Department of Plant Pathology, North Dakota State University, Fargo 58105.
Plant Dis. 2018 Feb;102(2):349-358. doi: 10.1094/PDIS-06-17-0852-RE. Epub 2017 Dec 18.
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 F129L 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 F129L 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.
琥珀酸脱氢酶抑制剂 (SDHI) 和醌外抑制剂 (QoI) 杀菌剂化学物质的应用是防治早疫病的主要策略,早疫病是由茄丝核菌引起的。茄丝核菌对 QoI 的抗性归因于 F129L 突变,而对 SDHI 的抗性则由三个 AsSdh 基因上的五个不同的已知点突变赋予。总共从 2013 年到 2015 年在 11 个州收集了 1323 个分离物,以确定这些突变的时空频率分布。实时聚合酶链反应 (PCR) 用于检测 F129L 突变的存在。使用针对 AsSdhB、AsSdhC 或 AsSdhD 基因中点突变的 SDHI 多重 PCR 以及检测 AsSdhB 中点突变的错配扩增分析 PCR 对 SDHI 抗性分离物进行分子检测。我们研究小组之前的工作确定,在 AsSdhB 基因的密码子 278 处组氨酸取代酪氨酸 (H278Y) 或精氨酸 (H278R) 的取代是最常见的突变,在 2011 年至 2012 年收集的分别为 46%和 21%的茄丝核菌分离物中检测到,均匀分布在六个采样州中。相比之下,2013 年至 2015 年,AsSdhC 基因中组氨酸取代精氨酸 (H134R) 的取代是最常见的突变,在 36%的分离物中鉴定到,而在 2011 年至 2012 年的分离物中只有 7.5%。到 2015 年,在茄丝核菌种群中检测到 AsSdhD 基因中组氨酸取代精氨酸 (H133R) 和天冬氨酸取代谷氨酸 (D123E) 的取代分别为 16%和 12%,并且在广泛的州中回收了这些取代,而在 2011 年至 2012 年收集的分离物中,这两种取代分别为 15%和 1.5%。总体而言,SDHI 和 QoI 抗性分离物在所有年份均以高频率检测到,具有显著的空间变异性。未来的研究将调查这些结果是否归因于寄生适应性的差异。