4.4 Article

An integrative view of the toxic potential of Conophis lineatus (Dipsadidae: Xenodontinae), a medically relevant rear-fanged snake

期刊

TOXICON
卷 205, 期 -, 页码 38-52

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.toxicon.2021.11.009

关键词

Road guarder; Duvernoy 's venom gland; RNA-Seq; Venomics; Venom characterization; Envenomation

资金

  1. National Science Foundation [DEB 1822417, DEB 1638902]
  2. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [2016/50127-5, 2018/26520-4]
  3. Consejo Nacional de Ciencia y Tecnologia (CONACYT) [247437]
  4. Clemson University
  5. [NSF DBI-1701713]
  6. [NSF DBI-1701714]

向作者/读者索取更多资源

Traditional research has focused on front-fanged snake families, but venom is now recognized as a widespread trait among snakes. Despite historical neglect, an analysis of a particular species' venom gland transcriptome revealed new insights, including atypical venom components. This study provides a comprehensive venom characterization of a medically important snake species, shedding light on the effects and evolution of its venom.
Most traditional research on snake venoms has focused on front-fanged snake families (Viperidae, Elapidae, and Atractaspididae). However, venom is now generally accepted as being a much more broadly possessed trait within snakes, including species traditionally considered harmless. Unfortunately, due to historical inertia and methodological challenges, the toxin repertoires of non-front-fanged snake families (e.g., Colubridae, Dipsadidae, and Natricidae) have been heavily neglected despite the knowledge of numerous species capable of inflicting medically relevant envenomations. Integrating proteomic data for validation, we perform a de novo assembly and analysis of the Duvernoy's venom gland transcriptome of the Central American Road Guarder (Dipsadidae: Xenodontinae: Conophis lineatus), a species known for its potent bite. We identified 28 putative toxin transcripts from 13 toxin families in the Duvernoy's venom gland transcriptome, comprising 63.7% of total transcriptome expression. In addition to ubiquitous snake toxin families, we proteomically confirmed several atypical venom components. The most highly expressed toxins (55.6% of total toxin expression) were recently described snake venom matrix metalloproteases (svMMPs), with 48.0% of svMMP expression contributable to a novel svMMP isoform. We investigate the evolution of the new svMMP isoform in the context of rear-fanged snakes using phylogenetics. Finally, we examine the morphology of the venom apparatus using mu CT and explore how the venom relates to autecology and the highly hemorrhagic effects seen in human envenomations. Importantly, we provide the most complete venom characterization of this medically relevant snake species to date, producing insights into the effects and evolution of its venom, and point to future research directions to better understand the venoms of 'harmless' non-front-fanged snakes.

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