Abstract

OH-CATH is a novel cathelicidin identified from king cobra. It showed strong antibacterial activity against various bacteria in the presence of 1% NaCl and no haemolytic activity toward human red blood cells even at a high concentration. OH-CATH might serve as model molecules for the development of antimicrobial drugs. Understanding the action mechanism of OH-CATH and the reason for its selectivity against microbes is very important for this purpose. The bactericidal effect of the king cobra antimicrobial peptide OH-CATH on Gram-negative Escherichia coli (ATCC 25922) is observed by scanning electron microscopy (SEM) and transmitted electron microscopy (TEM). The SEM and TEM results suggested that the bactericidal mechanism of OH-CATH against Escherichia coli happened in three steps. Firstly, OH-CATH attached to the negatively charged bacterial wall by positively charged amino acid residues. In the second step, the accumulated OH-CATH aggregated and damaged the bacteria membrane in a pore-forming manner. In the last step, with the damage of cell permeability, the contents of the cells were released and eventually cells died.

Highlights

  • OH-CATH is a novel cathelicidin identified from king cobra

  • The scanning electron microscopy (SEM) and transmitted electron microscopy (TEM) results suggested that the bactericidal mechanism of OH-CATH against Escherichia coli happened in three steps

  • OH-CATH is a new member of cathelicidin antimicrobial peptides characterized from Elapidae king cobra snake

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Summary

Introduction

OH-CATH is a novel cathelicidin identified from king cobra. It showed strong antibacterial activity against various bacteria in the presence of 1% NaCl and no haemolytic activity toward human red blood cells even at a high concentration. OH-CATH, the deduced mature cathelicidin from king cobra, showed strong antibacterial activity against various tested bacteria with minimal inhibitory concentration of 1−20 g/mL in the presence of 1% NaCl. the peptide showed no haemolytic activity toward human red blood cells even at a high dose of 200 g/mL.

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Conclusion

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