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基于PCR的番茄细菌性斑点病和细菌性叶斑病病原菌诊断检测方法的开发与评估

Development and Evaluation of PCR-Based Diagnostic Assays for the Bacterial Speck and Bacterial Spot Pathogens of Tomato.

作者信息

Cuppels Diane A, Louws Frank J, Ainsworth Teresa

机构信息

Agriculture and Agri-Food Canada, London, ON, N5V 4T3 Canada.

Department of Plant Pathology, North Carolina State University, Raleigh 27695.

出版信息

Plant Dis. 2006 Apr;90(4):451-458. doi: 10.1094/PD-90-0451.

Abstract

Bacterial speck and bacterial spot lesions can easily be confused with each other and with those formed by other tomato pathogens. To facilitate disease diagnosis, we developed and evaluated polymerase chain reaction (PCR)-based lesion assays using crude DNA extracts and primer sets COR1/2 (bacterial speck) and BSX1/2 (bacterial spot). All 29 pathogenic Pseudomonas syringae pv. tomato strains tested produced a 689-bp amplicon with COR1/2; 28 of the 37 geographically diverse bacterial spot-causing xanthomonad (BSX) strains that were tested generated the 579-bp BSX1/2 amplicon. The detection limit with plant samples was 30 to 50 CFU/reaction. In a 6-year study, the COR1/2 PCR assay diverged from the culture-based classical assay for only 3 of 70 bacterial speck lesion samples collected from Ontario greenhouses and tomato fields; the BSX1/2 assay was positive for 112 of the 124 confirmed bacterial spot lesions sampled. The majority (66%) of the BSX strains isolated from these lesions belonged to group D; the 12 strains that were BSX1/2-negative belonged to group C. Group D strains produced a 425-bp PCR product with crude DNA extracts but a 579-bp product with purified DNA; the former was identical to the latter except that it was missing 150 bp from the middle of the 579-bp sequence.

摘要

番茄细菌性斑点病和细菌性叶斑病的病斑很容易相互混淆,也容易与由其他番茄病原体形成的病斑混淆。为便于疾病诊断,我们开发并评估了基于聚合酶链反应(PCR)的病斑检测方法,该方法使用粗DNA提取物以及COR1/2引物对(用于检测细菌性斑点病)和BSX1/2引物对(用于检测细菌性叶斑病)。所有测试的29株致病性丁香假单胞菌番茄致病变种菌株用COR1/2引物对均产生了一条689bp的扩增子;在测试的37株来自不同地理区域的引起细菌性叶斑病的黄单胞菌(BSX)菌株中,有28株产生了579bp的BSX1/2扩增子。对植物样品的检测限为30至50CFU/反应。在一项为期6年的研究中,从安大略省温室和番茄田采集的70个细菌性斑点病斑样品中,只有3个样品的COR1/2 PCR检测结果与基于培养的经典检测结果不同;在124个已确诊的细菌性叶斑病斑样品中,有112个样品的BSX1/2检测呈阳性。从这些病斑中分离出的大多数(66%)BSX菌株属于D组;12株BSX1/2检测呈阴性的菌株属于C组。D组菌株用粗DNA提取物产生一条425bp的PCR产物,但用纯化DNA产生一条579bp的产物;前者与后者相同,只是在579bp序列的中间缺失了150bp。

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