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Genome‐wide identification of fitness determinants in the Xanthomonas campestris bacterial pathogen during early stages of plant infection
Plant diseases are an important threat to food production. While major pathogenicity determinants required for disease have been extensively studied, less is known on how pathogens thrive during host colonization, especially at early infection stages. Here, we used randomly barcoded‐transposon inser...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9543026/ https://www.ncbi.nlm.nih.gov/pubmed/35706385 http://dx.doi.org/10.1111/nph.18313 |
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author | Luneau, Julien S. Baudin, Maël Quiroz Monnens, Thomas Carrère, Sébastien Bouchez, Olivier Jardinaud, Marie‐Françoise Gris, Carine François, Jonas Ray, Jayashree Torralba, Babil Arlat, Matthieu Lewis, Jennifer D. Lauber, Emmanuelle Deutschbauer, Adam M. Noël, Laurent D. Boulanger, Alice |
author_facet | Luneau, Julien S. Baudin, Maël Quiroz Monnens, Thomas Carrère, Sébastien Bouchez, Olivier Jardinaud, Marie‐Françoise Gris, Carine François, Jonas Ray, Jayashree Torralba, Babil Arlat, Matthieu Lewis, Jennifer D. Lauber, Emmanuelle Deutschbauer, Adam M. Noël, Laurent D. Boulanger, Alice |
author_sort | Luneau, Julien S. |
collection | PubMed |
description | Plant diseases are an important threat to food production. While major pathogenicity determinants required for disease have been extensively studied, less is known on how pathogens thrive during host colonization, especially at early infection stages. Here, we used randomly barcoded‐transposon insertion site sequencing (RB‐TnSeq) to perform a genome‐wide screen and identify key bacterial fitness determinants of the vascular pathogen Xanthomonas campestris pv campestris (Xcc) during infection of the cauliflower host plant (Brassica oleracea). This high‐throughput analysis was conducted in hydathodes, the natural entry site of Xcc, in xylem sap and in synthetic media. Xcc did not face a strong bottleneck during hydathode infection. In total, 181 genes important for fitness were identified in plant‐associated environments with functional enrichment in genes involved in metabolism but only few genes previously known to be involved in virulence. The biological relevance of 12 genes was independently confirmed by phenotyping single mutants. Notably, we show that XC_3388, a protein with no known function (DUF1631), plays a key role in the adaptation and virulence of Xcc possibly through c‐di‐GMP‐mediated regulation. This study revealed yet unsuspected social behaviors adopted by Xcc individuals when confined inside hydathodes at early infection stages. |
format | Online Article Text |
id | pubmed-9543026 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95430262022-10-14 Genome‐wide identification of fitness determinants in the Xanthomonas campestris bacterial pathogen during early stages of plant infection Luneau, Julien S. Baudin, Maël Quiroz Monnens, Thomas Carrère, Sébastien Bouchez, Olivier Jardinaud, Marie‐Françoise Gris, Carine François, Jonas Ray, Jayashree Torralba, Babil Arlat, Matthieu Lewis, Jennifer D. Lauber, Emmanuelle Deutschbauer, Adam M. Noël, Laurent D. Boulanger, Alice New Phytol Research Plant diseases are an important threat to food production. While major pathogenicity determinants required for disease have been extensively studied, less is known on how pathogens thrive during host colonization, especially at early infection stages. Here, we used randomly barcoded‐transposon insertion site sequencing (RB‐TnSeq) to perform a genome‐wide screen and identify key bacterial fitness determinants of the vascular pathogen Xanthomonas campestris pv campestris (Xcc) during infection of the cauliflower host plant (Brassica oleracea). This high‐throughput analysis was conducted in hydathodes, the natural entry site of Xcc, in xylem sap and in synthetic media. Xcc did not face a strong bottleneck during hydathode infection. In total, 181 genes important for fitness were identified in plant‐associated environments with functional enrichment in genes involved in metabolism but only few genes previously known to be involved in virulence. The biological relevance of 12 genes was independently confirmed by phenotyping single mutants. Notably, we show that XC_3388, a protein with no known function (DUF1631), plays a key role in the adaptation and virulence of Xcc possibly through c‐di‐GMP‐mediated regulation. This study revealed yet unsuspected social behaviors adopted by Xcc individuals when confined inside hydathodes at early infection stages. John Wiley and Sons Inc. 2022-07-02 2022-10 /pmc/articles/PMC9543026/ /pubmed/35706385 http://dx.doi.org/10.1111/nph.18313 Text en © 2022 The Authors. New Phytologist © 2022 New Phytologist Foundation. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Luneau, Julien S. Baudin, Maël Quiroz Monnens, Thomas Carrère, Sébastien Bouchez, Olivier Jardinaud, Marie‐Françoise Gris, Carine François, Jonas Ray, Jayashree Torralba, Babil Arlat, Matthieu Lewis, Jennifer D. Lauber, Emmanuelle Deutschbauer, Adam M. Noël, Laurent D. Boulanger, Alice Genome‐wide identification of fitness determinants in the Xanthomonas campestris bacterial pathogen during early stages of plant infection |
title | Genome‐wide identification of fitness determinants in the Xanthomonas campestris bacterial pathogen during early stages of plant infection |
title_full | Genome‐wide identification of fitness determinants in the Xanthomonas campestris bacterial pathogen during early stages of plant infection |
title_fullStr | Genome‐wide identification of fitness determinants in the Xanthomonas campestris bacterial pathogen during early stages of plant infection |
title_full_unstemmed | Genome‐wide identification of fitness determinants in the Xanthomonas campestris bacterial pathogen during early stages of plant infection |
title_short | Genome‐wide identification of fitness determinants in the Xanthomonas campestris bacterial pathogen during early stages of plant infection |
title_sort | genome‐wide identification of fitness determinants in the xanthomonas campestris bacterial pathogen during early stages of plant infection |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9543026/ https://www.ncbi.nlm.nih.gov/pubmed/35706385 http://dx.doi.org/10.1111/nph.18313 |
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