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The plant host environment influences competitive interactions between bacterial pathogens

Bacteria compete for resources in diverse environments using an array of antagonistic strategies, including the production of narrow‐spectrum protein antibacterials termed bacteriocins. Although significant research has focused on bacteriocin‐mediated dynamics in culture environments, little researc...

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Autores principales: Ehau‐Taumaunu, Hanareia, Hockett, Kevin L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9796116/
https://www.ncbi.nlm.nih.gov/pubmed/35700743
http://dx.doi.org/10.1111/1758-2229.13103
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author Ehau‐Taumaunu, Hanareia
Hockett, Kevin L.
author_facet Ehau‐Taumaunu, Hanareia
Hockett, Kevin L.
author_sort Ehau‐Taumaunu, Hanareia
collection PubMed
description Bacteria compete for resources in diverse environments using an array of antagonistic strategies, including the production of narrow‐spectrum protein antibacterials termed bacteriocins. Although significant research has focused on bacteriocin‐mediated dynamics in culture environments, little research has explored bacteriocin‐mediated dynamics within a host context, particularly in plant environments. Here, we show that a bacterial plant pathogen, Pseudomonas syringae pv. syringae (Psy), expresses a bacteriocin both in culture and in leaf apoplast when co‐inoculated with a bacteriocin‐sensitive competitor, P. syringae pv. phaseolicola (Pph). Although there is an observable negative effect of the bacteriocin on the Pph population at most time points both in culture and in the leaf apoplast, a bacteriocin‐mediated benefit to Psy was only observed when the producing strain was co‐infiltrated at a low population frequency (1:9) into the leaf apoplast. At 6 days post‐infiltration, Psy achieved an eightfold population increase compared to a bacteriocin‐deficient mutant in the apoplast. No bacteriocin‐mediated benefit for Psy was observed under the culture conditions tested. Additionally, we found that the bacteriocin‐mediated benefit for Psy was dependent on the Type III Secretion System. Taken together, our results demonstrate that the fitness benefit of bacteriocin‐mediated antagonism is influenced by interactions within the host plant.
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spelling pubmed-97961162022-12-30 The plant host environment influences competitive interactions between bacterial pathogens Ehau‐Taumaunu, Hanareia Hockett, Kevin L. Environ Microbiol Rep Brief Reports Bacteria compete for resources in diverse environments using an array of antagonistic strategies, including the production of narrow‐spectrum protein antibacterials termed bacteriocins. Although significant research has focused on bacteriocin‐mediated dynamics in culture environments, little research has explored bacteriocin‐mediated dynamics within a host context, particularly in plant environments. Here, we show that a bacterial plant pathogen, Pseudomonas syringae pv. syringae (Psy), expresses a bacteriocin both in culture and in leaf apoplast when co‐inoculated with a bacteriocin‐sensitive competitor, P. syringae pv. phaseolicola (Pph). Although there is an observable negative effect of the bacteriocin on the Pph population at most time points both in culture and in the leaf apoplast, a bacteriocin‐mediated benefit to Psy was only observed when the producing strain was co‐infiltrated at a low population frequency (1:9) into the leaf apoplast. At 6 days post‐infiltration, Psy achieved an eightfold population increase compared to a bacteriocin‐deficient mutant in the apoplast. No bacteriocin‐mediated benefit for Psy was observed under the culture conditions tested. Additionally, we found that the bacteriocin‐mediated benefit for Psy was dependent on the Type III Secretion System. Taken together, our results demonstrate that the fitness benefit of bacteriocin‐mediated antagonism is influenced by interactions within the host plant. John Wiley & Sons, Inc. 2022-06-14 2022-10 /pmc/articles/PMC9796116/ /pubmed/35700743 http://dx.doi.org/10.1111/1758-2229.13103 Text en © 2022 The Authors. Environmental Microbiology Reports published by Society for Applied Microbiology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Brief Reports
Ehau‐Taumaunu, Hanareia
Hockett, Kevin L.
The plant host environment influences competitive interactions between bacterial pathogens
title The plant host environment influences competitive interactions between bacterial pathogens
title_full The plant host environment influences competitive interactions between bacterial pathogens
title_fullStr The plant host environment influences competitive interactions between bacterial pathogens
title_full_unstemmed The plant host environment influences competitive interactions between bacterial pathogens
title_short The plant host environment influences competitive interactions between bacterial pathogens
title_sort plant host environment influences competitive interactions between bacterial pathogens
topic Brief Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9796116/
https://www.ncbi.nlm.nih.gov/pubmed/35700743
http://dx.doi.org/10.1111/1758-2229.13103
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