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Association between genotypic diversity and biofilm production in group B Streptococcus

BACKGROUND: Group B Streptococcus (GBS) is a leading cause of sepsis and meningitis and an important factor in premature and stillbirths. Biofilm production has been suggested to be important for GBS pathogenesis alongside many other elements, including phylogenetic lineage and virulence factors, su...

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Autores principales: Parker, Robert E., Laut, Clare, Gaddy, Jennifer A., Zadoks, Ruth N., Davies, H. Dele, Manning, Shannon D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4875601/
https://www.ncbi.nlm.nih.gov/pubmed/27206613
http://dx.doi.org/10.1186/s12866-016-0704-9
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author Parker, Robert E.
Laut, Clare
Gaddy, Jennifer A.
Zadoks, Ruth N.
Davies, H. Dele
Manning, Shannon D.
author_facet Parker, Robert E.
Laut, Clare
Gaddy, Jennifer A.
Zadoks, Ruth N.
Davies, H. Dele
Manning, Shannon D.
author_sort Parker, Robert E.
collection PubMed
description BACKGROUND: Group B Streptococcus (GBS) is a leading cause of sepsis and meningitis and an important factor in premature and stillbirths. Biofilm production has been suggested to be important for GBS pathogenesis alongside many other elements, including phylogenetic lineage and virulence factors, such as pili and capsule type. A complete understanding of the confluence of these components, however, is lacking. To identify associations between biofilm phenotype, pilus profile and lineage, 293 strains from asymptomatic carriers, invasive disease cases, and bovine mastitis cases, were assessed for biofilm production using an in vitro assay. RESULTS: Multilocus sequence type (ST) profile, pilus island profile, and isolate source were associated with biofilm production. Strains from invasive disease cases and/or belonging to the ST-17 and ST-19 lineages were significantly more likely to form weak biofilms, whereas strains producing strong biofilms were recovered more frequently from individuals with asymptomatic colonization. CONCLUSIONS: These data suggest that biofilm production is a lineage-specific trait in GBS and may promote colonization of strains representing lineages other than STs 17 and 19. The findings herein also demonstrate that biofilms must be considered in the treatment of pregnant women, particularly for women with heavy GBS colonization. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12866-016-0704-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-48756012016-05-22 Association between genotypic diversity and biofilm production in group B Streptococcus Parker, Robert E. Laut, Clare Gaddy, Jennifer A. Zadoks, Ruth N. Davies, H. Dele Manning, Shannon D. BMC Microbiol Research Article BACKGROUND: Group B Streptococcus (GBS) is a leading cause of sepsis and meningitis and an important factor in premature and stillbirths. Biofilm production has been suggested to be important for GBS pathogenesis alongside many other elements, including phylogenetic lineage and virulence factors, such as pili and capsule type. A complete understanding of the confluence of these components, however, is lacking. To identify associations between biofilm phenotype, pilus profile and lineage, 293 strains from asymptomatic carriers, invasive disease cases, and bovine mastitis cases, were assessed for biofilm production using an in vitro assay. RESULTS: Multilocus sequence type (ST) profile, pilus island profile, and isolate source were associated with biofilm production. Strains from invasive disease cases and/or belonging to the ST-17 and ST-19 lineages were significantly more likely to form weak biofilms, whereas strains producing strong biofilms were recovered more frequently from individuals with asymptomatic colonization. CONCLUSIONS: These data suggest that biofilm production is a lineage-specific trait in GBS and may promote colonization of strains representing lineages other than STs 17 and 19. The findings herein also demonstrate that biofilms must be considered in the treatment of pregnant women, particularly for women with heavy GBS colonization. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12866-016-0704-9) contains supplementary material, which is available to authorized users. BioMed Central 2016-05-20 /pmc/articles/PMC4875601/ /pubmed/27206613 http://dx.doi.org/10.1186/s12866-016-0704-9 Text en © The Author(s). 2016 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
Parker, Robert E.
Laut, Clare
Gaddy, Jennifer A.
Zadoks, Ruth N.
Davies, H. Dele
Manning, Shannon D.
Association between genotypic diversity and biofilm production in group B Streptococcus
title Association between genotypic diversity and biofilm production in group B Streptococcus
title_full Association between genotypic diversity and biofilm production in group B Streptococcus
title_fullStr Association between genotypic diversity and biofilm production in group B Streptococcus
title_full_unstemmed Association between genotypic diversity and biofilm production in group B Streptococcus
title_short Association between genotypic diversity and biofilm production in group B Streptococcus
title_sort association between genotypic diversity and biofilm production in group b streptococcus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4875601/
https://www.ncbi.nlm.nih.gov/pubmed/27206613
http://dx.doi.org/10.1186/s12866-016-0704-9
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