Jin Yong Ju, Jo Dawon, Kwon Soon-Wo, Jee Samnyu, Kim Jeong-Seon, Raman Jegadeesh, Kim Soo-Jin
Agricultural Microbiology Division, National Institute of Agricultural Sciences, Rural Development Administration, Wanju 54875, Korea.
Highland Agriculture Research Institute, National Institute of Crop Science, Rural Development Administration, Pyeongchang 25342, Korea.
Plant Pathol J. 2022 Dec;38(6):656-664. doi: 10.5423/PPJ.OA.09.2022.0138. Epub 2022 Dec 1.
Pectobacterium odoriferum is the primary causative agent in Kimchi cabbage soft-rot diseases. The pathogenic bacteria Pectobacterium genera are responsible for significant yield losses in crops. However, P. odoriferum shares a vast range of hosts with P. carotovorum, P. versatile, and P. brasiliense, and has similar biochemical, phenotypic, and genetic characteristics to these species. Therefore, it is essential to develop a P. odoriferum- specific diagnostic method for soft-rot disease because of the complicated diagnostic process and management as described above. Therefore, in this study, to select P. odoriferum-specific genes, species-specific genes were selected using the data of the P. odoriferum JK2.1 whole genome and similar bacterial species registered with NCBI. Thereafter, the specificity of the selected gene was tested through blast analysis. We identified novel species-specific genes to detect and quantify targeted P. odoriferum and designed specific primer sets targeting HAD family hydrolases. It was confirmed that the selected primer set formed a specific amplicon of 360 bp only in the DNA of P. odoriferum using 29 Pectobacterium species and related species. Furthermore, the population density of P. odoriferum can be estimated without genomic DNA extraction through SYBR Green-based real-time quantitative PCR using a primer set in plants. As a result, the newly developed diagnostic method enables rapid and accurate diagnosis and continuous monitoring of soft-rot disease in Kimchi cabbage without additional procedures from the plant tissue.
恶臭果胶杆菌是泡菜白菜软腐病的主要致病因子。果胶杆菌属的病原菌会导致农作物大幅减产。然而,恶臭果胶杆菌与胡萝卜软腐果胶杆菌、多能果胶杆菌和巴西果胶杆菌有着广泛的寄主范围,并且在生化、表型和遗传特征上与这些物种相似。因此,鉴于上述复杂的诊断过程和管理,开发一种针对恶臭果胶杆菌的软腐病诊断方法至关重要。因此,在本研究中,为了选择恶臭果胶杆菌特异性基因,利用恶臭果胶杆菌JK2.1全基因组数据和NCBI注册的相似细菌物种数据来选择物种特异性基因。此后,通过比对分析测试所选基因的特异性。我们鉴定出了用于检测和定量目标恶臭果胶杆菌的新的物种特异性基因,并设计了针对HAD家族水解酶的特异性引物组。使用29种果胶杆菌属物种及相关物种证实,所选引物组仅在恶臭果胶杆菌的DNA中形成了一个360 bp的特异性扩增子。此外,使用植物中的引物组通过基于SYBR Green的实时定量PCR,无需提取基因组DNA即可估计恶臭果胶杆菌的种群密度。结果,新开发的诊断方法能够在无需对植物组织进行额外操作的情况下,快速、准确地诊断和持续监测泡菜白菜的软腐病。