Matson Michael E H, Small Ian M, Fry William E, Judelson Howard S
First and fourth authors: Department of Plant Pathology and Microbiology, University of California, Riverside, CA 92521; and second and third authors: Section of Plant Pathology and Plant-Microbe Biology, Cornell University, Ithaca, NY 14853.
Phytopathology. 2015 Dec;105(12):1594-600. doi: 10.1094/PHYTO-05-15-0129-R. Epub 2015 Nov 9.
Prior work has shown that the inheritance of resistance to metalaxyl, an oomycete-specific fungicide, is complex and may involve multiple genes. Recent research indicated that a single nucleotide polymorphism (SNP) in the gene encoding RPA190, the largest subunit of RNA polymerase I, confers resistance to metalaxyl (or mefenoxam) in some isolates of the potato late blight pathogen Phytophthora infestans. Using both DNA sequencing and high resolution melt assays for distinguishing RPA190 alleles, we show here that the SNP is absent from certain resistant isolates of P. infestans from North America, Europe, and Mexico. The SNP is present in some members of the US-23 and US-24 clonal lineages, but these tend to be fairly sensitive to the fungicide based on artificial media and field test data. Diversity in the level of sensitivity, RPA190 genotype, and RPA190 copy number was observed in these lineages but were uncorrelated. Controlled laboratory crosses demonstrated that RPA190 did not cosegregate with metalaxyl resistance from a Mexican and British isolate. We conclude that while metalaxyl may be used to control many contemporary strains of P. infestans, an assay based on RPA190 will not be sufficient to diagnose the sensitivity levels of isolates.
先前的研究表明,对卵菌特异性杀菌剂甲霜灵的抗性遗传较为复杂,可能涉及多个基因。最近的研究表明,编码RNA聚合酶I最大亚基RPA190的基因中的单核苷酸多态性(SNP)赋予了马铃薯晚疫病病原菌致病疫霉的某些分离株对甲霜灵(或精甲霜灵)的抗性。通过使用DNA测序和高分辨率熔解分析来区分RPA190等位基因,我们在此表明,来自北美、欧洲和墨西哥的某些致病疫霉抗性分离株中不存在该SNP。该SNP存在于US-23和US-24克隆谱系的一些成员中,但根据人工培养基和田间试验数据,这些成员对该杀菌剂往往相当敏感。在这些谱系中观察到了敏感性水平、RPA190基因型和RPA190拷贝数的多样性,但它们之间没有相关性。受控的实验室杂交表明,RPA190与来自墨西哥和英国分离株的甲霜灵抗性不共分离。我们得出结论,虽然甲霜灵可用于控制许多当代致病疫霉菌株,但基于RPA190的检测不足以诊断分离株的敏感性水平。