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Snake Cathelicidin from Bungarus fasciatus Is a Potent Peptide Antibiotics
BACKGROUND: Cathelicidins are a family of antimicrobial peptides acting as multifunctional effector molecules of innate immunity, which are firstly found in mammalians. Recently, several cathelicidins have also been found from chickens and fishes. No cathelicidins from other non-mammalian vertebrate...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2528936/ https://www.ncbi.nlm.nih.gov/pubmed/18795096 http://dx.doi.org/10.1371/journal.pone.0003217 |
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author | Wang, Yipeng Hong, Jing Liu, Xiuhong Yang, Hailong Liu, Rui Wu, Jing Wang, Aili Lin, Donghai Lai, Ren |
author_facet | Wang, Yipeng Hong, Jing Liu, Xiuhong Yang, Hailong Liu, Rui Wu, Jing Wang, Aili Lin, Donghai Lai, Ren |
author_sort | Wang, Yipeng |
collection | PubMed |
description | BACKGROUND: Cathelicidins are a family of antimicrobial peptides acting as multifunctional effector molecules of innate immunity, which are firstly found in mammalians. Recently, several cathelicidins have also been found from chickens and fishes. No cathelicidins from other non-mammalian vertebrates have been reported. PRINCIPAL FINDINGS: In this work, a cathelicidin-like antimicrobial peptide named cathelicidin-BF has been purified from the snake venoms of Bungarus fasciatus and its cDNA sequence was cloned from the cDNA library, which confirm the presence of cathelicidin in reptiles. As other cathelicidins, the precursor of cathelicidin-BF has cathelin-like domain at the N terminus and carry the mature cathelicidin-BF at the C terminus, but it has an atypical acidic fragment insertion between the cathelin-like domain and the C-terminus. The acidic fragment is similar to acidic domains of amphibian antimicrobial precursors. Phylogenetic analysis revealed that the snake cathelicidin had the nearest evolution relationship with platypus cathelicidin. The secondary structure of cathelicidin-BF investigated by CD and NMR spectroscopy in the presence of the helicogenic solvent TFE is an amphipathic α-helical conformation as many other cathelicidins. The antimicrobial activities of cathelicidin BF against forty strains of microorganisms were tested. Cathelicidin-BF efficiently killed bacteria and some fungal species including clinically isolated drug-resistance microorganisms. It was especially active against Gram-negative bacteria. Furthermore, it could exert antimicrobial activity against some saprophytic fungus. No hemolytic and cytotoxic activity was observed at the dose of up to 400 µg/ml. Cathelicidin-BF could exist stably in the mice plasma for at least 2.5 hours. CONCLUSION: Discovery of snake cathelicidin with atypical structural and functional characterization offers new insights on the evolution of cathelicidins. Potent, broad spectrum, salt-independent antimicrobial activities make cathelicidin-BF an excellent candidate for clinical or agricultural antibiotics. |
format | Text |
id | pubmed-2528936 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-25289362008-09-16 Snake Cathelicidin from Bungarus fasciatus Is a Potent Peptide Antibiotics Wang, Yipeng Hong, Jing Liu, Xiuhong Yang, Hailong Liu, Rui Wu, Jing Wang, Aili Lin, Donghai Lai, Ren PLoS One Research Article BACKGROUND: Cathelicidins are a family of antimicrobial peptides acting as multifunctional effector molecules of innate immunity, which are firstly found in mammalians. Recently, several cathelicidins have also been found from chickens and fishes. No cathelicidins from other non-mammalian vertebrates have been reported. PRINCIPAL FINDINGS: In this work, a cathelicidin-like antimicrobial peptide named cathelicidin-BF has been purified from the snake venoms of Bungarus fasciatus and its cDNA sequence was cloned from the cDNA library, which confirm the presence of cathelicidin in reptiles. As other cathelicidins, the precursor of cathelicidin-BF has cathelin-like domain at the N terminus and carry the mature cathelicidin-BF at the C terminus, but it has an atypical acidic fragment insertion between the cathelin-like domain and the C-terminus. The acidic fragment is similar to acidic domains of amphibian antimicrobial precursors. Phylogenetic analysis revealed that the snake cathelicidin had the nearest evolution relationship with platypus cathelicidin. The secondary structure of cathelicidin-BF investigated by CD and NMR spectroscopy in the presence of the helicogenic solvent TFE is an amphipathic α-helical conformation as many other cathelicidins. The antimicrobial activities of cathelicidin BF against forty strains of microorganisms were tested. Cathelicidin-BF efficiently killed bacteria and some fungal species including clinically isolated drug-resistance microorganisms. It was especially active against Gram-negative bacteria. Furthermore, it could exert antimicrobial activity against some saprophytic fungus. No hemolytic and cytotoxic activity was observed at the dose of up to 400 µg/ml. Cathelicidin-BF could exist stably in the mice plasma for at least 2.5 hours. CONCLUSION: Discovery of snake cathelicidin with atypical structural and functional characterization offers new insights on the evolution of cathelicidins. Potent, broad spectrum, salt-independent antimicrobial activities make cathelicidin-BF an excellent candidate for clinical or agricultural antibiotics. Public Library of Science 2008-09-16 /pmc/articles/PMC2528936/ /pubmed/18795096 http://dx.doi.org/10.1371/journal.pone.0003217 Text en Wang et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Wang, Yipeng Hong, Jing Liu, Xiuhong Yang, Hailong Liu, Rui Wu, Jing Wang, Aili Lin, Donghai Lai, Ren Snake Cathelicidin from Bungarus fasciatus Is a Potent Peptide Antibiotics |
title | Snake Cathelicidin from Bungarus fasciatus Is a Potent Peptide Antibiotics |
title_full | Snake Cathelicidin from Bungarus fasciatus Is a Potent Peptide Antibiotics |
title_fullStr | Snake Cathelicidin from Bungarus fasciatus Is a Potent Peptide Antibiotics |
title_full_unstemmed | Snake Cathelicidin from Bungarus fasciatus Is a Potent Peptide Antibiotics |
title_short | Snake Cathelicidin from Bungarus fasciatus Is a Potent Peptide Antibiotics |
title_sort | snake cathelicidin from bungarus fasciatus is a potent peptide antibiotics |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2528936/ https://www.ncbi.nlm.nih.gov/pubmed/18795096 http://dx.doi.org/10.1371/journal.pone.0003217 |
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