AI Article Synopsis

  • The study investigates the biofilm-forming abilities of various clones of Staphylococcus aureus, focusing on both methicillin-sensitive (MSSA) and methicillin-resistant (MRSA) strains.
  • Different clones were analyzed for their adherence properties and slime production using modified Congo red agar and microtiter plate assays, revealing similarities within spa types but differences in slime production.
  • The research found that all tested clones contained the icaADBC genes, which are crucial for biofilm formation, while other MSCRAMM genes showed variable prevalence between the MSSA and MRSA groups.

Article Abstract

Clinical information about genotypically different clones of biofilm-producing Staphylococcus aureus is largely unknown. We examined whether different clones of methicillin-sensitive and methicillin-resistant S. aureus (MSSA and MRSA) differ with respect to staphylococcal microbial surface components recognizing adhesive matrix molecules (MSCRAMMs) in biofilm formation. The study used 60 different types of spa and determined the phenotypes, the prevalence of the 13 MSCRAMM, and biofilm genes for each clone. The current investigation was carried out using a modified Congo red agar (MCRA), a microtiter plate assay (MPA), polymerase chain reaction (PCR), and reverse transcriptase polymerase chain reaction (RT-PCR). Clones belonging to the same spa type were found to have similar properties in adheringto the polystyrene microtiter plate surface. However, their ability to produce slime on MCRA medium was different. PCR experiments showed that 60 clones of MSSA and MRSA were positive for 5 genes (out of 9 MSCRAMM genes). icaADBC genes were found to be present in all the 60 clones tested indicating a high prevalence, and these genes were equally distributed among the clones associated with MSSA and those with MRSA. The prevalence of other MSCRAMM genes among MSSA and MRSA clones was found to be variable. MRSA and MSSA gene expression (MSCRAMM and icaADBC) was confirmed by RT-PCR.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3372070PMC
http://dx.doi.org/10.1155/2012/976972DOI Listing

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