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Subinhibitory concentrations of pinocembrin exert anti‐ S taphylococcus aureus activity by reducing α ‐toxin expression
Author(s) -
Soromou L.W.,
Zhang Y.,
Cui Y.,
Wei M.,
Chen N.,
Yang X.,
Huo M.,
Baldé A.,
Guan S.,
Deng X.,
Wang D.
Publication year - 2013
Publication title -
journal of applied microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.889
H-Index - 156
eISSN - 1365-2672
pISSN - 1364-5072
DOI - 10.1111/jam.12221
Subject(s) - staphylococcus aureus , hemolysin , microbiology and biotechnology , pinocembrin , in vivo , biology , toxin , antibiotics , virulence , bacteria , biochemistry , genetics , flavonoid , gene , antioxidant
Aims Natural products have been used as potentially important sources of novel antibacterials in combating pathogenic S taphylococcus aureus isolates, a major problem around the world. In this study, we aimed to investigate the antibacterial effects of pinocembrin ( PNCB ) against S taph. aureus pneumonia in a murine model and its influence on the production of S taph. aureus α‐haemolysin ( H la ). Methods and Results The in vitro activities of PNCB on α‐haemolysin production were determined using haemolysis, Western blot and real‐time RT ‐ PCR assays. The viability and cytotoxicity assays were performed to evaluate the influence of PNCB on α‐toxin‐mediated injury of human alveolar epithelial cells. Moreover, through histopathologic analysis, we further determined the in vivo effects of PNCB on S taph. aureus pneumonia in a mouse model. In vitro , PNCB at low concentrations exhibited inhibitory activity against α‐haemolysin production and attenuated α‐haemolysin‐mediated cell injury. Furthermore, the in vivo findings demonstrated that PNCB protected mice from S taph. aureus pneumonia. Conclusions We have provided new evidence of the effects of PNCB , which suggest that PNCB attenuated α‐haemolysin‐mediated cell injury and protected mice from S taph. aureus pneumonia. Significance and Impact of the Study The findings indicate that PNCB may be used as a basis for anti‐ S taphylococcus agent.