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Pseudonajide Peptide Derived from Snake Venom Alters Cell Envelope Integrity Interfering on Biofilm Formation in Staphylococcus Epidermidis

Overview
Journal BMC Microbiol
Publisher Biomed Central
Specialty Microbiology
Date 2020 Aug 5
PMID 32746783
Citations 4
Authors
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Abstract

Background: The increase in bacterial resistance phenotype cases is a global health problem. New strategies must be explored by the scientific community in order to create new treatment alternatives. Animal venoms are a good source for antimicrobial peptides (AMPs), which are excellent candidates for new antimicrobial drug development. Cathelicidin-related antimicrobial peptides (CRAMPs) from snake venoms have been studied as a model for the design of new antimicrobial pharmaceuticals against bacterial infections.

Results: In this study we present an 11 amino acid-long peptide, named pseudonajide, which is derived from a Pseudonaja textilis venom peptide and has antimicrobial and antibiofilm activity against Staphylococcus epidermidis. Pseudonajide was selected based on the sequence alignments of various snake venom peptides that displayed activity against bacteria. Antibiofilm activity assays with pseudonajide concentrations ranging from 3.12 to 100 μM showed that the lowest concentration to inhibit biofilm formation was 25 μM. Microscopy analysis demonstrated that pseudonajide interacts with the bacterial cell envelope, disrupting the cell walls and membranes, leading to morphological defects in prokaryotes.

Conclusions: Our results suggest that pseudonajide's positives charges interact with negatively charged cell wall components of S. epidermidis, leading to cell damage and inhibiting biofilm formation.

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References
1.
Wang A, Athan E, Pappas P, Fowler Jr V, Olaison L, Pare C . Contemporary clinical profile and outcome of prosthetic valve endocarditis. JAMA. 2007; 297(12):1354-61. DOI: 10.1001/jama.297.12.1354. View

2.
Rupp M, Fey P, Heilmann C, Gotz F . Characterization of the importance of Staphylococcus epidermidis autolysin and polysaccharide intercellular adhesin in the pathogenesis of intravascular catheter-associated infection in a rat model. J Infect Dis. 2001; 183(7):1038-42. DOI: 10.1086/319279. View

3.
Kirchhoff C, Cypionka H . Propidium ion enters viable cells with high membrane potential during live-dead staining. J Microbiol Methods. 2017; 142:79-82. DOI: 10.1016/j.mimet.2017.09.011. View

4.
Donlan R . Biofilms: microbial life on surfaces. Emerg Infect Dis. 2002; 8(9):881-90. PMC: 2732559. DOI: 10.3201/eid0809.020063. View

5.
Casewell N, Wuster W, Vonk F, Harrison R, Fry B . Complex cocktails: the evolutionary novelty of venoms. Trends Ecol Evol. 2012; 28(4):219-29. DOI: 10.1016/j.tree.2012.10.020. View