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Hydrogen Peroxide Contributes to the Epithelial Cell Death Induced by the Oral Mitis Group of Streptococci
Members of the mitis group of streptococci are normal inhabitants of the commensal flora of the oral cavity and upper respiratory tract of humans. Some mitis group species, such as Streptococcus oralis and Streptococcus sanguinis, are primary colonizers of the human oral cavity. Recently, we found t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3909332/ https://www.ncbi.nlm.nih.gov/pubmed/24498253 http://dx.doi.org/10.1371/journal.pone.0088136 |
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author | Okahashi, Nobuo Sumitomo, Tomoko Nakata, Masanobu Sakurai, Atsuo Kuwata, Hirotaka Kawabata, Shigetada |
author_facet | Okahashi, Nobuo Sumitomo, Tomoko Nakata, Masanobu Sakurai, Atsuo Kuwata, Hirotaka Kawabata, Shigetada |
author_sort | Okahashi, Nobuo |
collection | PubMed |
description | Members of the mitis group of streptococci are normal inhabitants of the commensal flora of the oral cavity and upper respiratory tract of humans. Some mitis group species, such as Streptococcus oralis and Streptococcus sanguinis, are primary colonizers of the human oral cavity. Recently, we found that hydrogen peroxide (H(2)O(2)) produced by S. oralis is cytotoxic to human macrophages, suggesting that streptococcus-derived H(2)O(2) may act as a cytotoxin. Since epithelial cells provide a physical barrier against pathogenic microbes, we investigated their susceptibility to infection by H(2)O(2)-producing streptococci in this study. Infection by S. oralis and S. sanguinis was found to stimulate cell death of Detroit 562, Calu-3 and HeLa epithelial cell lines at a multiplicity of infection greater than 100. Catalase, an enzyme that catalyzes the decomposition of H(2)O(2), inhibited S. oralis cytotoxicity, and H(2)O(2) alone was capable of eliciting epithelial cell death. Moreover, S. oralis mutants lacking the spxB gene encoding pyruvate oxidase, which are deficient in H(2)O(2) production, exhibited reduced cytotoxicity toward Detroit 562 epithelial cells. In addition, enzyme-linked immunosorbent assays revealed that both S. oralis and H(2)O(2) induced interleukin-6 production in Detroit 562 epithelial cells. These results suggest that streptococcal H(2)O(2) is cytotoxic to epithelial cells, and promotes bacterial evasion of the host defense systems in the oral cavity and upper respiratory tracts. |
format | Online Article Text |
id | pubmed-3909332 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-39093322014-02-04 Hydrogen Peroxide Contributes to the Epithelial Cell Death Induced by the Oral Mitis Group of Streptococci Okahashi, Nobuo Sumitomo, Tomoko Nakata, Masanobu Sakurai, Atsuo Kuwata, Hirotaka Kawabata, Shigetada PLoS One Research Article Members of the mitis group of streptococci are normal inhabitants of the commensal flora of the oral cavity and upper respiratory tract of humans. Some mitis group species, such as Streptococcus oralis and Streptococcus sanguinis, are primary colonizers of the human oral cavity. Recently, we found that hydrogen peroxide (H(2)O(2)) produced by S. oralis is cytotoxic to human macrophages, suggesting that streptococcus-derived H(2)O(2) may act as a cytotoxin. Since epithelial cells provide a physical barrier against pathogenic microbes, we investigated their susceptibility to infection by H(2)O(2)-producing streptococci in this study. Infection by S. oralis and S. sanguinis was found to stimulate cell death of Detroit 562, Calu-3 and HeLa epithelial cell lines at a multiplicity of infection greater than 100. Catalase, an enzyme that catalyzes the decomposition of H(2)O(2), inhibited S. oralis cytotoxicity, and H(2)O(2) alone was capable of eliciting epithelial cell death. Moreover, S. oralis mutants lacking the spxB gene encoding pyruvate oxidase, which are deficient in H(2)O(2) production, exhibited reduced cytotoxicity toward Detroit 562 epithelial cells. In addition, enzyme-linked immunosorbent assays revealed that both S. oralis and H(2)O(2) induced interleukin-6 production in Detroit 562 epithelial cells. These results suggest that streptococcal H(2)O(2) is cytotoxic to epithelial cells, and promotes bacterial evasion of the host defense systems in the oral cavity and upper respiratory tracts. Public Library of Science 2014-01-31 /pmc/articles/PMC3909332/ /pubmed/24498253 http://dx.doi.org/10.1371/journal.pone.0088136 Text en © 2014 Okahashi 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Okahashi, Nobuo Sumitomo, Tomoko Nakata, Masanobu Sakurai, Atsuo Kuwata, Hirotaka Kawabata, Shigetada Hydrogen Peroxide Contributes to the Epithelial Cell Death Induced by the Oral Mitis Group of Streptococci |
title | Hydrogen Peroxide Contributes to the Epithelial Cell Death Induced by the Oral Mitis Group of Streptococci |
title_full | Hydrogen Peroxide Contributes to the Epithelial Cell Death Induced by the Oral Mitis Group of Streptococci |
title_fullStr | Hydrogen Peroxide Contributes to the Epithelial Cell Death Induced by the Oral Mitis Group of Streptococci |
title_full_unstemmed | Hydrogen Peroxide Contributes to the Epithelial Cell Death Induced by the Oral Mitis Group of Streptococci |
title_short | Hydrogen Peroxide Contributes to the Epithelial Cell Death Induced by the Oral Mitis Group of Streptococci |
title_sort | hydrogen peroxide contributes to the epithelial cell death induced by the oral mitis group of streptococci |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3909332/ https://www.ncbi.nlm.nih.gov/pubmed/24498253 http://dx.doi.org/10.1371/journal.pone.0088136 |
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