Pharmaceuticals (Apr 2021)

Antimicrobial Peptides as Potential Anti-Tubercular Leads: A Concise Review

  • Gabriel S. Oliveira,
  • Raquel P. Costa,
  • Paula Gomes,
  • Maria Salomé Gomes,
  • Tânia Silva,
  • Cátia Teixeira

DOI
https://doi.org/10.3390/ph14040323
Journal volume & issue
Vol. 14, no. 4
p. 323

Abstract

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Despite being considered a public health emergency for the last 25 years, tuberculosis (TB) is still one of the deadliest infectious diseases, responsible for over a million deaths every year. The length and toxicity of available treatments and the increasing emergence of multidrug-resistant strains of Mycobacterium tuberculosis renders standard regimens increasingly inefficient and emphasizes the urgency to develop new approaches that are not only cost- and time-effective but also less toxic. Antimicrobial peptides (AMP) are small cationic and amphipathic molecules that play a vital role in the host immune system by acting as a first barrier against invading pathogens. The broad spectrum of properties that peptides possess make them one of the best possible alternatives for a new “post-antibiotic” era. In this context, research into AMP as potential anti-tubercular agents has been driven by the increasing danger revolving around the emergence of extremely-resistant strains, the innate resistance that mycobacteria possess and the low compliance of patients towards the toxic anti-TB treatments. In this review, we will focus on AMP from various sources, such as animal, non-animal and synthetic, with reported inhibitory activity towards Mycobacterium tuberculosis.

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