Evidence map›Paper›PMID 41372907›Full record

ArticleMalaria journal2025

Trends and patterns of insecticide susceptibility of Anopheles gambiae between 2015 and 2020: implications for malaria vector control interventions in Ghana.

Andy Asafu-Adjaye, Joseph Chabi, Keziah Malm, Otubea Owusu Akrofi, Sylvester Coleman, Dominic B Dery, Yemane Yihdego, Kwadwo Kyereme Frempong, Sellase Pi-Bansa, Michelle Ayuritolya Asigbaase and 10 more

Abstract read
In one paragraph

Article in Malaria journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Andy Asafu-AdjayeVector Research Group, Department of Parasitology, Noguchi Memorial Institute for Medical Research, College of Health Sciences, University of Ghana, Legon, Ghana.
Joseph ChabiVector Research Group, Department of Parasitology, Noguchi Memorial Institute for Medical Research, College of Health Sciences, University of Ghana, Legon, Ghana.
Keziah MalmNational Malaria Elimination Programme (Formerly National Malaria Control Programme), Ghana Health Service, Accra, Ghana.
Otubea Owusu AkrofiNational Malaria Elimination Programme (Formerly National Malaria Control Programme), Ghana Health Service, Accra, Ghana.
Sylvester ColemanDepartment of Vector Biology, Liverpool School of Tropical Medicine, Liverpool, UK.
Dominic B DeryUSAID/PMI, No. 24 Fourth Circular Road, Cantonments, P.O. Box 1630, Accra, Ghana.
Yemane YihdegoDepartment of Vector Biology, Liverpool School of Tropical Medicine, Liverpool, UK.
Kwadwo Kyereme FrempongVector Research Group, Department of Parasitology, Noguchi Memorial Institute for Medical Research, College of Health Sciences, University of Ghana, Legon, Ghana. kfrempong@noguchi.ug.edu.gh.
Sellase Pi-BansaVector Research Group, Department of Parasitology, Noguchi Memorial Institute for Medical Research, College of Health Sciences, University of Ghana, Legon, Ghana.
Michelle Ayuritolya AsigbaaseVector Research Group, Department of Parasitology, Noguchi Memorial Institute for Medical Research, College of Health Sciences, University of Ghana, Legon, Ghana.
Rebecca PwaliaVector Research Group, Department of Parasitology, Noguchi Memorial Institute for Medical Research, College of Health Sciences, University of Ghana, Legon, Ghana.
Joannitta JoannidesVector Research Group, Department of Parasitology, Noguchi Memorial Institute for Medical Research, College of Health Sciences, University of Ghana, Legon, Ghana.
Kojo Yirenkyi SakyiVector Research Group, Department of Parasitology, Noguchi Memorial Institute for Medical Research, College of Health Sciences, University of Ghana, Legon, Ghana.
Osei Kwaku AkuokoVector Research Group, Department of Parasitology, Noguchi Memorial Institute for Medical Research, College of Health Sciences, University of Ghana, Legon, Ghana.
Joseph Harold Nyarko OseiVector Research Group, Department of Parasitology, Noguchi Memorial Institute for Medical Research, College of Health Sciences, University of Ghana, Legon, Ghana.
Duncan K AthinyaVestergaard Frandsen (E.A) Ltd, Nairobi, Kenya.
Aba Baffoe-WilmotNational Malaria Elimination Programme (Formerly National Malaria Control Programme), Ghana Health Service, Accra, Ghana.
Constance Bart-PlangeNational Malaria Elimination Programme (Formerly National Malaria Control Programme), Ghana Health Service, Accra, Ghana.
Daniel Adjei BoakyeVector Research Group, Department of Parasitology, Noguchi Memorial Institute for Medical Research, College of Health Sciences, University of Ghana, Legon, Ghana.
Samuel Kweku DadzieVector Research Group, Department of Parasitology, Noguchi Memorial Institute for Medical Research, College of Health Sciences, University of Ghana, Legon, Ghana. sdadzie@noguchi.ug.edu.gh.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe distribution and use of insecticide treated nets (ITNs) and indoor residual spraying (IRS) are the two main insecticide-based tools that have been scaled up in Ghana. Although insecticide resistance to different insecticides have been reported in parts of Ghana, there is little information on the status and extent of resistance in malaria vectors across different areas in the country. There was, therefore, a need to generate annual geographically specific insecticide resistance data to assist in the development of insecticide resistance management strategies in Ghana. This study presents five years data on monitoring of four classes of insecticides.

methodsStandard World Health Organization (WHO) insecticide susceptibility tube assays were carried out annually on adult female Anopheles gambiae reared from immature stages in 30 sentinel sites across Ghana each year from 2015 to 2020. Insecticide papers impregnated with seven insecticides in four classes were used for assays in the selected sites. PCR was performed to identify mosquito species and detect knock down resistance, kdr-west (L1014F) and acetylcholinesterase, ace-1 G119S gene mutations in forty randomly selected mosquitoes per site.

resultsHigh resistance to pyrethroids and DDT was detected in all the sites with a decrease in susceptibility over the years. The susceptibility of carbamates and organophosphates reduced in all the sites over the 5 years. Anopheles gambiae sensu stricto (s.s.) and Anopheles coluzzii represented the two-main species of the complex living in sympatry mostly in the southern sentinel sites, with Anopheles arabiensis in smaller numbers in the northern Sahelian sites. The target site resistance frequency was significantly higher for the L1014F compared to the G119S with variations across the sites.

conclusionFindings showed that resistance to deltamethrin, permethrin (pyrethroids), DDT (organochlorine) malathion and pirimiphos-methyl (organophosphates) and bendiocarb and propoxur (carbamates) was widespread in Ghana. There is high frequency of L1014F alleles (kdr-west) in all the sites with marginal increase for G119S ace-1 mutations. This highlights the need for continuous monitoring of the insecticide resistance of An. gambiae sensu lato in the country to ensure informed decision-making on resistance management strategies and choice of insecticides for malaria vector control in Ghana.

Indexed as

AnophelesInsecticide ResistanceInsecticidesMosquito ControlMosquito VectorsAnimalsFemaleGhanaMalariaInsecticidesAnopheles gambiaeG119SGhanaInsecticide resistanceKnockdown resistanceL1014FMalariaSusceptibility

Identifiers

PMID41372907
PMCPMC12794369

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.