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首页> 外文期刊>Plant Pathology >High-resolution melting analysis for rapid detection and characterization of Botrytis cinerea phenotypes resistant to fenhexamid and boscalid
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High-resolution melting analysis for rapid detection and characterization of Botrytis cinerea phenotypes resistant to fenhexamid and boscalid

机译:高分辨率熔解分析可快速检测和鉴定对苯六胺和硼鳞甲虫具有抗性的灰葡萄孢表型

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A novel, high-resolution melting (HRM) analysis was developed to detect single nucleotide polymorphisms (SNPs) associated with resistance to fenhexamid (hydroxyanilides) and boscalid (succinate dehydrogenase inhibitors) in Botrytis cinerea isolates. Thirty-six single-spore isolates arising from 13 phenotypes were selected and tested for fungicide sensitivity. Germ tube elongation assays showed two distinct sensitivity levels for each fungicide. Sequencing revealed that resistance to fenhexamid was due to a nucleotide change in the erg27 gene, resulting in an amino acid replacement of phenylalanine (F) with serine (S) or valine (V) at position 412 of the protein, whereas in isolates resistant to boscalid, a nucleotide change in the sdhB gene resulted in the replacement of histidine (H) with arginine (R) or tyrosine (Y) at position 272 of the respective protein. In each case, melting curve analysis generated three distinct profiles corresponding to the presence of each nucleotide in the targeted areas. HRM analysis successfully detected and differentiated the substitutions associated with resistance to both fungicides. In vitro bioassays, direct sequencing and high-resolution melting analysis showed a 100% correlation with detection of resistance. The results demonstrate the utility of HRM analysis as a potential molecular tool for routine detection of fungicide resistance using known polymorphic genes of B.cinerea populations.
机译:开发了一种新颖的高分辨率熔解(HRM)分析,以检测与灰葡萄孢分离物中对苯六胺(羟基苯胺)和硼化(琥珀酸脱氢酶抑制剂)的抗性相关的单核苷酸多态性(SNP)。选择了来自13个表型的36个单孢子分离株,并测试了其对杀菌剂的敏感性。胚芽管伸长试验显示每种杀菌剂有两个不同的敏感性水平。测序结果表明,对fenhexamid的抗性是由于erg27基因的核苷酸变化所致,导致该蛋白在412位氨基酸被丝氨酸(S)或缬氨酸(V)氨基酸置换为苯丙氨酸(F),而对在Boscalid中,sdhB基因的核苷酸变化导致相应蛋白质272位的精氨酸(R)或酪氨酸(Y)取代了组氨酸(H)。在每种情况下,解链曲线分析均产生了三个不同的谱,分别对应于目标区域中每个核苷酸的存在。 HRM分析成功检测并区分了对两种杀菌剂的抗性相关的取代。体外生物测定,直接测序和高分辨率熔解分析显示与耐药性检测具有100%的相关性。结果表明,HRM分析作为利用灰质双歧杆菌种群的已知多态性基因常规检测杀真菌剂抗性的潜在分子工具,具有实用性。

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