Abstract

Sunflower rust, which is incited by the fungus Puccinia helianthi Schwein., is the most common disease in Australia, Argentina, South Africa, and North America. Three independent genes, R 5 , R 4 , and R 13 with two alleles R 13a and R 13b , were discovered in sunflower and are promising sources of resistance to rust. R 5 was previously mapped to linkage group (LG) 2, and R 4 and R 13 were mapped to LG13 of the sunflower genome using simple sequence repeat (SSR) markers. The objective of this study was to finely map R 5 , R 4 , R 13a , and R 13b using newly developed single nucleotide polymorphism (SNP) markers in four F2 populations previously used for SSR mapping. Of the 67 LG2 SNP markers screened, two SNPs, SFW03654 and NSA_000267, flanked R 5 at a genetic distance of 0.6 and 1.2 cM, respectively. This flanking narrowed the genetic interval containing R 5 from 5.1 to 1.8 cM in length. A total of 69 LG13 SNP markers were analyzed in the R 4 , R 13a , and R 13b populations. In the R 4 consensus map, the gene R 4 was flanked by seven SNP loci; three co-segregating SNPs are on one side (0.7 cM proximal) and four on the other side (0.6 cM distal). Similarly, SNP markers that are tightly linked to both R 13a and R 13b were identified. R 13a was flanked by SNP markers at genetic distances of 0.4 and 0.2 cM. The SNP SFW00757 co-segregated with R 13b , and another three co-segregating SNPs were 2.4 cM proximal to R 13b . A total of 368 F2 plants from the cross between a resistant BC3F2 plant carrying R 5 with HA-R6 carrying R 13a were first screened by SSR markers to identify “double-resistant” lines. Twelve F2 plants were identified to be homozygous for a combination of R 5 and R 13a , which was further confirmed with additional SNP markers developed in the present study. The double-resistant line developed in this study may provide a source of durable resistance to manage rust in confection sunflower production and will help mitigate selection pressure on each gene by the pathogen.

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