Cargando…

Surface Dependent Inhibition of Mycobacterium abscessus by Diverse Pseudomonas aeruginosa Strains

Both Pseudomonas aeruginosa and Mycobacterium abscessus are bacteria that cause pulmonary infection in people with inflammatory lung disease, including individuals with cystic fibrosis (CF). These bacterial species inhabit the same environmental reservoirs (soil and water) and can be coisolated in t...

Descripción completa

Detalles Bibliográficos
Autores principales: Idosa, Ayantu W., Wozniak, Daniel J., Hall-Stoodley, Luanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9769778/
https://www.ncbi.nlm.nih.gov/pubmed/36394312
http://dx.doi.org/10.1128/spectrum.02471-22
_version_ 1784854446436515840
author Idosa, Ayantu W.
Wozniak, Daniel J.
Hall-Stoodley, Luanne
author_facet Idosa, Ayantu W.
Wozniak, Daniel J.
Hall-Stoodley, Luanne
author_sort Idosa, Ayantu W.
collection PubMed
description Both Pseudomonas aeruginosa and Mycobacterium abscessus are bacteria that cause pulmonary infection in people with inflammatory lung disease, including individuals with cystic fibrosis (CF). These bacterial species inhabit the same environmental reservoirs (soil and water) and can be coisolated in the lungs of people with CF. We investigated the interaction of these bacteria and found an antagonistic interaction favoring P. aeruginosa that was observed in biofilms but not in planktonic cultures. This antagonism extended to multiple P. aeruginosa strains and against Mycobacterium smegmatis. We tested known P. aeruginosa mutants for genes that can play roles in interbacterial contact-dependent (type III and type VI secretion systems) and contact-independent (quorum sensing, type II secretion) antagonism pathways to interrogate the mechanism of action. Our results indicate that well-known mechanisms of interbacterial competition are not responsible for the antagonism of P. aeruginosa toward M. abscessus, suggesting a novel antibacterial strategy. IMPORTANCE The biofilm lifestyle is favored by many organisms, and understanding interbacterial interactions that occur between coisolated bacterial species can provide new information regarding bacterial defense mechanisms and antibacterial targets. This may also provide insights into possible interbacterial interactions impacting host immunity during coinfection. Here, we investigate an antagonistic interaction favoring P. aeruginosa over M. abscessus exclusively in dual-species biofilms and not in liquid coculture.
format Online
Article
Text
id pubmed-9769778
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-97697782022-12-22 Surface Dependent Inhibition of Mycobacterium abscessus by Diverse Pseudomonas aeruginosa Strains Idosa, Ayantu W. Wozniak, Daniel J. Hall-Stoodley, Luanne Microbiol Spectr Research Article Both Pseudomonas aeruginosa and Mycobacterium abscessus are bacteria that cause pulmonary infection in people with inflammatory lung disease, including individuals with cystic fibrosis (CF). These bacterial species inhabit the same environmental reservoirs (soil and water) and can be coisolated in the lungs of people with CF. We investigated the interaction of these bacteria and found an antagonistic interaction favoring P. aeruginosa that was observed in biofilms but not in planktonic cultures. This antagonism extended to multiple P. aeruginosa strains and against Mycobacterium smegmatis. We tested known P. aeruginosa mutants for genes that can play roles in interbacterial contact-dependent (type III and type VI secretion systems) and contact-independent (quorum sensing, type II secretion) antagonism pathways to interrogate the mechanism of action. Our results indicate that well-known mechanisms of interbacterial competition are not responsible for the antagonism of P. aeruginosa toward M. abscessus, suggesting a novel antibacterial strategy. IMPORTANCE The biofilm lifestyle is favored by many organisms, and understanding interbacterial interactions that occur between coisolated bacterial species can provide new information regarding bacterial defense mechanisms and antibacterial targets. This may also provide insights into possible interbacterial interactions impacting host immunity during coinfection. Here, we investigate an antagonistic interaction favoring P. aeruginosa over M. abscessus exclusively in dual-species biofilms and not in liquid coculture. American Society for Microbiology 2022-11-17 /pmc/articles/PMC9769778/ /pubmed/36394312 http://dx.doi.org/10.1128/spectrum.02471-22 Text en Copyright © 2022 Idosa et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Idosa, Ayantu W.
Wozniak, Daniel J.
Hall-Stoodley, Luanne
Surface Dependent Inhibition of Mycobacterium abscessus by Diverse Pseudomonas aeruginosa Strains
title Surface Dependent Inhibition of Mycobacterium abscessus by Diverse Pseudomonas aeruginosa Strains
title_full Surface Dependent Inhibition of Mycobacterium abscessus by Diverse Pseudomonas aeruginosa Strains
title_fullStr Surface Dependent Inhibition of Mycobacterium abscessus by Diverse Pseudomonas aeruginosa Strains
title_full_unstemmed Surface Dependent Inhibition of Mycobacterium abscessus by Diverse Pseudomonas aeruginosa Strains
title_short Surface Dependent Inhibition of Mycobacterium abscessus by Diverse Pseudomonas aeruginosa Strains
title_sort surface dependent inhibition of mycobacterium abscessus by diverse pseudomonas aeruginosa strains
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9769778/
https://www.ncbi.nlm.nih.gov/pubmed/36394312
http://dx.doi.org/10.1128/spectrum.02471-22
work_keys_str_mv AT idosaayantuw surfacedependentinhibitionofmycobacteriumabscessusbydiversepseudomonasaeruginosastrains
AT wozniakdanielj surfacedependentinhibitionofmycobacteriumabscessusbydiversepseudomonasaeruginosastrains
AT hallstoodleyluanne surfacedependentinhibitionofmycobacteriumabscessusbydiversepseudomonasaeruginosastrains