Zhang Jiannan, Luo Jinyan, Chen Lei, Ahmed Temoor, Alotaibi Saqer S, Wang Yanli, Sun Guochang, Li Bin, An Qianli
State Key Laboratory of Rice Biology, Ministry of Agriculture Key Lab of Molecular Biology of Crop Pathogens and Insects, Zhejiang Province Key Laboratory of Biology of Crop Pathogens and Insects, Institute of Biotechnology, College of Agricultural and Biotechnology, Zhejiang University, Hangzhou 310058, China.
Department of Plant Quarantine, Shanghai Extension and Service Center of Agriculture Technology, Shanghai 201103, China.
Microorganisms. 2022 Jun 15;10(6):1223. doi: 10.3390/microorganisms10061223.
Bacterial panicle blight of rice or bacterial grain rot of rice is a worldwide rice disease. and are the causal agents. The early and accurate detection of seed-borne and is critical for domestic and international quarantine and effective control of the disease. Here, genomic analyses revealed that contains five phylogroups and the BG1 primer pair designed to target the 3'-end sequence of a gene encoding a Rhs family protein is specific to and two phylogroups within . Using the BG1 primer pair, a 138-bp DNA fragment was amplified only from the tested panicle blight pathogens and . An EvaGreen droplet digital PCR (dPCR) assay on detection and quantification of the two pathogens was developed from a SYBR Green real-time quantitative PCR (qPCR). The detection limits of the EvaGreen droplet dPCR on the two pathogens were identical at 2 × 10 colony forming units (CFU)∙mL from bacterial suspensions and 2 × 10 CFU∙seed from rice seeds. The EvaGreen droplet dPCR assay showed 10-fold detection sensitivity of the SYBR Green qPCR and could detect a single copy of the target gene in a 20-μL assay. Together, the SYBR Green qPCR assay allows for routine high-throughput detection of the panicle blight pathogens and the EvaGreen droplet dPCR assay provides a high-sensitive and high-accurate diagnostic method for quarantine of the pathogens.
水稻细菌性颖枯病或水稻细菌性谷粒腐烂病是一种世界性的水稻病害。[病原菌名称1]和[病原菌名称2]是其致病因子。对种子携带的[病原菌名称1]和[病原菌名称2]进行早期准确检测,对于国内外检疫和有效控制该病至关重要。在此,基因组分析表明[病原菌名称1]包含五个系统发育组,旨在靶向编码Rhs家族蛋白基因3′端序列设计的BG1引物对,对[病原菌名称1]以及[病原菌名称1]内的两个系统发育组具有特异性。使用BG1引物对,仅从测试的颖枯病病原菌[病原菌名称1]和[病原菌名称2]中扩增出一个138 bp的DNA片段。基于SYBR Green实时定量PCR(qPCR)开发了一种用于检测和定量这两种病原菌的EvaGreen液滴数字PCR(dPCR)检测方法。EvaGreen液滴dPCR对这两种病原菌的检测限相同,对于细菌悬液为2×10菌落形成单位(CFU)∙mL,对于水稻种子为2×10 CFU∙粒种子。EvaGreen液滴dPCR检测方法显示出比SYBR Green qPCR高10倍的检测灵敏度,并且在20 μL检测中能够检测到目标基因的单拷贝。总之,SYBR Green qPCR检测方法可用于颖枯病病原菌的常规高通量检测,而EvaGreen液滴dPCR检测方法为病原菌检疫提供了一种高灵敏度和高精度的诊断方法。