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From the wound to the bench: exoproteome interplay between wound-colonizing Staphylococcus aureus strains and co-existing bacteria

Wound-colonizing microorganisms can form complex and dynamic polymicrobial communities where pathogens and commensals may co-exist, cooperate or compete with each other. The present study was aimed at identifying possible interactions between different bacteria isolated from the same chronic wound o...

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Autores principales: García-Pérez, Andrea N., de Jong, Anne, Junker, Sabryna, Becher, Dörte, Chlebowicz, Monika A., Duipmans, José C., Jonkman, Marcel F., van Dijl, Jan Maarten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955179/
https://www.ncbi.nlm.nih.gov/pubmed/29233035
http://dx.doi.org/10.1080/21505594.2017.1395129
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author García-Pérez, Andrea N.
de Jong, Anne
Junker, Sabryna
Becher, Dörte
Chlebowicz, Monika A.
Duipmans, José C.
Jonkman, Marcel F.
van Dijl, Jan Maarten
author_facet García-Pérez, Andrea N.
de Jong, Anne
Junker, Sabryna
Becher, Dörte
Chlebowicz, Monika A.
Duipmans, José C.
Jonkman, Marcel F.
van Dijl, Jan Maarten
author_sort García-Pérez, Andrea N.
collection PubMed
description Wound-colonizing microorganisms can form complex and dynamic polymicrobial communities where pathogens and commensals may co-exist, cooperate or compete with each other. The present study was aimed at identifying possible interactions between different bacteria isolated from the same chronic wound of a patient with the genetic blistering disease epidermolysis bullosa (EB). Specifically, this involved two different isolates of the human pathogen Staphylococcus aureus, and isolates of Bacillus thuringiensis and Klebsiella oxytoca. Particular focus was attributed to interactions of S. aureus with the two other species, because of the high staphylococcal prevalence among chronic wounds. Intriguingly, upon co-cultivation, none of the wound isolates inhibited each other's growth. Since the extracellular proteome of bacterial pathogens is a reservoir of virulence factors, the exoproteomes of the staphylococcal isolates in monoculture and co-culture with B. thuringiensis and K. oxytoca were characterized by Mass Spectrometry to explore the inherent relationships between these co-exisiting bacteria. This revealed a massive reduction in the number of staphylococcal exoproteins upon co-culturing with K. oxytoca or B. thuringiensis. Interestingly, this decrease was particularly evident for extracellular proteins with a predicted cytoplasmic localization, which were recently implicated in staphylococcal virulence and epidemiology. Furthermore, our exoproteome analysis uncovered potential cooperativity between the two different S. aureus isolates. Altogether, the observed exoproteome variations upon co-culturing are indicative of unprecedented adaptive mechanisms that set limits to the production of secreted staphylococcal virulence factors.
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spelling pubmed-59551792018-05-21 From the wound to the bench: exoproteome interplay between wound-colonizing Staphylococcus aureus strains and co-existing bacteria García-Pérez, Andrea N. de Jong, Anne Junker, Sabryna Becher, Dörte Chlebowicz, Monika A. Duipmans, José C. Jonkman, Marcel F. van Dijl, Jan Maarten Virulence Research Paper Wound-colonizing microorganisms can form complex and dynamic polymicrobial communities where pathogens and commensals may co-exist, cooperate or compete with each other. The present study was aimed at identifying possible interactions between different bacteria isolated from the same chronic wound of a patient with the genetic blistering disease epidermolysis bullosa (EB). Specifically, this involved two different isolates of the human pathogen Staphylococcus aureus, and isolates of Bacillus thuringiensis and Klebsiella oxytoca. Particular focus was attributed to interactions of S. aureus with the two other species, because of the high staphylococcal prevalence among chronic wounds. Intriguingly, upon co-cultivation, none of the wound isolates inhibited each other's growth. Since the extracellular proteome of bacterial pathogens is a reservoir of virulence factors, the exoproteomes of the staphylococcal isolates in monoculture and co-culture with B. thuringiensis and K. oxytoca were characterized by Mass Spectrometry to explore the inherent relationships between these co-exisiting bacteria. This revealed a massive reduction in the number of staphylococcal exoproteins upon co-culturing with K. oxytoca or B. thuringiensis. Interestingly, this decrease was particularly evident for extracellular proteins with a predicted cytoplasmic localization, which were recently implicated in staphylococcal virulence and epidemiology. Furthermore, our exoproteome analysis uncovered potential cooperativity between the two different S. aureus isolates. Altogether, the observed exoproteome variations upon co-culturing are indicative of unprecedented adaptive mechanisms that set limits to the production of secreted staphylococcal virulence factors. Taylor & Francis 2018-03-01 /pmc/articles/PMC5955179/ /pubmed/29233035 http://dx.doi.org/10.1080/21505594.2017.1395129 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
García-Pérez, Andrea N.
de Jong, Anne
Junker, Sabryna
Becher, Dörte
Chlebowicz, Monika A.
Duipmans, José C.
Jonkman, Marcel F.
van Dijl, Jan Maarten
From the wound to the bench: exoproteome interplay between wound-colonizing Staphylococcus aureus strains and co-existing bacteria
title From the wound to the bench: exoproteome interplay between wound-colonizing Staphylococcus aureus strains and co-existing bacteria
title_full From the wound to the bench: exoproteome interplay between wound-colonizing Staphylococcus aureus strains and co-existing bacteria
title_fullStr From the wound to the bench: exoproteome interplay between wound-colonizing Staphylococcus aureus strains and co-existing bacteria
title_full_unstemmed From the wound to the bench: exoproteome interplay between wound-colonizing Staphylococcus aureus strains and co-existing bacteria
title_short From the wound to the bench: exoproteome interplay between wound-colonizing Staphylococcus aureus strains and co-existing bacteria
title_sort from the wound to the bench: exoproteome interplay between wound-colonizing staphylococcus aureus strains and co-existing bacteria
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955179/
https://www.ncbi.nlm.nih.gov/pubmed/29233035
http://dx.doi.org/10.1080/21505594.2017.1395129
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