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Review
. 2024 Sep 23;206(10):411.
doi: 10.1007/s00203-024-04133-x.

Antimicrobial peptide-based strategies to overcome antimicrobial resistance

Affiliations
Review

Antimicrobial peptide-based strategies to overcome antimicrobial resistance

Meetali Girdhar et al. Arch Microbiol. .

Abstract

Antibiotic resistance has emerged as a global threat, rendering the existing conventional treatment strategies ineffective. In view of this, antimicrobial peptides (AMPs) have proven to be potent alternative therapeutic interventions with a wide range of applications in clinical health. AMPs are small peptides produced naturally as a part of the innate immune responses against a broad range of bacterial, fungal and viral pathogens. AMPs present a myriad of advantages over traditional antibiotics, including their ability to target multiple sites, reduced susceptibility to resistance development, and high efficacy at low doses. These peptides have demonstrated notable potential in inhibiting microbes resistant to traditional antibiotics, including the notorious ESKAPE pathogens, recognized as the primary culprits behind nosocomial infections. AMPs, with their multifaceted benefits, emerge as promising candidates in the ongoing efforts to combat the escalating challenges posed by antibiotic resistance. This in-depth review provides a detailed discussion on AMPs, encompassing their classification, mechanism of action, and diverse clinical applications. Focus has been laid on combating newly emerging drug-resistant organisms, emphasizing the significance of AMPs in mitigating this pressing challenge. The review also illuminates potential future strategies that may be implemented to improve AMP efficacy, such as structural modifications and using AMPs in combination with antibiotics and matrix-inhibiting compounds.

Keywords: Antibiotics; Antimicrobial peptides; Biofilm inhibition; Drug resistance; Mechanism of action; Peptide-therapeutics.

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References

    1. Abi Khattar Z, Rejasse A, Destoumieux-Garzón D, Escoubas JM, Sanchis V, Lereclus D, Givaudan A, Kallassy M, Nielsen-Leroux C, Gaudriault S (2009) The dlt Operon of Bacillus cereus is required for resistance to cationic antimicrobial peptides and for virulence in insects. J Bacteriol 191:7063–7073. https://doi.org/10.1128/JB.00892-09 - DOI - PubMed - PMC
    1. Aggarwal R, Vaduganathan M, Chiu N, Bhatt DL (2021) Potential implications of the FDA approval of semaglutide for overweight and obese adults in the United States. Prog Cardiovasc Dis 68:97–98. https://doi.org/10.1016/j.pcad.2021.09.007 - DOI - PubMed
    1. Ahire JJ, Dicks LMT (2015) Nisin incorporated With 2,3-dihydroxybenzoic acid in nanofibers inhibits biofilm formation by a methicillin-resistant strain of Staphylococcus aureus. Probiotics Antimicrob Proteins 7:52–59. https://doi.org/10.1007/s12602-014-9171-5 - DOI - PubMed
    1. Alaoui Mdarhri H, Benmessaoud R, Yacoubi H, Seffar L, Guennouni Assimi H, Hamam M, Boussettine R, Filali-Ansari N, Lahlou FA, Diawara I, Ennaji MM, Kettani-Halabi M (2022) Alternatives therapeutic approaches to conventional antibiotics: advantages, limitations and potential application in medicine. Antibiot (Basel) 11:1826. https://doi.org/10.3390/antibiotics11121826 - DOI
    1. Arias M, Haney EF, Hilchie AL, Corcoran JA, Hyndman ME, Hancock REW, Vogel HJ (2020) Selective anticancer activity of synthetic peptides derived from the host defence peptide tritrpticin. Biochim Biophys Acta Biomembr 1862:183228. https://doi.org/10.1016/j.bbamem.2020.183228 - DOI - PubMed

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