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Polybacterial human disease: the ills of social networking

Polybacterial diseases involve multiple organisms that act collectively to facilitate disease progression. Although this phenomenon was highlighted early in the 20th century, recent technological advances in diagnostics have led to the appreciation that many infections are far more complex than orig...

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Detalles Bibliográficos
Autores principales: Short, Francesca L., Murdoch, Sarah L., Ryan, Robert P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Trends Journals 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4158425/
https://www.ncbi.nlm.nih.gov/pubmed/24938173
http://dx.doi.org/10.1016/j.tim.2014.05.007
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author Short, Francesca L.
Murdoch, Sarah L.
Ryan, Robert P.
author_facet Short, Francesca L.
Murdoch, Sarah L.
Ryan, Robert P.
author_sort Short, Francesca L.
collection PubMed
description Polybacterial diseases involve multiple organisms that act collectively to facilitate disease progression. Although this phenomenon was highlighted early in the 20th century, recent technological advances in diagnostics have led to the appreciation that many infections are far more complex than originally believed. Furthermore, it is apparent that although most treatments focus on the dominant bacterial species in an infection, other microbes, including commensals, can have a profound impact on both the response to therapy and virulence. Very little is known about the molecular mechanisms that underpin interactions between bacteria during such infections. Here, we discuss recent studies identifying and characterizing mechanisms of bacterial interaction and the biological processes they govern during certain diseases. We also highlight how possible strategies for targeting these interbacterial interactions may afford a route towards development of new therapies, with consequences for disease control.
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spelling pubmed-41584252014-09-10 Polybacterial human disease: the ills of social networking Short, Francesca L. Murdoch, Sarah L. Ryan, Robert P. Trends Microbiol Review Polybacterial diseases involve multiple organisms that act collectively to facilitate disease progression. Although this phenomenon was highlighted early in the 20th century, recent technological advances in diagnostics have led to the appreciation that many infections are far more complex than originally believed. Furthermore, it is apparent that although most treatments focus on the dominant bacterial species in an infection, other microbes, including commensals, can have a profound impact on both the response to therapy and virulence. Very little is known about the molecular mechanisms that underpin interactions between bacteria during such infections. Here, we discuss recent studies identifying and characterizing mechanisms of bacterial interaction and the biological processes they govern during certain diseases. We also highlight how possible strategies for targeting these interbacterial interactions may afford a route towards development of new therapies, with consequences for disease control. Elsevier Trends Journals 2014-09 /pmc/articles/PMC4158425/ /pubmed/24938173 http://dx.doi.org/10.1016/j.tim.2014.05.007 Text en © 2014 The Authors https://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Review
Short, Francesca L.
Murdoch, Sarah L.
Ryan, Robert P.
Polybacterial human disease: the ills of social networking
title Polybacterial human disease: the ills of social networking
title_full Polybacterial human disease: the ills of social networking
title_fullStr Polybacterial human disease: the ills of social networking
title_full_unstemmed Polybacterial human disease: the ills of social networking
title_short Polybacterial human disease: the ills of social networking
title_sort polybacterial human disease: the ills of social networking
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4158425/
https://www.ncbi.nlm.nih.gov/pubmed/24938173
http://dx.doi.org/10.1016/j.tim.2014.05.007
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