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Subinhibitory Concentrations of Mupirocin Stimulate Staphylococcus aureus Biofilm Formation by Upregulating cidA.
Jin, Ye; Guo, Yinjuan; Zhan, Qing; Shang, Yongpeng; Qu, Di; Yu, Fangyou.
Afiliação
  • Jin Y; Department of Laboratory Medicine, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
  • Guo Y; State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.
  • Zhan Q; Department of Laboratory Medicine, Shanghai Pulmonary Hospital of Tongji University School of Medicine, Shanghai, China.
  • Shang Y; Department of Laboratory Medicine, Shanghai Pulmonary Hospital of Tongji University School of Medicine, Shanghai, China.
  • Qu D; Key Laboratory of Medicine Molecular Virology of Ministry of Education and Ministry of Public Health, Shanghai Medical College of Fudan University, Shanghai, China.
  • Yu F; Key Laboratory of Medicine Molecular Virology of Ministry of Education and Ministry of Public Health, Shanghai Medical College of Fudan University, Shanghai, China dqu@shmu.edu.cn wzjxyfy@163.com.
Article em En | MEDLINE | ID: mdl-31932378
ABSTRACT
Previous studies have shown that the administration of antibiotics at subinhibitory concentrations stimulates biofilm formation by the majority of multidrug-resistant Staphylococcus aureus (MRSA) strains. Here, we investigated the effect of subinhibitory concentrations of mupirocin on biofilm formation by the community-associated (CA) mupirocin-sensitive MRSA strain USA300 and the highly mupirocin-resistant clinical S. aureus SA01 to SA05 isolates. We found that mupirocin increased the ability of MRSA cells to attach to surfaces and form biofilms. Confocal laser scanning microscopy (CLSM) demonstrated that mupirocin treatment promoted thicker biofilm formation, which also correlated with the production of extracellular DNA (eDNA). Furthermore, quantitative real-time PCR (RT-qPCR) results revealed that this effect was largely due to the involvement of holin-like and antiholin-like proteins (encoded by the cidA gene), which are responsible for modulating cell death and lysis during biofilm development. We found that cidA expression levels significantly increased by 6.05- to 35.52-fold (P < 0.01) after mupirocin administration. We generated a cidA-deficient mutant of the USA300 S. aureus strain. Exposure of the ΔcidA mutant to mupirocin did not result in thicker biofilm formation than that in the parent strain. We therefore hypothesize that the mupirocin-induced stimulation of S. aureus biofilm formation may involve the upregulation of cidA.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Staphylococcus aureus / Mupirocina / Antibacterianos Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Staphylococcus aureus / Mupirocina / Antibacterianos Idioma: En Ano de publicação: 2020 Tipo de documento: Article