Microbial Genomics Research Unit, National Center for Agricultural Utilization Research , Us Department of Agriculture, Agriculture research Service, Peoria, IL 61604, USA.
Phytopathology. 2010 Jan;100(1):58-71. doi: 10.1094/PHYTO-100-1-0058.
Sudden death syndrome (SDS) of soybean has become a serious constraint to the production of this crop in North and South America. Phenotypic and multilocus molecular phylogenetic analyses, as well as pathogenicity experiments, have demonstrated that four morphologically and phylogenetically distinct fusaria can induce soybean SDS. Published molecular diagnostic assays for the detection and identification of these pathogens have reported these pathogens as F. solani, F. solani f. sp. glycines, or F. solani f. sp. phaseoli, primarily because the species limits of these four pathogens were only recently resolved. In light of the recent discovery that soybean SDS and Phaseolus and mung bean root rot (BRR) are caused by four and two distinct species, respectively, multilocus DNA sequence analyses were conducted to assess whether any of the published molecular diagnostic assays were species-specific. Comparative DNA sequence analyses of the soybean SDS and BRR pathogens revealed that highly conserved regions of three loci were used in the design of these assays, and therefore none were species-specific based on our current understanding of species limits within the SDS-BRR clade. Prompted by this finding, we developed a high-throughput multilocus genotyping (MLGT) assay which accurately differentiated the soybean SDS and two closely related Phaseolus and mung BRR pathogens based on nucleotide polymorphism within the nuclear ribosomal intergenic spacer region rDNA and two anonymous intergenic regions designated locus 51 and 96. The single-well diagnostic assay, employing flow cytometry and a novel fluorescent microsphere array, was validated by independent multilocus molecular phylogenetic analysis of a 65 isolate design panel. The MLGT assay was used to reproducibly type a total of 262 soybean SDS and 9 BRR pathogens. The validated MLGT array provides a unique molecular diagnostic for the accurate identification and molecular surveillance of these economically important plant pathogens.
大豆猝死综合征(SDS)已成为北美和南美大豆生产的严重制约因素。表型和多位点分子系统发育分析以及致病性实验表明,四种形态和系统发育上不同的镰刀菌可引起大豆 SDS。已发表的用于检测和鉴定这些病原体的分子诊断检测方法将这些病原体报告为 F. solani、F. solani f. sp. glycines 或 F. solani f. sp. phaseoli,主要是因为这四种病原体的种间界限最近才得到解决。鉴于最近发现大豆 SDS 和菜豆及绿豆根腐病(BRR)分别由四种和两种不同的种引起,进行了多位点 DNA 序列分析,以评估任何已发表的分子诊断检测方法是否具有种特异性。对大豆 SDS 和 BRR 病原体的比较 DNA 序列分析表明,这些检测方法的设计使用了三个基因座的高度保守区域,因此,根据我们目前对 SDS-BRR 进化枝内种间界限的理解,它们都不是种特异性的。受此发现的启发,我们开发了一种高通量多位点基因分型(MLGT)检测方法,该方法基于核核糖体基因间隔区 rDNA 和两个命名为 51 号和 96 号的两个匿名基因间隔区的核苷酸多态性,准确地区分了大豆 SDS 和两种密切相关的菜豆和绿豆 BRR 病原体。该单孔诊断检测方法采用流式细胞术和新型荧光微球阵列,通过对 65 个分离株设计面板的独立多位点分子系统发育分析进行了验证。MLGT 检测方法用于可重复地对总共 262 种大豆 SDS 和 9 种 BRR 病原体进行分型。经验证的 MLGT 阵列为这些经济重要的植物病原体的准确鉴定和分子监测提供了独特的分子诊断方法。