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Group B streptococcus (GBS) is an important pathogen in human disease- but what about in cystic fibrosis?

BACKGROUND: Group B Streptococcus (GBS) is a common commensal capable of causing severe invasive infections. Most GBS infections occur in neonates (often as pneumonia). GBS can also cause infection in adults with diabetes and other immunological impairments but rarely leads to pneumonia in adults. G...

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Autores principales: Skolnik, Kate, Nguyen, Austin, Thornton, Christina S., Waddell, Barbara, Williamson, Tyler, Rabin, Harvey R., Parkins, Michael D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5625721/
https://www.ncbi.nlm.nih.gov/pubmed/28969684
http://dx.doi.org/10.1186/s12879-017-2729-6
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author Skolnik, Kate
Nguyen, Austin
Thornton, Christina S.
Waddell, Barbara
Williamson, Tyler
Rabin, Harvey R.
Parkins, Michael D.
author_facet Skolnik, Kate
Nguyen, Austin
Thornton, Christina S.
Waddell, Barbara
Williamson, Tyler
Rabin, Harvey R.
Parkins, Michael D.
author_sort Skolnik, Kate
collection PubMed
description BACKGROUND: Group B Streptococcus (GBS) is a common commensal capable of causing severe invasive infections. Most GBS infections occur in neonates (often as pneumonia). GBS can also cause infection in adults with diabetes and other immunological impairments but rarely leads to pneumonia in adults. GBS has occasionally been found in the sputum of Cystic Fibrosis (CF) patients, an inherited condition known for progressive lung disease. However, the epidemiology and clinical significance of GBS in CF are not understood. METHODS: We retrospectively reviewed a large single-centre adult CF population with an associated comprehensive, prospectively collected bacterial biobank beginning in 1978. We identified all individuals with GBS isolated from their sputum on at least one occasion. The primary outcome was risk of pulmonary exacerbation (PEx) at the time of the first GBS isolate compared to the preceding visit. Secondary outcomes included determining: prevalence of GBS infection in a CF population, whether GBS infections where transient or persistent, whether GBS strains were shared among patients, change in % predicted FEV(1) at the time of GBS isolate compared to the preceding visit, PEx frequency after the first GBS isolate, change in % predicted FEV(1) after the first GBS isolate, and complications of GBS infection. RESULTS: GBS was uncommon, infecting 3.5% (11/318) adults within our cohort. Only three individuals developed persistent GBS infection, all lasting > 12 months. There were no shared GBS strains among patients. PEx risk was not increased at initial GBS isolation (RR 5.0, CI 0.69–36.1, p=0.10). In the two years preceding initial GBS isolation compared to the two following years, there was no difference in PEx frequency (median 2, range 0–4 vs 1, range 0 to 5, respectively, p=0.42) or lung function decline, as measured by % predicted FEV(1), (median −1.0%, range −19 to 7% vs median −6.0%, range −18 to 22%, p=0.86). There were no invasive GBS infections. CONCLUSION: In adults with CF, GBS is uncommon and is generally a transient colonizer of the lower airways. Despite the presence of structural lung disease and impaired innate immunity in CF, incident GBS infection did not increase PEx risk, PEx frequency, rate of lung function decline, or other adverse clinical outcomes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12879-017-2729-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-56257212017-10-12 Group B streptococcus (GBS) is an important pathogen in human disease- but what about in cystic fibrosis? Skolnik, Kate Nguyen, Austin Thornton, Christina S. Waddell, Barbara Williamson, Tyler Rabin, Harvey R. Parkins, Michael D. BMC Infect Dis Research Article BACKGROUND: Group B Streptococcus (GBS) is a common commensal capable of causing severe invasive infections. Most GBS infections occur in neonates (often as pneumonia). GBS can also cause infection in adults with diabetes and other immunological impairments but rarely leads to pneumonia in adults. GBS has occasionally been found in the sputum of Cystic Fibrosis (CF) patients, an inherited condition known for progressive lung disease. However, the epidemiology and clinical significance of GBS in CF are not understood. METHODS: We retrospectively reviewed a large single-centre adult CF population with an associated comprehensive, prospectively collected bacterial biobank beginning in 1978. We identified all individuals with GBS isolated from their sputum on at least one occasion. The primary outcome was risk of pulmonary exacerbation (PEx) at the time of the first GBS isolate compared to the preceding visit. Secondary outcomes included determining: prevalence of GBS infection in a CF population, whether GBS infections where transient or persistent, whether GBS strains were shared among patients, change in % predicted FEV(1) at the time of GBS isolate compared to the preceding visit, PEx frequency after the first GBS isolate, change in % predicted FEV(1) after the first GBS isolate, and complications of GBS infection. RESULTS: GBS was uncommon, infecting 3.5% (11/318) adults within our cohort. Only three individuals developed persistent GBS infection, all lasting > 12 months. There were no shared GBS strains among patients. PEx risk was not increased at initial GBS isolation (RR 5.0, CI 0.69–36.1, p=0.10). In the two years preceding initial GBS isolation compared to the two following years, there was no difference in PEx frequency (median 2, range 0–4 vs 1, range 0 to 5, respectively, p=0.42) or lung function decline, as measured by % predicted FEV(1), (median −1.0%, range −19 to 7% vs median −6.0%, range −18 to 22%, p=0.86). There were no invasive GBS infections. CONCLUSION: In adults with CF, GBS is uncommon and is generally a transient colonizer of the lower airways. Despite the presence of structural lung disease and impaired innate immunity in CF, incident GBS infection did not increase PEx risk, PEx frequency, rate of lung function decline, or other adverse clinical outcomes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12879-017-2729-6) contains supplementary material, which is available to authorized users. BioMed Central 2017-10-02 /pmc/articles/PMC5625721/ /pubmed/28969684 http://dx.doi.org/10.1186/s12879-017-2729-6 Text en © The Author(s). 2017 Open AccessThis 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
Skolnik, Kate
Nguyen, Austin
Thornton, Christina S.
Waddell, Barbara
Williamson, Tyler
Rabin, Harvey R.
Parkins, Michael D.
Group B streptococcus (GBS) is an important pathogen in human disease- but what about in cystic fibrosis?
title Group B streptococcus (GBS) is an important pathogen in human disease- but what about in cystic fibrosis?
title_full Group B streptococcus (GBS) is an important pathogen in human disease- but what about in cystic fibrosis?
title_fullStr Group B streptococcus (GBS) is an important pathogen in human disease- but what about in cystic fibrosis?
title_full_unstemmed Group B streptococcus (GBS) is an important pathogen in human disease- but what about in cystic fibrosis?
title_short Group B streptococcus (GBS) is an important pathogen in human disease- but what about in cystic fibrosis?
title_sort group b streptococcus (gbs) is an important pathogen in human disease- but what about in cystic fibrosis?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5625721/
https://www.ncbi.nlm.nih.gov/pubmed/28969684
http://dx.doi.org/10.1186/s12879-017-2729-6
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