Inderbitzin Patrik, Davis R Michael, Bostock Richard M, Subbarao Krishna V
Department of Plant Pathology, University of California Davis, Davis, California, United States of America.
PLoS One. 2013 Jun 18;8(6):e65990. doi: 10.1371/journal.pone.0065990. Print 2013.
Accurate species identification is essential for effective plant disease management, but is challenging in fungi including Verticillium sensu stricto (Ascomycota, Sordariomycetes, Plectosphaerellaceae), a small genus of ten species that includes important plant pathogens. Here we present fifteen PCR assays for the identification of all recognized Verticillium species and the three lineages of the diploid hybrid V. longisporum. The assays were based on DNA sequence data from the ribosomal internal transcribed spacer region, and coding and non-coding regions of actin, elongation factor 1-alpha, glyceraldehyde-3-phosphate dehydrogenase and tryptophan synthase genes. The eleven single target (simplex) PCR assays resulted in amplicons of diagnostic size for V. alfalfae, V. albo-atrum, V. dahliae including V. longisporum lineage A1/D3, V. isaacii, V. klebahnii, V. nonalfalfae, V. nubilum, V. tricorpus, V. zaregamsianum, and Species A1 and Species D1, the two undescribed ancestors of V. longisporum. The four multiple target (multiplex) PCR assays simultaneously differentiated the species or lineages within the following four groups: Verticillium albo-atrum, V. alfalfae and V. nonalfalfae; Verticillium dahliae and V. longisporum lineages A1/D1, A1/D2 and A1/D3; Verticillium dahliae including V. longisporum lineage A1/D3, V. isaacii, V. klebahnii and V. tricorpus; Verticillium isaacii, V. klebahnii and V. tricorpus. Since V. dahliae is a parent of two of the three lineages of the diploid hybrid V. longisporum, no simplex PCR assay is able to differentiate V. dahliae from all V. longisporum lineages. PCR assays were tested with fungal DNA extracts from pure cultures, and were not evaluated for detection and quantification of Verticillium species from plant or soil samples. The DNA sequence alignments are provided and can be used for the design of additional primers.
准确的物种鉴定对于有效的植物病害管理至关重要,但在包括严格意义上的黄萎病菌(子囊菌门,粪壳菌纲,盘菌科)在内的真菌中具有挑战性,黄萎病菌是一个包含10个物种的小属,其中包括重要的植物病原体。在此,我们展示了15种PCR检测方法,用于鉴定所有已知的黄萎病菌物种以及二倍体杂种长孢黄萎病菌的三个谱系。这些检测方法基于核糖体内部转录间隔区、肌动蛋白、延伸因子1-α、甘油醛-3-磷酸脱氢酶和色氨酸合酶基因的编码区和非编码区的DNA序列数据。11种单靶点(单重)PCR检测方法产生了诊断大小的扩增子,用于鉴定苜蓿黄萎病菌、黑白轮枝菌、大丽轮枝菌(包括长孢黄萎病菌谱系A1/D3)、伊氏黄萎病菌、克莱巴氏黄萎病菌、非苜蓿黄萎病菌、云状黄萎病菌、三孢黄萎病菌、扎氏黄萎病菌,以及物种A1和物种D1,这两个未描述的长孢黄萎病菌祖先。4种多靶点(多重)PCR检测方法同时区分了以下四组中的物种或谱系:黑白轮枝菌、苜蓿黄萎病菌和非苜蓿黄萎病菌;大丽轮枝菌和长孢黄萎病菌谱系A1/D1、A1/D2和A1/D3;大丽轮枝菌(包括长孢黄萎病菌谱系A1/D3)、伊氏黄萎病菌、克莱巴氏黄萎病菌和三孢黄萎病菌;伊氏黄萎病菌、克莱巴氏黄萎病菌和三孢黄萎病菌。由于大丽轮枝菌是二倍体杂种长孢黄萎病菌三个谱系中两个谱系的亲本,因此没有单重PCR检测方法能够将大丽轮枝菌与所有长孢黄萎病菌谱系区分开来。PCR检测方法用纯培养物中的真菌DNA提取物进行了测试,未对从植物或土壤样品中检测和定量黄萎病菌物种进行评估。提供了DNA序列比对,可用于设计额外的引物。