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Extracellular DNA: A Nutritional Trigger of Mycoplasma bovis Cytotoxicity

Microbial access to host nutrients is a key factor of the host-pathogen interplay. With their nearly minimal genome, wall-less bacteria of the class Mollicutes have limited metabolic capacities and largely depend on host nutrients for their survival. Despite these limitations, host-restricted mycopl...

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Autores principales: Zhu, Xifang, Dordet-Frisoni, Emilie, Gillard, Lucie, Ba, Abou, Hygonenq, Marie-Claude, Sagné, Eveline, Nouvel, Laurent Xavier, Maillard, Renaud, Assié, Sébastien, Guo, Aizhen, Citti, Christine, Baranowski, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895004/
https://www.ncbi.nlm.nih.gov/pubmed/31849895
http://dx.doi.org/10.3389/fmicb.2019.02753
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author Zhu, Xifang
Dordet-Frisoni, Emilie
Gillard, Lucie
Ba, Abou
Hygonenq, Marie-Claude
Sagné, Eveline
Nouvel, Laurent Xavier
Maillard, Renaud
Assié, Sébastien
Guo, Aizhen
Citti, Christine
Baranowski, Eric
author_facet Zhu, Xifang
Dordet-Frisoni, Emilie
Gillard, Lucie
Ba, Abou
Hygonenq, Marie-Claude
Sagné, Eveline
Nouvel, Laurent Xavier
Maillard, Renaud
Assié, Sébastien
Guo, Aizhen
Citti, Christine
Baranowski, Eric
author_sort Zhu, Xifang
collection PubMed
description Microbial access to host nutrients is a key factor of the host-pathogen interplay. With their nearly minimal genome, wall-less bacteria of the class Mollicutes have limited metabolic capacities and largely depend on host nutrients for their survival. Despite these limitations, host-restricted mycoplasmas are widely distributed in nature and many species are pathogenic for humans and animals. Yet, only partial information is available regarding the mechanisms evolved by these minimal pathogens to meet their nutrients and the contribution of these mechanisms to virulence. By using the ruminant pathogen Mycoplasma bovis as a model system, extracellular DNA (eDNA) was identified as a limiting nutrient for mycoplasma proliferation under cell culture conditions. Remarkably, the growth-promoting effect induced by supplementation with eDNA was associated with important cytotoxicity for actively dividing host cells, but not confluent monolayers. To identify biological functions mediating M. bovis cytotoxicity, we produced a library of transposon knockout mutants and identified three critical genomic regions whose disruption was associated with a non-cytopathic phenotype. The coding sequences (CDS) disrupted in these regions pointed towards pyruvate metabolism as contributing to M. bovis cytotoxicity. Hydrogen peroxide was found responsible for eDNA-mediated M. bovis cytotoxicity, and non-cytopathic mutants were unable to produce this toxic metabolic compound. In our experimental conditions, no contact between M. bovis and host cells was required for cytotoxicity. Further analyses revealed important intra-species differences in eDNA-mediated cytotoxicity and H(2)O(2) production, with some strains displaying a cytopathic phenotype despite no H(2)O(2) production. Interestingly, the genome of strains PG45 and HB0801 were characterized by the occurrence of insertion sequences (IS) at close proximity to several CDSs found disrupted in non-cytopathic mutants. Since PG45 and HB0801 produced no or limited amount of H(2)O(2), IS-elements might influence H(2)O(2) production in M. bovis. These results confirm the multifaceted role of eDNA in microbial communities and further identify this ubiquitous material as a nutritional trigger of M. bovis cytotoxicity. M. bovis may thus take advantage of the multiple sources of eDNA in vivo to modulate its interaction with host cells, a way for this minimal pathogen to overcome its limited coding capacity.
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spelling pubmed-68950042019-12-17 Extracellular DNA: A Nutritional Trigger of Mycoplasma bovis Cytotoxicity Zhu, Xifang Dordet-Frisoni, Emilie Gillard, Lucie Ba, Abou Hygonenq, Marie-Claude Sagné, Eveline Nouvel, Laurent Xavier Maillard, Renaud Assié, Sébastien Guo, Aizhen Citti, Christine Baranowski, Eric Front Microbiol Microbiology Microbial access to host nutrients is a key factor of the host-pathogen interplay. With their nearly minimal genome, wall-less bacteria of the class Mollicutes have limited metabolic capacities and largely depend on host nutrients for their survival. Despite these limitations, host-restricted mycoplasmas are widely distributed in nature and many species are pathogenic for humans and animals. Yet, only partial information is available regarding the mechanisms evolved by these minimal pathogens to meet their nutrients and the contribution of these mechanisms to virulence. By using the ruminant pathogen Mycoplasma bovis as a model system, extracellular DNA (eDNA) was identified as a limiting nutrient for mycoplasma proliferation under cell culture conditions. Remarkably, the growth-promoting effect induced by supplementation with eDNA was associated with important cytotoxicity for actively dividing host cells, but not confluent monolayers. To identify biological functions mediating M. bovis cytotoxicity, we produced a library of transposon knockout mutants and identified three critical genomic regions whose disruption was associated with a non-cytopathic phenotype. The coding sequences (CDS) disrupted in these regions pointed towards pyruvate metabolism as contributing to M. bovis cytotoxicity. Hydrogen peroxide was found responsible for eDNA-mediated M. bovis cytotoxicity, and non-cytopathic mutants were unable to produce this toxic metabolic compound. In our experimental conditions, no contact between M. bovis and host cells was required for cytotoxicity. Further analyses revealed important intra-species differences in eDNA-mediated cytotoxicity and H(2)O(2) production, with some strains displaying a cytopathic phenotype despite no H(2)O(2) production. Interestingly, the genome of strains PG45 and HB0801 were characterized by the occurrence of insertion sequences (IS) at close proximity to several CDSs found disrupted in non-cytopathic mutants. Since PG45 and HB0801 produced no or limited amount of H(2)O(2), IS-elements might influence H(2)O(2) production in M. bovis. These results confirm the multifaceted role of eDNA in microbial communities and further identify this ubiquitous material as a nutritional trigger of M. bovis cytotoxicity. M. bovis may thus take advantage of the multiple sources of eDNA in vivo to modulate its interaction with host cells, a way for this minimal pathogen to overcome its limited coding capacity. Frontiers Media S.A. 2019-11-29 /pmc/articles/PMC6895004/ /pubmed/31849895 http://dx.doi.org/10.3389/fmicb.2019.02753 Text en Copyright © 2019 Zhu, Dordet-Frisoni, Gillard, Ba, Hygonenq, Sagné, Nouvel, Maillard, Assié, Guo, Citti and Baranowski. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Zhu, Xifang
Dordet-Frisoni, Emilie
Gillard, Lucie
Ba, Abou
Hygonenq, Marie-Claude
Sagné, Eveline
Nouvel, Laurent Xavier
Maillard, Renaud
Assié, Sébastien
Guo, Aizhen
Citti, Christine
Baranowski, Eric
Extracellular DNA: A Nutritional Trigger of Mycoplasma bovis Cytotoxicity
title Extracellular DNA: A Nutritional Trigger of Mycoplasma bovis Cytotoxicity
title_full Extracellular DNA: A Nutritional Trigger of Mycoplasma bovis Cytotoxicity
title_fullStr Extracellular DNA: A Nutritional Trigger of Mycoplasma bovis Cytotoxicity
title_full_unstemmed Extracellular DNA: A Nutritional Trigger of Mycoplasma bovis Cytotoxicity
title_short Extracellular DNA: A Nutritional Trigger of Mycoplasma bovis Cytotoxicity
title_sort extracellular dna: a nutritional trigger of mycoplasma bovis cytotoxicity
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895004/
https://www.ncbi.nlm.nih.gov/pubmed/31849895
http://dx.doi.org/10.3389/fmicb.2019.02753
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