Abstract

Summary Necrotic strains of bean common mosaic potyviruses are becoming increasingly problematic in bean growing areas of Africa and Europe. Pyramiding epistatic resistance genes provides the most effective long-term strategy for disease control against all known strains of the virus. Indirect selection using tightly linked markers should facilitate the breeding of desired epistatic resistance gene combinations. In common bean, the most effective strategy for broad spectrum control of the bean common mosaic potyviruses is to combine I and bc-3 genes. We describe the use of near-isogenic lines and segregating populations from different gene pools combined with bulked segregant analysis to identify markers tightly linked with the recessive bc-3 gene that conditions resistance to all strains of bean common mosaic necrosis virus. We identified a RAPD marker, OG6595, linked at 3.7 cM from the bc-3, and the marker was used to confirm the location of bc-3 gene on bean linkage group B6. A codominant AFLP marker, EACAMCGG-169/172 was identified and linked at 3.5 cM from the bc-3 and the AFLP and OG6595 markers flanked the bc-3 gene. The AFLP marker was converted to the STS marker SEACAMCGG-134/137 which showed co-segregation with the original AFLP marker. The 134 bp fragment associated with resistance was linked with the bc-3 gene present in a diverse group of bean genotypes except in two kidney bean lines. The OG6595 marker mapped on B6 supported independence of bc-3 from the I gene located on B2, which provides the opportunity to readily combine both genes in a single bean cultivar for broad spectrum resistance to bean common mosaic potyviruses.

Highlights

  • Bean Common Mosaic Virus (BCMV) and Bean Common Mosaic Necrosis Virus (BCMNV) are the most common and destructive potyviruses known to infect common bean (Phaseolus vulgaris L.) worldwide (Drijfhout, 1978; McKern et al, 1992)

  • The objectives of this study were to use near-isogenic lines (NILs), segregating populations and DNA from different bean gene pools combined with the bulked segregant analysis (BSA), to increase the opportunity of finding new markers linked to bc-3 gene using both RAPD and AFLP analyses

  • The Middle American gene pool was represented by a F4:7 recombinant inbred line (RIL) population derived from a cross between cultivars Bunsi with the I gene and Raven that carries the I, bc-3 gene combination (Kelly et al, 1994)

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Summary

Introduction

Bean Common Mosaic Virus (BCMV) and Bean Common Mosaic Necrosis Virus (BCMNV) are the most common and destructive potyviruses known to infect common bean (Phaseolus vulgaris L.) worldwide (Drijfhout, 1978; McKern et al, 1992). Both viruses are seedborne and transmitted by several aphid species in a non-persistent manner (Drijfhout, 1978). In East Africa where BCMNV is found in wild legumes (Sengooba et al, 1997; Spence & Walkey, 1995), the only effective way to control these viruses is to plant resistant cultivars, otherwise susceptible bean plants can become infected from alternate hosts, growing adjacent to bean fields (Coyne et al, 2003)

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