4.6 Article

Non-Native Peptides Capable of Pan-Activating the agr Quorum Sensing System across Multiple Specificity Groups of Staphylococcus epidermidis

Journal

ACS CHEMICAL BIOLOGY
Volume 16, Issue 6, Pages 1070-1078

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acschembio.1c00240

Keywords

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Funding

  1. NSF [CHE-1708714, DGE-1747503]
  2. NIH [AI153185, 1S10 OD020022-1]
  3. Merit Award from the Department of Veteran Affairs [I01 BX002711]
  4. UW-Madison NIH Chemistry-Biology Interface Training Program [T32 GM008505]
  5. UW-Madison NIH Biotechnology Training Program [T32 GM008349]

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Staphylococcus epidermidis is resistant to traditional antibiotics due to its ability to form biofilms and its involvement in pathogenesis through the agr quorum sensing system. Existing pan-group activators for the agr system in S. epidermidis have not been discovered, and further research on this topic is necessary.
Staphylococcus epidermidis is a leading cause of hospital-acquired infections. Traditional antibiotics have significantly reduced efficacy against this pathogen due to its ability to form biofilms on abiotic surfaces and drug resistance. The accessory gene regulator (agr) quorum sensing system is directly involved in S. epidermidis pathogenesis. Activation of agr is achieved via binding of the autoinducing peptide (AIP) signal to the extracellular sensor domain of its cognate receptor, AgrC. Divergent evolution has given rise to four agr specificity groups in S. epidermidis defined by the unique AIP sequence used by each group (AIPs-I-IV) with observed cross-group activities. As agr agonism has been shown to reduce biofilm growth in S. epidermidis, the development of pan-group activators of the agr system is of interest as a potential antivirulence strategy. To date, no synthetic compounds have been identified that are capable of appreciably activating the agr system of more than one specificity group of S. epidermidis or, to our knowledge, of any of the other Staphylococci. Here, we report the characterization of the structure-activity relationships for agr agonism by S. epidermidis AIP-II and AIP-III and the application of these new SAR data and those previously reported for AIP-I for the design and synthesis of the first multigroup agr agonists. These non-native peptides were capable of inducing the expression of critical biofilm dispersal agents (i.e., phenol-soluble modulins) in cell culture and represent new tools to study the role of quorum sensing in S. epidermidis infections.

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