Staphylococcus aureus (
S. aureus) is one of most common opportunistic pathogens and is attributed to several human infections. The increasing incidence of methicillin-resistant
S. aureus (MRSA) is a serious clinical threat for osteomyelitis crisis. The YycFG two-component system of
S. aureus regulates genes associated with biofilm formation. To investigate the potential role of an antisense
yycF RNA in the regulation of transcription levels of
yycF and associated effects on biofilm formation and pathogenicity, antisense
yycF (AS
yycF) RNA was detected by RT-PCR and 5′ RACE assays. AS
yycF overexpression mutants were constructed, and the biofilm biomass was determined by crystal violet microtiter assay and scanning electron microscopy (SEM). Quantitative RT-PCR and Western blotting analyses were used to detect whether AS
yycF overexpression inhibited the transcription and translation of biofilm-related genes. Then, a rat tibial infective model was used to evaluate the pathogenicity of AS
yycF overexpression in vivo. AS
yycF transcription led to reductions in YycF production and biofilm formation. Overexpression of AS
yycF inhibited the transcription and translation of biofilm-related genes. The sensitivity to vancomycin was improved in AS
yycF-overexpressing MRSA. Furthermore, AS
yycF inhibited MRSA invasion in a rat tibial infection model. From this study, the expression of the YycF protein was found to be inversely correlated with different levels of AS
yycF transcription. The biofilm biomass and pathogenicity decreased in the AS
yycF-overexpressing mutant. Thus, the current evidence may support AS
yycF as a supplementary strategy for managing
S. aureus and MRSA infections.
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