Discovery and development of singlenucleotide polymorphism markers for resistance to Striga gesnerioides in cowpea (Vigna unguiculata)

Introduction: The parasitic weed [Striga gesnerioides (Willd.) Vatke] is a principal biotic constraint to cowpea [Vigna unguiculata (L.) Walp.] production in West and Central Africa, causing severe yield reductions. Multiple races of S. gesnerioides exist across the cowpea-growing areas of the sub-r...

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Autores principales: Ongom, P.O., Fatokun, C., Boukar, O.
Formato: Journal Article
Lenguaje:Inglés
Publicado: Frontiers Media 2025
Materias:
Acceso en línea:https://hdl.handle.net/10568/177064
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author Ongom, P.O.
Fatokun, C.
Boukar, O.
author_browse Boukar, O.
Fatokun, C.
Ongom, P.O.
author_facet Ongom, P.O.
Fatokun, C.
Boukar, O.
author_sort Ongom, P.O.
collection Repository of Agricultural Research Outputs (CGSpace)
description Introduction: The parasitic weed [Striga gesnerioides (Willd.) Vatke] is a principal biotic constraint to cowpea [Vigna unguiculata (L.) Walp.] production in West and Central Africa, causing severe yield reductions. Multiple races of S. gesnerioides exist across the cowpea-growing areas of the sub-region. Past efforts identified some resistant sources and race-specific genes underpinning Striga resistance, but deployment of associated markers in breeding is limited. Here, we utilized a 51K cowpea iSelect single-nucleotide polymorphisms (SNPs) to decipher genomic regions underlying Striga resistance and explore marker conversion and validation for easy deployment. Method: The study used two-year phenotypic data on a minicore panel of 368 cowpea genotypes screened at two sites in Northern Nigeria. SNPs performances were verified and validated using two independent sets of 60 and 20 diverse genotypes respectively. Results: The minicore displayed apparent differences in response to the S. gesnerioides attack. A genome-wide scan uncovered a primary gene effect signal on chromosome Vu11 and minor regions on chromosomes Vu02, Vu03, Vu07, Vu09 and Vu10. The major effect region on Vu11 harbored a coil-coil nucleotide-binding site leucine-rich repeat (CC-NBS-LRR) protein, encoded by the RSG3–301 gene, previously implicated in race-specific resistance to S. gesnerioides in cowpea. The associated SNPs were successfully converted into Kompetitive Allele-Specific PCR (KASP) assays and validated using 20 independent diverse cowpea genotypes. Five KASP markers, snpVU00075, snpVU00076, snpVU00077, snpVU00078, and snpVU00079, depicted consistent and significant associations with the phenotype in the validation set.
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spelling CGSpace1770642025-12-08T10:29:22Z Discovery and development of singlenucleotide polymorphism markers for resistance to Striga gesnerioides in cowpea (Vigna unguiculata) Ongom, P.O. Fatokun, C. Boukar, O. cowpeas vigna unguiculata striga gesnerioides genes Introduction: The parasitic weed [Striga gesnerioides (Willd.) Vatke] is a principal biotic constraint to cowpea [Vigna unguiculata (L.) Walp.] production in West and Central Africa, causing severe yield reductions. Multiple races of S. gesnerioides exist across the cowpea-growing areas of the sub-region. Past efforts identified some resistant sources and race-specific genes underpinning Striga resistance, but deployment of associated markers in breeding is limited. Here, we utilized a 51K cowpea iSelect single-nucleotide polymorphisms (SNPs) to decipher genomic regions underlying Striga resistance and explore marker conversion and validation for easy deployment. Method: The study used two-year phenotypic data on a minicore panel of 368 cowpea genotypes screened at two sites in Northern Nigeria. SNPs performances were verified and validated using two independent sets of 60 and 20 diverse genotypes respectively. Results: The minicore displayed apparent differences in response to the S. gesnerioides attack. A genome-wide scan uncovered a primary gene effect signal on chromosome Vu11 and minor regions on chromosomes Vu02, Vu03, Vu07, Vu09 and Vu10. The major effect region on Vu11 harbored a coil-coil nucleotide-binding site leucine-rich repeat (CC-NBS-LRR) protein, encoded by the RSG3–301 gene, previously implicated in race-specific resistance to S. gesnerioides in cowpea. The associated SNPs were successfully converted into Kompetitive Allele-Specific PCR (KASP) assays and validated using 20 independent diverse cowpea genotypes. Five KASP markers, snpVU00075, snpVU00076, snpVU00077, snpVU00078, and snpVU00079, depicted consistent and significant associations with the phenotype in the validation set. 2025 2025-10-14T13:00:18Z 2025-10-14T13:00:18Z Journal Article https://hdl.handle.net/10568/177064 en Open Access application/pdf Frontiers Media Ongom, P.O., Fatokun, C. & Boukar, O. (2025). Discovery and development of single-nucleotide polymorphism markers for resistance to Striga gesnerioides in cowpea (Vigna unguiculata). Frontiers in Plant Science, 16: 1661440, 1-19.
spellingShingle cowpeas
vigna unguiculata
striga gesnerioides
genes
Ongom, P.O.
Fatokun, C.
Boukar, O.
Discovery and development of singlenucleotide polymorphism markers for resistance to Striga gesnerioides in cowpea (Vigna unguiculata)
title Discovery and development of singlenucleotide polymorphism markers for resistance to Striga gesnerioides in cowpea (Vigna unguiculata)
title_full Discovery and development of singlenucleotide polymorphism markers for resistance to Striga gesnerioides in cowpea (Vigna unguiculata)
title_fullStr Discovery and development of singlenucleotide polymorphism markers for resistance to Striga gesnerioides in cowpea (Vigna unguiculata)
title_full_unstemmed Discovery and development of singlenucleotide polymorphism markers for resistance to Striga gesnerioides in cowpea (Vigna unguiculata)
title_short Discovery and development of singlenucleotide polymorphism markers for resistance to Striga gesnerioides in cowpea (Vigna unguiculata)
title_sort discovery and development of singlenucleotide polymorphism markers for resistance to striga gesnerioides in cowpea vigna unguiculata
topic cowpeas
vigna unguiculata
striga gesnerioides
genes
url https://hdl.handle.net/10568/177064
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