Abstract
BackgroundA comprehensive evaluation of the -omic profiles of venom is important for understanding the potential function and evolution of snake venom. Here, we conducted an integrated multi-omics-analysis to unveil the venom-transcriptomic and venomic profiles in a same group of spine-bellied sea snakes (Hydrophis curtus) from the South China Sea, where the snake is a widespread species and might generate regionally-specific venom potentially harmful to human activities. The capacity of two heterologous antivenoms to immunocapture the H. curtus venom was determined for an in-depth evaluation of their rationality in treatment of H. curtus envenomation. In addition, a phylogenetic analysis by maximum likelihood was used to detect the adaptive molecular evolution of full-length toxin-coding unigenes.ResultsA total of 90,909,384 pairs of clean reads were generated via Illumina sequencing from a pooled cDNA library of six specimens, and yielding 148,121 unigenes through de novo assembly. Sequence similarity searching harvested 63,845 valid annotations, including 63,789 non-toxin-coding and 56 toxin-coding unigenes belonging to 22 protein families. Three protein families, three-finger toxins (3-FTx), phospholipase A2 (PLA2), and cysteine-rich secretory protein, were detected in the venom proteome. 3-FTx (27.15% in the transcriptome/41.94% in the proteome) and PLA2 (59.71%/49.36%) were identified as the most abundant families in the venom-gland transcriptome and venom proteome. In addition, 24 unigenes from 11 protein families were shown to have experienced positive selection in their evolutionary history, whereas four were relatively conserved throughout evolution. Commercial Naja atra antivenom exhibited a stronger capacity than Bungarus multicinctus antivenom to immunocapture H. curtus venom components, especially short neurotoxins, with the capacity of both antivenoms to immunocapture short neurotoxins being weaker than that for PLA2s.ConclusionsOur study clarified the venom-gland transcriptomic and venomic profiles along with the within-group divergence of a H. curtus population from the South China Sea. Adaptive evolution of most venom components driven by natural selection appeared to occur rapidly during evolutionary history. Notably, the utility of commercial N. atra and B. multicinctus antivenoms against H. curtus toxins was not comprehensive; thus, the development of species-specific antivenom is urgently needed.
Highlights
A comprehensive evaluation of the -omic profiles of venom is important for understanding the potential function and evolution of snake venom
The utility of commercial N. atra and B. multicinctus antivenoms against H. curtus toxins was not comprehensive; the development of species-specific antivenom is urgently needed
Sequencing and de novo assembly A total of 90,909,384 pairs of clean reads were filtered from 93,226,644 pairs of raw reads generated from Illumina sequencing of the venom gland cDNA library of H. curtus, derived from six H. curtus individuals captured as by-catch from the South China Sea, and assembled into 284,495 transcripts (N50/N90 = 1763/ 290) using Trinity
Summary
A comprehensive evaluation of the -omic profiles of venom is important for understanding the potential function and evolution of snake venom. The toxin-coding genes detected in the venom gland of the spine-bellied sea snake (Hydrophis curtus; formerly Lapemis curtus) are not well correlated with the secreted venom proteins [6, 8, 19]. Such a divergence is deduced according to the venom-gland transcriptomic and venom proteomic data on H. curtus specimens from different regions, and still requires in-depth verification using specimens from the same region
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