 ℃ 40 seconds, 72 ℃ 55 seconds, totally 40 circulations, last 72 ℃ are extended 3 minutes (establish blank one pipe simultaneously, blank only needs add after giving water 5 μ l mixings machine amplification on centrifugal 10 seconds of 10 000rpm in the reaction solution pipe).
(4) result judges: numerical value should not appear in the CT value of negative control; The CT value of positive control answers≤30; Then this tests to invalid as not satisfying above-mentioned condition.Detect sample CT value≤33 o'clock and be judged as the positive; Be judged as feminine gender when detecting sample CT value＞33 or not having numerical value.
(5) quantitative analysis: write down fluorescent value, the CT value of each sample, and obtain typical curve, calculate the Vibrio parahemolyticus copy number in each sample from computer.
The method that quantitative PCR detection kit of the present invention is used for detecting Vibrio parahemolyticus is to add the ring-like fluorescent molecular bacon probe of stem that is marked with reporter group (fluorophore) and quenching group (quencher) in the PCR reaction system, in the gene amplification process, PCR product and probe hybridization, according to resonance energy transfer phenomenon (fluorescence resonance energy transfer, FRET), reporter group and quencher group are separately, reporter group sends fluorescence and is detected, owing to adopt molecular beacon probe the PCR product is hybridized detection simultaneously, can detect by stopped pipe, conventional PCR product pollution and false-positive technical problem have been overcome, the use of the ring-like fluorescent molecular bacon probe of stem makes the specificity of detection better, can also carry out real-time quantitative to Vibrio parahemolyticus simultaneously and detect, be the developing direction of pathogenic micro-organism technique of gene detection.
Description of drawings
Fig. 1 is the corresponding relation figure of Vibrio parahemolyticus standard substance molecular beacon real-time quantitative PCR fluorescence intensity and cycle index
Fig. 2 is the canonical plotting of Vibrio parahemolyticus standard substance copy number logarithmic value and cycle index
The molecular beacon real-time quantitative PCR detected result figure of Fig. 3 for adopting this test kit that 15 kinds of bacteriums are carried out
Fig. 1, Fig. 2 and Fig. 3 all adopt ABI Prism7000 quantitative real time PCR Instrument and software kit thereof to obtain automatically.The CT value of the standard substance of different concns gradient is desirable as can be seen from result illustrated in figures 1 and 2, and linear correlation coefficient r is more than 0.99; From result shown in Figure 3 CT value≤30 of 2 strain Vibrio parahemolyticus and standard substance as can be seen, be judged as the positive, remaining bacterium and negative control CT value＞33 or do not have numerical value are judged as feminine gender.
Embodiment
Example 1
Described quantitative PCR detection kit is made up of following 7 pipes:
(1) PCR reaction tubes inner reaction tube liquid is made up of following component: 10 * Buffer damping fluid, 5 μ l, 25mM MgCl
2Solution 3 μ l, 1.25mMdNTP solution 8 μ l, 50 μ M upstream primers, 0.5 μ l, 50 μ M downstream primers, 0.5 μ l, 50 μ M ring molecule beacon probe 0.5 μ l and deionized water 27 μ l;
(2) treatment solution is made up of following component in the sample treatment solution pipe pipe: 0.5mol/LEDTA (PH8.0) 0.01ml, 1%SDS0.25ml, 20mg/ml Proteinase K 5 μ l and distilled water 0.235ml;
(3) the positive control pipe contains the reorganization positive plasmid DNA100 μ l of following insertion sequence;
(4) the negative control pipe includes the negative plasmid DNA 100 μ l of reorganization;
(5) the standard QC is 3, contains 10 respectively
7, 10
6, 10
5The reorganization positive plasmid DNA100 μ l of copy/ml;
(6) polysaccharase pipe 5U/ μ l Taq archaeal dna polymerase pipe 10 μ l;
(7) the deionization water pipe includes deionized water 100 μ l;
The production process and the preparation method of above-mentioned quantitative PCR detection kit are as follows:
The design of the first step specific gene primer and probe and synthetic
Go up the Vibrio parahemolyticus tdh gene order of announcing according to GenBank, adopt 4 PCR primers of Primer software design and the sub-beacon probe of 1 component, and at 5 ' end flag F AM of molecular beacon probe, 3 ' end mark DABCYL, primer and fluorescent probe are synthetic by Shanghai Bo Ya Bioisystech Co., Ltd.
Second each preparation and packing of forming of step PCR reaction solution
With 10 * Buffer damping fluid, 5 μ l, 25mM MgCl existing or that prepare
2Solution 3 μ l, 1.25mMdNTP solution 8 μ l, 50 μ M upstream primers, 0.5 μ l, 50 μ M downstream primers, 0.5 μ l, 50 μ M ring molecule beacon probe 0.5 μ l and deionized water 27 μ l join in the PCR reaction tubes of 0.2ml successively, and carry out mark.
The preparation and the packing of the 3rd step sample treatment solution
0.5mol/L EDTA (PH8.0) 0.01ml, the 1%SDS0.25ml, 20mg/ml Proteinase K 5 μ l and the distilled water 0.235ml that prepare are added in the sample treatment solution pipe.
Structure, purifying and the packing of the 4th step standard substance, positive control and negative control
Carry out the pcr amplification of Vibrio parahemolyticus according to a conventional method with the standard substance primer, the PCR reaction conditions is 94 ℃ of pre-sex change 5 minutes, each circulation comprises: 30 seconds, 55 ℃ annealing of 94 ℃ of sex change were extended 50 seconds for 45 seconds, 72 ℃, totally 40 circulations, and 72 ℃ were extended 5 minutes after the loop ends.PCR product size is 345bp.
The purification kit purifying that the PCR product provides through match Parkson, Beijing gene company limited, be cloned into the pGEM-T carrier, be transformed into the Top10 competent cell, smear containing on the flat board of Amp+/IPTG/X-gal, cultivated 12～16 hours, and chose hickie, propagation, upgrading grain, PCR are identified back preparation positive criteria product.
Concrete steps are as follows:
1. according to the pGEM-T carrier cloning system test kit operational requirement of Promega company, in the 0.5ml centrifuge tube, add 2 * Buffer5 μ l, pGEM-T carrier 1 μ l, T4 ligase enzyme 1 μ l, PCR purified product 3 μ l, with liquid-transfering gun pressure-vaccum mixing gently, 4 ℃ are spent the night.
2. get 2 μ l and connect product to the 1.5ml centrifuge tube, add the competent cell that 50 μ l have just melted, mixing gently, ice bath 20 minutes.
3.42 heat-shocked is 45～50 seconds in ℃ water bath, forbids shaking, rapid then ice bath 2 minutes.
4. add 950 μ l LB broth cultures, mixing, 37 ℃ of 150rpm shaking tables 1.5 hours.
5. contain 100 μ g/ μ l Ampicillin Trihydrate LB culture medium flat plates, after waiting to solidify, each dull and stereotyped 20 μ l X-gal (20 μ g/ μ l), 10 μ lIPTG (200 μ g/ μ l) of adding, get 100 μ l conversion fluid bed boards then, evenly smear with the paint daubs that high pressure is crossed, treat when slightly dry that the 37 ℃ of constant temperature incubator incubated overnight of putting upside down transform and the hickie bacterium colony successfully then occurs.
6. picking single day shift of colony inoculation contains to 5ml in the test tube of LB meat soup of Ampicillin Trihydrate (100 μ g/ μ l) from flat board, and 37 ℃ of 150rpm shaking tables carry out the mono-clonal enlarged culturing, to white floss occurring.
7. the specification sheets operation of the plasmid rapid extraction test kit that provides by Beijing ancient cooking vessel state Bioisystech Co., Ltd of the extraction of recombinant plasmid and purifying.The plasmid of purifying identifies with 0.8% agarose gel electrophoresis, and carries out PCR simultaneously and identify, can prepare reorganization positive plasmid DNA standard substance.
8. with 10 times of this recombinant plasmid dilutions, with the absorbancy of M75-B type ultraviolet spectrophotometer mensuration recombinant plasmid, OD
260=0.072, OD
280=0.039, OD
260/ OD
280=1.85, according to recombinant plasmid concentration=OD
260* extension rate * 50 can base of calculation product recombinant plasmid concentration be 36 μ g/ml, again according to containing 6.02 * 10 in plasmid molecule amount=(3000+345) * 324.5g/mol=1085453g/mol and every mole of sample
23Individual copy number, the copy number that obtains every milliliter of recombinant plasmid equals 1.997 * 10
13Positive plasmid is become 3 templates of overlapping different copy numbers, every pipe packing 100 μ l by 10 doubling dilutions.
Positive plasmid DNA is as positive control in reorganization, and the negative plasmid of recombinating is as negative control, every pipe packing 100 μ l.
The packing of the 5th step Taq archaeal dna polymerase and deionized water
5U/ μ l Taq archaeal dna polymerase 10 μ l branch is installed in the polysaccharase pipe; The deionized water branch installs in the deionized water pipe.
The 6th step was manipulated 1 part in specification sheets with 7 groups of pipes in above-mentioned five steps together with test kit, put into the reagent packing box on request, put dried-20 ℃ of preservations, and on the rocks placing in the bubble chamber transported.
The method that above-mentioned quantitative PCR detection kit is used to detect Vibrio parahemolyticus is:
(1) collection of sample to be tested and processing: get the broth culture 50 μ l of 15 kinds of bacteriums such as comprising Vibrio parahemolyticus, salmonella, intestinal bacteria in the laboratory, as sample.Or clinical (scene) will be correlated with sea-food 20 gram or add basic protein peptone incubated overnight after homogenate, with PBS by 1: 1 weight ratio mixing, 800rpm, centrifugal 1 minute, got supernatant 1200rpm centrifugal 5 minutes, abandon supernatant, suspend with 200 μ l PBS liquid, as sample.
After pending liquid thaws fully, get 50 μ l and add in the 0.5ml centrifuge tube, add sample to be tested 50 μ l again, mixing was placed 10 minutes for 37 ℃, and 100 ℃ were boiled 10 minutes then, centrifugal 10 seconds of 12000rpm, and supernatant liquor is as amplification template.This template can be preserved a week for 2～8 ℃, can preserve one month for-18 ℃.Negative control and positive control need not to handle, and directly get machine amplification on the 5 μ l.
(2) application of sample: get archaeal dna polymerase 0.5 μ l earlier and add (centrifugal 10 seconds of effective preceding 10 000rpm of need of archaeal dna polymerase and reaction solution) in the reaction solution pipe, each the 5 μ l of sample supernatant liquor, negative control, positive control and standard substance (needing mixing before adding) that get then after the processing add respectively in the reaction solution pipe, and 10000rpm went up the machine amplification in centrifugal 10 seconds behind the mixing.
(3) pcr amplification and real-time fluorescence detect: amplification program is 94 ℃ of pre-sex change 3 minutes, cycling condition be 94 ℃ 30 seconds, 55 ℃ 40 seconds, 72 ℃ 55 seconds, totally 40 circulations, last 72 ℃ are extended 3 minutes (establish blank one pipe simultaneously: blank only needs add behind the deionized water 3 μ l mixings machine amplification on centrifugal 10 seconds of the 10000rpm in the reaction solution pipe).
(4) result judges: numerical value should not appear in the CT value of negative control, and the CT value of positive control answers≤30, and then this tests to invalid as not satisfying above-mentioned condition.Detect sample CT value≤33 o'clock and be judged as the positive; Be judged as feminine gender when detecting sample CT value＞33 or not having numerical value.
(5) quantitative analysis: write down fluorescent value, the CT value of each sample, and obtain typical curve, calculate the Vibrio parahemolyticus copy number in each sample from computer.
Example 2:
In the described quantitative PCR detection kit in the pipe of positive control tube, negative control pipe, standard QC, polysaccharase pipe and deionization water pipe contained component all identical with example 1, the content of every pipe will be decided on the specification of test kit, promptly does how many person-portions and decides.Example 1 described quantitative PCR detection kit designs by 20 person-portions, and this enforcement and following embodiment can analogize (general knowledge that those of ordinary skills should know) by it.The inner reaction tube liquid of described PCR reaction tubes is made up of following component: 10 * Buffer damping fluid, 4 μ l, 25mM MgCl
2Solution 2 μ l, 1.25mMdNTP solution 4 μ l, 50 μ M upstream primers, 0.2 μ l, 50 μ M downstream primers, 0.2 μ l, 50 μ M ring molecule beacon probe 0.2 μ l and deionized water 34.4 μ l; Treatment solution is made up of following component in the pipe of described sample treatment solution pipe: 0.5mol/LEDTA (PH8.0) 0.008ml, 1%SDS0.20ml, 20mg/ml Proteinase K 5 μ l and distilled water 0.200ml.
The production process of above-mentioned quantitative PCR detection kit and preparation method's reference example 1 are implemented to get final product.
Because test kit of the present invention is a kind of improvement to the quantitative PCR detection kit of routine, therefore, this test kit is used to detect the method for Vibrio parahemolyticus, and those skilled in the art can independently be finished by the enlightenment of example 1 fully, need not to give unnecessary details.
Example 3:
Interior contained component of the pipe of positive control tube, negative control pipe, standard QC, polysaccharase pipe and deionization water pipe and content are all identical with example 1 in the described quantitative PCR detection kit.The inner reaction tube liquid of described PCR reaction tubes is made up of following component: 10 * Buffer damping fluid, 6 μ l, 25mM MgCl
2Solution 4 μ l, 1.25mMdNTP solution 8 μ l, 50 μ M upstream primers, 1.0 μ l, 50 μ M downstream primers, 1.0 μ l, 50 μ M ring molecule beacon probe 1.0 μ l and deionized water 24 μ l; Treatment solution is made up of following component in the pipe of described sample treatment solution pipe: 0.5mol/LEDTA (PH8.0) 0.012ml, 1%SDS0.30ml, 20mg/ml Proteinase K 8 μ l and distilled water 0.250ml;
The preparation of described quantitative PCR detection kit and being used to detects the method reference example 1 of Vibrio parahemolyticus and implements to get final product.
Claims (2)
1. quantitative PCR detection kit is characterized in that this test kit is made up of following test tube:
(1) PCR reaction tubes: inner reaction tube liquid is made by following parts by volume component: 4～6 parts of 10 * Buffer damping fluids, 25mM MgCl
22～4 parts of solution, 4～8 parts of 1.25mMdNTP solution, sequence are that 50 0.2～1.0 part of μ M upstream primer, the sequence of 5 '-TGGCTGACATCCTACATGAC-3 ' is that 50 0.2～1.0 part of μ M downstream primer, the sequence of 5 '-TCTTCACCAACAAAGTTAGC-3 ' is 50 0.2～1.0 part of μ M ring molecule beacon probe, 25～30 parts of the deionized waters of 5 '-FAM-CGAGCGGCTATAAGCACGGTCATTCTGCTGGCTCG-DABCYL-3 ';
(2) sample treatment solution pipe: treatment solution is made by following parts by volume component in the pipe: 200～250 parts of 8～12 parts of 0.5mol/LEDTA (PH8.0), 1%SDS200～300 part, 5～8 parts of 20mg/ml Proteinase Ks and distilled water;
(3) positive control pipe: reagent is the reorganization positive plasmid DNA of following insertion sequence in the pipe:
GGTCAATGTA?GAGGTCTCTG?ACTTTTGGAC?AAACCGTAAT?GTAAAAAGAA?AACCGTACAA
AGATGTTTAT?GGTCAATCAG?TATTCACAAC?GTCAGGTACT?AAATGGCTGA?CATCCTACAT
GACTGTGAAC?ATTAATGATA?AAGACTATAC?AATGGCAGCG?GTGTCTGGCT?ATAAGCACGG
TCATTCTGCT?GTGTTCGTAA?AATCAGATCA?AGTACAGCTT?CAACATTCCT?ATGATTCTGT
AGCTAACTTT?GTTGGTGAAG?ATGAAGATTC?TATTCCAAGT?AAAATGTATT?TGGATGAAAC
TCCAGAATAT?TTTGTTAATG?TAGAAGCATA?TGAGAGTGGT?AGTGG
(4) negative control pipe: reagent is the negative plasmid DNA of reorganization in the pipe;
(5) standard QC: reagent is respectively 10 in the pipe
7, 10
6, 10
5Each one of the reorganization positive plasmid DNA of copy/ml;
(6) polysaccharase pipe: reagent is 5U/ μ l Taq archaeal dna polymerase pipe in the pipe;
(7) deionization water pipe: reagent is deionized water in the pipe;
2. the quantitative PCR detection kit that claim 1 limited is used to detect the method for Vibrio parahemolyticus, it is characterized in that this method is made up of following steps in regular turn:
(1) collection of sample to be measured and processing: homogenate after getting sample 20 grams or adding basic protein peptone incubated overnight, press 1: 1 weight ratio mixing, 800rpm with PBS, centrifugal 1 minute, got supernatant 1200rpm centrifugal 5 minutes, abandon supernatant, suspend with 200 μ l PBS liquid, as sample.Get treatment solution 50 μ l and add in the 0.5ml centrifuge tube, add sample to be tested 50 μ l again, mixing was placed 10 minutes for 37 ℃, and 100 ℃ were boiled 10 minutes then, centrifugal 10 seconds of 12000rpm, and supernatant liquor is as amplification template;
(2) application of sample: get archaeal dna polymerase 0.5 μ l earlier and add in the reaction solution pipe, get each 5 μ l of amplification template, negative control, resistive contrast and standard substance then and add respectively in the reaction solution pipe, 10 000rpm went up the machine amplification in centrifugal 10 seconds behind the mixing;
(3) pcr amplification and real-time fluorescence detect: the PCR program is 94 ℃ of pre-sex change 3 minutes, cycling condition be 94 ℃ 30 seconds, 55 ℃ 40 seconds, 72 ℃ 55 seconds, totally 40 circulations, last 72 ℃ were extended 3 minutes, amplification and fluoroscopic examination are carried out simultaneously;
(4) result judges: numerical value should not appear in the CT value of negative control, and the CT value of positive control answers≤30, and then this tests to invalid as not satisfying above-mentioned condition; Detection sample CT value≤be judged as the positive at 33 o'clock is judged as feminine gender when detecting sample CT value＞33 or not having numerical value;
(5) quantitative analysis: write down the fluorescent value and the CT value of each sample, and obtain typical curve, calculate the Vibrio parahemolyticus copy number in each sample from computer.
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| CN106520962A (en) * | 2016-11-17 | 2017-03-22 | 中国水产科学研究院黑龙江水产研究所 | Aeromonas salmonicida SYBR Green I real-time quantitive PCR (Polymerase Chain Reaction) detection method and application thereof |
| CN106520962B (en) * | 2016-11-17 | 2019-11-01 | 中国水产科学研究院黑龙江水产研究所 | The SYBR Green I real-time quantitative PCR detection method of aeromonas salmonicida and its application |
| CN111518922A (en) * | 2019-09-02 | 2020-08-11 | 广东美格基因科技有限公司 | Fluorescent quantitative PCR method for detecting toxigenic vibrio parahaemolyticus and corresponding kit |
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