Tsang Laura H, Daily Sonja T, Weiss Elizabeth C, Smeltzer Mark S
Department of Microbiology and Immunology, University of Arkansas for Medical Sciences, 4301 W. Markham, Mail Slot 511, Little Rock, AR 72205, USA.
Infect Immun. 2007 Sep;75(9):4528-33. doi: 10.1128/IAI.00603-07. Epub 2007 Jun 4.
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.
为了研究traP(RNAIII激活肽的靶标)在金黄色葡萄球菌中的调控作用,我们在临床分离株UAMS-1和USA300中产生了traP突变。在这两种情况下,traP突变均未影响辅助基因调节因子(agr)的表达或形成生物膜的能力。我们也无法证实原型8325-4实验室菌株RN6390中的traP突变会导致agr表达降低、溶血活性降低或形成生物膜的能力改变。