CN102206714A - Degenerate primer, detection method and application for general RT-PCR detection of comovirinae subvirus - Google Patents
Degenerate primer, detection method and application for general RT-PCR detection of comovirinae subvirus Download PDFInfo
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Abstract
The invention discloses a degenerate primer, detection method and application for general RT-PCR detection of comovirinae subvirus. The degenerate primer consists of a forward degenerate primer of following sequence: SEQ ID No.1:5'-TGTGAYTAYWVNVVNTTYGATGG-3' and a reverse degenerate primer of following sequence: SEQ ID No.2:5' -YTTRTCHBTVCCATCVGTAAT-3', wherein, Y,C,T,W,A,G,N,R,B and H satisfy the following relation: Y=C/T, W=A/T, V=G/A/C, N=A/G/C/T, R=A/G, B=G/T and H=A/T/C. The primer disclosed in the invention has good versatility, and the detection method is accurate and rapid, providing a guarantee of security of import and export.
Description
Technical field
The present invention relates to the general RT-PCR of a kind of cowpea mosaic virus subfamily virus detects with degenerated primer, detection method and application thereof.
Background technology
The cowpea mosaic virus subfamily (
Comovirinae) belong to class picornavirus order (
Picornavirales), association cowpea Viraceae (
Secoviridae) in a subfamily, comprise Comovirus (
Comovirus), fabavirus belong to (
Fabavirus) and Nepovirus (
Nepovirus) wait 3 Tobamovirus, have 53 kinds of viruses.To be a class cause the virus of important threat to agriculture production safety to cowpea mosaic virus subfamily virus, and multiple virus has host range very widely, and can cause the various crop heavy losses.According to " People's Republic of China (PRC) enter the territory Plant Quarantine harmful organism register " that announced in 2007, the kind that is listed in the venereal disease poison of quarantining in this virus subfamily has: arabis mosaic virus (
Arabis mosaic virus, ArMV), broad bean dyeing virus (
Broad bean stain virus, BBSV), bean pod mottle virus (
Bean pod mottle virus, BPMV), cowpea severe mosaic virus (
Cowpea severe mosaic virus, CPSMV), peach rosette mosaic virus (
Peach rosette mosaic virus, PRMV), nepovirus (
Tobacco ringspot virus, TRSV), tomato black ring virus (
Tomato black ring virus, TBRV), annulus zonatus (
Tomato ringspot virus, ToRSV), totally 8 kinds.Maliogka in 2004 etc. set up Comoviridae (
Comoviridae) the nido RT-PCR of (being present cowpea mosaic virus subfamily) viral general detection, but yet there are no conventional general RT-PCR detection method.The present application people seeks the conservative region on the RNA1 genome of cowpea mosaic virus subfamily again, according to conservative region sequence redesign pair of degenerate primers, by reverse transcription (reverse transcription, RT) and polymerase chain reaction technology (polymerase chain reaction, PCR) set up the general RT-PCR detection method of cowpea mosaic virus subfamily, reaction finishes the location determination result of back according to the specific amplification dna fragmentation, and carries out viral species according to the sequencing result and identify.
Summary of the invention
The object of the present invention is to provide the general RT-PCR of a kind of cowpea mosaic virus subfamily virus to detect with degenerated primer, detection method and application thereof.Primer versatility of the present invention is good, detection method quick and precisely, for imports and exports safety provides assurance.
In order to reach above-mentioned purpose, solution of the present invention is:
The general RT-PCR of a kind of cowpea mosaic virus subfamily virus detects and uses degenerated primer, is made up of forward and reverse primer, and the nucleotide sequence of its forward primer is seen SEQ ID No.1:5 '-TGTGAYTAYWVNVVNTTYGATGG-3 '; The nucleotide sequence of reverse primer is seen SEQ ID No.2:5 '-YTTRTCHBTVCCATCVGTAAT-3 '; Wherein, Y=C/T, W=A/T, V=G/A/C, N=A/G/C/T, R=A/G, B=G/T/C, H=A/T/C.
The detection method that the general RT-PCR of a kind of cowpea mosaic virus subfamily virus detects, comprise the steps: that with the total RNA of sample be template, utilize above-mentioned primer to carry out the RT-PCR amplification, reaction finishes back detected through gel electrophoresis amplified production, according to the location determination result of amplification of DNA fragments, all can detect the dna fragmentation of 407 ~ 451 bp in the illness blade.
Described RT-PCR reaction comprises reverse transcription and two processes of pcr amplification.
The temperature of reverse transcription reaction is 42 ℃ in the reaction process of described RT-PCR, and the elder generation of pcr amplification carries out 5 circulations with 42 ℃ of annealing temperatures, carries out 30 circulations with 50 ℃ of annealing temperatures then, and elongating temperature is 72 ℃.
Beneficial effect of the present invention is: the present invention is according to cowpea mosaic virus subfamily viral RNA 1 genome sequence design primer, and the general RT-PCR that this primer can be used for cowpea mosaic virus subfamily virus detects.Whether detection method of the present invention judgement sample rapidly and accurately has cowpea mosaic virus subfamily virus, and the primer versatility is good, detection method quick and precisely, for imports and exports safety provides assurance.
Description of drawings
Fig. 1 is the specificity test-results of the general RT-PCR method of cowpea mosaic virus subfamily virus to various subfamily viruses, comprise 9 kinds of Nepoviruses (
Nepovirus) virus, 7 kinds of Comoviruses (
Comovirus) virus and a kind of broad bean wilt virus belong to (
Fabavirus) virus.Promptly, 1 is arabis mosaic virus (ArMV) isolate 1 sick leaf, 2 is the sick leaf of nepovirus (TRSV), 3 is annulus zonatus (ToRSV) isolate 1 sick leaf, 4 is the sick leaf of cherry leaf roll virus (CLRV), 5 is the sick leaf of tobacco black ring virus (TBRV), 6 is the sick leaf of peach rosette mosaic virus (PRMV), 7 is the sick leaf of grapevine fanleaf virus (GFLV), 8 is the sick leaf of myrtillin leave mottle virus (BLMoV), 9 is the sick leaf of raspberry ring spot virus (RpRSV), 10 is the sick leaf of bean pod mottle virus (BPMV), 11 is cowpea mosaic virus (CPMV) isolate 1 sick leaf, 12 is cowpea severe mosaic virus (CPSMV) isolate 1 sick leaf, 13 is the sick leaf of broad bean dyeing virus (BBSV), 14 is the sick leaf of Flos Cucurbitae mosaic virus (SqMV), 15 is the sick leaf of red clover mottle virus (RCMV), 16 is No. 1 (BBWV1) sick leaf of broad bean wilt virus, 17 is the sick leaf of radish mosaic virus (RaMV), 18 is annulus zonatus (ToRSV) isolate 2 sick leaves, 19 is annulus zonatus (ToRSV) isolate 3 sick leaves, 20 is cowpea mosaic virus (CPMV) isolate 2 sick leaves, 21 is cowpea severe mosaic virus (CPSMV) isolate 2 sick leaves, 22 is arabis mosaic virus (ArMV) isolate 2 sick leaves, 23 is arabis mosaic virus (ArMV) isolate 3 sick leaves, and M is the DNA Mark of 100 bp.
Fig. 2 uses the result that the general RT-PCR method of cowpea mosaic virus subfamily virus detects healthy host plant.1-10 is respectively the healthy leaves of langenaria siceria, common cigarette, tomato, cucumber, pumpkin, Dolichos lablab, broad bean, cowpea, watermelon, lily.
Fig. 3 uses the result that the general RT-PCR method of cowpea mosaic virus subfamily virus detects the Bulbus Lilii syndrome leaf.1 is the detected result of healthy lily blade, and 2-6 is the detected result of morbidity lily blade, and 7 is blank, and M is the DNA Mark of 100 bp.
Embodiment
Following embodiment is used for further specifying of the present invention, but is not used for limiting the scope of the invention.
1. design of primers is with synthetic
According to the RNA1 genome sequence design primer of the downright bad stunt virus (CNSV) of sago cycas in the cowpea mosaic virus subfamily, grapevine chrome mosaic nepovirus (GCMV), GFLV, Ribes nigrum L. degeneration virus (BRV), RaMV, SqMV, BPMV, RCMV, CPMV, CPSMV, BBWV1, broad bean wilt virus No. 2 (BBWV2), ArMV, TRSV, GFLV, RpRSV, TBRV, beet ring spot virus (BRSV), PRMV, ToRSV virus, primer sequence is:
SEQ ID No.1(upstream): 5 '-TGTGAYTAYWVNVVNTTYGATGG-3 ';
SEQ ID No.2(downstream): 5 '-YTTRTCHBTVCCATCVGTAAT-3 '.
For ease of order-checking, in primer, introduce universal sequencing primer thing BCABESTTM Sequencing Primer RV-M and M13-47(underscore respectively), primer sequence is:
SEQ?ID?No.1（Comov-sf-F2）：5′-
GAGCGGATAACAATTTCACACAGG?TGTGAYTAYWVNVVNTTYGATGG-3′
SEQ?ID?No.2（Comov-sf-R2）：5′-
CGCCAGGGTTTTCCCAGTCACGAC?YTTRTCHBTVCCATCVGTAAT-3′
2. the extraction of total RNA
1) get 0.1 g plant incidence of leaf, add the TRIzol(American I nvitrogen company of 1 ml) reagent, move in the 1.5 ml centrifuge tubes of sterilization, keep 5 min under the room temperature;
2) add 0.2 ml chloroform, thermal agitation 15 s, at room temperature keep 2-15 min then after, 4 ℃, centrifugal 15 min of 12000 g;
3) with the upper water phase transition in 1.5 new ml centrifuge tubes, add 0.5 ml Virahol, put upside down mixing, keep 15 min under the room temperature;
4) 4 ℃, centrifugal 10 min of 12000 g, RNA will form precipitation in the sidewall and the bottom of pipe;
5) outwell supernatant liquor, add 75% washing with alcohol precipitation, 4 ℃ then, centrifugal 5 min(of 7500 g suspend as precipitation, then use 12000 g centrifugal), discard ethanol;
6) be deposited under the room temperature after the thorough drying, be dissolved in 40 μ l dH
2O(DEPC handles) in ,-20 ℃ of preservations are standby.
3.RT-PCR the foundation of amplification method
With total RNA is template, carries out the RT-PCR reaction.20 μ L reaction systems are carried out reverse transcription reaction, promptly add 6.75 μ L DEPC treating water, the total RNA of 4 μ L, the oligo of 1 μ L (d T) in the reaction tubes of 0.2 mL
15Primer (10 μ mol/L) (precious biotechnology (Dalian) company limited), 1 μ L dNTP mixture (10 mmol/L) (is specially dATP, dGTP, dTTP and four kinds of mixtures of dCTP, treasured biotechnology (Dalian) company limited), in 65 ℃ of maintenance 5 min, transfer to quenching 5min on ice rapidly behind the mixing; In reaction tubes, add 2 μ L DTT(dithiothreitol (DTT) then, U.S. Pu Luomaige company) (0.1 mmol/L), 4 μ L, 5 * reverse transcription damping fluid (U.S. Pu Luomaige company), 1 μ L RNA enzyme inhibitors (40 U/ μ L) (precious biotechnology (Dalian) company limited), 0.25 μ L ThermoScript II (200 U/ μ L) (U.S. Pu Luomaige company), 42 ℃ of reaction 50 min; Obtain reverse transcription product cDNA after 72 ℃ of 15 min deactivation ThermoScript II.
The PCR reaction system is 25 μ L, promptly in the PCR of 0.2 mL reaction tubes, add 13.25 μ L DEPC treating water, 3 μ L cDNA, 2 μ L forward primer SEQ ID No.1(10 μ mol/L), 2 μ L reverse primer SEQ ID No.2(10 μ mol/L), the precious biotechnology (Dalian) of 10 * PCR damping fluid, 2.5 μ L(company limited), 2 μ L dNTP mixtures (2.5 mmol/L), 0.25 μ L Taq archaeal dna polymerase (5 U/ μ L) precious biotechnology (Dalian) company limited).Reaction conditions is: 95 ℃ of pre-sex change 3 min; 94 ℃ of sex change 50 s, 42 ℃ of annealing 50 s, 72 ℃ of extension 50 s, 5 circulations; Follow 94 ℃ of sex change 50 s, 50 ℃ of annealing 50 s, 72 ℃ of extension 50 s, 30 circulations; Last 72 ℃ are extended 7 min.On the PCR instrument, finish.
PCR reaction finishes laggard row agarose gel electrophoresis and detects, and judges in the sample whether contain cowpea mosaic virus subfamily virus according to the dna fragmentation of 407 ~ 451 bp that whether increase.Whether present embodiment detection method judgement sample rapidly and accurately has cowpea mosaic virus subfamily virus, carries out kind according to sequence and identifies, for imports and exports safety provides assurance.The general RT-PCR of cowpea mosaic virus subfamily virus detects with degenerated primer further can make the general RT-PCR detection kit of cowpea mosaic virus subfamily virus.
The versatility of the general RT-PCR method of cowpea mosaic virus subfamily detects
Get arabis mosaic virus (ArMV), nepovirus (TRSV), annulus zonatus (ToRSV), cherry leaf roll virus (CLRV), tobacco black ring virus (TBRV), peach rosette mosaic virus (PRMV), grapevine fanleaf virus (GFLV), raspberry ring spot virus (RpRSV), myrtillin leave mottle virus (BLMoV), bean pod mottle virus (BPMV), cowpea mosaic virus (CPMV), cowpea severe mosaic virus (CPSMV), broad bean dyeing virus (BBSV), Flos Cucurbitae mosaic virus (SqMV), red clover mottle virus (RCMV), radish mosaic virus (RaMV), broad bean wilt virus 1(BBWV1) 17 kinds of viruses such as, 24 sick leaves of isolate, extract total RNA respectively by embodiment 1 method, carry out RT-PCR amplification, agarose gel electrophoresis detected result by the method for embodiment 1 again.All detect the dna fragmentation of 407 ~ 451 bp as a result in the blade of infective virus.Detected result as shown in Figure 1.Show that the RT-PCR method of foundation can be used for the detection of different virus kind in this subfamily, have good versatility, can be used for the general detection of cowpea mosaic virus subfamily virus.
The general RT-PCR method of cowpea mosaic virus subfamily specific detection
Get the healthy leaves of plants such as langenaria siceria, common tobacco leaf, tomato, cucumber, pumpkin, Dolichos lablab, broad bean, cowpea, watermelon, lily, extract total RNA respectively, carry out the RT-PCR amplification by the method for embodiment 1 again, carry out specific detection by embodiment 1 method.Detected result as shown in Figure 2.The general RT-PCR method that shows foundation can't produce cross reaction with the host plant of virus, has good specificity, the requirement of coincidence detection.
The general RT-PCR method of cowpea mosaic virus subfamily the application in lily virus detects
Get lily blade, extract total RNA respectively, use primer Comov-sf-F2 and Comov-sf-R2, carry out the RT-PCR amplification, detect application by the method for embodiment 1 by embodiment 1 method with similar viral symptom.Detected result as shown in Figure 3.Dna fragmentation to amplification directly checks order, and sequential analysis is indicated as arabis mosaic virus (ArMV).The general RT-PCR method that shows foundation can be used for the rapid detection of cowpea mosaic virus subfamily virus in the sample such as lily and identifies.
Sequence table
＜110〉Inspection and Quarantine Center of Xiamen Entry-Exit Inspection and Quarantine Bureau
＜120〉the general RT-PCR of cowpea mosaic virus subfamily virus detects and uses degenerated primer
<130>
<160> 2
<170> PatentIn?version?？
<210> 1
<211> 23
<212> DNA
＜213〉artificial sequence
<400> 1
TGTGAYTAYW?VNVVNTTYGA?TGG 23
<210> 2
<211> 21
<212> DNA
＜213〉artificial sequence
<400> 2
YTTRTCHBTV?CCATCVGTAA?T 21
Claims (6)
1. the general RT-PCR of cowpea mosaic virus subfamily virus detects and uses degenerated primer, it is characterized in that being made up of forward and reverse primer, and the nucleotide sequence of its forward primer is seen SEQ ID No.1:5 '-TGTGAYTAYWVNVVNTTYGATGG-3 '; The nucleotide sequence of reverse primer is seen SEQ ID No.2:5 '-YTTRTCHBTVCCATCVGTAAT-3 '; Wherein, Y=C/T, W=A/T, V=G/A/C, N=A/G/C/T, R=A/G, B=G/T/C, H=A/T/C.
2. detection method that the general RT-PCR of cowpea mosaic virus subfamily as claimed in claim 1 virus detects, it is characterized in that comprising the steps: that with the total RNA of sample be template, utilize above-mentioned primer to carry out the RT-PCR amplification, reaction finishes back detected through gel electrophoresis amplified production, according to the location determination result of amplification of DNA fragments, all can detect the dna fragmentation of 407 ~ 451 bp in the illness blade.
3. the detection method that the general RT-PCR of a kind of cowpea mosaic virus subfamily virus as claimed in claim 2 detects, it is characterized in that: described RT-PCR reaction comprises reverse transcription and two processes of pcr amplification.
4. the detection method that the general RT-PCR of a kind of cowpea mosaic virus subfamily virus as claimed in claim 3 detects, it is characterized in that: the temperature of reverse transcription reaction is 42 ℃ in the reaction process of described RT-PCR, earlier carry out 5 circulations during pcr amplification with 42 ℃ of annealing temperatures, carry out 30 circulations with 50 ℃ of annealing temperatures then, elongating temperature is 72 ℃.
5. application of the general RT-PCR detection of cowpea mosaic virus subfamily virus usefulness degenerated primer according to claim 1, it is characterized in that: described primer carries out RT-PCR amplification back to behind the further sequencing of the dna fragmentation that is increased to the total RNA of sample, the kind of energy Rapid identification cowpea mosaic virus subfamily virus.
One kind according to claim 1 the general RT-PCR of cowpea mosaic virus subfamily virus detect application with degenerated primer, it is characterized in that: the general RT-PCR of described cowpea mosaic virus subfamily virus detects with degenerated primer and can be applied to the viral general RT-PCR detection kit of cowpea mosaic virus subfamily.
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106148567A (en) * | 2016-07-08 | 2016-11-23 | 厦门出入境检验检疫局检验检疫技术中心 | A kind of cowpea mosaic virus subfamily virus wide spectrum detection kit and method thereof |
| CN106191303A (en) * | 2016-07-08 | 2016-12-07 | 厦门出入境检验检疫局检验检疫技术中心 | A kind of Flos Cucurbitae mosaic virus real-time fluorescence RT PCR detection kit and method thereof |
| CN107058611A (en) * | 2016-12-19 | 2017-08-18 | 云南农业大学 | A kind of viral universal detector primer of Tobamovirus and its method |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101215611A (en) * | 2008-01-11 | 2008-07-09 | 中华人民共和国厦门出入境检验检疫局 | Primer for detecting southern cowpea mosaic virus |
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2011
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Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101215611A (en) * | 2008-01-11 | 2008-07-09 | 中华人民共和国厦门出入境检验检疫局 | Primer for detecting southern cowpea mosaic virus |
Non-Patent Citations (4)
| Title |
|---|
| ROSA FELICIA E, ET AL: "Biological, serological and molecular comparison between isolates of Cowpea severe mosaic virus", 《TROPICAL PLANT PATHOLOGY》 * |
| 李彬 等: "一种豇豆重花叶病毒RT - PCR检测方法的研究", 《植物检疫》 * |
| 李彬 等: "豇豆花叶病毒和黑眼豇豆花叶病毒RT-Realtime PCR及IC-RT-Realtime PCR检测方法研究", 《南京农业大学学报》 * |
| 董菁 等: "应用简并引物检测南方菜豆花叶病毒属病毒", 《植物保护学报》 * |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106148567A (en) * | 2016-07-08 | 2016-11-23 | 厦门出入境检验检疫局检验检疫技术中心 | A kind of cowpea mosaic virus subfamily virus wide spectrum detection kit and method thereof |
| CN106191303A (en) * | 2016-07-08 | 2016-12-07 | 厦门出入境检验检疫局检验检疫技术中心 | A kind of Flos Cucurbitae mosaic virus real-time fluorescence RT PCR detection kit and method thereof |
| CN106191303B (en) * | 2016-07-08 | 2019-07-02 | 厦门出入境检验检疫局检验检疫技术中心 | A kind of pumpkin mosaic virus real-time fluorescent RT-PCR detection reagent box and its method |
| CN107058611A (en) * | 2016-12-19 | 2017-08-18 | 云南农业大学 | A kind of viral universal detector primer of Tobamovirus and its method |
| CN107058611B (en) * | 2016-12-19 | 2020-02-04 | 云南农业大学 | Universal detection primer for tobacco mosaic virus and method thereof |
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