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A genome-wide scan for genes under balancing selection in the plant pathogen Ralstonia solanacearum
BACKGROUND: Plant pathogens are under significant selective pressure by the plant host. Consequently, they are expected to have adapted to this condition or contribute to evading plant defenses. In order to acquire long-term fitness, plant bacterial pathogens are usually forced to maintain advantage...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6580516/ https://www.ncbi.nlm.nih.gov/pubmed/31208326 http://dx.doi.org/10.1186/s12862-019-1456-6 |
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author | Castillo, José A. Agathos, Spiros N. |
author_facet | Castillo, José A. Agathos, Spiros N. |
author_sort | Castillo, José A. |
collection | PubMed |
description | BACKGROUND: Plant pathogens are under significant selective pressure by the plant host. Consequently, they are expected to have adapted to this condition or contribute to evading plant defenses. In order to acquire long-term fitness, plant bacterial pathogens are usually forced to maintain advantageous genetic diversity in populations. This strategy ensures that different alleles in the pathogen’s gene pool are maintained in a population at frequencies larger than expected under neutral evolution. This selective process, known as balancing selection, is the subject of this work in the context of a common bacterial phytopathogen. We performed a genome-wide scan of Ralstonia solanacearum species complex, an aggressive plant bacterial pathogen that shows broad host range and causes a devastating disease called ‘bacterial wilt’. RESULTS: Using a sliding window approach, we analyzed 57 genomes from three phylotypes of the R. solanacearum species complex to detect signatures of balancing selection. A total of 161 windows showed extreme values in three summary statistics of population genetics: Tajima’s D, θ(w) and Fu & Li’s D*. We discarded any confounding effects due to demographic events by means of coalescent simulations of genetic data. The prospective windows correspond to 78 genes with known function that map in any of the two main replicons (1.7% of total number of genes). The candidate genes under balancing selection are related to primary metabolism and other basal activities (51.3%) or directly associated to virulence (48.7%), the latter being involved in key functions targeted to dismantle plant defenses or to participate in critical stages in the pathogenic process. CONCLUSIONS: We identified various genes under balancing selection that play a significant role in basic metabolism as well as in virulence of the R. solanacearum species complex. These genes are useful to understand and monitor the evolution of bacterial pathogen populations and emerge as potential candidates for future treatments to induce specific plant immune responses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12862-019-1456-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6580516 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65805162019-06-24 A genome-wide scan for genes under balancing selection in the plant pathogen Ralstonia solanacearum Castillo, José A. Agathos, Spiros N. BMC Evol Biol Research Article BACKGROUND: Plant pathogens are under significant selective pressure by the plant host. Consequently, they are expected to have adapted to this condition or contribute to evading plant defenses. In order to acquire long-term fitness, plant bacterial pathogens are usually forced to maintain advantageous genetic diversity in populations. This strategy ensures that different alleles in the pathogen’s gene pool are maintained in a population at frequencies larger than expected under neutral evolution. This selective process, known as balancing selection, is the subject of this work in the context of a common bacterial phytopathogen. We performed a genome-wide scan of Ralstonia solanacearum species complex, an aggressive plant bacterial pathogen that shows broad host range and causes a devastating disease called ‘bacterial wilt’. RESULTS: Using a sliding window approach, we analyzed 57 genomes from three phylotypes of the R. solanacearum species complex to detect signatures of balancing selection. A total of 161 windows showed extreme values in three summary statistics of population genetics: Tajima’s D, θ(w) and Fu & Li’s D*. We discarded any confounding effects due to demographic events by means of coalescent simulations of genetic data. The prospective windows correspond to 78 genes with known function that map in any of the two main replicons (1.7% of total number of genes). The candidate genes under balancing selection are related to primary metabolism and other basal activities (51.3%) or directly associated to virulence (48.7%), the latter being involved in key functions targeted to dismantle plant defenses or to participate in critical stages in the pathogenic process. CONCLUSIONS: We identified various genes under balancing selection that play a significant role in basic metabolism as well as in virulence of the R. solanacearum species complex. These genes are useful to understand and monitor the evolution of bacterial pathogen populations and emerge as potential candidates for future treatments to induce specific plant immune responses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12862-019-1456-6) contains supplementary material, which is available to authorized users. BioMed Central 2019-06-17 /pmc/articles/PMC6580516/ /pubmed/31208326 http://dx.doi.org/10.1186/s12862-019-1456-6 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Castillo, José A. Agathos, Spiros N. A genome-wide scan for genes under balancing selection in the plant pathogen Ralstonia solanacearum |
title | A genome-wide scan for genes under balancing selection in the plant pathogen Ralstonia solanacearum |
title_full | A genome-wide scan for genes under balancing selection in the plant pathogen Ralstonia solanacearum |
title_fullStr | A genome-wide scan for genes under balancing selection in the plant pathogen Ralstonia solanacearum |
title_full_unstemmed | A genome-wide scan for genes under balancing selection in the plant pathogen Ralstonia solanacearum |
title_short | A genome-wide scan for genes under balancing selection in the plant pathogen Ralstonia solanacearum |
title_sort | genome-wide scan for genes under balancing selection in the plant pathogen ralstonia solanacearum |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6580516/ https://www.ncbi.nlm.nih.gov/pubmed/31208326 http://dx.doi.org/10.1186/s12862-019-1456-6 |
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