Abstract

Venoms have evolved over a hundred times in animals. Venom toxins are thought to evolve mostly by recruitment of endogenous proteins with physiological functions. Here we report phylogenetic analyses of venom proteome-annotated venom gland transcriptome data, assisted by genomic analyses, to show that centipede venoms have recruited at least five gene families from bacterial and fungal donors, involving at least eight horizontal gene transfer events. These results establish centipedes as currently the only known animals with venoms used in predation and defence that contain multiple gene families derived from horizontal gene transfer. The results also provide the first evidence for the implication of horizontal gene transfer in the evolutionary origin of venom in an animal lineage. Three of the bacterial gene families encode virulence factors, suggesting that horizontal gene transfer can provide a fast track channel for the evolution of novelty by the exaptation of bacterial weapons into animal venoms.

Highlights

  • Venoms have evolved over a hundred times in animals

  • Horizontal gene transfer (HGT) between kingdoms and domains of life has contributed to the evolution of a diversity of novel adaptive traits in animals, including the ability of bdelloid rotifers to withstand desiccation, the ability of springtails to feed on decaying organic matter, and the ability of plant-parasitic nematodes to degrade plant cell walls[1,2,3,4,5,6,7]

  • We show that multiple HGTs have stocked centipede venom arsenals throughout their evolution

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Summary

Introduction

Venoms have evolved over a hundred times in animals. Venom toxins are thought to evolve mostly by recruitment of endogenous proteins with physiological functions.

Results
Conclusion
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