Identification of a novel LysR family transcriptional regulator controlling acquisition of sulfur sources in Acinetobacter baumannii.

L-cysteine biosynthesis from inorganic sulfur represents a major mechanism by which reduced sulfur is incorporated into organic compounds. Cysteine biosynthesis and regulation is well characterized in E. coli. However, the regulation of sulfur metabolism in Acinetobacter baumannii is only partly understood, with the LysR type regulator, GigC known to control some aspects of sulfur reduction. In this study, we have used transcriptomics and bioinformatic analyses to characterize a novel LysR-type transcriptional regulator encoded by ABUW_1016 (cbl), in a highly multidrug-resistant and virulent isolate of Acinetobacter baumannii. We have shown that Cbl is involved in controlling the expression of the genes required for uptake and reduction of various sulfur sources in A. baumannii. We have identified the global regulon of Cbl and proposed a model of cysteine biosynthesis and its regulation by Cbl and GigC in A. baumannii.