Abstract

Background: The venom of bamboo vipers (Trimeresurus stejnegeri - TS), commonly found in Taiwan, contains deadly hemotoxins that cause severe envenomation. Equine-derived antivenom is a specific treatment against snakebites, but its production costs are high and there are some inevitable side effects. The aim of the present work is to help in the development of an affordable and more endurable therapeutic strategy for snakebites. Methods: T. stejnegeri venom proteins were inactivated by glutaraldehyde in order to immunize hens for polyclonal immunoglobulin (IgY) antibodies production. After IgY binding assays, two antibody libraries were constructed expressing single-chain variable fragment (scFv) antibodies joined by the short or long linker for use in phage display antibody technology. Four rounds of biopanning were carried out. The selected scFv antibodies were then further tested for their binding activities and neutralization assays to TS proteins.Results: Purified IgY from egg yolk showed the specific binding ability to TS proteins. The dimensions of these two libraries contain 2.4 × 107 and 6.8 × 107 antibody clones, respectively. An increase in the titers of eluted phage indicated anti-TS clones remarkably enriched after 2nd panning. The analysis based on the nucleotide sequences of selected scFv clones indicated that seven groups of short linkers and four groups of long linkers were identified. The recombinant scFvs showed significant reactivity to TS venom proteins and a cross-reaction to Trimeresurus mucrosquamatus venom proteins. In in vivo studies, the data demonstrated that anti-TS IgY provided 100% protective effects while combined scFvs augmented partial survival time of mice injected with a lethal amount of TS proteins. Conclusion: Chickens were excellent hosts for the production of neutralization antibodies at low cost. Phage display technology is available for generation of monoclonal antibodies against snake venom proteins. These antibodies could be applied in the development of diagnostic kits or as an alternative for snakebite envenomation treatment in the near future.

Highlights

  • The venom of bamboo vipers (Trimeresurus stejnegeri – TS), commonlyKeywords: Trimeresurus stejnegeri immunoglobulin Y (IgY) antibody Phage display technology Single-chain variable fragment antibody found in Taiwan, contains deadly hemotoxins that cause severe envenomation

  • The data demonstrated that anti-TS IgY provided 100% protective effects while combined single-chain variable fragment (scFv) augmented partial survival time of mice injected with a lethal amount of TS proteins

  • Phage display technology is available for generation of monoclonal antibodies against snake venom proteins

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Summary

Introduction

The venom of bamboo vipers (Trimeresurus stejnegeri – TS), commonly. Snakebite is a worldwide medical problem, in tropical or subtropical areas including Taiwan. An estimation of 125,000 deaths are reported due to snakebites every year [1,2,3,4]. It is believed that the number of cases are underestimated because most snakebites occur in remote or rural areas. Asian Trimeresurus snakes are one of the most diverse adaptive groups of venomous pit vipers [5], which include a monophyletic cluster of over 30 species. The members of the Trimeresurus family diversify rapidly in ecology, life-evolution, and individual behavior [6]. Trimeresurus stejnegeri (TS; formerly Trimeresurus gramineus), known as green bamboo vipers, are best recognized for their remarkable similarity in morphology

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