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Detection of sdhB Gene Mutations in SDHI-Resistant Isolates of Botrytis cinerea Using High Resolution Melting (HRM) Analysis

机译:使用高分辨率熔解(HRM)分析检测灰葡萄孢的SDHI抗性分离株中sdhB基因突变

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摘要

Botrytis cinerea, is a high risk pathogen for fungicide resistance development. Pathogen’ resistance to SDHIs is associated with several mutations in sdh gene. The diversity of mutations and their differential effect on cross-resistance patterns among SDHIs and the fitness of resistant strains necessitate the availability of a tool for their rapid identification. This study was initiated to develop and validate a high-resolution melting (HRM) analysis for the identification of P225H/F/L//T, N230I, and H272L/R/Y mutations. Based on the sequence of sdhB subunit of resistant and sensitive isolates, a universal primer pair was designed. The specificity of the HRM analysis primers was verified to ensure against the cross-reaction with other fungal species and its sensitivity was evaluated using concentrations of known amounts of mutant’s DNA. The melting curve analysis generated nine distinct curve profiles, enabling the discrimination of all the four mutations located at codon 225, the N230I mutation, the three mutations located in codon 272, and the non-mutated isolates (isolates of wild-type sensitivity). Similar results were obtained when DNA was extracted directly from artificially inoculated strawberry fruit. The method was validated by monitoring the presence of sdhB mutations in samples of naturally infected strawberry fruits and stone fruit rootstock seedling plants showing damping-off symptoms. HRM analysis data were compared with a standard PIRA–PCR technique and an absolute agreement was observed suggesting that in both populations the H272R mutation was the predominant one, while H272Y, N230I, and P225H were detected in lower frequencies. The results of the study suggest that HRM analysis can be a useful tool for sensate, accurate, and rapid identification of several sdhB mutations in B. cinerea and it is expected to contribute in routine fungicide resistance monitoring or assessments of the effectiveness of anti-resistance strategies implemented in crops heavily treated with botryticides.
机译:灰葡萄孢(Botrytis cinerea)是产生抗真菌剂的高风险病原体。病原体对SDHIs的抵抗力与sdh基因的多个突变有关。突变的多样性及其对SDHIs中交叉耐药模式的不同影响以及耐药菌株的适应性使得有必要提供一种快速鉴定它们的工具。启动这项研究是为了开发和验证用于鉴定P225H / F / L // T,N230I和H272L / R / Y突变的高分辨率熔解(HRM)分析。基于抗性和敏感菌株的sdhB亚基序列,设计了通用引物对。验证了HRM分析引物的特异性,以确保不会与其他真菌物种发生交叉反应,并使用已知量的突变体DNA的浓度评估了其敏感性。熔解曲线分析产生了九种不同的曲线图,从而能够区分位于密码子225的所有四个突变,N230I突变,位于密码子272的三个突变以及未突变的分离株(野生型敏感性分离株)。直接从人工接种的草莓果实中提取DNA可获得相似的结果。该方法通过监测自然阻尼的草莓果实和核果砧木幼苗植物样品中sdhB突变的存在而得到验证。将HRM分析数据与标准PIRA-PCR技术进行比较,并观察到绝对一致,这表明在两个种群中H272R突变是主要突变,而H272Y,N230I和P225H的检出频率较低。研究结果表明,HRM分析可以成为敏感,准确和快速鉴定灰质芽孢杆菌中几个sdhB突变的有用工具,并且有望有助于常规杀真菌剂耐药性监测或抗耐药性评估大量使用杀菌剂处理的农作物中实施的策略。

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