McCuiston Jamie L, Hudson Laura C, Subbotin Sergei A, Davis Eric L, Warfield Colleen Y
Graduate Students, Professor and Assistant Professor, Department of Plant Pathology, NC State University, Raleigh, NC 27695 Plant Pest Diagnostic Center, California Department of Food and Agriculture, 3294 Meadowview Road, Sacramento, CA 95832 Current Address: University of California Cooperative Extension, 80 Stone Pine Road, Suite 100, Half Moon Bay, CA 94019.
J Nematol. 2007 Dec;39(4):343-55.
A PCR-based diagnostic assay was developed for early detection and identification of Aphelenchoides fragariae directly in host plant tissues using the species-specific primers AFragFl and AFragRl that amplify a 169-bp fragment in the internal transcribed spacer (ITS1) region of ribosomal DNA. These species-specific primers did not amplify DNA from Aphelenchoides besseyi or Aphelenchoides ritzemabosi. The PCR assay was sensitive, detecting a single nematode in a background of plant tissue extract. The assay accurately detected A. fragariae in more than 100 naturally infected, ornamental plant samples collected in North Carolina nurseries, garden centers and landscapes, including 50 plant species not previously reported as hosts of Aphelenchoides spp. The detection sensitivity of the PCR-based assay was higher for infected yet asymptomatic plants when compared to the traditional, water extraction method for Aphelenchoides spp. detection. The utility of using NaOH extraction for rapid preparation of total DNA from plant samples infected with A. fragariae was demonstrated.
开发了一种基于聚合酶链反应(PCR)的诊断检测方法,用于直接在寄主植物组织中早期检测和鉴定草莓滑刃线虫。该方法使用物种特异性引物AFragFl和AFragRl,它们能在核糖体DNA的内部转录间隔区(ITS1)扩增出一段169 bp的片段。这些物种特异性引物不能扩增来自贝西滑刃线虫或里氏滑刃线虫的DNA。该PCR检测方法灵敏,能在植物组织提取物背景中检测到单个线虫。该检测方法准确地检测出在北卡罗来纳州苗圃、园艺中心和景观中采集的100多个自然感染的观赏植物样本中的草莓滑刃线虫,其中包括50种以前未被报道为滑刃线虫寄主的植物物种。与传统的用于检测滑刃线虫的水提取方法相比,基于PCR的检测方法对感染但无症状的植物检测灵敏度更高。证明了使用氢氧化钠提取法从感染草莓滑刃线虫的植物样本中快速制备总DNA的实用性。