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Infection and Immunity, September 2007, p. 4528-4533, Vol. 75, No. 9
0019-9567/07/$08.00+0 doi:10.1128/IAI.00603-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Department of Microbiology and Immunology, University of Arkansas for Medical Sciences, 4301 W. Markham, Little Rock, Arkansas 72205
Received 27 April 2007/ Returned for modification 14 May 2007/ Accepted 25 May 2007
To investigate the regulatory role of traP (target of RNAIII-activating peptide) in Staphylococcus aureus, we generated traP mutations in the clinical isolates UAMS-1 and USA300. In neither case did mutation of traP affect expression of the accessory gene regulator (agr) or the ability to form a biofilm. We were also unable to confirm that mutation of traP in the prototype 8325-4 laboratory strain RN6390 results in reduced expression of agr, reduced hemolytic activity, or an altered capacity to form a biofilm.
Published ahead of print on 4 June 2007.
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