AI Article Synopsis

  • Culex quinquefasciatus mosquitoes are key vectors for diseases but lack sufficient data on their biology and resistance to insecticides.
  • A study in Yaoundé, Cameroon, found that most populations of Cx. quinquefasciatus showed significant resistance to multiple insecticides, with mortality rates between 0-89%.
  • The resistance is linked to genetic mutations and overexpression of certain genes, indicating a complicated biological response that could reduce the effectiveness of existing pest control methods and highlights the need for new integrated strategies.

Article Abstract

Culex mosquitoes particularly Culex quinquefasciatus are important arboviral and filariasis vectors, however despite this important epidemiological role, there is still a paucity of data on their bionomics. The present study was undertaken to assess the insecticide resistance status of Cx. quinquefasciatus populations from four districts of Yaoundé (Cameroon). All Culex quinquefasciatus populations except one displayed high resistance to bendiocarb and malathion with mortalities ranging from 0 to 89% while high resistance intensity against both permethrin and deltamethrin was recorded. Molecular analyses revealed high frequencies of the ACE-1 G119S mutation (ranging from 0 to 33%) and kdr L1014F allele (ranging from 55 to 74%) in all Cx. quinquefasciatus populations. Significant overexpression was detected for cytochrome P450s genes CYP6AA7 and CYP6Z10, as well as for Esterase A and Esterase B genes. The total cuticular hydrocarbon content, a proxy of cuticular resistance, was significantly increased (compared to the S-lab strain) in one population. The study confirms strong insecticide resistance mediated by different mechanisms in Cx. quinquefasciatus populations from the city of Yaoundé. The expansion of insecticide resistance in Culex populations could affect the effectiveness of current vector control measures and stress the need for the implementation of integrated vector control strategies in urban settings.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8017000PMC
http://dx.doi.org/10.1038/s41598-021-86850-7DOI Listing

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