| Literature DB >> 32679168 |
Parvin Abraham1, Leny Jose2, Tessy Thomas Maliekal3, R Ajay Kumar2, K Santhosh Kumar4.
Abstract
Tuberculosis (TB) is a devastating infectious disease that causes a high rate of mortality. Drugs with new modes of action are needed to overcome this scenario. Cationic antibacterial peptides can serve as a potential alternative to existing TB drugs as they target the entire bacterial membrane for activity, thereby reducing the probability of development of drug resistance. In this study, we report anti-tuberculosis activity of B1CTcu5, a peptide that belongs to brevinin-1 family of antimicrobial peptides. This peptide possesses potent in vitro inhibitory activity against M. tuberculosis at 12.5 μg/mL but was not active against M. smegmatis. B1CTcu5 successfully eliminated intracellular mycobacteria without inducing cytotoxicity to the human macrophages at the concentrations tested. This peptide can be used as a template to design peptide-based anti-tubercular agents.Entities:
Keywords: B1CTcu5; Cationic antibacterial peptides; Macrophage; Mycobacterium tuberculosis
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Year: 2020 PMID: 32679168 DOI: 10.1016/j.peptides.2020.170373
Source DB: PubMed Journal: Peptides ISSN: 0196-9781 Impact factor: 3.750