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首页> 外文期刊>Frontiers in Microbiology >Suspension Array for Multiplex Detection of Eight Fungicide-Resistance Related Alleles in Botrytis cinerea
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Suspension Array for Multiplex Detection of Eight Fungicide-Resistance Related Alleles in Botrytis cinerea

机译:悬浮阵列用于多重检测中八个抗药性相关的等位基因

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A simple and high-throughput assay to detect fungicide resistance is required for large-scale monitoring of the emergence of resistant strains of Botrytis cinerea . Using suspension array technology performed on a Bio-Plex 200 System, we developed a single-tube allele-specific primer extension assay that can simultaneously detect eight alleles in one reaction. These eight alleles include E198 and 198A of the β-Tubulin gene ( BenA ), H272 and 272Y of the Succinate dehydrogenase iron–sulfur subunit gene ( SdhB) , I365 and 365S of the putative osmosensor histidine kinase gene ( BcOS1 ), and F412 and 412S of the 3-ketoreductase gene ( erg27 ). This assay was first established and optimized with eight plasmid templates containing the DNA sequence variants BenA- E198, BenA- 198A, SdhB- H272, SdhB- 272Y, BcOS1- I365, BcOS1- 365S, erg27 -F412, and erg27 -412S. Results indicated that none of the probes showed cross-reactivity with one another. The minimum limit of detection for these genotypes was one copy per test. Four mutant plasmids were mixed with 10 ng/μL wild-type genomic DNA in different ratios. Detection sensitivity of mutant loci was 0.45% for BenA- E198A, BcOS1- I365S, and erg27 -F412S, and was 4.5% for SdhB- H272Y. A minimum quantity of 0.1 ng of genomic DNA was necessary to obtain reliable results. This is the first reported assay that can simultaneously detect mutations in BenA , SdhB , BcOS1 , and erg27 .
机译:为了大规模监测灰葡萄孢的抗性菌株的出现,需要一种简单且高通量的检测杀真菌剂抗性的方法。使用在Bio-Plex 200系统上执行的悬浮阵列技术,我们开发了一种单管等位基因特异性引物延伸测定法,可以在一个反应​​中同时检测八个等位基因。这八个等位基因包括β-微管蛋白基因(BenA)的E198和198A,琥珀酸脱氢酶铁硫亚基基因(SdhB)的H272和272Y,假定的渗透压传感器组氨酸激酶基因(BcOS1)的I365和365S,以及F412和3-酮还原酶基因(erg27)的412S。首先用包含DNA序列变体BenA-E198,BenA-198A,SdhB-H272,SdhB-272Y,BcOS1-1365,BcOS1-365S,erg27-F412和erg27-412S的8个质粒模板建立和优化该测定法。结果表明,没有一种探针显示出彼此的交叉反应性。这些基因型的最低检测限是每次检测一份。将四个突变质粒与10 ng /μL野生型基因组DNA以不同比例混合。对于BenA-E198A,BcOS1-I365S和erg27-F412S,突变基因座的检测灵敏度为0.45%,对SdhB-H272Y为4.5%。为了获得可靠的结果,最少需要0.1 ng的基因组DNA。这是首次报道的可同时检测BenA,SdhB,BcOS1和erg27突变的检测方法。

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