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首页> 外文期刊>Plant Disease >Spatial and Temporal Distribution of Mutations Conferring QoI and SDHI Resistance in Alternaria solani Across the United States
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Spatial and Temporal Distribution of Mutations Conferring QoI and SDHI Resistance in Alternaria solani Across the United States

机译:美国横跨美国altaria solani的Qoi和Sdhi抗性的空间和时间分布

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The application of succinate dehydrogenase inhibiting (SDHI) and quinone outside inhibiting (QoI) fungicide chemistries is a primary tactic in the management of early blight of potato, caused by Alternaria solani. Resistance to QoIs in A. solani has been attributed to the F129 L mutation, while resistance to SDHIs is conferred by five different known point mutations on three AsSdh genes. In total, 1,323 isolates were collected from 2013 through 2015 across 11 states to determine spatial and temporal frequency distribution of these mutations. A real-time polymerase chain reaction (PCR) was used to detect the presence of the F129 L mutation. Molecular detection of SDHI-resistant isolates was performed using SDH multiplex PCR specific for point mutations in AsSdhB, AsSdhC, or AsSdhD genes and mismatch amplification analysis PCR detecting the point mutations in AsSdhB. Previous work in our research group determined that substitutions of histidine for tyrosine (H278Y) or arginine (H278R) at codon 278 on the AsSdhB gene were the most prevalent mutations, detected in 46 and 21% of A. solani isolates, respectively, collected in 2011 to 2012, and uniformly distributed among six sampled states. In contrast, the substitution of histidine for arginine (H134R) at codon 134 in the AsSdhC gene was the most prevalent mutation in 2013 through 2015, identified in 36% of isolates, compared with 7.5% of isolates recovered in 2011 to 2012. Substitutions of histidine for arginine (H133R) at codon 133 and aspartic acid for glutamic acid (D123E) at codon 123 in the AsSdhD gene were detected in 16 and 12%, respectively, in the A. solani population by 2015 and were recovered across a wide range of states, compared with 15 and 1.5% of isolates collected in 2011 to 2012, respectively. Overall, SDHI- and QoI-resistant isolates were detected at high frequencies across all years, with evidence of significant spatial variability. Future research will investigate whether these results are due to differences in parasitic fitness.
机译:琥珀酸脱氢酶抑制(SDHI)和醌外的应用外部抑制(QOI)杀菌剂化学物质是在aleralaria solani引起的马铃薯早期枯萎的主要策略。 A.Solani中的抗琼脂血管致力于F129 L突变,而对三种ASSH基因的五种不同的已知点突变赋予抗SDHIS的抵抗力。总共从2013年到2015年收集了1,323个分离株,以确定这些突变的空间和时间频率分布。使用实时聚合酶链反应(PCR)检测F129 L突变的存在。使用SDH多重PCR特异于ASSDHB,ASSDHC或ASSDHD基因中的点突变和检测ASSDHB中的点突变的点突变进行SDHI多重PCR进行SDHI多重PCR的分子检测。在我们的研究组中,确定酪氨酸(H278Y)或精氨酸(H278R)的组氨酸的替代物在Codon 278上的ASSHB基因中的替代品分别在46和21%的A. solani分离物中检测到最普遍的突变。 2011年至2012年,并在六个采样状态下均匀分布。相反,在ASSDHC基因中的密码子134处的精氨酸(H134R)的组氨酸替代于2013年至2015年的最普遍突变,其在36%的分离株中鉴定,而2011年至2012年的分离株7.5%的分离物。替代在2015年A.Solani人群中分别在16%和12%中检测到Codon 133和Codon酸(D123e)的精氨酸133和谷氨酸(D123e)的谷氨酸(D123e)的组氨酸。各国,与2011年至2012年收集的15%和1.5%的分离物相比。总体而言,在全年的高频下检测到总体,耐频性分离物,具有显着的空间变异性的证据。未来的研究将调查这些结果是否是由于寄生体的差异。

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