CN102154279A - Detection method and specific SCAR (sequenced characterized amplified region) marker of tilletia controversa kuhn (TCK) - Google Patents
Detection method and specific SCAR (sequenced characterized amplified region) marker of tilletia controversa kuhn (TCK) Download PDFInfo
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Abstract
The invention relates to a detection method and a specific SCAR (sequenced characterized amplified region) marker of tilletia controversa kuhn (TCK). The SCAR marker is a nucleotide sequence shown as Seq No.5, and can provide a plurality of primers for TCK detected by a PCR (polymerase chain reaction). The detection sensitivity of high-specific primer TCKSF2/TCKSR2 designed according to SCAR marked sequence can reach 1ng/25 mu l, thus TCK can be identified from multiple similar bacterial strains.
Description
The present patent application is application number " 200910085151.0 ", the applying date " on June 2nd, 2009 ", name is called the dividing an application of Chinese invention patent application of " a kind of special gene sequence of T contraversa, specific SCAR label and PCR detection method ".
Technical field:
The invention belongs to biological technical field, relate to a kind of detection method and specific SCAR label of T contraversa.
Technical background
T contraversa (Tilletia controversa K ü hn, abbreviation TCK) dwarf bunt of wheat that causes is a kind of important international quarantine venereal disease evil, Wheat Production had crushing harm, also be one of main species of China adventive invasion research (Wang Yuan. dwarf bunt of wheat bacterium [M]. China's Plant Quarantine harmful organism a collection of selected materials that enters the territory, animal and plant quarantine bureau of the People's Republic of China (PRC) and Plant Quarantine Test Office, Ministry of Agriculture compile, Beijing: Chinese agriculture press, 1997,95～98).The production loss that causes in the popular time of dwarf bunt of wheat is generally 20～50%, can reach 75～90% when serious, even total crop failure.Germ resistance is extremely strong, and its winter spore can survive in soil 3～7 years, is wrapped in the winter spore in the mycoceicidum even can maintains vigour to reach more than 10 years.This disease is taken precautions against so there are 15 countries to classify it as Quarantine Objects in the world in case generation is difficult to control or elimination.China classifies this disease as the external Quarantine Objects of one class always since the sixties in 20th century.In Tilletia foetida, TCK is very similar on morphology to its sibling species wheat net fungus tilletia, wheat light Tilletia foetida etc., is difficult to difference.
Traditional disease screening, detection method mainly are the characteristics according to cause of disease morphology, physiology and biochemistry, and not only process is loaded down with trivial details, the time cycle is long, and poor accuracy, precision are not high.Therefore, utilize molecular biology method to differentiate that quickly and accurately T contraversa has important significance for theories and practical value.(Ferreira M.A. such as Ferreira in 1996, Tooley P.W., Hatziloukas E.etc.Isolation of a species specific mitochondrial DNA sequence for identification of Tilletia indica, the Karnal bunt of wheat fungus[J] .Application Environment Microbiology, 1996,62:87～93) first round pcr is introduced into the evaluation of India's bunt (Tilletia indicaMitra), they have selected the EcoR I fragment of a 2.3kb of India's Tilletia foetida Mitochondrial DNA to clone and check order, and the Auele Specific Primer Ti1/Ti4 of design has identified the seal raw meat from 25 kinds of bunt bacteria strains.In addition, (Smith O.P. such as Smith, Peterson G.L.Beck R.J.etc.Development of a PCR-based method for identification of Tilletia indica, causal agent of karnal bunt of wheat[J] .Phytopathology, 1996,86:115～122) by cloning the Dra I fragment of India's Tilletia foetida Mitochondrial DNA, carried out sequential analysis, two cover Oligonucleolide primers have been designed to Ti17/M1 and Ti17/M2, can from India's Tilletia foetida, amplify size respectively for 825bp and 118bp specific fragment, also realize detection evaluation work India's bunt.(Frederick R.D. such as Frederic in 2000, Snyder K.E., Tooley P.W.Identification and Differentiation of Tilletia indica and T.walkeri using the Polymerase Chain Reaction[J] .Phytopathology, 2000,90:951-960.) having designed 5 pairs of Auele Specific Primer and 3 pairs of Auele Specific Primers according to mitochondrial difference at the rye grass Tilletia foetida at India's Tilletia foetida, India's Tilletia foetida bacterial strain and the strain of rye grass raw meat powder bacterium germ can be differentiated from its relative genus kind respectively.(Zhang Jingyu such as Zhang Jingyu, Zhang Zhengguang, Zheng Xiaobo, Deng. the Molecular Detection of tilletia indica mitra [J]. the hi-tech communication, 2004,1:31～36) utilize the difference on the rrna ITS sequence in 20 kinds of Tilletia genus, to design a pair of Auele Specific Primer T1/T2, T.indica and T.walkeri can be made a distinction from other kind, then designed a pair of Auele Specific Primer M1/M2 according to the difference between T.indica and the T.walkeri plastosome again, the two can be made a distinction, in order to make reaction more sensitive, set up the sleeve type PCR technology, so that simpler authentication method is provided.(Liang Hong such as Liang Hong, Peng Youliang, Zhang Guozhen, Deng. the amplification and the sequential analysis [J] thereof in 3 kinds of quarantine property of Tilletia fungi rDNA 2IGS district. Plant Pathology, 2006,36 (5): 407-412), designed a pair of Auele Specific Primer, wheat light Tilletia foetida bacterial strain can have been differentiated from its relative genus kind according to ribosomal IGS1 zone properties.2004 high-strength (high-strength. the Molecular Detection of dwarf bunt of wheat [D]. Changsha, Agricultural University Of Hunan, 2004) utilize the RAPD technology to find a band that wheat net fungus tilletia bacterial strain and T contraversa bacterial strain can be different from other ustilago strain, but it's a pity and between short Tilletia foetida and net fungus tilletia, do not find discrepant band, fail the two is separated.Zhou Yeqin in 2006, Liu Suping etc. (Zhou Yeqin, Liu Suping, Zhou Guoliang, etc. the monospore of paddy rice bunt bacterium detects [J].Plant Quarantine, 2006,20:38～41) use universal primer Ti11/Ti14 and two couples of Auele Specific Primer (Hor2/Hor9 of rrna ITS sequence; Hm1/Hm5) in conjunction with having set up the sleeve type PCR technology, the paddy rice Tilletia foetida can be demarcated out.Old ten thousand power in this laboratory, Liu Taiguo, Liu Jianhua utilize the AFLP technology, found the specific fragment of T contraversa, T contraversa can be made a distinction from its relative genus kind, this technology has obtained national inventing patent, the patent No. is: 200510080073.7, but do not report the sensitivity of its detection, in customs quarantine control, do not use as yet.
ISSR is meant that Oligonucleolide primers that utilization designs based on SSR detects one section short dna sequence difference between 2 SSR, and its advantage is to carry out genome fingerprinting map and to make up under the situation without any the molecular biology research basis; Can detect a plurality of SSR seat simultaneously; The DNA consumption is few; Dominance or codominance.The ISSR mark can be used for filling rare interruption of some RFLP marks or clear area in the genetic map, therefore, also obtains more application gradually in the QTL location.Do not see as yet based on the ISSR method both at home and abroad at present and obtain the report that Auele Specific Primer detects T contraversa.
Summary of the invention:
The present invention is single according to the method that present molecular biology method detects T contraversa, sensitivity is not high, detect the narrower present situation of sample range, a kind of detection method and specific SCAR label of T contraversa are provided, be used to detect the wheat Tilletia foetida, have good, highly sensitive, the easy and simple to handle advantage fast of specificity.
The specific SCAR label of a kind of T contraversa (Tilletia controversa K ü hn) is shown in its nucleotide sequence Seq No.5.
A kind of detection method of dwarf bunt of wheat is characterized in that according to the nucleotide sequence shown in the Seq No.5 design primer template to be measured that increases,
Described primer is:
Forward primer TCKSF2:5 '-TTG CTG GCT CTT CGC CCT GA-3,
Reverse primer TCKSR2:5 '-TTG CCC GTC TTG CGG TTG AT-3 '.
The present invention is based on the specific gene sequence of the T contraversa of ISSR acquisition, the ustilago sample wide material sources that adopted amount to 51 bacterial strains: 14 T contraversas (T.controversa K ü hn, TCK) bacterial strains; (wherein 1 comes from Czech (TFL 6) to 6 wheat light Tilletia foetidas, different areas in all the other 5 countries of origin for T.foetidaLiro, TFL) bacterial strain; (major part comes from the U.S. to 24 wheat net fungus tilletias for T.cariesTul., TCT) bacterial strain, and 1 comes from Czech (TCT24), and other 5 kinds of fungal bacterial strains not of the same race.Present ustilago region in vogue has been contained in these 51 sample sources substantially, 100 ISSR primers announcing with Canadian Columbia University carry out the Auele Specific Primer screening to these bacterial strains, wherein primer I SSR859 can stably amplify the fragment of 670bp in T contraversa, ISSR818 can stably amplify the fragment of 952bp and 867bp in T contraversa, and does not find this band in the pathogenic fungi of 37 bacterial strains of the Tilletia foetida of all the other two kinds of nearly edge and other contrast.Therefore, determine that it is the distinctive nucleotide sequence of T contraversa.By reclaiming above-mentioned 3 DNA fragment specific of order-checking, obtain these segmental nucleotide sequence informations, as Seq No.1, No.2 is shown in the No.3.
Because the Seq No.1 that the present invention obtains, No.2, the nucleotide sequence shown in the No.3 are the peculiar gene fragments of T contraversa, therefore, according to the Auele Specific Primer of this sequences Design, T contraversa can be distinguished from its sibling species and be come.The gene fragment that these primers increased out can be used as the SCAR mark of T contraversa.
Auele Specific Primer TCKSF (1-3)/TCKSR (1-3) that the present invention is designed, its nucleotide sequence is shown in Seq No. (7-12), can highly sensitive, with high specificity T contraversa is differentiated out, this has Seq No.4 to the gene fragment that primer increased out, No.5, nucleotide sequence shown in the No.6, its size is respectively 372bp, 496bp and 419bp, can be used as the preferred SCAR mark of T contraversa.
The present invention detects in the PCR method of T contraversa, because when detecting preclinical seed or seedling, its bacterium of carrying amount is considerably less, in the DNA of seed or seedling co-extracted, the DNA ratio of germ is extremely low, and is very high to specificity, the susceptibility requirement of primer.Therefore, the PCR reaction system adopts high specific SCAR mark such as Seq No.4, No.5, the nucleotide sequence design high specific shown in the No.6, the primer of highly sensitive identification detect as long as the gene fragment that these primer amplifications come out is convenient to sepharose.The preferred TCKSF of the present invention (1-2)/TCKSR (1-2) is as detecting primer, and its detection sensitivity all can reach 1ng/25 μ l.
T contraversa DNA fragment specific Seq No.1 provided by the invention, No.2, No.3 and the high specific and highly sensitive SCAR mark such as the Seq No.4 that obtain according to the nucleotide sequence of these specific fragments, No.5, nucleotide sequence shown in the No.6, can be round pcr detection dwarf bunt of wheat provides multiple primer to select.Detection sensitivity according to a pair of high specific primer TCKSF (the 1-2)/TCKSR (1-2) of SCAR flag sequence design can reach 1ng/25 μ l.Therefore, PCR method provided by the invention be used to detect the wheat Tilletia foetida have save time, accurately, the sensitive advantage, utilized " a kind of T contraversa detect PCR method " (patent No.: 200510080073.7 of AFLP technical research in the past with respect to this laboratory; Contriver: Chen Wanquan etc., 2007), have higher detection sensitivity and reliability.This method can be applicable to that T contraversa the carry disease germs detection of wheat seeds sample and the diagnosis of dwarf bunt of wheat are had higher actual application value.
Description of drawings
Fig. 1: ISSR859 primer screening
Wherein M is standard DNA molecule marker (DNA marker DL2000); 1-8 is respectively T contraversa and (is encoded to TCK1, TCK2, TCK3, TCK4, TCK5, TCK6, TCK7, TCK8), 9-12 is respectively wheat light Tilletia foetida and (is encoded to TFL1, TFL2, TFL3, TFL4), 13-16 is respectively the wheat net fungus tilletia and (is encoded to TCT1, TCT2, TCT3, TCT4).
Fig. 2: the checking of specific SCAR label
Wherein M is standard DNA molecule marker (DNA marker DL 2000); 1-14 is respectively 14 bacterial strains of T contraversa and (is encoded to TCK1, TCK2, TCK3, TCK4, TCK5, TCK6, TCK7, TCK8, TCK9, TCK10, TCK11, TCK12, TCK13, TCK14), 15-38 is respectively 24 bacterial strains of wheat net fungus tilletia and (is encoded to TCT1, TCT2, TCT3, TCT4, TCT5, TCT6, TCT7, TCT8, TCT9, TCT10, TCT11, TCT12, TCT13, TCT14, TCT15, TCT16, TCT17, TCT18, TCT19, TCT20, TCT21, TCT22, TCT23, TCT24), 39-44 (is not encoded to TFL1, TFL2 for wheat light Tilletia foetida, TFL3, TFL4, TFL5, TFL6), 45 are the diffusing black ustilago of wheat, and 46 is grain of rice ustilago, and 47 is the sugarcane ustilago, and 48 is the sorghum smut bacterium, 49,50 is Sporisorium reilianum, and 51 is wheat stripe rust, and 52 is distilled water.
Fig. 3: the sensitivity of Auele Specific Primer TCKSF1/TCKSR1 detects
Wherein M is standard DNA molecule marker (DNAmarkerDL 2,000); 1-10 is respectively T contraversa (TCK9) different concns gradient, is respectively 100ng, 50ng, 20ng, 10ng, 5ng, 1ng, 100pg, 10pg, 1pg, 0.1pg (25 μ l).
Fig. 4: ISSR818 primer screening
Wherein 1 is standard DNA molecule marker (DNAmarkerDL2000); 2-5 be respectively T contraversa (be encoded to TCK2, TCK6, TCK7, TCK10), 6-9 be respectively wheat light Tilletia foetida (be encoded to TFL1, TFL2, TFL3, TFL4), 10-12 be respectively the wheat net fungus tilletia (be encoded to TCT1, TCT2, TCT3).
Fig. 5: the checking of specific SCAR label
Wherein 1,25,26,50 is standard DNA molecule marker (DNAmarkerDL2000); 2-9 is respectively 8 bacterial strains of T contraversa and (is encoded to TCK1, TCK2, TCK5, TCK6, TCK7, TCK8, TCK9, TCK10), 10-17 is respectively 8 bacterial strains of wheat net fungus tilletia and (is encoded to TCT1, TCT2, TCT3, TCT4, TCT5, TCT6, TCT7, TCT8), 18-23 (is not encoded to TFL1, TFL2 for 6 bacterial strains of wheat light Tilletia foetida, TFL3, TFL4, TFL5, TFL6), 24,27-28 is the wheat loose smut, 29-33 is the sugarcane ustilago, and 34-36 is the sorghum smut bacterium, and 37-40 is a Sporisorium reilianum, 41-42 is a wheat stripe rust, 43-44 is a puccinia triticinia, and 45-46 is a red rust, and 47 is wheat powdery mildew, 48 is gibberella saubinetii, and 49 is distilled water.
Fig. 6: the sensitivity of Auele Specific Primer TCKSF2/TCKSR2 detects
Wherein M is standard DNA molecule marker (DNA marker DL 2,000); 2-12 is respectively the gradient of T contraversa (TCK6) different concns, is respectively 60ng, 50ng, 30ng, 20ng, 10ng, 5ng, 1ng, 100pg, 10pg, 1pg, 0pg (25 μ l).
Fig. 7: the checking of specific SCAR label
Wherein 1,25,26,50 is standard DNA molecule marker (DNA marker DL 2000); 2-9 is respectively 8 bacterial strains of T contraversa and (is encoded to TCK1, TCK2, TCK5, TCK6, TCK7, TCK8, TCK9, TCK10), 10-17 is respectively 8 bacterial strains of wheat net fungus tilletia and (is encoded to TCT1, TCT2, TCT3, TCT4, TCT5, TCT6, TCT7, TCT8), 18-23 (is not encoded to TFL1, TFL2 for 6 bacterial strains of wheat light Tilletia foetida, TFL3, TFL4, TFL5, TFL6), 24,27-28 is the wheat loose smut, 29-33 is the sugarcane ustilago, and 34-36 is the sorghum smut bacterium, and 37-40 is a Sporisorium reilianum, 41-42 is a wheat stripe rust, 43-44 is a puccinia triticinia, and 45-46 is a red rust, and 47 is wheat powdery mildew, 48 is gibberella saubinetii, and 49 is distilled water.
Fig. 8: the sensitivity of Auele Specific Primer TCKSF3/TCKSR3 detects
Wherein M is standard DNA molecule marker (DNAmarkerDL 2,000); 1-10 is respectively the gradient of T contraversa (TCK7) different concns, is respectively 100ng, 90ng, 80ng, 70ng, 60ng, 50ng, 40ng, 30ng, 20ng, 10ng, 5ng, 1ng, 100pg, 10pg (25 μ l).
Embodiment
The present invention is described in further detail below in conjunction with example.
Experiment material of the present invention:
(wherein 12 bacterium sources are in the U.S. for T.controversa K ü hn, TCK) totally 14 bacterial strains, and 2 bacterial strains are provided by professor Wang Zhongkang of University Of Chongqing for T contraversa; (wherein 1 is derived from Czech to wheat light Tilletia foetida for T.foetida Liro, TFL) totally 6 bacterial strains, and different areas in all the other 5 countries of origin are by the sick group harvesting of Plant Protection institute, Chinese Academy of Agricultral Sciences wheat; The wheat net fungus tilletia (T.caries Tul., TCT) totally 24 bacterial strains, except that 1 from the Czech, all the other provide by professor Wang Zhongkang of University Of Chongqing; Wheat loose smut (Ustilago tritici); grain of rice ustilago (Neovossia horrida); sugarcane ustilago (U.scitaminea); Chinese sorghum axle ustilago (Sphacelotheca crueuta); Sporisorium reilianum (S.reiliana); wheat stripe rust (Puccnia striiformis); puccinia triticinia (P.triticina); red rust (P.graminis); wheat powdery mildew (Erysiphe graminis); gibberella saubinetiis (Fusarium graminearum) etc. are by the sick group harvesting of Plant Protection institute, Chinese Academy of Agricultral Sciences wheat, can provide as non-commercial experiment with (seeing Table 1) to the public.
The employed bacterial strain material of this experiment of table 1
Main agents:
Taq DNAPolymerase, dNTP, Mg
2+, plasmid extraction kit purchases in sky root biochemical technology company; Cloning vector pMD18-T, IPTG, X-Gal purchase in precious biotechnology company limited; The sepharose test kit is purchased in AXYGEN; The ISSR primer is synthetic by Shanghai bio-engineering corporation according to the ISSR sequence that Canadian Columbia University announces.
Embodiment 1: the specific ISSR Auele Specific Primer of screening T contraversa
The extraction of 11 T contraversa DNA
The CTAB/SDS method of application enhancements is extracted the DNA of T contraversa.
(1) The pretreatment: get one of ustilago mycoceicidum (approximately 10mg) crushing and join in the sterilization screw socket centrifuge tube of 2ml, add 25mg diatomite, the 250mg diameter 1mm granulated glass sphere of sterilize, the vortex instrument shakes mixing.Place-20 ℃ to spend the night.
(2) water-bath: the 660 μ l SDS/CTAB that add preheating in the centrifuge tube extract damping fluid and 5 μ l Proteinase K solution, vortex instrument mixing, 65 ℃ of water bath with thermostatic control 1h
(3) grind: put centrifuge tube in quick nucleic acid extraction instrument MP FastPrep-24, establish 6.5M/s, 10s handles 1 time.
(4) extracting: get supernatant liquor, add equal-volume chloroform/primary isoamyl alcohol mixing solutions (24: 1), 4 ℃, the centrifugal 10min of 15493 * g.Change supernatant liquor to new centrifuge tube, repeat extraction procedure again 2 times
(5) remove RNA: get supernatant liquor to new centrifuge tube, add 5 μ l 10mg/ml RNA enzymes, behind 37 ℃ of water bath with thermostatic control 1-2h, extracting is once again by extractive step.
(6) precipitation: change supernatant liquor to new centrifuge tube, add 0.6 times of pre-cold isopropanol of volume mixing gently, preserved 1 hour for 4 ℃.The centrifugal 10min of 15493 * g.Abandon supernatant liquor.
(7) washing:,, wash 2 times with the liquid-transfering gun flushing for adding 200 μ l precoolings, 70% ethanol.
The centrifugal 5min of 15493 * g, deposit D NA.
(8) dissolving: behind the vacuum-drying 10min, DNA is dissolved in 20 μ l TE solution ,-20 ℃ of preservations.
The screening of (the SCAR mark) 1.2 of T contraversa specificity ISSR labeled primer
From 100 ISSR primers that Canadian Columbia University announces, select wherein 40, all T contraversas, wheat net fungus tilletia, wheat light Tilletia foetida are screened by optimizing the good reaction system and the optimum annealing temperature of each primer.Screen the specific fragment that amplifies T contraversa (Fig. 1) that primer UBC859 can be stable.
The ISSR-PCR reaction system: adopt the PCR reaction system of 25 μ l, proportioning is as follows: 10 * PCR-buffer, 2.5 μ l, Mg
2+2 μ l (25mM), dNTPs 0.25 μ l (10mM), 3 μ l (10 μ M) primer (ISSR859:5 '-TGT GTG TGT GTG TGTGRC-3 '; ISSR818:5 '-TGT GTG TGT GTG TGT GRC-3 ') Taq DNA polymerase 0.4 μ l (2.5U/ μ l), template DNA 1.5 μ l (20ng/ μ l), the sterilization distilled water is supplied 25 μ l.On MJ research pcr amplification instrument, increase.
The pcr amplification condition is 94 ℃ of 1min; 94 ℃ of 1min, 48 ℃ of (annealing temperature is chosen by the optimum temps of different primers) 1min, 72 ℃ of 2min, 40 circulations; 72 ℃ are extended 5min; 4 ℃ of forever.Behind the pcr amplification, get 5 μ l amplified productions and add 1 μ l sample loading buffer electrophoresis on 1.5% sepharose, as electrophoretic buffer, electrophoresis is 2 hours under the 100V with 1 * TAE, with EB dyeing, and observation and photograph under ultraviolet lamp.As Fig. 1.
Determine that through amplification repeatedly polymorphism is more stable with primer I SSR859 and ISSR818, primer I SSR859 as can be seen from Fig. 1 and Fig. 4, ISSR818 amplification T contraversa colony obtains the DNA fragment specific of 670bp, 952bp and 867bp.This fragment is cut down from sepharose, use the DNA of AXYGEN company reclaim test kit to specific fragment reclaim with purifying after, product behind the purifying is connected on the pMD18-T carrier, the PCR product is with after carrier is connected, be transformed among the E.coli and clone, with sequencing primer on the carrier and restriction enzyme plasmid is detected respectively.The recombinant plasmid that shows as positive colony is transferred to Shanghai bio-engineering corporation carry out sequencing.
670bp, the 952bp that measures and the complete sequence of 867bp T contraversa specific fragment are shown in Seq No.1, Seq No.2 and Seq No.3.
Embodiment 2 T contraversa specific fragment sequencings and acquisition specific SCAR label
The sequence sequencing result of the T contraversa specific fragment that obtains according to embodiment 1 is analyzed comparison with DNAMAN 5.2.2 software to sequence, and is designed specialization SCAR primer TCKSF (1-3)/TCKSR (1-3) of three couples of TCK respectively.These primers can amplify the band of 372bp, 496bp and 419bp respectively in all TCK bacterial strains, and in wheat light Tilletia foetida, wheat net fungus tilletia without any amplified production such as Fig. 2,5,7.Therefore, above-mentioned 3 specific SCAR labels that fragment is the wheat Tilletia foetida.
Primer TCKSF (1-3) and TCKSR (1-3) sequence are as follows:
TCKSF1(5’-TGGTGGTCG?GGAAAGATTAGA-3’)
TCKSR1(5’-GGGACGAAG?GCATCAAGAAG-3’)
TCKSF2(5’-TTG?CTG?GCT?CTT?CGC?CCT?GA-3’)
TCKSR2(5’-TTG?CCC?GTC?TTG?CGG?TTGAT-3’)
TCKSF3(5’-CACACACACACAGGAAGCA-3’)
TCKSR3(5’-CGAGGAAGCAGACAAGGCAT-3’)
Embodiment 3: the checking of T contraversa specific SCAR label
T contraversa specific SCAR label primer TCKSF (1-3)/TCKSR (1-3) that the present invention makes up is synthetic by Shanghai bio-engineering corporation, the amplification reaction system cumulative volume of specific SCAR label is 25 μ l, wherein contain 10 * PCR-buffer, 2.5 μ l, Mg
2+2 μ l (25mM), dNTPs 0.3 μ l (10mM), each 1 μ l (10 μ M) of TCKSF (1-3)/TCKSR (1-3), Taq DNA polymerase 0.3 μ l (2.5U/ μ l), template DNA (DNA that T contraversa and wheat light Tilletia foetida, wheat net fungus tilletia extract) 1 μ l (20ng/ μ l), the sterilization distilled water is supplied 25 μ l.
The pcr amplification condition is 94 ℃ of 5min; 94 ℃ of 30Sec, TCKSF1,3/TCKSR1,3 55 ℃ of 30 Sec (60 ℃ of 30 Sec of TCKSF2/TCKSR2), 72 ℃ of 1min, 30 circulations; 72 ℃ are extended 10min; 4 ℃ of forever.Behind the pcr amplification, get 5 μ l amplified productions and add 1 μ l sample loading buffer electrophoresis on 1.0% sepharose, electrophoresis is 1 hour under the 100V, with EB dyeing, adopts the analysis of taking a picture of the gel analysis system of Bio-Rad company.
As Fig. 2, can in all T contraversas, obtain the specific SCAR label fragment of 372bp with primer TCKSF1/TCKSR1, as 1-14 swimming lane among Fig. 2, and the wheat net fungus tilletia, 15-38 swimming lane among Fig. 2), wheat light Tilletia foetida, 39-44 swimming lane among Fig. 2 does not obtain corresponding amplified fragments in the 45-51 swimming lane of loose smut of wheat bacterium, grain of rice ustilago, sugarcane ustilago, sorghum smut bacterium, maize head dust-brand, wheat stripe rust.As Fig. 5 and Fig. 7, T contraversa can obtain the specific SCAR label fragment of 496bp and 419bp respectively, as 2-9 swimming lane among Fig. 5, and 2-8 swimming lane among Fig. 7.Illustrate that the constructed SCAR mark of the present invention is the high specific SCAR mark of T contraversa.Auele Specific Primer according to this SCAR indicia designs can be used for detecting T contraversa.
Embodiment 4: the sensitivity of Auele Specific Primer detects
Because the Auele Specific Primer of specific SCAR label design has high specific and highly sensitive, the present invention directly selects for use the primer of this SCAR mark of amplification to detect the Auele Specific Primer of wheat Tilletia foetida as PCR.Detect its sensitivity by following experiment.
The TCK template DNA is diluted to 100ng/ μ l, 50ng/ μ l, 20ng/ μ l, 10ng/ μ l, 5ng/ μ l, 1ng/ μ l, 100pg/ μ l, 10pg/ μ l, 1pg/ μ l, 0.1pg/ μ l respectively, in each reaction system, adds 1 μ l and dilute good dna profiling and carry out PCR.The PCR system detects with agarose gel electrophoresis behind the PCR with embodiment 3.The result shows that TCKSF1/TCKSR1 all can amplify the band of 372bp in the scope of template amount 1～100ng, as shown in Figure 3; TCKSF2/TCKSR2 all can amplify the band of 496bp in the scope of template amount 1～60ng, as shown in Figure 6, TCKSF3/TCKSR3 all can amplify the band of 419bp in the scope of template amount 5～100ng, as shown in Figure 8.
The present invention filters out the exclusive specific fragment of TCK by the ISSR molecular marker method, and success change into stable specific SCAR label, wherein TCKSF (1-2)/TCKSR (1-2) can effectively detect TCK when minimum template content 1ng, and not amplification on wheat light Tilletia foetida, wheat net fungus tilletia.Illustrate that the T contraversa specific SCAR label that the present invention makes up has higher accuracy and reliability, can be used for the rapid molecular detection of T contraversa according to the primer of its design.
Claims (3)
1. the specific SCAR label of a T contraversa (Tilletia controversa K ü hn) is characterized in that having the nucleotide sequence shown in Seq No.5.
2. the detection method of a dwarf bunt of wheat is characterized in that coming pcr amplification template to be measured according to the design of the nucleotide sequence shown in Seq No.5 primer.
3. detection method according to claim 2, described primer is:
Forward primer TCKSF2:5 '-TTG CTG GCT CTT CGC CCT GA-3,
Reverse primer TCKSR2:5 '-TTG CCC GTC TTG CGG TTG AT-3.
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Cited By (4)
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| CN104221648A (en) * | 2013-08-13 | 2014-12-24 | 中国农业科学院植物保护研究所 | Method for cultivating tilletia controversa kuhn disease plants in indoor environments |
| CN105331602A (en) * | 2015-10-29 | 2016-02-17 | 中国农业科学院植物保护研究所 | Method for detecting Tilletia controversa Kuhn in soil by QPCR (quantitative polymerase chain reaction) |
| CN105331713A (en) * | 2015-11-10 | 2016-02-17 | 中国农业科学院植物保护研究所 | Method for detecting TCK (trichloroK) winter spores in soil by microdroplet digital PCR (ddPCR) |
| CN112961935A (en) * | 2021-03-11 | 2021-06-15 | 中国农业科学院植物保护研究所 | SCAR marker primer for detecting Tilletia controversa Kuhn and application thereof |
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| CN100392102C (en) * | 2005-06-29 | 2008-06-04 | 中国农业科学院植物保护研究所 | PCR method for detecting T contraversa |
| CN101328496B (en) * | 2008-07-11 | 2011-02-02 | 天津出入境检验检疫局动植物与食品检测中心 | Detection method of three Tilletia foetida similar species on Perennial ryegrass |
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| CN104221648A (en) * | 2013-08-13 | 2014-12-24 | 中国农业科学院植物保护研究所 | Method for cultivating tilletia controversa kuhn disease plants in indoor environments |
| CN104221648B (en) * | 2013-08-13 | 2017-01-18 | 中国农业科学院植物保护研究所 | Method for obtaining Tilletia controversa Kuhn disease-causing plants through indoor culture |
| CN105331602A (en) * | 2015-10-29 | 2016-02-17 | 中国农业科学院植物保护研究所 | Method for detecting Tilletia controversa Kuhn in soil by QPCR (quantitative polymerase chain reaction) |
| CN105331713A (en) * | 2015-11-10 | 2016-02-17 | 中国农业科学院植物保护研究所 | Method for detecting TCK (trichloroK) winter spores in soil by microdroplet digital PCR (ddPCR) |
| CN112961935A (en) * | 2021-03-11 | 2021-06-15 | 中国农业科学院植物保护研究所 | SCAR marker primer for detecting Tilletia controversa Kuhn and application thereof |
| CN112961935B (en) * | 2021-03-11 | 2022-03-29 | 中国农业科学院植物保护研究所 | SCAR marker primer for detecting Tilletia controversa Kuhn and application thereof |
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