Instituto de Conservación y Mejora de la Agrodiversidad Valenciana (COMAV-UPV), Universitat Politècnica de València, Camino de Vera s/n, 46022 Valencia, Spain.
Centro de Biotecnología y Genómica de Plantas UPM-INIA and E.T.S. Ingeniería Agronómica, Alimentaria y de Biosistemas, Universidad Politécnica de Madrid, 28031 Madrid, Spain.
Int J Mol Sci. 2024 Aug 15;25(16):8880. doi: 10.3390/ijms25168880.
Tomato leaf curl New Delhi virus (ToLCNDV) is a begomovirus causing significant melon () crop losses globally. This study aims to map the ToLCNDV resistance in the PI 414723 melon accession, previously identified and characterized through phenotypic studies, thereby exploring shared genomic regions with the established resistant source WM-7. In the present study, WM-7 and PI 414723 were crossed with the susceptible accessions 'Rochet' and 'Blanco' respectively, to generate F hybrids. These hybrids were self-pollinated to generate the populations for mapping the ToLCNDV resistance region and designing markers for marker-assisted selection. Disease evaluation included visual symptom scoring, viral-load quantification and tissue printing. Genotyping-by-sequencing and SNP markers were used for quantitative trait loci (QTL) mapping. For genetic analysis, qPCR and bulked segregant RNA-seq (BSR-seq) were performed. Gene expression was assessed using RNA-seq, and qRT-PCR was used for confirmation. The research narrows the candidate region for resistance in WM-7 and identifies overlapping QTLs on chromosome 11 in PI 414723, found in the region of the DNA primase large subunit. BSR-seq and expression analyses highlight potential regulatory roles of chromosome 2 in conferring resistance. Differential expression was confirmed for six genes in the candidate region on chromosome 2. This study confirms the existence of common resistance genes in PI 414723 and WM-7.
番茄黄曲叶病毒(ToLCNDV)是一种引起瓜类作物全球减产的伴随病毒。本研究旨在对先前通过表型研究鉴定和表征的 PI 414723 甜瓜品系中的 ToLCNDV 抗性进行作图,从而探索与已建立的抗性来源 WM-7 共享的基因组区域。在本研究中,WM-7 和 PI 414723 分别与易感品种 'Rochet' 和 'Blanco' 杂交,产生 F1 杂种。这些杂种自交产生用于绘制 ToLCNDV 抗性区域和设计用于标记辅助选择的标记的群体。疾病评估包括视觉症状评分、病毒载量定量和组织印刷。基因分型测序和 SNP 标记用于数量性状位点(QTL)作图。用于遗传分析的 qPCR 和批量分离 RNA-seq(BSR-seq)。使用 RNA-seq 评估基因表达,并使用 qRT-PCR 进行确认。该研究缩小了 WM-7 中抗性的候选区域,并确定了 PI 414723 中第 11 号染色体上的重叠 QTL,该区域位于 DNA 引物酶大亚基。BSR-seq 和表达分析突出了第 2 号染色体在赋予抗性方面的潜在调节作用。在候选区域的六个基因在染色体 2 上的差异表达得到了确认。本研究证实了 PI 414723 和 WM-7 中存在共同的抗性基因。