Oxygen as a Virulence Determinant in Polymicrobial Infections

ABSTRACT Infections caused by multiple organisms, or polymicrobial infections, are likely more common than is broadly appreciated. Interaction among microbial communities (and with their host) can change the infection landscape by subverting immunity, providing nutrients and inhibiting competing mic...

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Autores principales: Elizabeth M. Selleck, Michael S. Gilmore
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Publicado: American Society for Microbiology 2016
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spelling oai:doaj.org-article:52ebf317a0fc43b7bf815281152c696c2021-11-15T15:50:19ZOxygen as a Virulence Determinant in Polymicrobial Infections10.1128/mBio.01249-162150-7511https://doaj.org/article/52ebf317a0fc43b7bf815281152c696c2016-09-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mBio.01249-16https://doaj.org/toc/2150-7511ABSTRACT Infections caused by multiple organisms, or polymicrobial infections, are likely more common than is broadly appreciated. Interaction among microbial communities (and with their host) can change the infection landscape by subverting immunity, providing nutrients and inhibiting competing microbes. Stacy et al. (A. Stacy, D. Fleming, R. J. Lamont, K. P. Rumbaugh, and M. Whiteley, mBio 7:e00782-16, 2016, http://dx.doi.org/10.1128/mBio.00782-16) described a novel mechanism that results in synergistic growth of oral microbes Aggregatibacter actinomycetemcomitans and Streptococcus gordonii. The authors used whole-genome fitness profiling by transposon sequencing (Tn-seq) to identify genes differentially required for growth in vitro versus in a mono- or coinfection in a thigh abscess model. They found that coinfection with S. gordonii allowed A. actinomycetemcomitans to shift from an anaerobic to an aerobic mode of growth. This shift involved the production of a terminal electron acceptor H2O2 by S. gordonii and increased A. actinomycetemcomitans persistence—an interaction termed “cross-respiration.”Elizabeth M. SelleckMichael S. GilmoreAmerican Society for MicrobiologyarticleMicrobiologyQR1-502ENmBio, Vol 7, Iss 4 (2016)
institution DOAJ
collection DOAJ
language EN
topic Microbiology
QR1-502
spellingShingle Microbiology
QR1-502
Elizabeth M. Selleck
Michael S. Gilmore
Oxygen as a Virulence Determinant in Polymicrobial Infections
description ABSTRACT Infections caused by multiple organisms, or polymicrobial infections, are likely more common than is broadly appreciated. Interaction among microbial communities (and with their host) can change the infection landscape by subverting immunity, providing nutrients and inhibiting competing microbes. Stacy et al. (A. Stacy, D. Fleming, R. J. Lamont, K. P. Rumbaugh, and M. Whiteley, mBio 7:e00782-16, 2016, http://dx.doi.org/10.1128/mBio.00782-16) described a novel mechanism that results in synergistic growth of oral microbes Aggregatibacter actinomycetemcomitans and Streptococcus gordonii. The authors used whole-genome fitness profiling by transposon sequencing (Tn-seq) to identify genes differentially required for growth in vitro versus in a mono- or coinfection in a thigh abscess model. They found that coinfection with S. gordonii allowed A. actinomycetemcomitans to shift from an anaerobic to an aerobic mode of growth. This shift involved the production of a terminal electron acceptor H2O2 by S. gordonii and increased A. actinomycetemcomitans persistence—an interaction termed “cross-respiration.”
format article
author Elizabeth M. Selleck
Michael S. Gilmore
author_facet Elizabeth M. Selleck
Michael S. Gilmore
author_sort Elizabeth M. Selleck
title Oxygen as a Virulence Determinant in Polymicrobial Infections
title_short Oxygen as a Virulence Determinant in Polymicrobial Infections
title_full Oxygen as a Virulence Determinant in Polymicrobial Infections
title_fullStr Oxygen as a Virulence Determinant in Polymicrobial Infections
title_full_unstemmed Oxygen as a Virulence Determinant in Polymicrobial Infections
title_sort oxygen as a virulence determinant in polymicrobial infections
publisher American Society for Microbiology
publishDate 2016
url https://doaj.org/article/52ebf317a0fc43b7bf815281152c696c
work_keys_str_mv AT elizabethmselleck oxygenasavirulencedeterminantinpolymicrobialinfections
AT michaelsgilmore oxygenasavirulencedeterminantinpolymicrobialinfections
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