Antimicrobial peptides properties beyond growth inhibition and bacterial killing

PeerJ. 2022 Jan 21:10:e12667. doi: 10.7717/peerj.12667. eCollection 2022.

Abstract

Antimicrobial peptides (AMPs) are versatile molecules with broad antimicrobial activity produced by representatives of the three domains of life. Also, there are derivatives of AMPs and artificial short peptides that can inhibit microbial growth. Beyond killing microbes, AMPs at grow sub-inhibitory concentrations also exhibit anti-virulence activity against critical pathogenic bacteria, including ESKAPE pathogens. Anti-virulence therapies are an alternative to antibiotics since they do not directly affect viability and growth, and they are considered less likely to generate resistance. Bacterial biofilms significantly increase antibiotic resistance and are linked to establishing chronic infections. Various AMPs can kill biofilm cells and eradicate infections in animal models. However, some can inhibit biofilm formation and promote dispersal at sub-growth inhibitory concentrations. These examples are discussed here, along with those of peptides that inhibit the expression of traits controlled by quorum sensing, such as the production of exoproteases, phenazines, surfactants, toxins, among others. In addition, specific targets that are determinants of virulence include secretion systems (type II, III, and VI) responsible for releasing effector proteins toxic to eukaryotic cells. This review summarizes the current knowledge on the anti-virulence properties of AMPs and the future directions of their research.

Keywords: Adyuvants; Antimicrobial peptide; Bioflm; Secretion systems; Toxin-Antitoxin; Virulence.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Bacterial Agents / pharmacology
  • Antimicrobial Cationic Peptides* / pharmacology
  • Antimicrobial Peptides*
  • Bacteria / metabolism

Substances

  • Antimicrobial Cationic Peptides
  • Antimicrobial Peptides
  • Anti-Bacterial Agents

Grants and funding

Ana María Fernández-Presas is funded by PAPITT, DGAPA, UNAM, Mexico City, grant #IN218419, Rodolfo García-Contreras is funded by CONACYT grant CB 2017-2018 number A1-S-8530 and by PAPITT UNAM grant number IN214218. Israel Castillo Júarez is funded by Cátedras-CONACyT program. Blanca Esther Blancas-Luciano is supported by CONACYT grant # 424031 for her doctoral studies. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.