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The Q225P Mutation in SigB Promotes Membrane Vesicle Formation in Staphylococcus aureus
Both Gram-positive and Gram-negative bacteria release nano-sized lipid bilayered particles, known as membrane vesicles (MVs), into external environments. Although MVs play a variety of roles in bacterial physiology and pathogenesis, the mechanisms underlying MV formation in Gram-positive microorgani...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8804369/ https://www.ncbi.nlm.nih.gov/pubmed/35103842 http://dx.doi.org/10.1007/s00284-022-02772-1 |
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author | Qiao, Li Yang, Yi Zhu, Keting Rao, Yifan Li, Gang Rao, Xiancai Li, Ming Zhou, Renjie |
author_facet | Qiao, Li Yang, Yi Zhu, Keting Rao, Yifan Li, Gang Rao, Xiancai Li, Ming Zhou, Renjie |
author_sort | Qiao, Li |
collection | PubMed |
description | Both Gram-positive and Gram-negative bacteria release nano-sized lipid bilayered particles, known as membrane vesicles (MVs), into external environments. Although MVs play a variety of roles in bacterial physiology and pathogenesis, the mechanisms underlying MV formation in Gram-positive microorganisms such as Staphylococcus aureus remain obscure. Bacterial MV production can be induced in response to stress conditions, and the alternative sigma factor B (SigB) functions as a central regulator of the stress response in Gram-positive bacteria. In a previous study, we demonstrated that the SigB(Q225P) substitution mutation in S. aureus promotes biofilm formation. Here, we report that the SigB(Q225P) mutation also increases MV production in this important pathogen. LacZ reporter assays and electrophoretic mobility shift assays showed that the Q225P substitution reduces SigB binding to the promoter region of the thermonuclease gene (nuc), resulting in a significant reduction in Nuc expression. Deletion of nuc markedly enhances S. aureus MV generation, possibly due to the accumulation of nucleic acids. These results are not only important for understanding MV biogenesis in S. aureus, but also useful for the development of a S. aureus MV-based platform for MV application. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00284-022-02772-1. |
format | Online Article Text |
id | pubmed-8804369 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-88043692022-02-01 The Q225P Mutation in SigB Promotes Membrane Vesicle Formation in Staphylococcus aureus Qiao, Li Yang, Yi Zhu, Keting Rao, Yifan Li, Gang Rao, Xiancai Li, Ming Zhou, Renjie Curr Microbiol Article Both Gram-positive and Gram-negative bacteria release nano-sized lipid bilayered particles, known as membrane vesicles (MVs), into external environments. Although MVs play a variety of roles in bacterial physiology and pathogenesis, the mechanisms underlying MV formation in Gram-positive microorganisms such as Staphylococcus aureus remain obscure. Bacterial MV production can be induced in response to stress conditions, and the alternative sigma factor B (SigB) functions as a central regulator of the stress response in Gram-positive bacteria. In a previous study, we demonstrated that the SigB(Q225P) substitution mutation in S. aureus promotes biofilm formation. Here, we report that the SigB(Q225P) mutation also increases MV production in this important pathogen. LacZ reporter assays and electrophoretic mobility shift assays showed that the Q225P substitution reduces SigB binding to the promoter region of the thermonuclease gene (nuc), resulting in a significant reduction in Nuc expression. Deletion of nuc markedly enhances S. aureus MV generation, possibly due to the accumulation of nucleic acids. These results are not only important for understanding MV biogenesis in S. aureus, but also useful for the development of a S. aureus MV-based platform for MV application. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00284-022-02772-1. Springer US 2022-02-01 2022 /pmc/articles/PMC8804369/ /pubmed/35103842 http://dx.doi.org/10.1007/s00284-022-02772-1 Text en © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Article Qiao, Li Yang, Yi Zhu, Keting Rao, Yifan Li, Gang Rao, Xiancai Li, Ming Zhou, Renjie The Q225P Mutation in SigB Promotes Membrane Vesicle Formation in Staphylococcus aureus |
title | The Q225P Mutation in SigB Promotes Membrane Vesicle Formation in Staphylococcus aureus |
title_full | The Q225P Mutation in SigB Promotes Membrane Vesicle Formation in Staphylococcus aureus |
title_fullStr | The Q225P Mutation in SigB Promotes Membrane Vesicle Formation in Staphylococcus aureus |
title_full_unstemmed | The Q225P Mutation in SigB Promotes Membrane Vesicle Formation in Staphylococcus aureus |
title_short | The Q225P Mutation in SigB Promotes Membrane Vesicle Formation in Staphylococcus aureus |
title_sort | q225p mutation in sigb promotes membrane vesicle formation in staphylococcus aureus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8804369/ https://www.ncbi.nlm.nih.gov/pubmed/35103842 http://dx.doi.org/10.1007/s00284-022-02772-1 |
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