Cargando…

Deciphering how plant pathogenic bacteria disperse and meet: Molecular epidemiology of Xanthomonas citri pv. citri at microgeographic scales in a tropical area of Asiatic citrus canker endemicity

Although some plant pathogenic bacteria represent a significant threat to agriculture, the determinants of their ecological success and evolutionary potential are still poorly understood. Refining our understanding of bacterial strain circulation at small spatial scales and the biological significan...

Descripción completa

Detalles Bibliográficos
Autores principales: Pruvost, Olivier, Boyer, Karine, Ravigné, Virginie, Richard, Damien, Vernière, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708428/
https://www.ncbi.nlm.nih.gov/pubmed/31462912
http://dx.doi.org/10.1111/eva.12788
_version_ 1783446008805457920
author Pruvost, Olivier
Boyer, Karine
Ravigné, Virginie
Richard, Damien
Vernière, Christian
author_facet Pruvost, Olivier
Boyer, Karine
Ravigné, Virginie
Richard, Damien
Vernière, Christian
author_sort Pruvost, Olivier
collection PubMed
description Although some plant pathogenic bacteria represent a significant threat to agriculture, the determinants of their ecological success and evolutionary potential are still poorly understood. Refining our understanding of bacterial strain circulation at small spatial scales and the biological significance and evolutionary consequences of co‐infections are key questions. The study of bacterial population biology can be challenging, because it requires high‐resolution markers that can be genotyped with a high throughput. Here, we overcame this difficulty for Xanthomonas citri pv. citri, a genetically monomorphic bacterium causing Asiatic citrus canker (ACC). Using a genotyping method that did not require cultivating the bacterium or purifying DNA, we deciphered the pathogen's spatial genetic structure at several microgeographic scales, down to single lesion, in a situation of ACC endemicity. In a grove where copper was recurrently applied for ACC management, copper‐susceptible and copper‐resistant X. citri pv. citri coexisted and the bacterial population structured as three genetic clusters, suggesting a polyclonal contamination. The range of spatial dependency, estimated for the two largest clusters, was four times greater for the cluster predominantly composed of copper‐resistant bacteria. Consistently, the evenness value calculated for this cluster was indicative of increased transmission. Linkage disequilibrium was high even at a tree scale, probably due to a combination of clonality and admixture. Approximately 1% of samples exhibited within‐lesion multilocus polymorphism, explained at least in part by polyclonal infections. Canker lesions, which are of major biological significance as an inoculum source, may also represent a preferred niche for horizontal gene transfer. This study points out the potential of genotyping data for estimating the range of spatial dependency of plant bacterial pathogens, an important parameter for guiding disease management strategies.
format Online
Article
Text
id pubmed-6708428
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-67084282019-08-28 Deciphering how plant pathogenic bacteria disperse and meet: Molecular epidemiology of Xanthomonas citri pv. citri at microgeographic scales in a tropical area of Asiatic citrus canker endemicity Pruvost, Olivier Boyer, Karine Ravigné, Virginie Richard, Damien Vernière, Christian Evol Appl Original Articles Although some plant pathogenic bacteria represent a significant threat to agriculture, the determinants of their ecological success and evolutionary potential are still poorly understood. Refining our understanding of bacterial strain circulation at small spatial scales and the biological significance and evolutionary consequences of co‐infections are key questions. The study of bacterial population biology can be challenging, because it requires high‐resolution markers that can be genotyped with a high throughput. Here, we overcame this difficulty for Xanthomonas citri pv. citri, a genetically monomorphic bacterium causing Asiatic citrus canker (ACC). Using a genotyping method that did not require cultivating the bacterium or purifying DNA, we deciphered the pathogen's spatial genetic structure at several microgeographic scales, down to single lesion, in a situation of ACC endemicity. In a grove where copper was recurrently applied for ACC management, copper‐susceptible and copper‐resistant X. citri pv. citri coexisted and the bacterial population structured as three genetic clusters, suggesting a polyclonal contamination. The range of spatial dependency, estimated for the two largest clusters, was four times greater for the cluster predominantly composed of copper‐resistant bacteria. Consistently, the evenness value calculated for this cluster was indicative of increased transmission. Linkage disequilibrium was high even at a tree scale, probably due to a combination of clonality and admixture. Approximately 1% of samples exhibited within‐lesion multilocus polymorphism, explained at least in part by polyclonal infections. Canker lesions, which are of major biological significance as an inoculum source, may also represent a preferred niche for horizontal gene transfer. This study points out the potential of genotyping data for estimating the range of spatial dependency of plant bacterial pathogens, an important parameter for guiding disease management strategies. John Wiley and Sons Inc. 2019-04-10 /pmc/articles/PMC6708428/ /pubmed/31462912 http://dx.doi.org/10.1111/eva.12788 Text en © 2019 The Authors. Evolutionary Applications published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Pruvost, Olivier
Boyer, Karine
Ravigné, Virginie
Richard, Damien
Vernière, Christian
Deciphering how plant pathogenic bacteria disperse and meet: Molecular epidemiology of Xanthomonas citri pv. citri at microgeographic scales in a tropical area of Asiatic citrus canker endemicity
title Deciphering how plant pathogenic bacteria disperse and meet: Molecular epidemiology of Xanthomonas citri pv. citri at microgeographic scales in a tropical area of Asiatic citrus canker endemicity
title_full Deciphering how plant pathogenic bacteria disperse and meet: Molecular epidemiology of Xanthomonas citri pv. citri at microgeographic scales in a tropical area of Asiatic citrus canker endemicity
title_fullStr Deciphering how plant pathogenic bacteria disperse and meet: Molecular epidemiology of Xanthomonas citri pv. citri at microgeographic scales in a tropical area of Asiatic citrus canker endemicity
title_full_unstemmed Deciphering how plant pathogenic bacteria disperse and meet: Molecular epidemiology of Xanthomonas citri pv. citri at microgeographic scales in a tropical area of Asiatic citrus canker endemicity
title_short Deciphering how plant pathogenic bacteria disperse and meet: Molecular epidemiology of Xanthomonas citri pv. citri at microgeographic scales in a tropical area of Asiatic citrus canker endemicity
title_sort deciphering how plant pathogenic bacteria disperse and meet: molecular epidemiology of xanthomonas citri pv. citri at microgeographic scales in a tropical area of asiatic citrus canker endemicity
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708428/
https://www.ncbi.nlm.nih.gov/pubmed/31462912
http://dx.doi.org/10.1111/eva.12788
work_keys_str_mv AT pruvostolivier decipheringhowplantpathogenicbacteriadisperseandmeetmolecularepidemiologyofxanthomonascitripvcitriatmicrogeographicscalesinatropicalareaofasiaticcitruscankerendemicity
AT boyerkarine decipheringhowplantpathogenicbacteriadisperseandmeetmolecularepidemiologyofxanthomonascitripvcitriatmicrogeographicscalesinatropicalareaofasiaticcitruscankerendemicity
AT ravignevirginie decipheringhowplantpathogenicbacteriadisperseandmeetmolecularepidemiologyofxanthomonascitripvcitriatmicrogeographicscalesinatropicalareaofasiaticcitruscankerendemicity
AT richarddamien decipheringhowplantpathogenicbacteriadisperseandmeetmolecularepidemiologyofxanthomonascitripvcitriatmicrogeographicscalesinatropicalareaofasiaticcitruscankerendemicity
AT vernierechristian decipheringhowplantpathogenicbacteriadisperseandmeetmolecularepidemiologyofxanthomonascitripvcitriatmicrogeographicscalesinatropicalareaofasiaticcitruscankerendemicity