» Articles » PMID: 26581678

Insecticide Resistance Profile of Anopheles Gambiae from a Phase II Field Station in Cové, Southern Benin: Implications for the Evaluation of Novel Vector Control Products

Overview
Journal Malar J
Publisher Biomed Central
Specialty Tropical Medicine
Date 2015 Nov 20
PMID 26581678
Citations 40
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Novel indoor residual spraying (IRS) and long-lasting insecticidal net (LLIN) products aimed at improving the control of pyrethroid-resistant malaria vectors have to be evaluated in Phase II semi-field experimental studies against highly pyrethroid-resistant mosquitoes. To better understand their performance it is necessary to fully characterize the species composition, resistance status and resistance mechanisms of the vector populations in the experimental hut sites.

Methods: Bioassays were performed to assess phenotypic insecticide resistance in the malaria vector population at a newly constructed experimental hut site in Cové, a rice growing area in southern Benin, being used for WHOPES Phase II evaluation of newly developed LLIN and IRS products. The efficacy of standard WHOPES-approved pyrethroid LLIN and IRS products was also assessed in the experimental huts. Diagnostic genotyping techniques and microarray studies were performed to investigate the genetic basis of pyrethroid resistance in the Cové Anopheles gambiae population.

Results: The vector population at the Cové experimental hut site consisted of a mixture of Anopheles coluzzii and An. gambiae s.s. with the latter occurring at lower frequencies (23 %) and only in samples collected in the dry season. There was a high prevalence of resistance to pyrethroids and DDT (>90 % bioassay survival) with pyrethroid resistance intensity reaching 200-fold compared to the laboratory susceptible An. gambiae Kisumu strain. Standard WHOPES-approved pyrethroid IRS and LLIN products were ineffective in the experimental huts against this vector population (8-29 % mortality). The L1014F allele frequency was 89 %. CYP6P3, a cytochrome P450 validated as an efficient metabolizer of pyrethroids, was over-expressed.

Conclusion: Characterizing pyrethroid resistance at Phase II field sites is crucial to the accurate interpretation of the performance of novel vector control products. The strong levels of pyrethroid resistance at the Cové experimental hut station make it a suitable site for Phase II experimental hut evaluations of novel vector control products, which aim for improved efficacy against pyrethroid-resistant malaria vectors to WHOPES standards. The resistance genes identified can be used as markers for further studies investigating the resistance management potential of novel mixture LLIN and IRS products tested at the site.

Citing Articles

The experimental hut efficacy of next-generation insecticide-treated nets against pyrethroid-resistant malaria vectors after 12, 24 and 36 months of household use in Benin.

Agbevo A, Syme T, Fagbohoun J, Fongnikin A, Ahoga J, Accrombessi M Malar J. 2024; 23(1):388.

PMID: 39695690 PMC: 11656845. DOI: 10.1186/s12936-024-05199-0.


Phenotypic evidence of deltamethrin resistance and identification of selective sweeps in Anopheles mosquitoes on the Bijagós Archipelago, Guinea-Bissau.

Moss S, Jones R, Pretorius E, Teixeira da Silva E, Higgins M, Kristan M Sci Rep. 2024; 14(1):22840.

PMID: 39354094 PMC: 11445403. DOI: 10.1038/s41598-024-73996-3.


Laboratory evaluation of the regeneration time, efficacy and wash-resistance of PermaNet Dual (a deltamethrin-chlorfenapyr net) against susceptible and pyrethroid-resistant strains of Anopheles gambiae sensu lato.

Syme T, Ndombidje B, Todjinou D, Ariori V, Ngufor C PLoS One. 2024; 19(8):e0298513.

PMID: 39208123 PMC: 11361417. DOI: 10.1371/journal.pone.0298513.


Malaria prevalence and transmission in the Zakpota sub-district of central Benin: baseline characteristics for a community randomised trial of a new insecticide for indoor residual spraying.

Govoetchan R, Fongnikin A, Hueha C, Ahoga J, Boko C, Syme T Parasit Vectors. 2024; 17(1):303.

PMID: 38997729 PMC: 11245802. DOI: 10.1186/s13071-024-06342-1.


Identifying suitable methods for evaluating the sterilizing effects of pyriproxyfen on adult malaria vectors: a comparison of the oviposition and ovary dissection methods.

Myers A, Fagbohoun J, Houetohossou G, Ndombidje B, Govoetchan R, Todjinou D Malar J. 2024; 23(1):164.

PMID: 38789998 PMC: 11127354. DOI: 10.1186/s12936-024-04983-2.


References
1.
Fanello C, Santolamazza F, Della Torre A . Simultaneous identification of species and molecular forms of the Anopheles gambiae complex by PCR-RFLP. Med Vet Entomol. 2003; 16(4):461-4. DOI: 10.1046/j.1365-2915.2002.00393.x. View

2.
Bass C, Nikou D, Donnelly M, Williamson M, Ranson H, Ball A . Detection of knockdown resistance (kdr) mutations in Anopheles gambiae: a comparison of two new high-throughput assays with existing methods. Malar J. 2007; 6:111. PMC: 1971715. DOI: 10.1186/1475-2875-6-111. View

3.
Tungu P, Magesa S, Maxwell C, Malima R, Masue D, Sudi W . Evaluation of PermaNet 3.0 a deltamethrin-PBO combination net against Anopheles gambiae and pyrethroid resistant Culex quinquefasciatus mosquitoes: an experimental hut trial in Tanzania. Malar J. 2010; 9:21. PMC: 2817703. DOI: 10.1186/1475-2875-9-21. View

4.
Essandoh J, Yawson A, Weetman D . Acetylcholinesterase (Ace-1) target site mutation 119S is strongly diagnostic of carbamate and organophosphate resistance in Anopheles gambiae s.s. and Anopheles coluzzii across southern Ghana. Malar J. 2013; 12:404. PMC: 3842805. DOI: 10.1186/1475-2875-12-404. View

5.
Asidi A, NGuessan R, Akogbeto M, Curtis C, Rowland M . Loss of household protection from use of insecticide-treated nets against pyrethroid-resistant mosquitoes, benin. Emerg Infect Dis. 2012; 18(7):1101-6. PMC: 3376816. DOI: 10.3201/eid1807.120218. View