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Updated: May 24, 2025

Extraction of Venom and Venom Gland Microdissections from Spiders for Proteomic and Transcriptomic Analyses
Published on: November 3, 2014
Transcriptomic and proteomic analyses reveals the diverse venom composition of the spider Neoscona shillongensis
Wenhao Yin1, Yongming You1, Luke R Tembrock2
1Yunnan Provincial Key Laboratory of Entomological Biopharmaceutical Research & Development, College of Pharmacy, Dali University, Dali, Yunnan, 671000, China; National Local Joint Engineering Research Centre for the Development of Medicinal Specialty Insects, Dali University, Dali, Yunnan, 671000, China.
Abstract:
Neoscona shillongensis (Araneidae), also known as the Shillong orb-weaving spider, is a species that constructs a typically shaped round web, is inactive during the daytime and comes out at dusk to forage, primarily preying on flying insects such as mosquitoes, flies, and moths. This spider serves as an important natural enemy of agricultural and forest pests. Neoscona shillongensis primarily uses its web to capture prey, but its venom also plays a crucial role in subduing and processing prey. To date, no research has been conducted on the composition of N. shillongensis venom. In This study, conducted high-throughput sequencing on the venom gland transcriptome and the venom gland extract proteome. A cDNA library of the venom gland tissue of N. shillongensis was constructed, yielding over 62 million reads, which were assembled into 90,481 sequences, predicting 171 toxin-like sequences, including 94 peptide toxins and 77 protein toxins. Furthermore, proteomic analyses of the venom gland extract samples identified 53 peptides and proteins, including 23 peptide toxins and 30 enzymes or proteins such as acetylcholinesterase, hyaluronidase, and astacin-like metalloproteases. The results revealed that the toxin composition of N. shillongensis is diverse and complex. This study provides essential baseline data for further research on the evolution and physiological activity of spider venom, as well as the potential development of pharmaceutical compounds therefrom.

