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Molecular and chemical dialogues in bacteria-protozoa interactions

Protozoan predation of bacteria can significantly affect soil microbial community composition and ecosystem functioning. Bacteria possess diverse defense strategies to resist or evade protozoan predation. For soil-dwelling Pseudomonas species, several secondary metabolites were proposed to provide p...

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Autores principales: Song, Chunxu, Mazzola, Mark, Cheng, Xu, Oetjen, Janina, Alexandrov, Theodore, Dorrestein, Pieter, Watrous, Jeramie, van der Voort, Menno, Raaijmakers, Jos M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4542665/
https://www.ncbi.nlm.nih.gov/pubmed/26246193
http://dx.doi.org/10.1038/srep12837
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author Song, Chunxu
Mazzola, Mark
Cheng, Xu
Oetjen, Janina
Alexandrov, Theodore
Dorrestein, Pieter
Watrous, Jeramie
van der Voort, Menno
Raaijmakers, Jos M.
author_facet Song, Chunxu
Mazzola, Mark
Cheng, Xu
Oetjen, Janina
Alexandrov, Theodore
Dorrestein, Pieter
Watrous, Jeramie
van der Voort, Menno
Raaijmakers, Jos M.
author_sort Song, Chunxu
collection PubMed
description Protozoan predation of bacteria can significantly affect soil microbial community composition and ecosystem functioning. Bacteria possess diverse defense strategies to resist or evade protozoan predation. For soil-dwelling Pseudomonas species, several secondary metabolites were proposed to provide protection against different protozoan genera. By combining whole-genome transcriptome analyses with (live) imaging mass spectrometry (IMS), we observed multiple changes in the molecular and chemical dialogues between Pseudomonas fluorescens and the protist Naegleria americana. Lipopeptide (LP) biosynthesis was induced in Pseudomonas upon protozoan grazing and LP accumulation transitioned from homogeneous distributions across bacterial colonies to site-specific accumulation at the bacteria-protist interface. Also putrescine biosynthesis was upregulated in P. fluorescens upon predation. We demonstrated that putrescine induces protozoan trophozoite encystment and adversely affects cyst viability. This multifaceted study provides new insights in common and strain-specific responses in bacteria-protozoa interactions, including responses that contribute to bacterial survival in highly competitive soil and rhizosphere environments.
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spelling pubmed-45426652015-09-01 Molecular and chemical dialogues in bacteria-protozoa interactions Song, Chunxu Mazzola, Mark Cheng, Xu Oetjen, Janina Alexandrov, Theodore Dorrestein, Pieter Watrous, Jeramie van der Voort, Menno Raaijmakers, Jos M. Sci Rep Article Protozoan predation of bacteria can significantly affect soil microbial community composition and ecosystem functioning. Bacteria possess diverse defense strategies to resist or evade protozoan predation. For soil-dwelling Pseudomonas species, several secondary metabolites were proposed to provide protection against different protozoan genera. By combining whole-genome transcriptome analyses with (live) imaging mass spectrometry (IMS), we observed multiple changes in the molecular and chemical dialogues between Pseudomonas fluorescens and the protist Naegleria americana. Lipopeptide (LP) biosynthesis was induced in Pseudomonas upon protozoan grazing and LP accumulation transitioned from homogeneous distributions across bacterial colonies to site-specific accumulation at the bacteria-protist interface. Also putrescine biosynthesis was upregulated in P. fluorescens upon predation. We demonstrated that putrescine induces protozoan trophozoite encystment and adversely affects cyst viability. This multifaceted study provides new insights in common and strain-specific responses in bacteria-protozoa interactions, including responses that contribute to bacterial survival in highly competitive soil and rhizosphere environments. Nature Publishing Group 2015-08-06 /pmc/articles/PMC4542665/ /pubmed/26246193 http://dx.doi.org/10.1038/srep12837 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Song, Chunxu
Mazzola, Mark
Cheng, Xu
Oetjen, Janina
Alexandrov, Theodore
Dorrestein, Pieter
Watrous, Jeramie
van der Voort, Menno
Raaijmakers, Jos M.
Molecular and chemical dialogues in bacteria-protozoa interactions
title Molecular and chemical dialogues in bacteria-protozoa interactions
title_full Molecular and chemical dialogues in bacteria-protozoa interactions
title_fullStr Molecular and chemical dialogues in bacteria-protozoa interactions
title_full_unstemmed Molecular and chemical dialogues in bacteria-protozoa interactions
title_short Molecular and chemical dialogues in bacteria-protozoa interactions
title_sort molecular and chemical dialogues in bacteria-protozoa interactions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4542665/
https://www.ncbi.nlm.nih.gov/pubmed/26246193
http://dx.doi.org/10.1038/srep12837
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