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Species Interaction and Selective Carbon Addition During Antibiotic Exposure Enhances Bacterial Survival

Biofilms are multifaceted and robust microbiological systems that enable microorganisms to withstand a multitude of environmental stresses and expand their habitat range. We have shown previously that nutritional status alters antibiotic susceptibility in a mixed-species biofilm. To further elucidat...

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Autores principales: Jackson, Lindsay M. D., Kroukamp, Otini, Yeung, William C., Ronan, Evan, Liss, Steven N., Wolfaardt, Gideon M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895500/
https://www.ncbi.nlm.nih.gov/pubmed/31849882
http://dx.doi.org/10.3389/fmicb.2019.02730
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author Jackson, Lindsay M. D.
Kroukamp, Otini
Yeung, William C.
Ronan, Evan
Liss, Steven N.
Wolfaardt, Gideon M.
author_facet Jackson, Lindsay M. D.
Kroukamp, Otini
Yeung, William C.
Ronan, Evan
Liss, Steven N.
Wolfaardt, Gideon M.
author_sort Jackson, Lindsay M. D.
collection PubMed
description Biofilms are multifaceted and robust microbiological systems that enable microorganisms to withstand a multitude of environmental stresses and expand their habitat range. We have shown previously that nutritional status alters antibiotic susceptibility in a mixed-species biofilm. To further elucidate the effects of nutrient addition on inter-species dynamics and whole-biofilm susceptibility to high-dose streptomycin exposures, a CO(2) Evolution Measurement System was used to monitor the metabolic activity of early steady state pure-culture and mixed-species biofilms containing Pseudomonas aeruginosa and Stenotrophomonas maltophilia, with and without added carbon. Carbon supplementation was needed for biofilm recovery from high-dose streptomycin exposures when P. aeruginosa was either the dominant community member in a mixed-species biofilm (containing predominantly P. aeruginosa and S. maltophilia) or as a pure culture. By contrast, S. maltophilia biofilms could recover from high-dose streptomycin exposures without the need for carbon addition during antibiotic exposure. Metagenomic analysis revealed that even when inocula were dominated by Pseudomonas, the relative abundance of Stenotrophomonas increased upon biofilm development to ultimately become the dominant species post-streptomycin exposure. The combined metabolic and metagenomic results demonstrated the relevance of inter-species influence on survival and that nutritional status has a strong influence on the survival of P. aeruginosa dominated biofilms.
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spelling pubmed-68955002019-12-17 Species Interaction and Selective Carbon Addition During Antibiotic Exposure Enhances Bacterial Survival Jackson, Lindsay M. D. Kroukamp, Otini Yeung, William C. Ronan, Evan Liss, Steven N. Wolfaardt, Gideon M. Front Microbiol Microbiology Biofilms are multifaceted and robust microbiological systems that enable microorganisms to withstand a multitude of environmental stresses and expand their habitat range. We have shown previously that nutritional status alters antibiotic susceptibility in a mixed-species biofilm. To further elucidate the effects of nutrient addition on inter-species dynamics and whole-biofilm susceptibility to high-dose streptomycin exposures, a CO(2) Evolution Measurement System was used to monitor the metabolic activity of early steady state pure-culture and mixed-species biofilms containing Pseudomonas aeruginosa and Stenotrophomonas maltophilia, with and without added carbon. Carbon supplementation was needed for biofilm recovery from high-dose streptomycin exposures when P. aeruginosa was either the dominant community member in a mixed-species biofilm (containing predominantly P. aeruginosa and S. maltophilia) or as a pure culture. By contrast, S. maltophilia biofilms could recover from high-dose streptomycin exposures without the need for carbon addition during antibiotic exposure. Metagenomic analysis revealed that even when inocula were dominated by Pseudomonas, the relative abundance of Stenotrophomonas increased upon biofilm development to ultimately become the dominant species post-streptomycin exposure. The combined metabolic and metagenomic results demonstrated the relevance of inter-species influence on survival and that nutritional status has a strong influence on the survival of P. aeruginosa dominated biofilms. Frontiers Media S.A. 2019-11-29 /pmc/articles/PMC6895500/ /pubmed/31849882 http://dx.doi.org/10.3389/fmicb.2019.02730 Text en Copyright © 2019 Jackson, Kroukamp, Yeung, Ronan, Liss and Wolfaardt. 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
Jackson, Lindsay M. D.
Kroukamp, Otini
Yeung, William C.
Ronan, Evan
Liss, Steven N.
Wolfaardt, Gideon M.
Species Interaction and Selective Carbon Addition During Antibiotic Exposure Enhances Bacterial Survival
title Species Interaction and Selective Carbon Addition During Antibiotic Exposure Enhances Bacterial Survival
title_full Species Interaction and Selective Carbon Addition During Antibiotic Exposure Enhances Bacterial Survival
title_fullStr Species Interaction and Selective Carbon Addition During Antibiotic Exposure Enhances Bacterial Survival
title_full_unstemmed Species Interaction and Selective Carbon Addition During Antibiotic Exposure Enhances Bacterial Survival
title_short Species Interaction and Selective Carbon Addition During Antibiotic Exposure Enhances Bacterial Survival
title_sort species interaction and selective carbon addition during antibiotic exposure enhances bacterial survival
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895500/
https://www.ncbi.nlm.nih.gov/pubmed/31849882
http://dx.doi.org/10.3389/fmicb.2019.02730
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