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Transcriptome analysis of the biofilm formed by methicillin-susceptible Staphylococcus aureus
Biofilm formation is regarded as one of the major determinants in the prevalence of methicillin-resistant Staphylococcus aureus (MRSA) as pathogens of medical device-related infection. However, methicillin-susceptible S. aureus (MSSA) can also form biofilm in vitro and such biofilms are resistant to...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4493712/ https://www.ncbi.nlm.nih.gov/pubmed/26149474 http://dx.doi.org/10.1038/srep11997 |
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author | Tan, Xiaojuan Qin, Nan Wu, Chunyan Sheng, Jiyang Yang, Rui Zheng, Beiwen Ma, Zhanshan Liu, Lin Peng, Xinhua Jia, Aiqun |
author_facet | Tan, Xiaojuan Qin, Nan Wu, Chunyan Sheng, Jiyang Yang, Rui Zheng, Beiwen Ma, Zhanshan Liu, Lin Peng, Xinhua Jia, Aiqun |
author_sort | Tan, Xiaojuan |
collection | PubMed |
description | Biofilm formation is regarded as one of the major determinants in the prevalence of methicillin-resistant Staphylococcus aureus (MRSA) as pathogens of medical device-related infection. However, methicillin-susceptible S. aureus (MSSA) can also form biofilm in vitro and such biofilms are resistant to vancomycin. Hence, researching the possible mechanisms of MSSA biofilm formation is urgent and necessary. Here, we used S. aureus ATCC25923 as the model strain, and studied gene expression profiles in biofilms after the treatment of ursolic acid and resveratrol using RNA-seq technology. The results showed that only ursolic acid could inhibit biofilm formation, which differed from their applied on the multiple clinical drugs resistant MRSA biofilm. RNA-seq data was validated by examining the expression of six genes involved in biofilm formation by qRT-PCR. These data analysis indicated that the mechanism of the MSSA biofilm formation was different from that of the MRSA, due to absence of accessory gene regulator (agr) function. These findings suggest that biofilms of S. aureus with agr dysfunction may be more resistant than those with agr function. Therefore, the infection from clinical MSSA may be recalcitrant once forming biofilm. Further study is necessary to uncover the mechanisms of biofilm formation in other clinical S. aureus. |
format | Online Article Text |
id | pubmed-4493712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-44937122015-07-09 Transcriptome analysis of the biofilm formed by methicillin-susceptible Staphylococcus aureus Tan, Xiaojuan Qin, Nan Wu, Chunyan Sheng, Jiyang Yang, Rui Zheng, Beiwen Ma, Zhanshan Liu, Lin Peng, Xinhua Jia, Aiqun Sci Rep Article Biofilm formation is regarded as one of the major determinants in the prevalence of methicillin-resistant Staphylococcus aureus (MRSA) as pathogens of medical device-related infection. However, methicillin-susceptible S. aureus (MSSA) can also form biofilm in vitro and such biofilms are resistant to vancomycin. Hence, researching the possible mechanisms of MSSA biofilm formation is urgent and necessary. Here, we used S. aureus ATCC25923 as the model strain, and studied gene expression profiles in biofilms after the treatment of ursolic acid and resveratrol using RNA-seq technology. The results showed that only ursolic acid could inhibit biofilm formation, which differed from their applied on the multiple clinical drugs resistant MRSA biofilm. RNA-seq data was validated by examining the expression of six genes involved in biofilm formation by qRT-PCR. These data analysis indicated that the mechanism of the MSSA biofilm formation was different from that of the MRSA, due to absence of accessory gene regulator (agr) function. These findings suggest that biofilms of S. aureus with agr dysfunction may be more resistant than those with agr function. Therefore, the infection from clinical MSSA may be recalcitrant once forming biofilm. Further study is necessary to uncover the mechanisms of biofilm formation in other clinical S. aureus. Nature Publishing Group 2015-07-07 /pmc/articles/PMC4493712/ /pubmed/26149474 http://dx.doi.org/10.1038/srep11997 Text en Copyright © 2015, 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 Tan, Xiaojuan Qin, Nan Wu, Chunyan Sheng, Jiyang Yang, Rui Zheng, Beiwen Ma, Zhanshan Liu, Lin Peng, Xinhua Jia, Aiqun Transcriptome analysis of the biofilm formed by methicillin-susceptible Staphylococcus aureus |
title | Transcriptome analysis of the biofilm formed by methicillin-susceptible Staphylococcus aureus |
title_full | Transcriptome analysis of the biofilm formed by methicillin-susceptible Staphylococcus aureus |
title_fullStr | Transcriptome analysis of the biofilm formed by methicillin-susceptible Staphylococcus aureus |
title_full_unstemmed | Transcriptome analysis of the biofilm formed by methicillin-susceptible Staphylococcus aureus |
title_short | Transcriptome analysis of the biofilm formed by methicillin-susceptible Staphylococcus aureus |
title_sort | transcriptome analysis of the biofilm formed by methicillin-susceptible staphylococcus aureus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4493712/ https://www.ncbi.nlm.nih.gov/pubmed/26149474 http://dx.doi.org/10.1038/srep11997 |
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