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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
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.
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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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