Nov 2026· J. Amer. Soc. Hort. Sci.· 0 citations· 28 references
TL;DR
The genomic position of Ipcr is refined and candidate genes that may condition susceptibility are highlighted, providing valuable targets for functional validation and breeding strategies to eliminate suppressive alleles and develop durable resistance to P. capsici.
Abstract
Phytophthora capsici
is a destructive pathogen of pepper (
Capsicum annuum
L.), causing severe yield losses worldwide. Although resistance loci derived from the
C. annuum
landrace CM334 have been widely deployed, durable resistance remains elusive due to complex inheritance and the reported
Inhibitor of P. capsici resistance
(
Ipcr
) gene that suppresses resistance. We investigated the inheritance and genomic location of
Ipcr
using an F
2
population derived from a hybridization between CM334 and NMCA10399. Disease evaluations with a virulent
P. capsici
isolate revealed segregation did not deviate from a 3:13 ratio, consistent with dominant suppression epistasis. Bulk segregant analysis with quantitative trait loci sequencing identified a major susceptibility-associated interval on chromosome 3 (107.6 to 113.4 Mb) significantly associated with susceptibility, in which ΔSNP index values reached –0.62 and G′ statistics exceeded significance thresholds, consistent with dominant suppression of resistance. Candidate gene analysis within this region revealed loci with potential roles in defense regulation, including a CLAVATA3/ESR-related protein, calmodulin-binding protein 60, ASC1-like protein, MLO-like gene, and PBS1-like kinase. These findings refine the genomic position of
Ipcr
and highlight candidate genes that may condition susceptibility, providing valuable targets for functional validation and breeding strategies to eliminate suppressive alleles and develop durable resistance to
P. capsici
in pepper.
The refined QTLs and associated developed SSR markers can be utilized to accelerate marker-assisted introgression breeding for anthracnose fruit rot disease resistance.
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