Development of an Inhibition Enzyme-Linked Immunosorbent Assay (ELISA) Prototype for Detecting Cytotoxic Three-Finger Toxins (3FTxs) in African Spitting Cobra Venoms

The administration of toxin-specific therapy in snake envenoming is predicated on improved diagnostic techniques capable of detecting specific venom toxins. Various serological tests have been used in detecting snakebite envenoming. Comparatively, enzyme-linked immunosorbent assay (ELISA) has been s...

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Veröffentlicht in:Molecules (Basel, Switzerland) Switzerland), 2022-01, Vol.27 (3), p.888
Hauptverfasser: Manson, Ernest Z, Mutinda, Kyama C, Gikunju, Joseph K, Bocian, Aleksandra, Hus, Konrad K, Petrílla, Vladimír, Legáth, Jaroslav, Kimotho, James H
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Sprache:eng
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Zusammenfassung:The administration of toxin-specific therapy in snake envenoming is predicated on improved diagnostic techniques capable of detecting specific venom toxins. Various serological tests have been used in detecting snakebite envenoming. Comparatively, enzyme-linked immunosorbent assay (ELISA) has been shown to offer a wider practical application. We report an inhibition ELISA for detecting three-finger toxin (3FTx) proteins in venoms of African spitting cobras. The optimized assay detected 3FTxs in (including other sp.) venoms, spiked samples, and venom-challenged mice samples. In venoms of sp., the assay showed inhibition, implying the detection of 3FTxs, but showed little or no inhibition in non- sp. In mice-spiked samples, one-way ANOVA results showed that the observed inhibition was not statistically significant between spiked samples and negative control ( -value = 0.164). Similarly, the observed differences in inhibition between venom-challenged and negative control samples were not statistically significant ( -value = 0.9109). At an LOD of 0.01 µg/mL, the assay was able to confirm the presence of 3FTxs in the samples. Our results show a proof of concept for the use of an inhibition ELISA model as a tool for detecting 3FTxs in the venoms of African spitting cobra snakes.
ISSN:1420-3049
1420-3049
DOI:10.3390/molecules27030888