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Changes in microbiota during experimental human Rhinovirus infection

BACKGROUND: Human Rhinovirus (HRV) is responsible for the majority of common colds and is frequently accompanied by secondary bacterial infections through poorly understood mechanisms. We investigated the effects of experimental human HRV serotype 16 infection on the upper respiratory tract microbio...

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Autores principales: Hofstra, J. J., Matamoros, S., van de Pol, M. A., de Wever, B., Tanck, M. W., Wendt-Knol, H., Deijs, M., van der Hoek, L., Wolthers, K. C., Molenkamp, R., Visser, C. E., Sterk, P. J., Lutter, R., de Jong, M. D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4659412/
https://www.ncbi.nlm.nih.gov/pubmed/26271750
http://dx.doi.org/10.1186/s12879-015-1081-y
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author Hofstra, J. J.
Matamoros, S.
van de Pol, M. A.
de Wever, B.
Tanck, M. W.
Wendt-Knol, H.
Deijs, M.
van der Hoek, L.
Wolthers, K. C.
Molenkamp, R.
Visser, C. E.
Sterk, P. J.
Lutter, R.
de Jong, M. D.
author_facet Hofstra, J. J.
Matamoros, S.
van de Pol, M. A.
de Wever, B.
Tanck, M. W.
Wendt-Knol, H.
Deijs, M.
van der Hoek, L.
Wolthers, K. C.
Molenkamp, R.
Visser, C. E.
Sterk, P. J.
Lutter, R.
de Jong, M. D.
author_sort Hofstra, J. J.
collection PubMed
description BACKGROUND: Human Rhinovirus (HRV) is responsible for the majority of common colds and is frequently accompanied by secondary bacterial infections through poorly understood mechanisms. We investigated the effects of experimental human HRV serotype 16 infection on the upper respiratory tract microbiota. METHODS: Six healthy volunteers were infected with HRV16. We performed 16S ribosomal RNA-targeted pyrosequencing on throat swabs taken prior, during and after infection. We compared overall community diversity, phylogenetic structure of the ecosystem and relative abundances of the different bacteria between time points. RESULTS: During acute infection strong trends towards increases in the relative abundances of Haemophilus parainfluenzae and Neisseria subflava were observed, as well as a weaker trend towards increases of Staphylococcus aureus. No major differences were observed between day-1 and day 60, whereas differences between subjects were very high. CONCLUSIONS: HRV16 infection is associated with the increase of three genera known to be associated with secondary infections following HRV infections. The observed changes of upper respiratory tract microbiota could help explain why HRV infection predisposes to bacterial otitis media, sinusitis and pneumonia. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-015-1081-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-46594122015-11-26 Changes in microbiota during experimental human Rhinovirus infection Hofstra, J. J. Matamoros, S. van de Pol, M. A. de Wever, B. Tanck, M. W. Wendt-Knol, H. Deijs, M. van der Hoek, L. Wolthers, K. C. Molenkamp, R. Visser, C. E. Sterk, P. J. Lutter, R. de Jong, M. D. BMC Infect Dis Research Article BACKGROUND: Human Rhinovirus (HRV) is responsible for the majority of common colds and is frequently accompanied by secondary bacterial infections through poorly understood mechanisms. We investigated the effects of experimental human HRV serotype 16 infection on the upper respiratory tract microbiota. METHODS: Six healthy volunteers were infected with HRV16. We performed 16S ribosomal RNA-targeted pyrosequencing on throat swabs taken prior, during and after infection. We compared overall community diversity, phylogenetic structure of the ecosystem and relative abundances of the different bacteria between time points. RESULTS: During acute infection strong trends towards increases in the relative abundances of Haemophilus parainfluenzae and Neisseria subflava were observed, as well as a weaker trend towards increases of Staphylococcus aureus. No major differences were observed between day-1 and day 60, whereas differences between subjects were very high. CONCLUSIONS: HRV16 infection is associated with the increase of three genera known to be associated with secondary infections following HRV infections. The observed changes of upper respiratory tract microbiota could help explain why HRV infection predisposes to bacterial otitis media, sinusitis and pneumonia. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-015-1081-y) contains supplementary material, which is available to authorized users. BioMed Central 2015-08-14 /pmc/articles/PMC4659412/ /pubmed/26271750 http://dx.doi.org/10.1186/s12879-015-1081-y Text en © Hofstra et al. 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Hofstra, J. J.
Matamoros, S.
van de Pol, M. A.
de Wever, B.
Tanck, M. W.
Wendt-Knol, H.
Deijs, M.
van der Hoek, L.
Wolthers, K. C.
Molenkamp, R.
Visser, C. E.
Sterk, P. J.
Lutter, R.
de Jong, M. D.
Changes in microbiota during experimental human Rhinovirus infection
title Changes in microbiota during experimental human Rhinovirus infection
title_full Changes in microbiota during experimental human Rhinovirus infection
title_fullStr Changes in microbiota during experimental human Rhinovirus infection
title_full_unstemmed Changes in microbiota during experimental human Rhinovirus infection
title_short Changes in microbiota during experimental human Rhinovirus infection
title_sort changes in microbiota during experimental human rhinovirus infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4659412/
https://www.ncbi.nlm.nih.gov/pubmed/26271750
http://dx.doi.org/10.1186/s12879-015-1081-y
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