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Commensal Staphylococcus epidermidis Defends against Staphylococcus aureus through SaeRS Two-Component System

[Image: see text] Staphylococcus aureus is a high-virulent Gram-positive pathogen that is responsible for a serious of diseases. The emergence of antibiotic-resistant S. aureus poses a significant challenge in terms of treatment. The recent research on the human microbiome suggested that the applica...

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Autores principales: Nurxat, Nadira, Wang, Lili, Wang, Qichen, Li, Shujing, Jin, Chen, Shi, Yaran, Wulamu, Ayjiamali, Zhao, Na, Wang, Yanan, Wang, Hua, Li, Min, Liu, Qian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10210170/
https://www.ncbi.nlm.nih.gov/pubmed/37251147
http://dx.doi.org/10.1021/acsomega.3c00263
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author Nurxat, Nadira
Wang, Lili
Wang, Qichen
Li, Shujing
Jin, Chen
Shi, Yaran
Wulamu, Ayjiamali
Zhao, Na
Wang, Yanan
Wang, Hua
Li, Min
Liu, Qian
author_facet Nurxat, Nadira
Wang, Lili
Wang, Qichen
Li, Shujing
Jin, Chen
Shi, Yaran
Wulamu, Ayjiamali
Zhao, Na
Wang, Yanan
Wang, Hua
Li, Min
Liu, Qian
author_sort Nurxat, Nadira
collection PubMed
description [Image: see text] Staphylococcus aureus is a high-virulent Gram-positive pathogen that is responsible for a serious of diseases. The emergence of antibiotic-resistant S. aureus poses a significant challenge in terms of treatment. The recent research on the human microbiome suggested that the application of commensal bacteria is a new strategy for combating pathogenic infections. Staphylococcus epidermidis, one of the most abundant species in the nasal microbiome, is able to inhibit the colonization of S. aureus. However, during bacterial competition, S. aureus undergoes evolutionary changes to adapt to the diverse environment. Our study has demonstrated that the nasal colonized S. epidermidis possesses the ability to inhibit the hemolytic activity of S. aureus. Moreover, we deciphered another layer of mechanism to inhibit S. aureus colonization by S. epidermidis. The active component present in the cell-free culture of S. epidermidis was found to significantly reduce the hemolytic activity of S. aureus in SaeRS- and Agr-dependent manner. Specifically, the hemolytic inhibition on the S. aureus Agr-I type by S. epidermidis is primarily dependent on the SaeRS two-component system. The active component is characterized as a small molecule that is heat sensitive and protease resistant. Critically, S. epidermidis significantly inhibit the virulence of S. aureus in a mouse skin abscess model, suggesting that the active compound could potentially be used as a therapeutic agent for managing S. aureus infections.
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spelling pubmed-102101702023-05-26 Commensal Staphylococcus epidermidis Defends against Staphylococcus aureus through SaeRS Two-Component System Nurxat, Nadira Wang, Lili Wang, Qichen Li, Shujing Jin, Chen Shi, Yaran Wulamu, Ayjiamali Zhao, Na Wang, Yanan Wang, Hua Li, Min Liu, Qian ACS Omega [Image: see text] Staphylococcus aureus is a high-virulent Gram-positive pathogen that is responsible for a serious of diseases. The emergence of antibiotic-resistant S. aureus poses a significant challenge in terms of treatment. The recent research on the human microbiome suggested that the application of commensal bacteria is a new strategy for combating pathogenic infections. Staphylococcus epidermidis, one of the most abundant species in the nasal microbiome, is able to inhibit the colonization of S. aureus. However, during bacterial competition, S. aureus undergoes evolutionary changes to adapt to the diverse environment. Our study has demonstrated that the nasal colonized S. epidermidis possesses the ability to inhibit the hemolytic activity of S. aureus. Moreover, we deciphered another layer of mechanism to inhibit S. aureus colonization by S. epidermidis. The active component present in the cell-free culture of S. epidermidis was found to significantly reduce the hemolytic activity of S. aureus in SaeRS- and Agr-dependent manner. Specifically, the hemolytic inhibition on the S. aureus Agr-I type by S. epidermidis is primarily dependent on the SaeRS two-component system. The active component is characterized as a small molecule that is heat sensitive and protease resistant. Critically, S. epidermidis significantly inhibit the virulence of S. aureus in a mouse skin abscess model, suggesting that the active compound could potentially be used as a therapeutic agent for managing S. aureus infections. American Chemical Society 2023-05-08 /pmc/articles/PMC10210170/ /pubmed/37251147 http://dx.doi.org/10.1021/acsomega.3c00263 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Nurxat, Nadira
Wang, Lili
Wang, Qichen
Li, Shujing
Jin, Chen
Shi, Yaran
Wulamu, Ayjiamali
Zhao, Na
Wang, Yanan
Wang, Hua
Li, Min
Liu, Qian
Commensal Staphylococcus epidermidis Defends against Staphylococcus aureus through SaeRS Two-Component System
title Commensal Staphylococcus epidermidis Defends against Staphylococcus aureus through SaeRS Two-Component System
title_full Commensal Staphylococcus epidermidis Defends against Staphylococcus aureus through SaeRS Two-Component System
title_fullStr Commensal Staphylococcus epidermidis Defends against Staphylococcus aureus through SaeRS Two-Component System
title_full_unstemmed Commensal Staphylococcus epidermidis Defends against Staphylococcus aureus through SaeRS Two-Component System
title_short Commensal Staphylococcus epidermidis Defends against Staphylococcus aureus through SaeRS Two-Component System
title_sort commensal staphylococcus epidermidis defends against staphylococcus aureus through saers two-component system
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10210170/
https://www.ncbi.nlm.nih.gov/pubmed/37251147
http://dx.doi.org/10.1021/acsomega.3c00263
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