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10.1038/srep11997

http://scihub22266oqcxt.onion/10.1038/srep11997
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C4493712!4493712!26149474
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suck abstract from ncbi


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pmid26149474      Sci+Rep 2015 ; 5 (ä): ä
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  • Transcriptome analysis of the biofilm formed by methicillin-susceptible Staphylococcus aureus #MMPMID26149474
  • Tan X; Qin N; Wu C; Sheng J; Yang R; Zheng B; Ma Z; Liu L; Peng X; Jia A
  • Sci Rep 2015[]; 5 (ä): ä PMID26149474show ga
  • 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.
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