Transcriptional Regulation of the virR Operon of the Intracellular Pathogen Rhodococcus equi

School of Biomolecular and Biomedical Science and Conway Institute, University College Dublin, Dublin 4, Ireland

^* To whom correspondence should be addressed. Email: wim.meijer{at}ucd.ie.

	Abstract

The virR operon, located on the virulence plasmid of the intracellular pathogen Rhodococcus equi, contains 5 genes, two of which (virR and orf8) encode transcriptional regulators. The first gene of the operon (virR), encoding a LysR type transcriptional regulator, is transcribed at a constitutive low level, whereas the four downstream genes are induced by low pH and high growth temperature. Differential regulation of the virR operon genes could not be explained by differential mRNA stability as there were no major differences in mRNA half-lifes of the transcripts representing each of the five genes within the virR operon. Transcription of virR is driven by the P_virR promoter with a transcription start of 53 bp upstream of the virR initiation codon. The four genes downstream of virR are transcribed from P_virR and from a second promoter P_orf5, located 585 bp downstream of the virR initiation codon. VirR binds to a site overlapping the initiation codon of virR resulting in negative autoregulation of the virR gene, explaining its low constitutive transcription level. The P_orf5 promoter is induced by high temperature and low pH, thus explaining the observed differential gene expression of the virR operon. VirR has a positive effect on P_orf5 activity, whereas the response regulator encoded by orf8 is not involved in regulating transcription of the virR operon. The P_virR promoter is strikingly similar to those recognized by the principal sigma factors of Streptomyces and Mycobacterium, whereas the P_orf5 promoter does not share sequence similarity with P_virR. This suggests that P_orf5 is recognized by an alternative sigma factor.