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用于区分菲利普斯异皮线虫和燕麦异皮线虫的种特异性PCR检测方法

Species-Specific PCR Assays for Differentiating Heterodera filipjevi and H. avenae.

作者信息

Yan Guiping, Smiley Richard W, Okubara Patricia A, Skantar Andrea M

机构信息

Oregon State University, Columbia Basin Agricultural Research Center, Pendleton 97801.

United States Department of Agriculture-Agricultural Research Service (USDA-ARS), Root Disease and Biological Control Research Unit, Pullman, WA 99164-6430.

出版信息

Plant Dis. 2013 Dec;97(12):1611-1619. doi: 10.1094/PDIS-01-13-0064-RE.

Abstract

Heterodera avenae and H. filipjevi are economically important cyst nematodes that restrict production of cereal crops in the Pacific Northwest United States and elsewhere in the world. Identification of these two species is critical for recommending and implementing effective management practices. Primers were designed from the internal transcribed spacer (ITS) regions of H. avenae and H. filipjevi ribosomal DNA. The primers were highly specific when examined on target isolates but did not amplify DNA from nontarget Heterodera, Globodera, Meloidogyne, Pratylenchus, and other nematode species tested. Polymerase chain reaction (PCR) and amplification conditions were established, and H. avenae and H. filipjevi were clearly distinguished by PCR fragments of 242 and 170 bp, respectively. Robust PCR amplification was achieved with DNA extracted from a single egg or second-stage juvenile (J2) using a laboratory-made worm lysis buffer, and DNA from 0.5 egg or J2 using a commercial kit. The PCR assays were successfully employed for differentiation of H. filipjevi and H. avenae populations collected from eight locations in three Pacific Northwest states. This is the first report of a species-specific ITS PCR assay to detect and identify H. filipjevi. The assays for both species will enhance diagnosis of cereal cyst nematode species in infested fields.

摘要

燕麦异皮线虫和菲利普异皮线虫是具有重要经济意义的孢囊线虫,它们限制了美国太平洋西北部以及世界其他地区谷类作物的产量。鉴别这两个物种对于推荐和实施有效的管理措施至关重要。引物是根据燕麦异皮线虫和菲利普异皮线虫核糖体DNA的内转录间隔区(ITS)设计的。这些引物在检测目标分离株时具有高度特异性,但不会扩增来自非目标异皮线虫属、球孢囊线虫属、根结线虫属、短体线虫属以及其他所测试线虫物种的DNA。建立了聚合酶链反应(PCR)及扩增条件,燕麦异皮线虫和菲利普异皮线虫可分别通过242 bp和170 bp的PCR片段清晰区分。使用自制的线虫裂解缓冲液从单个卵或二龄幼虫(J2)中提取的DNA以及使用商业试剂盒从0.5个卵或J2中提取的DNA均实现了稳健的PCR扩增。PCR检测方法成功用于区分从太平洋西北部三个州的八个地点采集的菲利普异皮线虫和燕麦异皮线虫种群。这是关于一种用于检测和鉴定菲利普异皮线虫的物种特异性ITS PCR检测方法的首次报道。这两种线虫的检测方法将提高对受侵染田地中谷类孢囊线虫物种的诊断能力。

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