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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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Autores principales: Manson, Ernest Z., Mutinda, Kyama C., Gikunju, Joseph K., Bocian, Aleksandra, Hus, Konrad K., Petrílla, Vladimír, Legáth, Jaroslav, Kimotho, James H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8838685/
https://www.ncbi.nlm.nih.gov/pubmed/35164152
http://dx.doi.org/10.3390/molecules27030888
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author Manson, Ernest Z.
Mutinda, Kyama C.
Gikunju, Joseph K.
Bocian, Aleksandra
Hus, Konrad K.
Petrílla, Vladimír
Legáth, Jaroslav
Kimotho, James H.
author_facet Manson, Ernest Z.
Mutinda, Kyama C.
Gikunju, Joseph K.
Bocian, Aleksandra
Hus, Konrad K.
Petrílla, Vladimír
Legáth, Jaroslav
Kimotho, James H.
author_sort Manson, Ernest Z.
collection PubMed
description 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 N. ashei (including other Naja sp.) venoms, spiked samples, and venom-challenged mice samples. In venoms of Naja sp., the assay showed inhibition, implying the detection of 3FTxs, but showed little or no inhibition in non-Naja sp. In mice-spiked samples, one-way ANOVA results showed that the observed inhibition was not statistically significant between spiked samples and negative control (p-value = 0.164). Similarly, the observed differences in inhibition between venom-challenged and negative control samples were not statistically significant (p-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.
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spelling pubmed-88386852022-02-13 Development of an Inhibition Enzyme-Linked Immunosorbent Assay (ELISA) Prototype for Detecting Cytotoxic Three-Finger Toxins (3FTxs) in African Spitting Cobra Venoms Manson, Ernest Z. Mutinda, Kyama C. Gikunju, Joseph K. Bocian, Aleksandra Hus, Konrad K. Petrílla, Vladimír Legáth, Jaroslav Kimotho, James H. Molecules Article 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 N. ashei (including other Naja sp.) venoms, spiked samples, and venom-challenged mice samples. In venoms of Naja sp., the assay showed inhibition, implying the detection of 3FTxs, but showed little or no inhibition in non-Naja sp. In mice-spiked samples, one-way ANOVA results showed that the observed inhibition was not statistically significant between spiked samples and negative control (p-value = 0.164). Similarly, the observed differences in inhibition between venom-challenged and negative control samples were not statistically significant (p-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. MDPI 2022-01-28 /pmc/articles/PMC8838685/ /pubmed/35164152 http://dx.doi.org/10.3390/molecules27030888 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Manson, Ernest Z.
Mutinda, Kyama C.
Gikunju, Joseph K.
Bocian, Aleksandra
Hus, Konrad K.
Petrílla, Vladimír
Legáth, Jaroslav
Kimotho, James H.
Development of an Inhibition Enzyme-Linked Immunosorbent Assay (ELISA) Prototype for Detecting Cytotoxic Three-Finger Toxins (3FTxs) in African Spitting Cobra Venoms
title Development of an Inhibition Enzyme-Linked Immunosorbent Assay (ELISA) Prototype for Detecting Cytotoxic Three-Finger Toxins (3FTxs) in African Spitting Cobra Venoms
title_full Development of an Inhibition Enzyme-Linked Immunosorbent Assay (ELISA) Prototype for Detecting Cytotoxic Three-Finger Toxins (3FTxs) in African Spitting Cobra Venoms
title_fullStr Development of an Inhibition Enzyme-Linked Immunosorbent Assay (ELISA) Prototype for Detecting Cytotoxic Three-Finger Toxins (3FTxs) in African Spitting Cobra Venoms
title_full_unstemmed Development of an Inhibition Enzyme-Linked Immunosorbent Assay (ELISA) Prototype for Detecting Cytotoxic Three-Finger Toxins (3FTxs) in African Spitting Cobra Venoms
title_short Development of an Inhibition Enzyme-Linked Immunosorbent Assay (ELISA) Prototype for Detecting Cytotoxic Three-Finger Toxins (3FTxs) in African Spitting Cobra Venoms
title_sort development of an inhibition enzyme-linked immunosorbent assay (elisa) prototype for detecting cytotoxic three-finger toxins (3ftxs) in african spitting cobra venoms
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8838685/
https://www.ncbi.nlm.nih.gov/pubmed/35164152
http://dx.doi.org/10.3390/molecules27030888
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