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A single mutation in the GSTe2 gene allows tracking of metabolically based insecticide resistance in a major malaria vector

Jacob M Riveron1, Cristina Yunta12, Sulaiman S Ibrahim1, Rousseau Djouaka3, Helen Irving1, Benjamin D Menze14, Hanafy M Ismail1, Janet Hemingway1, Hilary Ranson1, Armando Albert2 and Charles S Wondji1*

Author Affiliations

1 Vector Biology Department, Liverpool School of Tropical Medicine, Pembroke Place, Liverpool L3 5QA, United Kingdom

2 Departamento de Cristalografía y Biología Estructural, Instituto de Química-Física “Rocasolano”, CSIC, C/Serrano 119 Madrid E-28006, Spain

3 International Institute of Tropical Agriculture, 08 BP 0932 Cotonou, Benin

4 Organisation de Coordination pour la lutte contre les Endémies en Afrique Centrale, PO Box 288, Yaoundé, Cameroon

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Genome Biology 2014, 15:R27  doi:10.1186/gb-2014-15-2-r27

Published: 25 February 2014

Abstract

Background

Metabolic resistance to insecticides is the biggest threat to the continued effectiveness of malaria vector control. However, its underlying molecular basis, crucial for successful resistance management, remains poorly characterized.

Results

Here, we demonstrate that the single amino acid change L119F in an upregulated glutathione S-transferase gene, GSTe2, confers high levels of metabolic resistance to DDT in the malaria vector Anopheles funestus. Genome-wide transcription analysis revealed that GSTe2 was the most over-expressed detoxification gene in DDT and permethrin-resistant mosquitoes from Benin. Transgenic expression of GSTe2 in Drosophila melanogaster demonstrated that over-transcription of this gene alone confers DDT resistance and cross-resistance to pyrethroids. Analysis of GSTe2 polymorphism established that the point mutation is tightly associated with metabolic resistance to DDT and its geographical distribution strongly correlates with DDT resistance patterns across Africa. Functional characterization of recombinant GSTe2 further supports the role of the L119F mutation, with the resistant allele being more efficient at metabolizing DDT than the susceptible one. Importantly, we also show that GSTe2 directly metabolizes the pyrethroid permethrin. Structural analysis reveals that the mutation confers resistance by enlarging the GSTe2 DDT-binding cavity, leading to increased DDT access and metabolism. Furthermore, we show that GSTe2 is under strong directional selection in resistant populations, and a restriction of gene flow is observed between African regions, enabling the prediction of the future spread of this resistance.

Conclusions

This first DNA-based metabolic resistance marker in mosquitoes provides an essential tool to track the evolution of resistance and to design suitable resistance management strategies.