Instance-Wise Contrastive Graph Neural Network Enables the Discovery of Novel Aedes aegypti Larvicidal Compounds

Abstract Aedes aegypti remains a major arboviral vector, making larval control a critical strategy to reduce mosquito populations. However, resistance to commercial larvicides has reduced the long-term effectiveness of current interventions, reinforcing the need for new compounds with improved potency and selectivity. Here, we present an instance-wise contrastive graph neural network (GNN) framework to accelerate the discovery of novel larvicidal compounds. The model was trained on a curated data set of 556 organic compounds organized into LC50-derived multitask classification thresholds and integrated Transformer-inspired graph learning with whole-molecule and fragment-level contrastive regularization. This model achieved strong held-out performance, with global AUC = 0.95 ± 0.01, PR-AUC = 0.93 ± 0.01, MCC = 0.77 ± 0.03, and G-mean = 0.88 ± 0.02, outperforming conventional machine learning and graph-based baselines. Predictive uncertainty analysis and counterfactual maps further supported the interpretation of threshold-sensitive predictions and substructural contribution patterns. The model was applied to screen 1.3 million compounds, resulting in 10 candidates for experimental validation. Three compounds showed measurable larvicidal activity against A. aegypti larvae. Among them, LC-79 emerged as the most promising hit, with 2-day and 5-day LC50 values of 0.24 μg/mL (0.66 μM) and 0.05 μg/mL (0.13 μM), respectively, an IE50 of 0.06 μg/mL (0.16 μM), and rapid larval mortality (LT50 = 1.10 days at 1 μg/mL). LC-79 also showed no measurable acute toxicity to Daphnia magna at the highest tested concentration [EC50–48h > 43 μg/mL (> 119 μM)], resulting in selectivity indices > 180 and > 860 relative to its 2-day and 5-day LC50 values. Overall, this study demonstrates that contrastive graph learning can move beyond retrospective larvicide modeling to experimentally validated hit discovery, identifying LC-79 as a potent and preliminarily selective acylthiourea larvicide candidate for further mechanism-of-action, resistance, and semifield evaluation.

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Journal
Journal of Chemical Information and Modeling
Published
2026-10-30
DOI
https://doi.org/10.1021/acs.jcim.6c02558
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

Instance-Wise Contrastive Graph Neural Network Enables the Discovery of Novel Aedes aegypti Larvicidal Compounds

Sumbal Saba, Vinícius Alexandre Fiaia Costa, Christian Luz, Gisele Augusto Rodrigues de Oliveira et al.
2 links
Journal of Chemical Information and Modeling
Computational Drug Discovery Methods
article

Instance-Wise Contrastive Graph Neural Network Enables the Discovery of Novel Aedes aegypti Larvicidal Compounds

Sumbal Saba, Vinícius Alexandre Fiaia Costa, Christian Luz, Gisele Augusto Rodrigues de Oliveira, Eugene N. Muratov, Rodolpho C. Braga, Jamal Rafique, Bruna Cassimiro Batista, Bruno Junior Neves, Holli‐Joi Martin, Juscelino Rodrigues, Karine Santana Lúcio da Costa, Carolina da Silva Pereira, Amanda Santana Silva, Luana Bafutto Manchein, Gustavo Henrique Garcia Caldeira
article en

Abstract

Abstract Aedes aegypti remains a major arboviral vector, making larval control a critical strategy to reduce mosquito populations. However, resistance to commercial larvicides has reduced the long-term effectiveness of current interventions, reinforcing the need for new compounds with improved potency and selectivity. Here, we present an instance-wise contrastive graph neural network (GNN) framework to accelerate the discovery of novel larvicidal compounds. The model was trained on a curated data set of 556 organic compounds organized into LC50-derived multitask classification thresholds and integrated Transformer-inspired graph learning with whole-molecule and fragment-level contrastive regularization. This model achieved strong held-out performance, with global AUC = 0.95 ± 0.01, PR-AUC = 0.93 ± 0.01, MCC = 0.77 ± 0.03, and G-mean = 0.88 ± 0.02, outperforming conventional machine learning and graph-based baselines. Predictive uncertainty analysis and counterfactual maps further supported the interpretation of threshold-sensitive predictions and substructural contribution patterns. The model was applied to screen 1.3 million compounds, resulting in 10 candidates for experimental validation. Three compounds showed measurable larvicidal activity against A. aegypti larvae. Among them, LC-79 emerged as the most promising hit, with 2-day and 5-day LC50 values of 0.24 μg/mL (0.66 μM) and 0.05 μg/mL (0.13 μM), respectively, an IE50 of 0.06 μg/mL (0.16 μM), and rapid larval mortality (LT50 = 1.10 days at 1 μg/mL). LC-79 also showed no measurable acute toxicity to Daphnia magna at the highest tested concentration [EC50–48h > 43 μg/mL (> 119 μM)], resulting in selectivity indices > 180 and > 860 relative to its 2-day and 5-day LC50 values. Overall, this study demonstrates that contrastive graph learning can move beyond retrospective larvicide modeling to experimentally validated hit discovery, identifying LC-79 as a potent and preliminarily selective acylthiourea larvicide candidate for further mechanism-of-action, resistance, and semifield evaluation.

Journal of Chemical Information and Modeling
University of North Carolina at Chapel Hill (US), Universidade Federal da Paraíba (BR), Universidade Federal de Goiás (BR)
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Conselho Nacional de Desenvolvimento Científico e Tecnológico, Fundação de Amparo à Pesquisa do Estado de Goiás
Good health and well-being
Openalex Percentile: Top 14%
Computational Drug Discovery Methods
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