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Foreign peptide triggers boost in pneumococcal metabolism and growth
BACKGROUND: Nonencapsulated Streptococcus pneumoniae bacteria are successful colonizers of the human nasopharynx and often possess genes aliB-like ORF 1 and 2 in place of capsule genes. AliB-like ORF 2 binds peptide FPPQSV, found in Prevotella species, resulting in enhanced colonization. How this re...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870813/ https://www.ncbi.nlm.nih.gov/pubmed/29580217 http://dx.doi.org/10.1186/s12866-018-1167-y |
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author | Nasher, Fauzy Förster, Sunniva Yildirim, Efe C. Grandgirard, Denis Leib, Stephen L. Heller, Manfred Hathaway, Lucy J. |
author_facet | Nasher, Fauzy Förster, Sunniva Yildirim, Efe C. Grandgirard, Denis Leib, Stephen L. Heller, Manfred Hathaway, Lucy J. |
author_sort | Nasher, Fauzy |
collection | PubMed |
description | BACKGROUND: Nonencapsulated Streptococcus pneumoniae bacteria are successful colonizers of the human nasopharynx and often possess genes aliB-like ORF 1 and 2 in place of capsule genes. AliB-like ORF 2 binds peptide FPPQSV, found in Prevotella species, resulting in enhanced colonization. How this response is mediated is so far unknown. RESULTS: Here we show that the peptide increases expression of genes involved in release of host carbohydrates, carbohydrate uptake and carbohydrate metabolism. In particular, the peptide increased expression of 1,5-anhydro-D-fructose reductase, a metabolic enzyme of an alternative starch and glycogen degrading pathway found in many organisms, in both transcriptomic and proteomic data. The peptide enhanced pneumococcal growth giving a competitive advantage to a strain with aliB-like ORF 2, over its mutant lacking the gene. Possession of aliB-like ORF 2 did not affect release of inflammatory cytokine CXCL8 from epithelial cells in culture and the nonencapsulated wild type strain was not able to establish disease or inflammation in an infant rat model of meningitis. CONCLUSIONS: We propose that AliB-like ORF 2 confers an advantage in colonization by enhancing carbohydrate metabolism resulting in a boost in growth. This may explain the widespread presence of aliB-like ORF 2 in the nonencapsulated pneumococcal population in the human nasopharynx. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12866-018-1167-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5870813 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58708132018-03-29 Foreign peptide triggers boost in pneumococcal metabolism and growth Nasher, Fauzy Förster, Sunniva Yildirim, Efe C. Grandgirard, Denis Leib, Stephen L. Heller, Manfred Hathaway, Lucy J. BMC Microbiol Research Article BACKGROUND: Nonencapsulated Streptococcus pneumoniae bacteria are successful colonizers of the human nasopharynx and often possess genes aliB-like ORF 1 and 2 in place of capsule genes. AliB-like ORF 2 binds peptide FPPQSV, found in Prevotella species, resulting in enhanced colonization. How this response is mediated is so far unknown. RESULTS: Here we show that the peptide increases expression of genes involved in release of host carbohydrates, carbohydrate uptake and carbohydrate metabolism. In particular, the peptide increased expression of 1,5-anhydro-D-fructose reductase, a metabolic enzyme of an alternative starch and glycogen degrading pathway found in many organisms, in both transcriptomic and proteomic data. The peptide enhanced pneumococcal growth giving a competitive advantage to a strain with aliB-like ORF 2, over its mutant lacking the gene. Possession of aliB-like ORF 2 did not affect release of inflammatory cytokine CXCL8 from epithelial cells in culture and the nonencapsulated wild type strain was not able to establish disease or inflammation in an infant rat model of meningitis. CONCLUSIONS: We propose that AliB-like ORF 2 confers an advantage in colonization by enhancing carbohydrate metabolism resulting in a boost in growth. This may explain the widespread presence of aliB-like ORF 2 in the nonencapsulated pneumococcal population in the human nasopharynx. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12866-018-1167-y) contains supplementary material, which is available to authorized users. BioMed Central 2018-03-27 /pmc/articles/PMC5870813/ /pubmed/29580217 http://dx.doi.org/10.1186/s12866-018-1167-y Text en © The Author(s). 2018 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 Nasher, Fauzy Förster, Sunniva Yildirim, Efe C. Grandgirard, Denis Leib, Stephen L. Heller, Manfred Hathaway, Lucy J. Foreign peptide triggers boost in pneumococcal metabolism and growth |
title | Foreign peptide triggers boost in pneumococcal metabolism and growth |
title_full | Foreign peptide triggers boost in pneumococcal metabolism and growth |
title_fullStr | Foreign peptide triggers boost in pneumococcal metabolism and growth |
title_full_unstemmed | Foreign peptide triggers boost in pneumococcal metabolism and growth |
title_short | Foreign peptide triggers boost in pneumococcal metabolism and growth |
title_sort | foreign peptide triggers boost in pneumococcal metabolism and growth |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870813/ https://www.ncbi.nlm.nih.gov/pubmed/29580217 http://dx.doi.org/10.1186/s12866-018-1167-y |
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