Abstract
The saw-scaled viper Echis carinatus, one of the “Big Four” causes of snakebites in India,
is found from Sri Lanka to eastern Iraq. To investigate clinical reports regarding the
limited efficacy of Indian polyvalent antivenom (IPAV) against envenomation in Echis
carinatus sochureki (ECS) in northwestern India, we obtained 22 snakes from three locations
in Rajasthan and identified 148–174 toxin isoforms belonging to 21–25 toxin families in their
venom using a bottom-up proteomics approach. All samples showed a high abundance
of snake venom metalloproteinases (SVMPs), particularly SVMP class III. Other major
components were phospholipases A2, L-amino-acid oxidases, snake venom serine proteases
and snaclecs (C-type lectins). Variation in venom composition among locations in Rajasthan,
compared to E. c. carinatus (ECC) from southern India, was primarily due to differences
in the relative abundance of these toxin families. Recognition of all venom components
by IPAV was poor at lower antivenom concentrations. Notably, SVMP classes II and III
were poorly recognized at all venom-to-antivenom ratios in all ECS venoms, and a plasma
clotting assay revealed poor neutralization of procoagulant activity. This collaborative
study highlights the need for the development of regional antivenoms to effectively treat
snakebites in northwestern India.
is found from Sri Lanka to eastern Iraq. To investigate clinical reports regarding the
limited efficacy of Indian polyvalent antivenom (IPAV) against envenomation in Echis
carinatus sochureki (ECS) in northwestern India, we obtained 22 snakes from three locations
in Rajasthan and identified 148–174 toxin isoforms belonging to 21–25 toxin families in their
venom using a bottom-up proteomics approach. All samples showed a high abundance
of snake venom metalloproteinases (SVMPs), particularly SVMP class III. Other major
components were phospholipases A2, L-amino-acid oxidases, snake venom serine proteases
and snaclecs (C-type lectins). Variation in venom composition among locations in Rajasthan,
compared to E. c. carinatus (ECC) from southern India, was primarily due to differences
in the relative abundance of these toxin families. Recognition of all venom components
by IPAV was poor at lower antivenom concentrations. Notably, SVMP classes II and III
were poorly recognized at all venom-to-antivenom ratios in all ECS venoms, and a plasma
clotting assay revealed poor neutralization of procoagulant activity. This collaborative
study highlights the need for the development of regional antivenoms to effectively treat
snakebites in northwestern India.
| Original language | English |
|---|---|
| Article number | 54 |
| Pages (from-to) | 1-18 |
| Number of pages | 18 |
| Journal | Toxins |
| Volume | 18 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 21 Jan 2026 |