Rapid, label-free surface plasmon resonance discrimination between Bothrops and Crotalus venoms using clinical antivenom as the capture reagent

Snake envenoming is recognized as a global health problem, affecting thousands of people every year. One of the main challenges in addressing this issue is the correct identification and treatment of these envenomations, particularly in locations where people do not have easy access to hospitals. In Brazil, the genus Bothrops is responsible for the majority of envenomations, followed by Crotalus. This study reports a simple methodology for detecting crude venom from snakes of the genus Bothrops, through interaction with their corresponding antibodies, using a high-sensitivity optical biosensor. The protocol consists of adding antibodies (present in the commercial antivenom) to the sensor surface, followed by the addition of Crotalus venom (nonspecific), and then Bothrops venom (specific), resulting in changes in the refractive index, to evaluate cross reactions between them. Different concentrations of raw venom from snakes of the genus Bothrops and Crotalus were tested, starting with a concentration of 6.784 [Formula: see text]gmL-1 and progressing until reaching the minimum detectable concentration. The binding capacity of venom to antivenom was investigated at two concentrations of antivenom: 5 [Formula: see text]gmL-1 and 50 [Formula: see text]gmL-1. Both antivenom and snake venoms were solubilized in phosphate-buffered saline (PBS). The results show an accurate detection of the antigen of interest (Bothrops venom), tested at different concentrations. The biosensor was able to detect venom up to a concentration of 0.848 [Formula: see text]gmL-1. In addition, no interference from nonspecific binding between the Bothrops antivenom and Crotalus venom was detected. The detection of specific venom (Bothrops) occurred in a satisfactory time (up to 14 minutes). The results provide evidence that the biosensor and the methodology employed can be considered a diagnostic model under development, which can help health workers to better identify and treat envenomated people.

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Publication Details

Journal
PLoS neglected tropical diseases
Published
2026-01-06
DOI
https://doi.org/10.1371/journal.pntd.0013501
Primary Topic
Venomous Animal Envenomation and Studies
Type
article
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article

Rapid, label-free surface plasmon resonance discrimination between Bothrops and Crotalus venoms using clinical antivenom as the capture reagent

J. S. Vasconcelos, K Soledad Encalada Luna, Arthur Melo, Antonio M. N. Lima et al.
PLoS neglected tropical diseases
Venomous Animal Envenomation and Studies
article

Rapid, label-free surface plasmon resonance discrimination between Bothrops and Crotalus venoms using clinical antivenom as the capture reagent

J. S. Vasconcelos, K Soledad Encalada Luna, Arthur Melo, Antonio M. N. Lima, Ely S. F. Borges, Fernanda C. C. L. Loureiro
article en

Abstract

Snake envenoming is recognized as a global health problem, affecting thousands of people every year. One of the main challenges in addressing this issue is the correct identification and treatment of these envenomations, particularly in locations where people do not have easy access to hospitals. In Brazil, the genus Bothrops is responsible for the majority of envenomations, followed by Crotalus. This study reports a simple methodology for detecting crude venom from snakes of the genus Bothrops, through interaction with their corresponding antibodies, using a high-sensitivity optical biosensor. The protocol consists of adding antibodies (present in the commercial antivenom) to the sensor surface, followed by the addition of Crotalus venom (nonspecific), and then Bothrops venom (specific), resulting in changes in the refractive index, to evaluate cross reactions between them. Different concentrations of raw venom from snakes of the genus Bothrops and Crotalus were tested, starting with a concentration of 6.784 [Formula: see text]gmL-1 and progressing until reaching the minimum detectable concentration. The binding capacity of venom to antivenom was investigated at two concentrations of antivenom: 5 [Formula: see text]gmL-1 and 50 [Formula: see text]gmL-1. Both antivenom and snake venoms were solubilized in phosphate-buffered saline (PBS). The results show an accurate detection of the antigen of interest (Bothrops venom), tested at different concentrations. The biosensor was able to detect venom up to a concentration of 0.848 [Formula: see text]gmL-1. In addition, no interference from nonspecific binding between the Bothrops antivenom and Crotalus venom was detected. The detection of specific venom (Bothrops) occurred in a satisfactory time (up to 14 minutes). The results provide evidence that the biosensor and the methodology employed can be considered a diagnostic model under development, which can help health workers to better identify and treat envenomated people.

PLoS neglected tropical diseasesVol. 20(1)
Universidade Estadual da Paraíba (BR), Universidade Federal da Paraíba (BR), Universidade Federal do Rio Grande do Norte (BR), Universidade Federal de Campina Grande (BR), Instituto Federal do Maranhão (BR), Universidade Federal do Maranhão (BR)
Reduced inequalities, Peace, Justice and strong institutions
Openalex Percentile: Top 96%
Venomous Animal Envenomation and Studies
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