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Suspension Array for Multiplex Detection of Eight Fungicide-Resistance Related Alleles in Botrytis cinerea

机译:悬浮检测灰葡萄孢中8种抗药性相关等位基因的多重检测

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摘要

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8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-酮还原酶基因的412S(erg27)。首先使用包含DNA序列变体BenA-E198,BenA-198A,SdhB-H272,SdhB-272Y,BcOS1-I365,BcOS1-365S,erg27-F412和erg27-412S的8个质粒模板建立并优化该测定法。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%,对于 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 erg27 的突变的检测方法。

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