Abstract

The accessory gene regulator (agr) quorum-sensing system is an important global regulatory system of Staphylococcus aureus and contributes to its pathogenicity. The S. aureus agr system is divided into four agr groups based on the amino acid polymorphisms of AgrB, AgrD, and AgrC. The agr activation is group-specific, resulting in variations in agr activity and pathogenicity among the four agr groups. Strains with divergent agr system always have different phenotypes. In the present report, we, respectively, exchanged the agr system of a certain S. aureus with other three agr alleles and assessed the corresponding phenotypes of these congenic strains. Replacement of the agr system led to significant variations in hemolytic activity, protein expression, and virulence gene expression comparing with that of the parental strain. Interestingly, we found that the biological characteristics of these agr congenic strains in the same strain background were highly similar to each other, and the allele-dependent differences of the agr systems were weakened. These findings indicate that the allele-dependent agr predilections of S. aureus are determined by some factors in addition to the polymorphisms of AgrB, AgrD, and AgrC. Future studies may reveal the novel mechanism to improve our understanding of the agr network.

Highlights

  • The accessory gene regulator quorum-sensing system, a globe transcriptional regulator of Staphylococcus aureus, plays a key role in its pathogenesis and resistance (Bernabè et al, 2021) and has been intensively studied to aid drug and vaccine development (Tan et al, 2018)

  • The agr systems were divided into four agr groups named agrBDC genes of Newman strain (agrI), agrII, agrIII, and agrIV in S. aureus (Wang and Muir, 2016)

  • S. aureus Newman and N315 were selected for agr congenic strains construction to assess the effects of divergent agr alleles

Read more

Summary

Introduction

The accessory gene regulator (agr) quorum-sensing system, a globe transcriptional regulator of Staphylococcus aureus, plays a key role in its pathogenesis and resistance (Bernabè et al, 2021) and has been intensively studied to aid drug and vaccine development (Tan et al, 2018). The agr locus comprises two adjacent transcripts, RNAII and RNAIII, which are controlled by P2 and P3 promoters, respectively (Ji et al, 1995). RNAII is composed of four genes, agrB, agrD, agrC, and agrA (Novick et al, 1995). AgrD encodes the propeptide for an autoinducing peptide (AIP). AgrB encodes an endopeptidase that is the processor of AIP. When agr system is activated, AIP propeptide is processed to an octapeptide by AgrB and secreted to extracellular space (Queck et al, 2008). As AIP reaches a threshold, the membrane-bound histidine kinase AgrC autophosphorylates and becomes activated, which leads to the phosphorylation of its cognate response regulator, AgrA

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call