A Novel and Advanced Diagnostic Approach toward Paracidovorax citrulli Causing Bacterial Fruit Blotch in Watermelon by Direct SYBR Green Real-Time PCR Assay.

IF 1.8 3区 农林科学 Q2 PLANT SCIENCES Plant Pathology Journal Pub Date : 2024-12-01 DOI:10.5423/PPJ.OA.08.2024.0125
Hyeonheui Ham, Bang Wool Lee, Kyongnim Kim, Woohyung Lee, Yong Hwan Lee, Dong Suk Park
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Abstract

Bacterial fruit blotch (BFB) caused by Paracidovorax citrulli is a devastating disease in cucurbit hosts such as watermelon. P. citrulli is a seed-borne pathogen, and contaminated seeds are the primary inoculum. Because it is difficult to control BFB after the emergence of the disease, it is essential to detect the pathogen and remove infected plant materials, including seeds, in the early stages. In this study, we developed a direct SYBR Green real-time polymerase chain reaction (PCR) method using a new species-specific marker for detecting P. citrulli with high specificity and sensitivity. The genome information of P. citrulli and related species was collected and compared to retrieve the P. citrulli-specific gene. The primer set RS01560-164 was designed based on the selected gene and tested for specificity and sensitivity using cloned DNA, genomic DNA, cell suspension, and suspensions obtained from infected watermelon cotyledons. Our primer set detected only P. citrulli from the closely related species with a detection limit of cloned DNA at 1.46 × 103 copies/µl, gDNA at 500 fg/µl, and cell suspension at 1.4 × 104 cfu/ml by real-time PCR. Our method also detected P. citrulli from diseased plants without the need for a DNA extraction phase. Therefore, the primer set and real-time PCR methods newly developed in this study could be applied for the specific detection of P. citrulli in plants or seeds with high sensitivity and robustness, providing the potential to manage BFB in cucurbits.

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直接SYBR绿色实时荧光定量PCR法诊断西瓜细菌性果斑病的新方法
细菌性水果斑病是西瓜等瓜类寄主的一种毁灭性病害。瓜霉是一种种子传播的病原菌,被污染的种子是主要的接种物。由于BFB出现病害后难以控制,因此必须在早期检测病原体并清除受感染的植物材料,包括种子。本研究利用一种新的种特异性标记,建立了一种直接SYBR Green实时聚合酶链反应(PCR)方法,用于瓜氨酸的检测,具有较高的特异性和敏感性。本研究收集了甜瓜属植物及其近缘种的基因组信息,并对其进行比对,以检索甜瓜属植物的特异性基因。根据所选基因设计引物RS01560-164,并利用克隆DNA、基因组DNA、细胞悬液和感染西瓜子叶的悬液进行特异性和敏感性检测。我们的引物只检测到近缘种的瓜氨酸,克隆DNA检测限为1.46 × 103 copies/µl, gDNA检测限为500 fg/µl,细胞悬液检测限为1.4 × 104 cfu/ml。我们的方法也可以在不需要DNA提取阶段的情况下从患病植物中检测到瓜氨酸。因此,本研究新建立的引物集和实时PCR方法具有较高的灵敏度和鲁棒性,可用于植物或种子中对瓜脯杆菌的特异性检测,为管理瓜脯杆菌提供了可能。
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来源期刊
Plant Pathology Journal
Plant Pathology Journal 生物-植物科学
CiteScore
4.90
自引率
4.30%
发文量
71
审稿时长
12 months
期刊介绍: Information not localized
期刊最新文献
Functional Analysis of KPvRxLR27, a Novel Plasmopara viticola Effector from a Korean Isolate, and Its Role in Hypersensitive Response. Characterization and Biocontrol Efficacy of Bacillus velezensis GYUN-1190 against Apple Bitter Rot. A Novel and Advanced Diagnostic Approach toward Paracidovorax citrulli Causing Bacterial Fruit Blotch in Watermelon by Direct SYBR Green Real-Time PCR Assay. Characterization of Tomato Seed Endophytic Bacteria as Growth Promoters and Potential Biocontrol Agents. Construction and Characterization of a Full-Length Infectious cDNA Clone of a Strain of Watermelon Mosaic Virus Isolated from Melon.
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