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Role of the ESAT-6 secretion system in virulence of the emerging community-associated Staphylococcus aureus lineage ST398
Novel Staphylococcus aureus clones continue to emerge that cause infections in otherwise healthy people. One example is the sequence type (ST) 398 lineage, which we show here is increasing in importance as a significant cause of community-associated (CA) human infections in China. We have a profound...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4844983/ https://www.ncbi.nlm.nih.gov/pubmed/27112266 http://dx.doi.org/10.1038/srep25163 |
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author | Wang, Yanan Hu, Mo Liu, Qian Qin, Juanxiu Dai, Yingxin He, Lei Li, Tianming Zheng, Bing Zhou, Fan Yu, Kaiwen Fang, Jingyuan Liu, Xiaoyun Otto, Michael Li, Min |
author_facet | Wang, Yanan Hu, Mo Liu, Qian Qin, Juanxiu Dai, Yingxin He, Lei Li, Tianming Zheng, Bing Zhou, Fan Yu, Kaiwen Fang, Jingyuan Liu, Xiaoyun Otto, Michael Li, Min |
author_sort | Wang, Yanan |
collection | PubMed |
description | Novel Staphylococcus aureus clones continue to emerge that cause infections in otherwise healthy people. One example is the sequence type (ST) 398 lineage, which we show here is increasing in importance as a significant cause of community-associated (CA) human infections in China. We have a profound lack of understanding about what determines the considerable virulence potential of such newly emerging clones. Information about the contribution to virulence of the more recently discovered ESAT-6 secretion system (ESS) has remained particularly scarce. The Chinese ST398 isolates exhibited significantly increased expression of ESS genes as compared to predominant hospital-associated clones, which we found is likely due to increased expression of the accessory gene regulator (Agr) system and control of ESS by Agr. Importantly, deletion of essB in ST398 resulted in significantly reduced resistance to neutrophil killing and decreased virulence in murine skin and blood infection models. Our results demonstrate a key function of ESS in promoting virulence and mechanisms of resistance to innate host defense in an important emerging CA-S. aureus lineage. They suggest that ESS has a so far underestimated role in promoting aggressive virulence and epidemiological success of S. aureus. |
format | Online Article Text |
id | pubmed-4844983 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48449832016-04-29 Role of the ESAT-6 secretion system in virulence of the emerging community-associated Staphylococcus aureus lineage ST398 Wang, Yanan Hu, Mo Liu, Qian Qin, Juanxiu Dai, Yingxin He, Lei Li, Tianming Zheng, Bing Zhou, Fan Yu, Kaiwen Fang, Jingyuan Liu, Xiaoyun Otto, Michael Li, Min Sci Rep Article Novel Staphylococcus aureus clones continue to emerge that cause infections in otherwise healthy people. One example is the sequence type (ST) 398 lineage, which we show here is increasing in importance as a significant cause of community-associated (CA) human infections in China. We have a profound lack of understanding about what determines the considerable virulence potential of such newly emerging clones. Information about the contribution to virulence of the more recently discovered ESAT-6 secretion system (ESS) has remained particularly scarce. The Chinese ST398 isolates exhibited significantly increased expression of ESS genes as compared to predominant hospital-associated clones, which we found is likely due to increased expression of the accessory gene regulator (Agr) system and control of ESS by Agr. Importantly, deletion of essB in ST398 resulted in significantly reduced resistance to neutrophil killing and decreased virulence in murine skin and blood infection models. Our results demonstrate a key function of ESS in promoting virulence and mechanisms of resistance to innate host defense in an important emerging CA-S. aureus lineage. They suggest that ESS has a so far underestimated role in promoting aggressive virulence and epidemiological success of S. aureus. Nature Publishing Group 2016-04-26 /pmc/articles/PMC4844983/ /pubmed/27112266 http://dx.doi.org/10.1038/srep25163 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Wang, Yanan Hu, Mo Liu, Qian Qin, Juanxiu Dai, Yingxin He, Lei Li, Tianming Zheng, Bing Zhou, Fan Yu, Kaiwen Fang, Jingyuan Liu, Xiaoyun Otto, Michael Li, Min Role of the ESAT-6 secretion system in virulence of the emerging community-associated Staphylococcus aureus lineage ST398 |
title | Role of the ESAT-6 secretion system in virulence of the emerging community-associated Staphylococcus aureus lineage ST398 |
title_full | Role of the ESAT-6 secretion system in virulence of the emerging community-associated Staphylococcus aureus lineage ST398 |
title_fullStr | Role of the ESAT-6 secretion system in virulence of the emerging community-associated Staphylococcus aureus lineage ST398 |
title_full_unstemmed | Role of the ESAT-6 secretion system in virulence of the emerging community-associated Staphylococcus aureus lineage ST398 |
title_short | Role of the ESAT-6 secretion system in virulence of the emerging community-associated Staphylococcus aureus lineage ST398 |
title_sort | role of the esat-6 secretion system in virulence of the emerging community-associated staphylococcus aureus lineage st398 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4844983/ https://www.ncbi.nlm.nih.gov/pubmed/27112266 http://dx.doi.org/10.1038/srep25163 |
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