Zhao Fangzhou, Wang Yanan, Cheng Wei, Antwi-Boasiako Augustine, Yan Wenkai, Zhang Chunting, Gao Xuewen, Kong Jiejie, Liu Wusheng, Zhao Tuanjie
Key Laboratory of Biology and Genetics Improvement of Soybean, Ministry of Agriculture/Zhongshan Biological Breeding Laboratory (ZSBBL)/National Innovation Platform for Soybean Breeding and Industry-Education Integration/State Key Laboratory of Crop Genetics & Germplasm Enhancement and Utilization/College of Agriculture, Nanjing Agricultural University, Nanjing 210095, China.
Institute of Industrial Crops, Shandong Academy of Agricultural Sciences, Jinan 250100, China.
Plant Dis. 2025 Feb;109(2):341-351. doi: 10.1094/PDIS-01-24-0162-RE. Epub 2025 Feb 3.
Bacterial blight caused by pv. (Psg) is a widespread foliar disease. Although four pv. () to () genes that have been observed to segregate in a Mendelian pattern have been reported to confer resistance to Psg in soybean, the genetic basis of quantitative resistance to bacterial blight in soybean remains unclear. In the present study, the Psg resistance of two soybean association panels consisting of 573 and 213 lines, respectively, was phenotyped in multiple environments in 2014 to 2016. Genome-wide association study was performed using two models, FarmCPU and BLINK, to identify Psg resistance loci. A total of 40 soybean varieties with high level of Psg resistance were identified, and 14 quantitative trait loci (QTLs) were detected on 12 soybean chromosomes. These QTLs were identified for the first time. The majority of the QTLs were detected only in one or the other association panels, while was detected in both association panels for at least one growing season. A total of 46 candidate Psg resistance genes were identified from the , , and loci based on gene function annotation. In addition, we found the genomic region covering and harbored the synteny with a genomic region on chromosome 15 and identified 16 nucleotide binding site-leucine-rich repeat () genes as the candidate Psg resistance genes from the synteny blocks. This study provides new information for dissecting the genetic control of Psg resistance in soybean.
由丁香假单胞菌大豆致病变种(Psg)引起的细菌性疫病是一种广泛发生的叶部病害。尽管已有报道称4个以孟德尔模式分离的丁香假单胞菌大豆致病变种(Psg)抗性基因可使大豆对Psg产生抗性,但大豆对细菌性疫病数量抗性的遗传基础仍不清楚。在本研究中,分别由573个和213个品系组成的两个大豆关联群体的Psg抗性在2014年至2016年的多个环境中进行了表型鉴定。使用FarmCPU和BLINK两种模型进行全基因组关联研究,以鉴定Psg抗性位点。共鉴定出40个对Psg具有高抗性水平的大豆品种,并在12条大豆染色体上检测到14个数量性状位点(QTL)。这些QTL是首次被鉴定出来。大多数QTL仅在其中一个关联群体中被检测到,而qPsg-12-1在两个关联群体中至少在一个生长季节被检测到。基于基因功能注释,从qPsg-1-1、qPsg-3-1和qPsg-12-1位点共鉴定出46个候选Psg抗性基因。此外,我们发现覆盖qPsg-1-1和qPsg-3-1的基因组区域与15号染色体上的一个基因组区域存在共线性,并从共线性区域中鉴定出16个核苷酸结合位点富含亮氨酸重复序列(NBS-LRR)基因作为候选Psg抗性基因。本研究为剖析大豆对Psg抗性的遗传控制提供了新信息。