4.6 Article

Antimicrobial peptides properties beyond growth inhibition and bacterial killing

Journal

PEERJ
Volume 10, Issue -, Pages -

Publisher

PEERJ INC
DOI: 10.7717/peerj.12667

Keywords

Antimicrobial peptide; Virulence; Bioflm; Secretion systems; Toxin-Antitoxin; Adyuvants

Funding

  1. PAPITT, DGAPA, UNAM, Mexico City [IN218419]
  2. CONACYT [CB 2017-2018, A1-S-8530, 424031]
  3. PAPITT UNAM [IN214218]
  4. Catedras-CONACyT program

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Antimicrobial peptides (AMPs) have broad antimicrobial activity and can inhibit microbial growth. In addition to their bactericidal effects, AMPs also have anti-virulence activity against pathogenic bacteria, including those in biofilms. Understanding the mechanisms behind AMPs' anti-virulence properties is important for developing alternative therapeutic strategies to combat antibiotic resistance.
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.

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