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Author Spotlight: Optimizing Scorpion Venom Extraction for Antivenom Production
Published on: October 6, 2023
Cross-reactivity and inhibition myotoxic effects induced by Bothrops snake venoms using specific polyclonal
Lamartine L Melo1, Mirian M Mendes2, Lívia M Alves3
1Instituto de Biologia, Universidade Federal de Uberlândia, Av. Pará, 1720, Campus Umuarama, Bloco 2D, Uberlândia, MG, 38400-902, Brazil; Instituto de Genética e Bioquímica, Universidade Federal de Uberlândia, Av. Pará, 1720, Campus Umuarama, Bloco 2E, Uberlândia, MG, 38400-902, Brazil.
Abstract:
Polyclonal antibodies raised in Balb-c mice against BnSP-7, a Lys-49 phospholipase A2, were used to measure cross reactivity against other snake venoms. Using ELISA, these antibodies were able to recognize PLA2s isoforms present in venoms of botropic snakes at 1:6400, 1:3200 and 1:100 ratios (w/w). These antibodies highly recognized proteins of low molecular weight (∼14,000) from crude snake venom Bp and Bm by Western Blotting. PLA2 these venoms, by alignment of primary structures demonstrated high identity with BnSP-7 PLA2, especially in the C-terminal region. However, the crude snake venom Bd and Bj, showed low recognition. The PLA2 activity of Bothrops pauloensis, Bothrops moojeni venoms or BpPLA2-TXI was inhibited significantly when anti-BnSP-7 antibodies were incubated at 1:10 and 1:20 ratios (venoms or toxin:anti-BnSP-7, w/w), respectively. The myotoxic effect induced by the same venoms was also reduced significantly at 1:1, 1:10 and 1:20 ratios, by decreased creatine kinase levels. The anti-PLA2 polyclonal antibodies effectively recognized PLA2s from Bothrops pauloensis and Bothrops moojeni venoms, and neutralized specific catalytic and myotoxic activity.
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