Deciphering the Molecular Diversity of an Ant Venom Peptidome through a Venomics Approach

peer-reviewed · Journal of Proteome Research · 2018

peer-reviewed · Journal of Proteome Research · 2018. Axel Touchard et al. The peptide toxins in the venoms of small invertebrates such as stinging ants have rarely been studied due to…
Date 2018-10-05
Type peer-reviewed
Venue Journal of Proteome Research
Publisher American Chemical Society (ACS)
Contribution downstream-application
DOI 10.1021/acs.jproteome.8b00452
Citations (OpenAlex) 38
Venue 2-year citedness 3.83

Abstract

The peptide toxins in the venoms of small invertebrates such as stinging ants have rarely been studied due to the limited amount of venom available per individual. We used a venomics strategy to identify the molecular diversity of the venom peptidome for the myrmicine ant Tetramorium bicarinatum. The methodology included (i) peptidomics, in which the venom peptides are sequenced through a de novo mass spectrometry approach or Edman degradation; (ii) transcriptomics, based on RT-PCR-cloning and DNA sequencing; and (iii) the data mining of the RNA-seq in the available transcriptome. Mass spectrometry analysis revealed about 2800 peptides in the venom. However, the de novo sequencing suggested that most of these peptides arose from processing or the artifactual fragmentations of full-length mature peptides. These peptides, called “myrmicitoxins”, are produced by a limited number of genes. Thirty-seven peptide precursors were identified and classified into three superfamilies. These precursors are related to pilosulin, secapin or are new ant venom prepro-peptides. The mature myrmicitoxins display sequence homologies with antimicrobial, cytolytic and neurotoxic peptides. The venomics strategy enabled several post-translational modifications in some peptides such as O-glycosylation to be identified. This study provides novel insights into the molecular diversity and evolution of ant venoms.

Authors

  1. Axel Touchard · AgroParisTech, Biochimie et Toxicologie des Substances Bioactives, Centre National de la Recherche Scientifique, Centre de Coopération Internationale en Recherche Agronomique pour le Développement, Ecologie des Forêts de Guyane, Institut National Universitaire Jean-François Champollion, Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement, Université de Toulouse
  2. Nathan Téné · Biochimie et Toxicologie des Substances Bioactives, Institut National Universitaire Jean-François Champollion, Université de Toulouse
  3. Philippe Chan Tchi Song · Institute for Research and Innovation in Biomedicine
  4. Benjamin Lefranc · Inserm, Normandie Université, Université de Rouen Normandie
  5. Jérôme Leprince · Inserm, Normandie Université, Université de Rouen Normandie
  6. Michel Treilhou · Biochimie et Toxicologie des Substances Bioactives, Institut National Universitaire Jean-François Champollion, Université de Toulouse
  7. Elsa Bonnafé · Biochimie et Toxicologie des Substances Bioactives, Institut National Universitaire Jean-François Champollion, Université de Toulouse

Methods and tools

  • Tetramorium bicarinatum ant venom peptidome: Venomics of the ant Tetramorium bicarinatum in which venom peptides were sequenced by de novo MS (PEAKS) or Edman and combined with transcriptomics to define 37 myrmicitoxin precursors in three superfamilies.

Methods it uses

  • PEAKS: Commercial DP-based de novo

Data deposited

  • Venomics reveals an ant venom peptidome — as deposited · PXD010451

Cited by (3)

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