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Function of BriC peptide in the pneumococcal competence and virulence portfolio
Streptococcus pneumoniae (pneumococcus) is an opportunistic pathogen that causes otitis media, sinusitis, pneumonia, meningitis and sepsis. The progression to this pathogenic lifestyle is preceded by asymptomatic colonization of the nasopharynx. This colonization is associated with biofilm formation...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6181422/ https://www.ncbi.nlm.nih.gov/pubmed/30308062 http://dx.doi.org/10.1371/journal.ppat.1007328 |
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author | Aggarwal, Surya D. Eutsey, Rory West-Roberts, Jacob Domenech, Arnau Xu, Wenjie Abdullah, Iman Tajer Mitchell, Aaron P. Veening, Jan-Willem Yesilkaya, Hasan Hiller, N. Luisa |
author_facet | Aggarwal, Surya D. Eutsey, Rory West-Roberts, Jacob Domenech, Arnau Xu, Wenjie Abdullah, Iman Tajer Mitchell, Aaron P. Veening, Jan-Willem Yesilkaya, Hasan Hiller, N. Luisa |
author_sort | Aggarwal, Surya D. |
collection | PubMed |
description | Streptococcus pneumoniae (pneumococcus) is an opportunistic pathogen that causes otitis media, sinusitis, pneumonia, meningitis and sepsis. The progression to this pathogenic lifestyle is preceded by asymptomatic colonization of the nasopharynx. This colonization is associated with biofilm formation; the competence pathway influences the structure and stability of biofilms. However, the molecules that link the competence pathway to biofilm formation are unknown. Here, we describe a new competence-induced gene, called briC, and demonstrate that its product promotes biofilm development and stimulates colonization in a murine model. We show that expression of briC is induced by the master regulator of competence, ComE. Whereas briC does not substantially influence early biofilm development on abiotic surfaces, it significantly impacts later stages of biofilm development. Specifically, briC expression leads to increases in biofilm biomass and thickness at 72h. Consistent with the role of biofilms in colonization, briC promotes nasopharyngeal colonization in the murine model. The function of BriC appears to be conserved across pneumococci, as comparative genomics reveal that briC is widespread across isolates. Surprisingly, many isolates, including strains from clinically important PMEN1 and PMEN14 lineages, which are widely associated with colonization, encode a long briC promoter. This long form captures an instance of genomic plasticity and functions as a competence-independent expression enhancer that may serve as a precocious point of entry into this otherwise competence-regulated pathway. Moreover, overexpression of briC by the long promoter fully rescues the comE-deletion induced biofilm defect in vitro, and partially in vivo. These findings indicate that BriC may bypass the influence of competence in biofilm development and that such a pathway may be active in a subset of pneumococcal lineages. In conclusion, BriC is a part of the complex molecular network that connects signaling of the competence pathway to biofilm development and colonization. |
format | Online Article Text |
id | pubmed-6181422 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-61814222018-10-26 Function of BriC peptide in the pneumococcal competence and virulence portfolio Aggarwal, Surya D. Eutsey, Rory West-Roberts, Jacob Domenech, Arnau Xu, Wenjie Abdullah, Iman Tajer Mitchell, Aaron P. Veening, Jan-Willem Yesilkaya, Hasan Hiller, N. Luisa PLoS Pathog Research Article Streptococcus pneumoniae (pneumococcus) is an opportunistic pathogen that causes otitis media, sinusitis, pneumonia, meningitis and sepsis. The progression to this pathogenic lifestyle is preceded by asymptomatic colonization of the nasopharynx. This colonization is associated with biofilm formation; the competence pathway influences the structure and stability of biofilms. However, the molecules that link the competence pathway to biofilm formation are unknown. Here, we describe a new competence-induced gene, called briC, and demonstrate that its product promotes biofilm development and stimulates colonization in a murine model. We show that expression of briC is induced by the master regulator of competence, ComE. Whereas briC does not substantially influence early biofilm development on abiotic surfaces, it significantly impacts later stages of biofilm development. Specifically, briC expression leads to increases in biofilm biomass and thickness at 72h. Consistent with the role of biofilms in colonization, briC promotes nasopharyngeal colonization in the murine model. The function of BriC appears to be conserved across pneumococci, as comparative genomics reveal that briC is widespread across isolates. Surprisingly, many isolates, including strains from clinically important PMEN1 and PMEN14 lineages, which are widely associated with colonization, encode a long briC promoter. This long form captures an instance of genomic plasticity and functions as a competence-independent expression enhancer that may serve as a precocious point of entry into this otherwise competence-regulated pathway. Moreover, overexpression of briC by the long promoter fully rescues the comE-deletion induced biofilm defect in vitro, and partially in vivo. These findings indicate that BriC may bypass the influence of competence in biofilm development and that such a pathway may be active in a subset of pneumococcal lineages. In conclusion, BriC is a part of the complex molecular network that connects signaling of the competence pathway to biofilm development and colonization. Public Library of Science 2018-10-11 /pmc/articles/PMC6181422/ /pubmed/30308062 http://dx.doi.org/10.1371/journal.ppat.1007328 Text en © 2018 Aggarwal et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Aggarwal, Surya D. Eutsey, Rory West-Roberts, Jacob Domenech, Arnau Xu, Wenjie Abdullah, Iman Tajer Mitchell, Aaron P. Veening, Jan-Willem Yesilkaya, Hasan Hiller, N. Luisa Function of BriC peptide in the pneumococcal competence and virulence portfolio |
title | Function of BriC peptide in the pneumococcal competence and virulence portfolio |
title_full | Function of BriC peptide in the pneumococcal competence and virulence portfolio |
title_fullStr | Function of BriC peptide in the pneumococcal competence and virulence portfolio |
title_full_unstemmed | Function of BriC peptide in the pneumococcal competence and virulence portfolio |
title_short | Function of BriC peptide in the pneumococcal competence and virulence portfolio |
title_sort | function of bric peptide in the pneumococcal competence and virulence portfolio |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6181422/ https://www.ncbi.nlm.nih.gov/pubmed/30308062 http://dx.doi.org/10.1371/journal.ppat.1007328 |
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