Quantitative trait loci detection of E dwardsiella tarda resistance in Japanese flounder Paralichthys olivaceus using bulked segregant analysis

被引:0
|
作者
王晓夏 [1 ,2 ]
徐文腾 [1 ]
刘洋 [1 ,3 ]
王磊 [1 ]
孙何军 [1 ,2 ]
陈松林 [1 ]
机构
[1] Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Function Laboratory for Marine Fisheries Science and Food Production Processes, National Lab for Ocean Science and Technology
[2] Nanjing Agricultural University
[3] College of Fisheries, Henan Normal University
[4] College of Marine Life Science, Shanghai Ocean University
基金
中国国家自然科学基金;
关键词
Paralichthys olivaceus; Edwardsiella tarda; disease resistance; simple sequence repeats(SSRs); bulked segregant analysis(BSA); quantitative trait loci(QTL);
D O I
暂无
中图分类号
S943 [各种鱼的病害、敌害及其防治];
学科分类号
0906 ;
摘要
In recent years, Edwardsiella tarda has become one of the most deadly pathogens of Japanese fl ounder( Paralichthys olivaceus), causing serious annual losses in commercial production. In contrast to the rapid advances in the aquaculture of P. o livaceus, the study of E. tarda resistance-related markers has lagged behind, hindering the development of a disease-resistant strain. Thus, a marker-trait association analysis was initiated, combining bulked segregant analysis(BSA) and quantitative trait loci(QTL) mapping. Based on 180 microsatellite loci across all chromosomes, 106 individuals from the F1333(♀: F0768 ×♂: F0915)(Nomenclature rule: F+year+family number) were used to detect simple sequence repeats(SSRs) and QTLs associated with E. tarda resistance. After a genomic scan, three markers(Scaffold 404-21589, Scaffold 404-21594 and Scaffold 270-13812) from the same linkage group(LG)-1 exhibited a signifi cant difference between DNA, pooled/bulked from the resistant and susceptible groups( P <0.001). Therefore, 106 individuals were genotyped using all the SSR markers in LG1 by single marker analysis. Two different analytical models were then employed to detect SSR markers with different levels of signifi cance in LG1, where 17 and 18 SSR markers were identifi ed, respectively. Each model found three resistance-related QTLs by composite interval mapping(CIM). These six QTLs, designated q E1–6, explained 16.0%–89.5% of the phenotypic variance. Two of the QTLs, q E-2 and q E-4, were located at the 66.7 c M region, which was considered a major candidate region for E. tarda resistance. This study will provide valuable data for further investigations of E. tarda resistance genes and facilitate the selective breeding of disease-resistant Japanese fl ounder in the future.
引用
收藏
页码:1297 / 1308
页数:12
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