Differential regulation of the virulence genes of Listeria monocytogenes by the transcriptional activator PrfA
- 1 June 1996
- journal article
- Published by Wiley in Molecular Microbiology
- Vol. 20 (6) , 1189-1198
- https://doi.org/10.1111/j.1365-2958.1996.tb02639.x
Abstract
The two Listeria monocytogenes strains EGD and NCTC 7973 display a different regulation pattern of their PrfA-dependent genes. All PrfA-dependent genes from L. monocytogenes NCTC 7973 are much more efficiently transcribed in brain-heart infusion medium than those from strain EGD. Transcription of these genes in EGD is, however, induced after shift into Minimal Essential Medium (MEM) to a level that is comparable to that of strain NCTC 7973. Expression of the internalin gene (inIA) is also influenced by PrfA, but only one (P2) out of three mapped promoters is strictly dependent on PrfA. In contrast to the other PrfA-regulated genes, transcription of inIA even from the P2 promoter is reduced in both strains after shift to MEM. The prfA deletion mutant SLCC 53 complemented with multiple copies of prfA synthesizes large amounts of monocistronic prfA transcript, but there is no concomitant increase in the transcripts of the PrfA-dependent genes. However, upon a shift into MEM, transcription of the PrfA-dependent genes (with the exception of the inIA gene) is highly induced even in the absence of de novo protein synthesis. The PrfA proteins of the two studied L. monocytogenes strains differ in their ability to activate PrfA-dependent genes. This difference is probably the result of amino acid exchange(s) in the C-terminal part of these proteins. Strain EGD supplemented with multiple copies of prfA-7973 shows a similar regulation of the PrfA-dependent genes as strain NCTC 7973, whereas multiple copies of prfA-EGD introduced into strain EGD hardly change the rate of transcription of the PrfA-dependent genes. Our data thus suggest that PrfA-mediated gene expression depends not only on the amount of the PrfA protein and the ‘quality’ of the putative PrfA-binding sites, but also on the ‘quality’ of the PrfA protein which seems to be influenced by its amino acid composition and by environmental parameters.Keywords
This publication has 43 references indexed in Scilit:
- Entry of Listeria monocytogenes into hepatocytes requires expression of InIB, a surface protein of the internalin multigene familyMolecular Microbiology, 1995
- Five Listeria monocytogenes genes preferentially expressed in infected mammalian cells: plcA, purH, purD, pyrE and an arginine ABC transporter gene, arpJMolecular Microbiology, 1994
- The virulence regulator protein of Listeria ivanovii is highly homologous to PrfA from Listeria monocytogenes and both belong to the Crp‐Fnr family of transcription regulatorsMolecular Microbiology, 1994
- Dual promoters of the Listeria monocytogenes prfA transcriptional activator appear essential in vitro but are redundant in vivoMolecular Microbiology, 1994
- Transcriptional regulation of prfA and PrfA‐regulated virulence genes in Listeria monocytogenesMolecular Microbiology, 1994
- Surface‐associated, PrfA‐regulated proteins of Listeria monocytogenes synthesized under stress conditionsMolecular Microbiology, 1993
- L. monocytogenes-induced actin assembly requires the actA gene product, a surface proteinCell, 1992
- Entry of L. monocytogenes into cells is mediated by internalin, a repeat protein reminiscent of surface antigens from gram-positive cocciCell, 1991
- Actin filaments and the growth, movement, and spread of the intracellular bacterial parasite, Listeria monocytogenes.The Journal of cell biology, 1989
- Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mpl8 and pUC19 vectorsGene, 1985