Repeated loss of the ability of a wild pepper disease resistance gene to function at high temperatures suggests that thermoresistance is a costly trait
- PMID: 37920100
- DOI: 10.1111/nph.19371
Repeated loss of the ability of a wild pepper disease resistance gene to function at high temperatures suggests that thermoresistance is a costly trait
Abstract
Specificity in plant-pathogen gene-for-gene (GFG) interactions is determined by the recognition of pathogen proteins by the products of plant resistance (R) genes. The evolutionary dynamics of R genes in plant-virus systems is poorly understood. We analyse the evolution of the L resistance locus to tobamoviruses in the wild pepper Capsicum annuum var. glabriusculum (chiltepin), a crop relative undergoing incipient domestication. The frequency, and the genetic and phenotypic diversity, of the L locus was analysed in 41 chiltepin populations under different levels of human management over its distribution range in Mexico. The frequency of resistance was lower in Cultivated than in Wild populations. L-locus genetic diversity showed a strong spatial structure with no isolation-by-distance pattern, suggesting environment-specific selection, possibly associated with infection by the highly virulent tobamoviruses found in the surveyed regions. L alleles differed in recognition specificity and in the expression of resistance at different temperatures, broad-spectrum recognition of P0 + P1 pathotypes and expression above 32°C being ancestral traits that were repeatedly lost along L-locus evolution. Overall, loss of resistance co-occurs with incipient domestication and broad-spectrum resistance expressed at high temperatures has apparent fitness costs. These findings contribute to understand the role of fitness trade-offs in plant-virus coevolution.
Keywords: Capsicum; Tobamovirus; evolution of resistance; gene-for-gene systems; plant-virus interactions; temperature-dependent resistance.
© 2023 The Authors New Phytologist © 2023 New Phytologist Foundation.
References
-
- Agrawal A, Lively CM. 2003. Modelling infection as a two-step process combining gene-for-gene and matching-allele genetics. Proceedings of the Royal Society of London. Series B: Biological Sciences 270: 323-334.
-
- Aguilar-Meléndez A, Morrell PL, Roose ML, Kim SC. 2009. Genetic diversity and structure in semiwild and domesticated chiles (Capsicum annuum; Solanaceae) from Mexico. American Journal of Botany 96: 1190-1202.
-
- Anderson DG, Kvie KS, Davydov VN, Røed KH. 2017. Maintaining genetic integrity of coexisting wild and domestic populations: genetic differentiation between wild and domestic Rangifer with long traditions of intentional interbreeding. Ecology and Evolution 7: 6790-6802.
-
- Anderson P, Cunningham AA, Patel NG, Morales FJ, Epstein PR, Daszak P. 2004. Emerging infectious diseases of plants: pathogen pollution, climate change and agrotechnology drivers. Trends in Ecology and Evolution 19: 535-544.
-
- Antignus Y, Lachman O, Pearlsman M, Maslenin L, Rosner A. 2008. A new pathotype of Pepper mild mottle virus (PMMoV) overcomes the L4 resistance genotype of pepper cultivars. Plant Disease 92: 1033-1037.
MeSH terms
Associated data
- Actions
- Actions
- Actions
- Actions
- Actions
- Actions
Grants and funding
LinkOut - more resources
Full Text Sources