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BotCl, the First Chlorotoxin-like Peptide Inhibiting Newcastle Disease Virus: The Emergence of a New Scorpion Venom AMPs Family
Newcastle disease virus (NDV) is one of the most serious contagions affecting domestic poultry and other avian species. It causes high morbidity and mortality, resulting in huge economic losses to the poultry industry worldwide. Despite vaccination, NDV outbreaks increase the need for alternative pr...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10254560/ https://www.ncbi.nlm.nih.gov/pubmed/37298831 http://dx.doi.org/10.3390/molecules28114355 |
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author | Jlassi, Abir Mekni-Toujani, Marwa Ferchichi, Asma Gharsallah, Charfeddine Malosse, Christian Chamot-Rooke, Julia ElAyeb, Mohamed Ghram, Abdeljelil Srairi-Abid, Najet Daoud, Salma |
author_facet | Jlassi, Abir Mekni-Toujani, Marwa Ferchichi, Asma Gharsallah, Charfeddine Malosse, Christian Chamot-Rooke, Julia ElAyeb, Mohamed Ghram, Abdeljelil Srairi-Abid, Najet Daoud, Salma |
author_sort | Jlassi, Abir |
collection | PubMed |
description | Newcastle disease virus (NDV) is one of the most serious contagions affecting domestic poultry and other avian species. It causes high morbidity and mortality, resulting in huge economic losses to the poultry industry worldwide. Despite vaccination, NDV outbreaks increase the need for alternative prevention and control means. In this study, we have screened fractions of Buthus occitanus tunetanus (Bot) scorpion venom and isolated the first scorpion peptide inhibiting the NDV multiplication. It showed a dose dependent effect on NDV growth in vitro, with an IC(50) of 0.69 µM, and a low cytotoxicity on cultured Vero cells (CC50 > 55 µM). Furthermore, tests carried out in specific pathogen-free embryonated chicken eggs demonstrated that the isolated peptide has a protective effect on chicken embryos against NDV, and reduced by 73% the virus titer in allantoic fluid. The N-terminal sequence, as well as the number of cysteine residues of the isolated peptide, showed that it belongs to the scorpion venom Chlorotoxin-like peptides family, which led us to designate it “BotCl”. Interestingly, at 10 µg/mL, BotCl showed an inhibiting effect three times higher than its analogue AaCtx, from Androctonus australis (Aa) scorpion venom, on NDV development. Altogether, our results highlight the chlorotoxin-like peptides as a new scorpion venom AMPs family. |
format | Online Article Text |
id | pubmed-10254560 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-102545602023-06-10 BotCl, the First Chlorotoxin-like Peptide Inhibiting Newcastle Disease Virus: The Emergence of a New Scorpion Venom AMPs Family Jlassi, Abir Mekni-Toujani, Marwa Ferchichi, Asma Gharsallah, Charfeddine Malosse, Christian Chamot-Rooke, Julia ElAyeb, Mohamed Ghram, Abdeljelil Srairi-Abid, Najet Daoud, Salma Molecules Article Newcastle disease virus (NDV) is one of the most serious contagions affecting domestic poultry and other avian species. It causes high morbidity and mortality, resulting in huge economic losses to the poultry industry worldwide. Despite vaccination, NDV outbreaks increase the need for alternative prevention and control means. In this study, we have screened fractions of Buthus occitanus tunetanus (Bot) scorpion venom and isolated the first scorpion peptide inhibiting the NDV multiplication. It showed a dose dependent effect on NDV growth in vitro, with an IC(50) of 0.69 µM, and a low cytotoxicity on cultured Vero cells (CC50 > 55 µM). Furthermore, tests carried out in specific pathogen-free embryonated chicken eggs demonstrated that the isolated peptide has a protective effect on chicken embryos against NDV, and reduced by 73% the virus titer in allantoic fluid. The N-terminal sequence, as well as the number of cysteine residues of the isolated peptide, showed that it belongs to the scorpion venom Chlorotoxin-like peptides family, which led us to designate it “BotCl”. Interestingly, at 10 µg/mL, BotCl showed an inhibiting effect three times higher than its analogue AaCtx, from Androctonus australis (Aa) scorpion venom, on NDV development. Altogether, our results highlight the chlorotoxin-like peptides as a new scorpion venom AMPs family. MDPI 2023-05-26 /pmc/articles/PMC10254560/ /pubmed/37298831 http://dx.doi.org/10.3390/molecules28114355 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Jlassi, Abir Mekni-Toujani, Marwa Ferchichi, Asma Gharsallah, Charfeddine Malosse, Christian Chamot-Rooke, Julia ElAyeb, Mohamed Ghram, Abdeljelil Srairi-Abid, Najet Daoud, Salma BotCl, the First Chlorotoxin-like Peptide Inhibiting Newcastle Disease Virus: The Emergence of a New Scorpion Venom AMPs Family |
title | BotCl, the First Chlorotoxin-like Peptide Inhibiting Newcastle Disease Virus: The Emergence of a New Scorpion Venom AMPs Family |
title_full | BotCl, the First Chlorotoxin-like Peptide Inhibiting Newcastle Disease Virus: The Emergence of a New Scorpion Venom AMPs Family |
title_fullStr | BotCl, the First Chlorotoxin-like Peptide Inhibiting Newcastle Disease Virus: The Emergence of a New Scorpion Venom AMPs Family |
title_full_unstemmed | BotCl, the First Chlorotoxin-like Peptide Inhibiting Newcastle Disease Virus: The Emergence of a New Scorpion Venom AMPs Family |
title_short | BotCl, the First Chlorotoxin-like Peptide Inhibiting Newcastle Disease Virus: The Emergence of a New Scorpion Venom AMPs Family |
title_sort | botcl, the first chlorotoxin-like peptide inhibiting newcastle disease virus: the emergence of a new scorpion venom amps family |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10254560/ https://www.ncbi.nlm.nih.gov/pubmed/37298831 http://dx.doi.org/10.3390/molecules28114355 |
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