A Genome Wide Association Study (GWAS) Identifies SNPs Associated with Resistance to Tobacco Rattle Virus (TRV) and Potato Mop-Top Virus (PMTV) in a Tetraploid Mapping Population of Potato

IF 1.2 4区 农林科学 Q3 AGRONOMY
Noelle L. Anglin, Shashi K. R. Yellarreddygari, Neil C. Gudmestad, Vidyasagar Sathuvalli, Charles R. Brown, Max Feldman, Walter S. De Jong, David S. Douches, Richard G. Novy, Joseph J. Coombs
{"title":"A Genome Wide Association Study (GWAS) Identifies SNPs Associated with Resistance to Tobacco Rattle Virus (TRV) and Potato Mop-Top Virus (PMTV) in a Tetraploid Mapping Population of Potato","authors":"Noelle L. Anglin,&nbsp;Shashi K. R. Yellarreddygari,&nbsp;Neil C. Gudmestad,&nbsp;Vidyasagar Sathuvalli,&nbsp;Charles R. Brown,&nbsp;Max Feldman,&nbsp;Walter S. De Jong,&nbsp;David S. Douches,&nbsp;Richard G. Novy,&nbsp;Joseph J. Coombs","doi":"10.1007/s12230-023-09933-3","DOIUrl":null,"url":null,"abstract":"<div><p><i>Potato mop top virus</i> (PMTV) and <i>Tobacco rattle virus</i> (TRV) are significant soil borne pathogens of potato vectored by powdery scab and stubby-root nematodes, respectively. These viruses adversely impact tuber quality with infected tubers displaying brown streaks in the flesh and/or necrotic arcs on the surface contributing to the rejection of tubers in commercial settings. Currently, limited agricultural control methods for PMTV are available to farmers outside of planting resistant genotypes and avoiding fields with its vector; however, for TRV chemical control of the nematode vector is an option. Field screening for susceptibility to PMTV and TRV identified ‘Castle Russet’ to be resistant to both PMTV and TRV. In order to localize virus resistance genes for the development of marker assisted selection, a tetraploid mapping population (A15001) was developed by hybridizing ‘Castle Russet’ x A06084-1TE (susceptible to both viruses) and its progeny were subsequently trialed for two years in fields known to be infested with PMTV and TRV (two separate disease trial sites) near Larimore, ND. The population was phenotyped for PMTV and TRV incidence and severity of necrotic tubers at two time points post-harvest (approximately 19 days after harvest and 89 days after storage) with several genotypes in the population showing little or no virus induced necrosis over the years of evaluation, making them useful as parents in hybridizations by the potato breeding community. Tubers produced from the population were further assayed for PMTV and TRV infection by testing tuber core samples with a quantitative polymerase chain reaction (qPCR) assay. The A15001 population and the parents, 241 individuals, were genotyped with the Illumina Infinium SolCAP V2 12K Potato SNP Array yielding 6,704 quality-filtered, informative SNP markers. A genome wide association study (GWAS) analysis revealed SNP markers on multiple chromosomes (1, 2, 3, 5, and 11) that were significantly associated with PMTV incidence and negative qPCR suggesting polygenic inheritance. Conversely, GWAS revealed a significant QTL on chromosome 9 associated with all TRV phenotypes indicative of a major gene contributing to TRV resistance. These data can guide the development of molecular markers to select genotypes resistant to PMTV and TRV in potato breeding programs.</p></div>","PeriodicalId":7596,"journal":{"name":"American Journal of Potato Research","volume":"101 1","pages":"1 - 16"},"PeriodicalIF":1.2000,"publicationDate":"2023-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Potato Research","FirstCategoryId":"97","ListUrlMain":"https://link.springer.com/article/10.1007/s12230-023-09933-3","RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"AGRONOMY","Score":null,"Total":0}
引用次数: 0

Abstract

Potato mop top virus (PMTV) and Tobacco rattle virus (TRV) are significant soil borne pathogens of potato vectored by powdery scab and stubby-root nematodes, respectively. These viruses adversely impact tuber quality with infected tubers displaying brown streaks in the flesh and/or necrotic arcs on the surface contributing to the rejection of tubers in commercial settings. Currently, limited agricultural control methods for PMTV are available to farmers outside of planting resistant genotypes and avoiding fields with its vector; however, for TRV chemical control of the nematode vector is an option. Field screening for susceptibility to PMTV and TRV identified ‘Castle Russet’ to be resistant to both PMTV and TRV. In order to localize virus resistance genes for the development of marker assisted selection, a tetraploid mapping population (A15001) was developed by hybridizing ‘Castle Russet’ x A06084-1TE (susceptible to both viruses) and its progeny were subsequently trialed for two years in fields known to be infested with PMTV and TRV (two separate disease trial sites) near Larimore, ND. The population was phenotyped for PMTV and TRV incidence and severity of necrotic tubers at two time points post-harvest (approximately 19 days after harvest and 89 days after storage) with several genotypes in the population showing little or no virus induced necrosis over the years of evaluation, making them useful as parents in hybridizations by the potato breeding community. Tubers produced from the population were further assayed for PMTV and TRV infection by testing tuber core samples with a quantitative polymerase chain reaction (qPCR) assay. The A15001 population and the parents, 241 individuals, were genotyped with the Illumina Infinium SolCAP V2 12K Potato SNP Array yielding 6,704 quality-filtered, informative SNP markers. A genome wide association study (GWAS) analysis revealed SNP markers on multiple chromosomes (1, 2, 3, 5, and 11) that were significantly associated with PMTV incidence and negative qPCR suggesting polygenic inheritance. Conversely, GWAS revealed a significant QTL on chromosome 9 associated with all TRV phenotypes indicative of a major gene contributing to TRV resistance. These data can guide the development of molecular markers to select genotypes resistant to PMTV and TRV in potato breeding programs.

Abstract Image

一项全基因组关联研究 (GWAS) 在一个马铃薯四倍体图谱群体中发现了与抗烟草纹枯病病毒 (TRV) 和马铃薯拖顶病毒 (PMTV) 有关的 SNPs
马铃薯拖把病毒(PMTV)和烟草瘤病毒(TRV)是马铃薯的重要土传病原体,分别由白粉病疮痂病和残根线虫传播。这些病毒会对块茎的质量产生不利影响,受感染的块茎果肉上会出现褐色条纹和/或表面出现坏死弧线,导致商业环境中块茎被拒收。目前,除了种植抗性基因型和避开有病媒的田地外,农民对 PMTV 的农业控制方法有限;但对 TRV 来说,线虫病媒的化学控制是一种选择。通过对 PMTV 和 TRV 的敏感性进行田间筛选,发现'Castle Russet'对 PMTV 和 TRV 均有抗性。为了定位病毒抗性基因以进行标记辅助选择,通过杂交'Castle Russet'×A06084-1TE(对两种病毒均敏感),培育出了一个四倍体制图群体(A15001),其后代随后在北达科他州拉里摩尔附近已知受 PMTV 和 TRV 侵染的田地(两个独立的病害试验点)进行了为期两年的试验。在收获后的两个时间点(收获后约 19 天和贮藏后 89 天),对该群体的 PMTV 和 TRV 发生率以及坏死块茎的严重程度进行了表型分析,在多年的评估过程中,该群体中的几个基因型几乎没有表现出病毒诱导的坏死,这使它们在马铃薯育种界的杂交中成为有用的亲本。通过使用定量聚合酶链式反应(qPCR)测定法检测块茎核心样本,对该群体生产的块茎进行了 PMTV 和 TRV 感染的进一步检测。利用 Illumina Infinium SolCAP V2 12K 马铃薯 SNP 阵列对 A15001 群体和亲本 241 个个体进行了基因分型,获得了 6704 个经过质量过滤的信息 SNP 标记。一项全基因组关联研究(GWAS)分析显示,多条染色体(1、2、3、5 和 11)上的 SNP 标记与 PMTV 发病率显著相关,qPCR 阴性表明是多基因遗传。相反,GWAS 发现第 9 号染色体上的一个显著 QTL 与所有 TRV 表型相关,表明有一个主要基因导致 TRV 抗性。这些数据可指导分子标记的开发,从而在马铃薯育种计划中筛选出抗 PMTV 和 TRV 的基因型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
American Journal of Potato Research
American Journal of Potato Research 农林科学-农艺学
CiteScore
3.40
自引率
6.70%
发文量
33
审稿时长
18-36 weeks
期刊介绍: The American Journal of Potato Research (AJPR), the journal of the Potato Association of America (PAA), publishes reports of basic and applied research on the potato, Solanum spp. It presents authoritative coverage of new scientific developments in potato science, including biotechnology, breeding and genetics, crop management, disease and pest research, economics and marketing, nutrition, physiology, and post-harvest handling and quality. Recognized internationally by contributors and readership, it promotes the exchange of information on all aspects of this fast-evolving global industry.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信