Venomics of the asp viper Vipera aspis aspis from France.


Journal

Journal of proteomics
ISSN: 1876-7737
Titre abrégé: J Proteomics
Pays: Netherlands
ID NLM: 101475056

Informations de publication

Date de publication:
30 04 2020
Historique:
received: 20 12 2019
revised: 13 02 2020
accepted: 18 02 2020
pubmed: 23 2 2020
medline: 22 6 2021
entrez: 23 2 2020
Statut: ppublish

Résumé

The asp viper Vipera aspis aspis is a venomous snake found in France, and despite its medical importance, the complete toxin repertoire produced is unknown. Here, we used a venomics approach to decipher the composition of its venom. Transcriptomic analysis revealed 80 venom-annotated sequences grouped into 16 gene families. Among the most represented toxins were snake venom metalloproteases (23%), phospholipases A2 (15%), serine proteases (13%), snake venom metalloprotease inhibitors (13%) and C-type lectins (12%). LC-MS of venoms revealed similar profiles regardless of the method of extraction (milking vs defensive bite). Proteomic analysis validated 57 venom-annotated transcriptomic sequences (>70%), including one for each of the 16 families, but also identified 7 sequences not initially annotated as venom proteins, including a serine protease, a disintegrin, a glutaminyl-peptide cyclotransferase, a proactivator polypeptide-like and 3 aminopeptidases. Interestingly, phospholipases A2 were the dominant proteins in the venom, among which included an ammodytoxin B-like sequence, which may explain the reported neurotoxicity following some asp viper envenomations. In total, 87 sequences were retrieved from the Vipera aspis aspis transcriptome and proteome, constituting a valuable resource that will help in understanding the toxinological basis of clinical signs of envenoming and for the mining of useful pharmacological compounds. BIOLOGICAL SIGNIFICANCE: The asp viper (Vipera aspis aspis) causes several hundred envenomations annually in France, including unusual cases with neurological signs, resulting in one death per year on average. Here, we performed a proteotranscriptomic analysis of V. a. aspis venom in order to provide a better understanding of its venom composition. We found that, as in other Vipera species, phospholipase A2 dominates in the venom, and the presence of a sequence related to ammodytoxin B may explain the reported neurotoxicity following some asp viper envenomations. Thus, this study will help in informing the toxinological basis of clinical signs of envenoming.

Identifiants

pubmed: 32087377
pii: S1874-3919(20)30075-0
doi: 10.1016/j.jprot.2020.103707
pii:
doi:

Substances chimiques

Viper Venoms 0
Phospholipases A2 EC 3.1.1.4
Metalloproteases EC 3.4.-

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

103707

Subventions

Organisme : Wellcome Trust
ID : 200517/Z/16/Z
Pays : United Kingdom

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Auteurs

Julien Giribaldi (J)

Institut des Biomolécules Max Mousseron, UMR 5247, Univ Montpellier, CNRS, Place Eugène Bataillon, 34095 Montpellier CEDEX 5, France.

Taline Kazandjian (T)

Centre for Snakebite Research and Interventions, Liverpool School of Tropical Medicine, Pembroke Place, Liverpool L3 5QA, UK.

Fernanda G Amorim (FG)

Laboratory of Mass Spectrometry, MolSys Research Unit, University of Liège, Liège, Belgium.

Gareth Whiteley (G)

Centre for Snakebite Research and Interventions, Liverpool School of Tropical Medicine, Pembroke Place, Liverpool L3 5QA, UK.

Simon C Wagstaff (SC)

Bioinformatics Unit, Liverpool School of Tropical Medicine, Pembroke Place, Liverpool L3 5QA, UK.

Guillaume Cazals (G)

Institut des Biomolécules Max Mousseron, UMR 5247, Univ Montpellier, CNRS, Place Eugène Bataillon, 34095 Montpellier CEDEX 5, France.

Christine Enjalbal (C)

Institut des Biomolécules Max Mousseron, UMR 5247, Univ Montpellier, CNRS, Place Eugène Bataillon, 34095 Montpellier CEDEX 5, France.

Loïc Quinton (L)

Laboratory of Mass Spectrometry, MolSys Research Unit, University of Liège, Liège, Belgium.

Nicholas R Casewell (NR)

Centre for Snakebite Research and Interventions, Liverpool School of Tropical Medicine, Pembroke Place, Liverpool L3 5QA, UK.

Sebastien Dutertre (S)

Institut des Biomolécules Max Mousseron, UMR 5247, Univ Montpellier, CNRS, Place Eugène Bataillon, 34095 Montpellier CEDEX 5, France. Electronic address: sebastien.dutertre@umontpellier.fr.

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Classifications MeSH