Ham Hyeonheui, Lee Bang Wool, Kim Kyongnim, Lee Woohyung, Lee Yong Hwan, Park Dong Suk
Crop Protection Division, National Institute of Agricultural Sciences, Rural Develop-ment Administration, Wanju 55365, Korea.
Microbial Safety Division, National Institute of Agricultural Sciences, Rural Develop-ment Administration, Wanju 55365, Korea.
Plant Pathol J. 2024 Dec;40(6):671-680. doi: 10.5423/PPJ.OA.08.2024.0125. Epub 2024 Dec 1.
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.
由西瓜嗜酸菌引起的细菌性果实斑点病(BFB)是西瓜等葫芦科寄主植物中的一种毁灭性病害。西瓜嗜酸菌是一种种传病原菌,受污染的种子是主要接种体。由于病害发生后难以控制BFB,因此在早期检测病原菌并清除包括种子在内的受感染植物材料至关重要。在本研究中,我们开发了一种直接SYBR Green实时聚合酶链反应(PCR)方法,使用一种新的种特异性标记物来高特异性和高灵敏度地检测西瓜嗜酸菌。收集并比较了西瓜嗜酸菌和相关物种的基因组信息,以检索西瓜嗜酸菌特异性基因。基于所选基因设计了引物对RS01560-164,并使用克隆DNA、基因组DNA、细胞悬液以及从受感染西瓜子叶中获得的悬液对其特异性和灵敏度进行了测试。通过实时PCR,我们的引物对仅从密切相关物种中检测到西瓜嗜酸菌,克隆DNA的检测限为1.46×103拷贝/µl,基因组DNA为500 fg/µl,细胞悬液为1.4×104 cfu/ml。我们的方法还能够从患病植物中检测到西瓜嗜酸菌,而无需进行DNA提取步骤。因此,本研究新开发的引物对和实时PCR方法可用于高灵敏度和稳健性地特异性检测植物或种子中的西瓜嗜酸菌,为管理葫芦科植物中的BFB提供了可能性。