Background: is a Gram-positive bacterium that causes severe illnesses in the human population. The capacity of strains to form biofilms on biotic and abiotic surfaces creates serious problems for treatment of hospital infections and has stimulated efforts to develop new means of specific protection or immunotherapy.

Material And Methods: We found that rabbit serum raised against crude concentrated liquid culture significantly decreased the development of staphylococcal biofilm . To discover the corresponding staphylococcal antigen, we used mass-spectrometry and molecular cloning and identified three major immunodominant proteins. They included α-haemolysin, serine proteinase SplB and surface protein G, known as adhesin SasG.

Results: Although according to literature data, all these proteins represent virulence factors of and play diverse and important roles in the pathogenesis of staphylococcal diseases, only SasG can be directly implicated into the biofilm formation because of its surface location on a staphylococcal cell. Indeed, rabbit serum directed against purified recombinant SasG, similar to serum against crude staphylococcal liquid culture, prevented the formation of a biofilm.

Conclusion: SasG can be considered as a target in an anti-biofilm drug development and a component of the vaccine or immunotherapeutic preparations directed against staphylococcal infections in humans.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5944129PMC
http://dx.doi.org/10.2174/1874285801812010094DOI Listing

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