Identification of a Staphylococcal AgrB Segment(s) Responsible for Group-Specific Processing of AgrD by Gene Swapping
Open Access
- 15 October 2004
- journal article
- research article
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 186 (20) , 6706-6713
- https://doi.org/10.1128/jb.186.20.6706-6713.2004
Abstract
The four gene products of the accessory gene regulator (agr) P2 operon of Staphylococcus aureus assemble a quorum-sensing system: AgrA and AgrC resemble a two-component signal transduction system, and AgrB and AgrD are required to produce an autoinducing peptide. Upon activation, this quorum-sensing system positively regulates the transcription of the P2 operon as well as the P3 operon, whose transcript, RNAIII, regulates the expression of virulence genes. Four groups of S. aureus have been identified based on the agr sequences and the group-specific interaction between the autoinducing peptide and AgrC. AgrB is a transmembrane protein involved in the processing of AgrD propeptide, and its interaction with AgrD is also group specific. In this study, a series of chimeric AgrBs were constructed by swapping between group I and group II AgrBs, and these mutants were used to analyze the group-specific segment(s) in AgrB that was responsible for AgrD processing. Our results revealed that the first transmembrane α-helix and the extracellular loop 1 of group I AgrB were decisive in the specific processing of group I AgrD. In contrast, two hydrophilic segments of group II AgrB played a crucial role in the group-specific processing of group II AgrD. We also found that several chimeric AgrBs were capable of processing AgrD from both groups, suggesting that all AgrB homologues may utilize the same or a similar mechanism in the processing of AgrDs.Keywords
This publication has 20 references indexed in Scilit:
- Membrane Anchoring of the AgrD N-terminal Amphipathic Region Is Required for Its Processing to Produce a Quorum-sensing Pheromone in Staphylococcus aureusJournal of Biological Chemistry, 2004
- Transmembrane Topology of AgrB, the Protein Involved in the Post-translational Modification of AgrD in Staphylococcus aureusJournal of Biological Chemistry, 2002
- Key Determinants of Receptor Activation in the agr Autoinducing Peptides of Staphylococcus aureusBiochemistry, 2002
- Reversible and Specific Extracellular Antagonism of Receptor-Histidine Kinase SignalingJournal of Biological Chemistry, 2002
- Exfoliatin-Producing Strains Define a Fourth agr Specificity Group in Staphylococcus aureusJournal of Bacteriology, 2000
- Theagr P2 operon: An autocatalytic sensory transduction system inStaphylococcus aureusMolecular Genetics and Genomics, 1995
- [32] Families of cysteine peptidasesPublished by Elsevier ,1994
- Improved method for electroporation ofStaphylococcus aureusFEMS Microbiology Letters, 1992
- Improved method for electroporation of Staphylococcus aureusFEMS Microbiology Letters, 1992
- [27] Genetic systems in StaphylococciPublished by Elsevier ,1991