Instituto de Biología Funcional y Genómica, Universidad de Salamanca, Consejo Superior de Investigaciones Científicas, 37007 Salamanca, Spain.
Departamento de Microbiología y Genética, Universidad de, Salamanca, 37007 Salamanca, Spain.
Plant Dis. 2022 Feb;106(2):676-684. doi: 10.1094/PDIS-08-21-1676-RE. Epub 2022 Feb 15.
Soft rot on potato tuber is a destructive disease caused by pathogenic bacterial species of the genera and . Accurate identification of the causal agent is necessary to ensure adequate disease management because different species may have distinct levels of aggressiveness and host range. One of the most important potato pathogens is , a highly heterogeneous species capable of infecting multiple hosts. The complexity of this species, until recently divided into several subspecies, has made it difficult to develop precise diagnostic tests. This study proposes a PCR assay based on the new pair of primers Pcar1F/R to facilitate the identification of potato isolates of according to the most recent taxonomic description of this species. The new primers were designed on a variable segment of the 16S rRNA gene and the intergenic spacer region of available DNA sequences from classical and recently established species in the genus . The results of the PCR analysis of genomic DNA from 32 and strains confirmed that the Pcar1F/R primers have sufficient nucleotide differences to discriminate between and other species associated with damage to potato crops, with the exception of , which improves the specificity of the currently available primers. The proposed assay was originally developed as a conventional PCR but was later adapted to the real-time PCR format for application in combination with the existing real-time PCR test for the potato-specific pathogen This should be useful for the routine diagnosis of potato soft rot.
马铃薯软腐病是一种由 和 属的病原菌引起的破坏性疾病。准确鉴定致病因子对于确保充分的疾病管理至关重要,因为不同的物种可能具有不同的侵袭性和宿主范围。最重要的马铃薯病原体之一是 ,它是一种高度异质的物种,能够感染多种宿主。由于该物种的复杂性,直到最近才被分为几个亚种,这使得开发精确的诊断测试变得困难。本研究提出了一种基于新引物对 Pcar1F/R 的 PCR 检测方法,根据该物种的最新分类描述,有助于鉴定马铃薯 菌株。新引物是根据 属中经典和最近建立的物种的 16S rRNA 基因和基因间间隔区的可变片段设计的。从 32 株 和 菌株的基因组 DNA 的 PCR 分析结果证实,Pcar1F/R 引物具有足够的核苷酸差异,可以区分 和与马铃薯作物损伤相关的其他 物种,除了 ,这提高了现有引物的特异性。该检测方法最初是作为常规 PCR 开发的,但后来被改编为实时 PCR 格式,与现有的马铃薯特异性病原体 实时 PCR 检测相结合应用。这对于马铃薯软腐病的常规诊断应该是有用的。