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Comparative analysis of viperidae venoms antibacterial profile: a short communication for proteomics. | LitMetric

Comparative analysis of viperidae venoms antibacterial profile: a short communication for proteomics.

Evid Based Complement Alternat Med

Departamento de Biologia Celular e Molecular, Laboratório de Antibióticos, Bioquímica e Modelagem Molecular (LABioMol), Instituto de Biologia, CEG, Universidade Federal Fluminense, CEP 24001-970, Niterói, Brazil.

Published: August 2012

AI Article Synopsis

  • Bacterial infections from drug-resistant strains are a major health issue and a leading cause of death, highlighting the need for new antibacterial agents.
  • Four snake venoms were tested against 10 resistant bacterial strains to explore their antibacterial potential.
  • The study found that the venoms of A. rhodostoma, B. atrox, and B. jararaca show promise as effective sources for developing new antibiotics, with potential for further pharmacological exploration.

Article Abstract

Bacterial infections involving multidrug-resistant strains are one of the ten leading causes of death and an important health problem in need for new antibacterial sources and agents. Herein, we tested and compared four snake venoms (Agkistrodon rhodostoma, Bothrops jararaca, B. atrox and Lachesis muta) against 10 Gram-positive and Gram-negative drug-resistant clinical bacteria strains to identify them as new sources of potential antibacterial molecules. Our data revealed that, as efficient as some antibiotics currently on the market (minimal inhibitory concentration (MIC) = 1-32 μg mL(-1)), A. rhodostoma and B. atrox venoms were active against Staphylococcus epidermidis and Enterococcus faecalis (MIC = 4.5 μg mL(-1)), while B. jararaca inhibited S. aureus growth (MIC = 13 μg ml(-1)). As genomic and proteomic technologies are improving and developing rapidly, our results suggested that A. rhodostoma, B. atrox and B. jararaca venoms and glands are feasible sources for searching antimicrobial prototypes for future design new antibiotics against drug-resistant clinical bacteria. They also point to an additional perspective to fully identify the pharmacological potential of these venoms by using different techniques.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3137867PMC
http://dx.doi.org/10.1093/ecam/nen052DOI Listing

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