Cargando…
Indirect Pathogenicity of Haemophilus influenzae and Moraxella catarrhalis in Polymicrobial Otitis Media Occurs via Interspecies Quorum Signaling
Otitis media (OM) is among the leading diseases of childhood and is caused by opportunists that reside within the nasopharynx, such as Haemophilus influenzae and Moraxella catarrhalis. As with most airway infections, it is now clear that OM infections involve multiple organisms. This study addresses...
Autores principales: | , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
American Society of Microbiology
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2925075/ https://www.ncbi.nlm.nih.gov/pubmed/20802829 http://dx.doi.org/10.1128/mBio.00102-10 |
_version_ | 1782185648688463872 |
---|---|
author | Armbruster, Chelsie E. Hong, Wenzhou Pang, Bing Weimer, Kristin E. D. Juneau, Richard A. Turner, James Swords, W. Edward |
author_facet | Armbruster, Chelsie E. Hong, Wenzhou Pang, Bing Weimer, Kristin E. D. Juneau, Richard A. Turner, James Swords, W. Edward |
author_sort | Armbruster, Chelsie E. |
collection | PubMed |
description | Otitis media (OM) is among the leading diseases of childhood and is caused by opportunists that reside within the nasopharynx, such as Haemophilus influenzae and Moraxella catarrhalis. As with most airway infections, it is now clear that OM infections involve multiple organisms. This study addresses the hypothesis that polymicrobial infection alters the course, severity, and/or treatability of OM disease. The results clearly show that coinfection with H. influenzae and M. catarrhalis promotes the increased resistance of biofilms to antibiotics and host clearance. Using H. influenzae mutants with known biofilm defects, these phenotypes were shown to relate to biofilm maturation and autoinducer-2 (AI-2) quorum signaling. In support of the latter mechanism, chemically synthesized AI-2 (dihydroxypentanedione [DPD]) promoted increased M. catarrhalis biofilm formation and resistance to antibiotics. In the chinchilla infection model of OM, polymicrobial infection promoted M. catarrhalis persistence beyond the levels seen in animals infected with M. catarrhalis alone. Notably, no such enhancement of M. catarrhalis persistence was observed in animals infected with M. catarrhalis and a quorum signaling-deficient H. influenzae luxS mutant strain. We thus conclude that H. influenzae promotes M. catarrhalis persistence within polymicrobial biofilms via interspecies quorum signaling. AI-2 may therefore represent an ideal target for disruption of chronic polymicrobial infections. Moreover, these results strongly imply that successful vaccination against the unencapsulated H. influenzae strains that cause airway infections may also significantly impact chronic M. catarrhalis disease by removing a reservoir of the AI-2 signal that promotes M. catarrhalis persistence within biofilm. |
format | Text |
id | pubmed-2925075 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | American Society of Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-29250752010-08-29 Indirect Pathogenicity of Haemophilus influenzae and Moraxella catarrhalis in Polymicrobial Otitis Media Occurs via Interspecies Quorum Signaling Armbruster, Chelsie E. Hong, Wenzhou Pang, Bing Weimer, Kristin E. D. Juneau, Richard A. Turner, James Swords, W. Edward mBio Research Article Otitis media (OM) is among the leading diseases of childhood and is caused by opportunists that reside within the nasopharynx, such as Haemophilus influenzae and Moraxella catarrhalis. As with most airway infections, it is now clear that OM infections involve multiple organisms. This study addresses the hypothesis that polymicrobial infection alters the course, severity, and/or treatability of OM disease. The results clearly show that coinfection with H. influenzae and M. catarrhalis promotes the increased resistance of biofilms to antibiotics and host clearance. Using H. influenzae mutants with known biofilm defects, these phenotypes were shown to relate to biofilm maturation and autoinducer-2 (AI-2) quorum signaling. In support of the latter mechanism, chemically synthesized AI-2 (dihydroxypentanedione [DPD]) promoted increased M. catarrhalis biofilm formation and resistance to antibiotics. In the chinchilla infection model of OM, polymicrobial infection promoted M. catarrhalis persistence beyond the levels seen in animals infected with M. catarrhalis alone. Notably, no such enhancement of M. catarrhalis persistence was observed in animals infected with M. catarrhalis and a quorum signaling-deficient H. influenzae luxS mutant strain. We thus conclude that H. influenzae promotes M. catarrhalis persistence within polymicrobial biofilms via interspecies quorum signaling. AI-2 may therefore represent an ideal target for disruption of chronic polymicrobial infections. Moreover, these results strongly imply that successful vaccination against the unencapsulated H. influenzae strains that cause airway infections may also significantly impact chronic M. catarrhalis disease by removing a reservoir of the AI-2 signal that promotes M. catarrhalis persistence within biofilm. American Society of Microbiology 2010-07-06 /pmc/articles/PMC2925075/ /pubmed/20802829 http://dx.doi.org/10.1128/mBio.00102-10 Text en Copyright © 2010 Armbruster et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported License (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Armbruster, Chelsie E. Hong, Wenzhou Pang, Bing Weimer, Kristin E. D. Juneau, Richard A. Turner, James Swords, W. Edward Indirect Pathogenicity of Haemophilus influenzae and Moraxella catarrhalis in Polymicrobial Otitis Media Occurs via Interspecies Quorum Signaling |
title | Indirect Pathogenicity of Haemophilus influenzae and Moraxella catarrhalis in Polymicrobial Otitis Media Occurs via Interspecies Quorum Signaling |
title_full | Indirect Pathogenicity of Haemophilus influenzae and Moraxella catarrhalis in Polymicrobial Otitis Media Occurs via Interspecies Quorum Signaling |
title_fullStr | Indirect Pathogenicity of Haemophilus influenzae and Moraxella catarrhalis in Polymicrobial Otitis Media Occurs via Interspecies Quorum Signaling |
title_full_unstemmed | Indirect Pathogenicity of Haemophilus influenzae and Moraxella catarrhalis in Polymicrobial Otitis Media Occurs via Interspecies Quorum Signaling |
title_short | Indirect Pathogenicity of Haemophilus influenzae and Moraxella catarrhalis in Polymicrobial Otitis Media Occurs via Interspecies Quorum Signaling |
title_sort | indirect pathogenicity of haemophilus influenzae and moraxella catarrhalis in polymicrobial otitis media occurs via interspecies quorum signaling |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2925075/ https://www.ncbi.nlm.nih.gov/pubmed/20802829 http://dx.doi.org/10.1128/mBio.00102-10 |
work_keys_str_mv | AT armbrusterchelsiee indirectpathogenicityofhaemophilusinfluenzaeandmoraxellacatarrhalisinpolymicrobialotitismediaoccursviainterspeciesquorumsignaling AT hongwenzhou indirectpathogenicityofhaemophilusinfluenzaeandmoraxellacatarrhalisinpolymicrobialotitismediaoccursviainterspeciesquorumsignaling AT pangbing indirectpathogenicityofhaemophilusinfluenzaeandmoraxellacatarrhalisinpolymicrobialotitismediaoccursviainterspeciesquorumsignaling AT weimerkristined indirectpathogenicityofhaemophilusinfluenzaeandmoraxellacatarrhalisinpolymicrobialotitismediaoccursviainterspeciesquorumsignaling AT juneauricharda indirectpathogenicityofhaemophilusinfluenzaeandmoraxellacatarrhalisinpolymicrobialotitismediaoccursviainterspeciesquorumsignaling AT turnerjames indirectpathogenicityofhaemophilusinfluenzaeandmoraxellacatarrhalisinpolymicrobialotitismediaoccursviainterspeciesquorumsignaling AT swordswedward indirectpathogenicityofhaemophilusinfluenzaeandmoraxellacatarrhalisinpolymicrobialotitismediaoccursviainterspeciesquorumsignaling |