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Mechanisms of hypervirulent Clostridium difficile ribotype 027 displacement of endemic strains: an epidemiological model

Following rapid, global clonal dominance of hypervirulent ribotypes, Clostridium difficile now constitutes the primary infectious cause of nosocomial diarrhoea. Evidence indicates at least three possible mechanisms of hypervirulence that facilitates the successful invasion of these atypical strains:...

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Autores principales: Yakob, Laith, Riley, Thomas V., Paterson, David L., Marquess, John, Magalhaes, Ricardo J. Soares, Furuya-Kanamori, Luis, Clements, Archie C.A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517512/
https://www.ncbi.nlm.nih.gov/pubmed/26218654
http://dx.doi.org/10.1038/srep12666
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author Yakob, Laith
Riley, Thomas V.
Paterson, David L.
Marquess, John
Magalhaes, Ricardo J. Soares
Furuya-Kanamori, Luis
Clements, Archie C.A.
author_facet Yakob, Laith
Riley, Thomas V.
Paterson, David L.
Marquess, John
Magalhaes, Ricardo J. Soares
Furuya-Kanamori, Luis
Clements, Archie C.A.
author_sort Yakob, Laith
collection PubMed
description Following rapid, global clonal dominance of hypervirulent ribotypes, Clostridium difficile now constitutes the primary infectious cause of nosocomial diarrhoea. Evidence indicates at least three possible mechanisms of hypervirulence that facilitates the successful invasion of these atypical strains: 1) increased infectiousness relative to endemic strains; 2) increased symptomatic disease rate relative to endemic strains; and 3) an ability to outcompete endemic strains in the host’s gut. Stochastic simulations of an infection transmission model demonstrate clear differences between the invasion potentials of C. difficile strains utilising the alternative hypervirulence mechanisms, and provide new evidence that favours certain mechanisms (1 and 2) more than others (3). Additionally, simulations illustrate that direct competition between strains (inside the host’s gut) is not a prerequisite for the sudden switching that has been observed in prevailing ribotypes; previously dominant C. difficile strains can be excluded by hypervirulent ribotypes through indirect (exploitative) competition.
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spelling pubmed-45175122015-07-30 Mechanisms of hypervirulent Clostridium difficile ribotype 027 displacement of endemic strains: an epidemiological model Yakob, Laith Riley, Thomas V. Paterson, David L. Marquess, John Magalhaes, Ricardo J. Soares Furuya-Kanamori, Luis Clements, Archie C.A. Sci Rep Article Following rapid, global clonal dominance of hypervirulent ribotypes, Clostridium difficile now constitutes the primary infectious cause of nosocomial diarrhoea. Evidence indicates at least three possible mechanisms of hypervirulence that facilitates the successful invasion of these atypical strains: 1) increased infectiousness relative to endemic strains; 2) increased symptomatic disease rate relative to endemic strains; and 3) an ability to outcompete endemic strains in the host’s gut. Stochastic simulations of an infection transmission model demonstrate clear differences between the invasion potentials of C. difficile strains utilising the alternative hypervirulence mechanisms, and provide new evidence that favours certain mechanisms (1 and 2) more than others (3). Additionally, simulations illustrate that direct competition between strains (inside the host’s gut) is not a prerequisite for the sudden switching that has been observed in prevailing ribotypes; previously dominant C. difficile strains can be excluded by hypervirulent ribotypes through indirect (exploitative) competition. Nature Publishing Group 2015-07-28 /pmc/articles/PMC4517512/ /pubmed/26218654 http://dx.doi.org/10.1038/srep12666 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Yakob, Laith
Riley, Thomas V.
Paterson, David L.
Marquess, John
Magalhaes, Ricardo J. Soares
Furuya-Kanamori, Luis
Clements, Archie C.A.
Mechanisms of hypervirulent Clostridium difficile ribotype 027 displacement of endemic strains: an epidemiological model
title Mechanisms of hypervirulent Clostridium difficile ribotype 027 displacement of endemic strains: an epidemiological model
title_full Mechanisms of hypervirulent Clostridium difficile ribotype 027 displacement of endemic strains: an epidemiological model
title_fullStr Mechanisms of hypervirulent Clostridium difficile ribotype 027 displacement of endemic strains: an epidemiological model
title_full_unstemmed Mechanisms of hypervirulent Clostridium difficile ribotype 027 displacement of endemic strains: an epidemiological model
title_short Mechanisms of hypervirulent Clostridium difficile ribotype 027 displacement of endemic strains: an epidemiological model
title_sort mechanisms of hypervirulent clostridium difficile ribotype 027 displacement of endemic strains: an epidemiological model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4517512/
https://www.ncbi.nlm.nih.gov/pubmed/26218654
http://dx.doi.org/10.1038/srep12666
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