Proteomics and antivenom immunoprofiling of Russell's viper ( Daboia siamensis ) venoms from Thailand and Indonesia

• Published in: The journal of venomous animals and toxins including tropical diseases Vol. 26; p. e20190048
• Main Authors: Lingam, Thava Malar Changra, Tan, Kae Yi, Tan, Choo Hock
• Format: Journal Article
• Language: English
• Published: Brazil Centro de Estudos de Venenos e Animais Peçonhentos 2020; Centro de Estudos de Venenos e Animais Peçonhentos (CEVAP/UNESP); SciELO
• Subjects: Antivenomics; Eastern Russell's viper; Neutralization; TOXICOLOGY; TROPICAL MEDICINE; Venomics; Venomics; Antivenomics; Eastern Russell's viper; Neutralization
• ISSN: 1678-9199; 1678-9199
• DOI: 10.1590/1678-9199-JVATITD-2019-0048

The Eastern Russell's viper, , is a WHO Category 1 medically important venomous snake. It has a wide but disjunct distribution in Southeast Asia. The specific antivenom, Monovalent Antivenom (DsMAV-Thailand) is produced in Thailand but not available in Indonesia, where a heterologous trivalent antivenom, Serum Anti Bisa Ular (SABU), is used instead. This study aimed to investigate the geographical venom variation of from Thailand (Ds-Thailand) and Indonesia (Ds-Indonesia), and the immunorecognition of the venom proteins by antivenoms. The venom proteins were decomplexed with reverse-phase high-performance liquid chromatography and sodium dodecyl sulfate-polyacrylamide gel electrophoresis, followed by in-solution tryptic digestion, nano-liquid chromatography-tandem mass spectrometry and protein identification. The efficacies of DsMAV-Thailand and SABU in binding the various venom fractions were assessed using an enzyme-linked immunosorbent assay optimized for immunorecognition profiling. The two most abundant protein families in Ds-Thailand venom are phospholipase A (PLA ) and Kunitz-type serine protease inhibitor (KSPI). Those abundant in Ds-Indonesia venom are PLA and serine protease. KSPI and vascular endothelial growth factor were detected in Ds-Thailand venom, whereas L-amino acid oxidase and disintegrin were present in Ds-Indonesia venom. Common proteins shared between the two included snaclecs, serine proteases, metalloproteinases, phosphodiesterases, 5'nucleotidases and nerve growth factors at varying abundances. DsMAV-Thailand exhibited strong immunorecognition of the major protein fractions in both venoms, but low immunoreactivity toward the low molecular weight proteins e.g. KSPI and disintegrins. On the other hand, SABU was virtually ineffective in binding all fractionated venom proteins. venoms from Thailand and Indonesia varied geographically in the protein subtypes and abundances. The venoms, nevertheless, shared conserved antigenicity that allowed effective immunorecognition by DsMAV-Thailand but not by SABU, consistent with the neutralization efficacy of the antivenoms. A specific, appropriate antivenom is needed in Indonesia to treat Russell's viper envenomation.