A New Approach Using the SYBR Green-Based Real-Time PCR Method for Detection of Soft Rot Pectobacterium odoriferum Associated with Kimchi Cabbage.

IF 1.8 3区 农林科学 Q2 PLANT SCIENCES
Yong Ju Jin, Dawon Jo, Soon-Wo Kwon, Samnyu Jee, Jeong-Seon Kim, Jegadeesh Raman, Soo-Jin Kim
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引用次数: 2

Abstract

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.

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基于SYBR绿色的实时荧光定量PCR检测泡菜软腐病臭乳杆菌的新方法
臭乳杆菌是白菜软腐病的主要病原菌。致病菌乳杆菌属是造成农作物产量损失的主要原因。然而,P. odoriferum与P. carotovorum、P. versatile和P. brasiliense共享广泛的寄主,并且与这些物种具有相似的生化、表型和遗传特征。因此,由于上述软腐病的诊断过程和管理都很复杂,因此有必要开发一种专门用于软腐病的诊断方法。因此,在本研究中,为了选择p.o odoriferum特异性基因,我们使用了p.o odoriferum JK2.1全基因组数据和NCBI中注册的类似细菌种的数据进行了种特异性基因的选择。然后,通过胚分析检测所选基因的特异性。我们发现了新的物种特异性基因来检测和量化靶向的臭臭草,并设计了针对HAD家族水解酶的特异性引物。结果表明,选取的引物仅在29个乳杆菌种及其近缘种的臭臭杆菌DNA中形成了360 bp的特异扩增子。此外,在不提取基因组DNA的情况下,利用SYBR green为基础的实时定量PCR技术,利用一组植物引物,可以估计P. odoriferum的种群密度。因此,新开发的诊断方法可以快速准确地诊断并持续监测泡菜软腐病,而无需从植物组织中进行额外的程序。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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
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