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From: Rufina Duncan <demersfr(*)globetrotter.net>
Date: Tue, 31 Jul 2007 11:39:43 -0500
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I know that, answered the boy, trembling, but WHY are you here? Because you have touched the Master Key of Electricity, and I must obey the laws of nature that compel me to respond to your summonsOne of the most intriguing areas of investigation is determining what impact quorum sensing has on the growth development and pathogenesis of staphylococcal biofilms. There is mounting evidence that the agr phenotype and expression patterns may influence several aspects of biofilm behavior including attachment of cells to surfaces biofilm dispersal and even the chronic nature of many biofilmassociated infections. Indeed many of the products involved in biofilm development including toxin surfaceassociated adhesins hemolysin and the autolysin AtlE in S. epidermidis are regulated by the agr system at least in vitro. Furthermore quorum sensing has been shown to be involved in biofilm development of several Grampositive and Gramnegative bacteria including Streptococcus mutans 32 and Pseudomonas aeruginosa 33.
Most infections of indwelling medical devices are caused by S. epidermidis an organism with few exotoxins and for which the ability to form biofilms is considered the primary virulence factor 2. Recently Vuong et al. 39 found that disruption of the agr locus in S. epidermidis resulted in increased attachment of the bacteria to polystyrene increased biofilm formation and higher expression of AtlE which enhances attachment to abiotic surfaces. They also confirmed that the clinical isolate S. epidermidis O47 the strain of choice for studying biofilm formation in S. epidermidis was an agr mutant. Interestingly agr did not regulate PIA expression. Received on Tue Jul 31 2007 - 20:27:38 EDT

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