Venomics Reveals Venom Complexity of the Piscivorous Cone Snail, Conus tulipa

Mriga Dutt (1) , Sébastien Dutertre (2) , Ai-Hua Jin (1) , Vincent Lavergne (3) , Paul Francis Alewood (1) , Richard James Lewis (1)

1 Institute for Molecular Bioscience
2 IBMM - Institut des Biomolécules Max Mousseron [Pôle Chimie Balard]
3 Centre Léon Bérard [Lyon]

The piscivorous cone snail Conus tulipa has evolved a net-hunting strategy, akin to the deadly Conus geographus, and is considered the second most dangerous cone snail to humans. Here, we present the first venomics study of C. tulipa venom using integrated transcriptomic and proteomic approaches. Parallel transcriptomic analysis of two C. tulipa specimens revealed striking differences in conopeptide expression levels (2.5-fold) between individuals, identifying 522 and 328 conotoxin precursors from 18 known gene superfamilies. Despite broad overlap at the superfamily level, only 86 precursors (11%) were common to both specimens. Conantokins (NMDA antagonists) from the superfamily B1 dominated the transcriptome and proteome of C. tulipa venom, along with superfamilies B2, A, O1, O3, con-ikot-ikot and conopressins, plus novel putative conotoxins precursors T1.3, T6.2, T6.3, T6.4 and T8.1. Thus, C. tulipa venom comprised both paralytic (putative ion channel modulating α-, ω-, μ-, δ-) and non-paralytic (conantokins, con-ikot-ikots, conopressins) conotoxins. This venomic study confirms the potential for non-paralytic conotoxins to contribute to the net-hunting strategy of C. tulipa.

Mots clés: conotoxin; Conus tulipa; intraspecific variation; venomics; transcriptomics; proteomics; conantokins; net hunting strategy; nirvana cabal; ion channel modulators

Domaines: Toxicologie; Génomique, Transcriptomique et Protéomique [q-bio.GN]

Mriga Dutt, Sébastien Dutertre, Ai-Hua Jin, Vincent Lavergne, Paul Francis Alewood, et al.. Venomics Reveals Venom Complexity of the Piscivorous Cone Snail, Conus tulipa. Marine drugs, 2019, 17 (1), pp.71. ⟨10.3390/md17010071⟩. ⟨hal-02307057⟩