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Journal Article Epublish

PubMed: 41204404 DOI: 10.1186/s12864-025-12229-x

Investigating the potential role of metabolic resistance genes in conferring cross-resistance to pyrethroids and polycyclic aromatic hydrocarbon pollutants in the major malaria vector Anopheles coluzzii.

BMC Genomics 26(1):1018

Authors: Abdullahi Muhammad, Sulaiman S Ibrahim, Hanafy M Ismail, Helen Irving, Mark J I Paine, Charles S Wondji

Affiliations

  • Vector Biology Department, Liverpool School of Tropical Medicine, Pembroke Place, Liverpool , L3 5QA, United Kingdom.
  • Centre for Biotechnology Research Bayero University, Kano, PMB 3011, Nigeria.
  • LSTM Research Unit, Centre for Research in Infectious Diseases (CRID), Yaoundé, Cameroon.
  • Department of Biochemistry, Bayero University, Kano, PMB 3011, Nigeria.
  • LSTM Research Unit, Centre for Research in Infectious Diseases (CRID), Yaoundé, Cameroon.
  • Vector Biology Department, Liverpool School of Tropical Medicine, Pembroke Place, Liverpool , L3 5QA, United Kingdom.

Abstract

BACKGROUND

Polycyclic aromatic hydrocarbons (PAHs) are a class of ubiquitous and recalcitrant environmental pollutants generated from petroleum activities and/or biological conversion of organic materials. Environmental exposure of mosquitoes to these pollutants can potentially select resistance to insecticides used in public health for vector control. To understand the cross-resistance potentials between PAHs and pyrethroid insecticides, microsomal fractions prepared from Anopheles coluzzii mosquitoes obtained from agricultural sites and a laboratory susceptible strain, Ngousso, were tested with three major PAHs - fluorene, fluoranthene and naphthalene. Recombinant P450s previously associated with pyrethroid resistance in Anopheles gambiae (CYPs 6M2, 6Z2, 6Z3, 9J5, 6P3, 6P4, 6P5, CYP9K1) and Anopheles funestus CYP6P9a were also used to investigate metabolism of the above PAHs alongside the microsome.

RESULTS

Microsomes prepared from pyrethroid-resistant Anopheles coluzzii significantly (P = 0.001, r = 0.99) depleted fluorene and fluoranthene with percentage depletions of 73%±0.5 and 43%0.0 ± 2.2, respectively. A Steady-state kinetic study demonstrated that the microsome has a high affinity for fluorene with a Km and turnover of 58.69 µM ± 20.47​ and 37.016 min- ± 3.67, respectively. On the other hand, significant metabolism of fluorene up to 47.9%±2.3 (P = 0.001, r = 0.99) and 52.8%±0.8 (P = 0.001, r = 0.97) depletions were observed with recombinant CYP6P3 and CYP6Z3, respectively. Other P450s showed little to no metabolism with fluorene. CYP6Z2 and CYP6Z3 metabolised fluoranthene with percentage depletions of 50.4%±4.9 (P = 0.003, r = 0.96) and 60.3% ±5.3 (P = 0.002, r = 0.84), respectively. However, no metabolism of naphthalene was observed with all the recombinant P450s used in this study.

CONCLUSION

This study demonstrates that P450 monooxygenases from the malaria vectors can metabolise PAHs, highlighting the potential of these environmental pollutants selecting the P450s, driving insecticide resistance in field populations of major malaria vectors.

MeSH

Genes, Malaria, Genomics, Environmental Pollutants, Polycyclic Aromatic Hydrocarbons, Hydrocarbons, Microsomes, Hydrocarbons, Aromatic, Insecticides