Fast track genetic improvement of ascochyta blight resistance and double podding in chickpea by marker-assisted backcrossing

• Published in: Theoretical and applied genetics 2013-06, Vol.126 (6), p.1639-1647
• Main Authors: Taran, B, Warkentin, T. D, Vandenberg, A
• Format: Article
• Language: English
• Subjects: Agricultural production; Agriculture; Ascochyta; Ascochyta rabiei; Ascomycota; backcrossing; Biochemistry; Biomedical and Life Sciences; Biotechnology; blight; Breeding - methods; Chickpea; chickpeas; Cicer - genetics; Cicer - microbiology; Cicer arietinum; Crosses, Genetic; Cultivars; Disease Resistance - genetics; Diseases and pests; Flowers - genetics; Flowers - growth & development; Fungi, Pathogenic; Genes; Genetic aspects; genetic background; genetic improvement; genetic markers; Germplasm; Health aspects; Life Sciences; microsatellite repeats; Microsatellite Repeats - genetics; Original Paper; Physiological aspects; Plant Biochemistry; Plant Breeding/Biotechnology; Plant Diseases - microbiology; Plant Genetics and Genomics; Plant immunology; Quantitative trait loci; Quantitative Trait Loci - genetics; Saskatchewan
• ISSN: 0040-5752; 1432-2242
• DOI: 10.1007/s00122-013-2080-2

Ascochyta blight (AB) caused by the fungus Ascochyta rabiei Pass. Lab. is one of the major diseases of chickpea worldwide and a constraint to production in western Canada. The use of varieties with high levels of resistance is considered the most economical solution for long-term ascochyta blight management in chickpea. QTL for resistance to ascochyta blight have been identified in chickpea. The availability of molecular markers associated with QTL for ascochyta blight resistant and double podding provides an opportunity to apply marker-assisted backcrossing to introgress the traits into adapted chickpea cultivars. In the present study, molecular markers that were linked to the QTL for ascochyta blight resistance and the double podding trait, and those unlinked to the resistance were used in foreground and background selection, respectively, in backcrosses between moderately resistant donors (CDC Frontier and CDC 425-14) and the adapted varieties (CDC Xena, CDC Leader and FLIP98-135C). The strategy included two backcrosses and selection for two QTL for ascochyta blight resistance and a locus associated with double podding. The fixation of the elite genetic background was monitored with 16–22 SSR markers to accelerate restoration of the genetic background at each backcross. By the BC₂F₁ generation, plants with improved ascochyta blight resistance and double podding were identified. The selected plants possessed the majority of elite parental type SSR alleles on all fragments analyzed except the segment of LG 4, LG 6 and LG 8 that possessed the target QTL. The results showed that the adapted variety could be efficiently converted into a variety with improved resistance in two backcross generations.