Gimode Winnie, Bao Kan, Fei Zhangjun, McGregor Cecilia
Institute for Plant Breeding, Genetics & Genomics, University of Georgia, 1111 Plant Sciences Bldg, Athens, GA, 30602, USA.
Boyce Thompson Institute for Plant Research, Cornell University, Ithaca, NY, 14853, USA.
Theor Appl Genet. 2021 Feb;134(2):573-584. doi: 10.1007/s00122-020-03715-9. Epub 2020 Nov 1.
We identified QTLs associated with gummy stem blight resistance in an interspecific F Citrullus population and developed marker assays for selection of the loci in watermelon. Gummy stem blight (GSB), caused by three Stagonosporopsis spp., is a devastating fungal disease of watermelon (Citrullus lanatus) and other cucurbits that can lead to severe yield losses. Currently, no commercial cultivars with genetic resistance to GSB in the field have been reported. Utilizing GSB-resistant cultivars would reduce yield losses, decrease the high cost of disease control, and diminish hazards resulting from frequent fungicide application. The objective of this study was to identify quantitative trait loci (QTLs) associated with GSB resistance in an F interspecific Citrullus mapping population (N = 178), derived from a cross between Crimson Sweet (C. lanatus) and GSB-resistant PI 482276 (C. amarus). The population was phenotyped by inoculating seedlings with Stagonosporopsis citrulli 12178A in the greenhouse in two separate experiments, each with three replications. We identified three QTLs (ClGSB3.1, ClGSB5.1 and ClGSB7.1) associated with GSB resistance, explaining between 6.4 and 21.1% of the phenotypic variation. The genes underlying ClGSB5.1 includes an NBS-LRR gene (ClCG05G019540) previously identified as a candidate gene for GSB resistance in watermelon. Locus ClGSB7.1 accounted for the highest phenotypic variation and harbors twenty-two candidate genes associated with disease resistance. Among them is ClCG07G013230, encoding an Avr9/Cf-9 rapidly elicited disease resistance protein, which contains a non-synonymous point mutation in the DUF761 domain that was significantly associated with GSB resistance. High throughput markers were developed for selection of ClGSB5.1 and ClGSB7.1. Our findings will facilitate the use of molecular markers for efficient introgression of the resistance loci and development of GSB-resistant watermelon cultivars.
我们在一个种间 F 西瓜属群体中鉴定出了与抗蔓枯病相关的数量性状基因座(QTL),并开发了标记分析方法用于在西瓜中选择这些基因座。蔓枯病(GSB)由三种西瓜壳针孢属真菌引起,是西瓜(Citrullus lanatus)和其他葫芦科作物的一种毁灭性真菌病害,可导致严重的产量损失。目前,尚未有在田间对 GSB 具有遗传抗性的商业品种报道。利用抗 GSB 的品种将减少产量损失,降低疾病控制的高昂成本,并减少频繁施用杀菌剂带来的危害。本研究的目的是在一个由 Crimson Sweet(C. lanatus)与抗 GSB 的 PI 482276(C. amarus)杂交产生的 F 种间西瓜属作图群体(N = 178)中鉴定与 GSB 抗性相关的数量性状基因座(QTL)。该群体在温室中通过用西瓜壳针孢 12178A 接种幼苗进行表型分析,共进行了两个独立实验,每个实验有三次重复。我们鉴定出了三个与 GSB 抗性相关的 QTL(ClGSB3.1、ClGSB5.1 和 ClGSB7.1),它们解释了 6.4%至 21.1%的表型变异。ClGSB5.1 位点的潜在基因包括一个先前被鉴定为西瓜抗 GSB 候选基因的 NBS-LRR 基因(ClCG05G019540)。ClGSB7.1 位点解释的表型变异最高,包含 22 个与抗病性相关的候选基因。其中有 ClCG07G013230,它编码一种 Avr9/Cf-9 快速引发抗病蛋白,该蛋白在 DUF761 结构域中存在一个与 GSB 抗性显著相关的非同义点突变。我们开发了高通量标记用于选择 ClGSB5.1 和 ClGSB7.1。我们的研究结果将有助于利用分子标记高效导入抗性基因座并培育抗 GSB 的西瓜品种。