AI Article Synopsis

  • The study investigates the origins of predatory and defensive venoms in cone snails, specifically focusing on the venoms of C. striatus specimens, highlighting their pharmacological significance.
  • Researchers used proteomic and transcriptomic methods to analyze different sections of the venom duct, identifying 370 conotoxin precursors and revealing that defensive venoms contained more inhibitory conotoxins while both types had excitatory κA-conotoxins.
  • The findings suggest that κA-conotoxins may have evolved through adaptive changes, allowing these snails to shift their feeding strategies from ancestral forms to targeting fish effectively.

Article Abstract

The venom duct origins of predatory and defensive venoms has not been studied for hook-and-line fish hunting cone snails despite the pharmacological importance of their venoms. To better understand the biochemistry and evolution of injected predatory and defensive venoms, we compared distal, central and proximal venom duct sections across three specimens of C. striatus (Pionoconus) using proteomic and transcriptomic approaches. A total of 370 conotoxin precursors were identified from the whole venom duct transcriptome. Milked defensive venom was enriched with a potent cocktail of proximally expressed inhibitory α-, ω- and μ-conotoxins compared to milked predatory venom. In contrast, excitatory κA-conotoxins dominated both the predatory and defensive venoms despite their distal expression, suggesting this class of conotoxin can be selectively expressed from the same duct segment in response to either a predatory or defensive stimuli. Given the high abundance of κA-conotoxins in the Pionoconus clade, we hypothesise that the κA-conotoxins have evolved through adaptive evolution following their repurposing from ancestral inhibitory A superfamily conotoxins to facilitate the dietary shift to fish hunting and species radiation in this clade.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8225645PMC
http://dx.doi.org/10.1038/s41598-021-91919-4DOI Listing

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