Evidence map›Paper›PMID 40730828›Full record

ArticleScientific reports2025

Novel insecticide resistance mutations associated with variable PBO synergy in Anopheles gambiae s.l. from the Democratic Republic of Congo.

Bethanie Pelloquin, Fiacre Agossa, Holly Acford-Palmer, Tiffany Clark, Sheila B Ogoma, Miriam Williams, Narcisse Basosila, Francis Watsenga, Emery Metelo, Richard M Oxborough and 14 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
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  3. Article
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

24 authors.

Bethanie PelloquinDepartment of Disease Control, Faculty of Infectious Tropical Diseases, London School of Hygiene and Tropical Medicine, London, UK. Bethanie.pelloquin1@alumni.lshtm.ac.uk.
Fiacre AgossaU.S. President's Malaria Initiative (PMI) Evolve Project, Abt Associates, MD, USA.
Holly Acford-PalmerDepartment of Infection Biology, Faculty of Infectious Tropical Diseases, London School of Hygiene and Tropical Medicine, London, UK.
Tiffany ClarkU.S. President's Malaria Initiative (PMI) Evolve Project, Abt Associates, MD, USA.
Sheila B OgomaU.S. President's Malaria Initiative (PMI) Evolve Project, Abt Associates, MD, USA.
Miriam WilliamsU.S. President's Malaria Initiative (PMI) Evolve Project, Abt Associates, MD, USA.
Narcisse BasosilaNational Malaria Control Program, Kinshasa, Democratic Republic of Congo.
Francis WatsengaInstitut National de Recherche Biomédicale, Kinshasa, Democratic Republic of Congo.
Emery MeteloInstitut National de Recherche Biomédicale, Kinshasa, Democratic Republic of Congo.
Richard M OxboroughParasitology and Vector Biology (PARAVEC) Laboratory, School of Public Health, University of Nevada, Las Vegas, USA.
Yibayiri Osee SanogoU.S. President's Malaria Initiative, U.S. Centers for Disease Control and Prevention, Kinshasa, Democratic Republic of Congo.
Ferdinand NtoyaU.S. President's Malaria Initiative, U.S. Centers for Disease Control and Prevention, Kinshasa, Democratic Republic of Congo.
Emma CollinsDepartment of Infection Biology, Faculty of Infectious Tropical Diseases, London School of Hygiene and Tropical Medicine, London, UK.
Sophie MossDepartment of Infection Biology, Faculty of Infectious Tropical Diseases, London School of Hygiene and Tropical Medicine, London, UK.
Charles McLoughlinDepartment of Disease Control, Faculty of Infectious Tropical Diseases, London School of Hygiene and Tropical Medicine, London, UK.
Monica CamposImperial College London, London, UK.
Jody PhelanDepartment of Infection Biology, Faculty of Infectious Tropical Diseases, London School of Hygiene and Tropical Medicine, London, UK.
Mark RowlandDepartment of Disease Control, Faculty of Infectious Tropical Diseases, London School of Hygiene and Tropical Medicine, London, UK.
Thomas WalkerSchool of Life Sciences, University of Warwick, Coventry, UK.
Noboru MinakawaDepartment of Vector Ecology and Environment, Institute of Tropical Medicine, Nagasaki University, Nagasaki, Japan.
Emile Zola ManzambiInstitut National de Recherche Biomédicale, Kinshasa, Democratic Republic of Congo.
Eric MukomenaNational Malaria Control Program, Kinshasa, Democratic Republic of Congo.
Susana CampinoDepartment of Infection Biology, Faculty of Infectious Tropical Diseases, London School of Hygiene and Tropical Medicine, London, UK.
Louisa A MessengerDepartment of Disease Control, Faculty of Infectious Tropical Diseases, London School of Hygiene and Tropical Medicine, London, UK. louisa.messenger@unlv.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Over-reliance on pyrethroid insecticides in insecticide-treated nets (ITNs) has imposed significant selection pressure for the evolution of insecticide resistance among major malaria vector species. In the Democratic Republic of Congo (DRC), the country with the second highest malaria burden globally, pyrethroid resistance is pervasive, but there is a paucity of information regarding the molecular mechanisms driving resistance. A clear understanding of the specificity of resistance mechanisms to individual insecticides and the likelihood of selecting for cross-resistance mechanisms is crucial for the development of new vector control tools. Anopheles gambiae s.l. populations from eight study sites across the DRC were phenotyped for resistance to alpha-cypermethrin, deltamethrin and permethrin, with and without pre-exposure to the synergist piperonyl butoxide (PBO), followed by multiplex amplicon sequencing. Phenotypic pyrethroid resistance and loss of PBO synergy was confirmed in all sites across the DRC. In An. gambiae s.s. four non-synonymous SNPs which have been previously associated with insecticide resistance were detected: gste2-L119V, vgsc-L995F, vgsc-L995S and rdl-A296G, while three were novel: gste2-T154S, ace1-N246T and ace1-P265L. Nationwide geographical trends in insecticide resistance mutation distribution, prevalence and selection were evident. In the West, near fixation of vgsc-L995F and almost complete absence of vgsc-L995S was observed, alongside low-moderate frequencies of rdl-A296G and gste2-L119V. Further East, the converse was apparent. Gste2-L119V was significantly associated with resistance to deltamethrin following PBO-pre-exposure, warranting functional validation to determine its putative role in reduced PBO synergy. Furthermore, gste2-T154S was implicated in deltamethrin and permethrin resistance but susceptibility to alpha-cypermethrin after PBO pre-exposure. Study findings comprise the most comprehensive overview of the prevalence of genetic markers of Anopheles insecticide resistance across the DRC and provide an important baseline for improved malaria vector control and the design of proactive insecticide resistance management strategies. Given the significant scale up in PBO-ITNs, with more than 58% of all ITNs delivered to sub-Saharan Africa in 2023 containing PBO, there is an urgent need to identify novel molecular markers to monitor changes in PBO synergy, which may be predicative of loss of intervention operational efficacy.

Indexed as

AnophelesInsecticide ResistanceInsecticidesMutationPesticide SynergistsPiperonyl ButoxideAnimalsDemocratic Republic of the CongoInsect ProteinsMalariaMosquito VectorsPolymorphism, Single NucleotidePyrethrinsInsecticidesInsect ProteinsPesticide SynergistsPiperonyl ButoxidePyrethrinsAmplicon sequencingAnopheles gambiaeDemocratic Republic of CongoPBO synergyPyrethroid resistanceSingle nucleotide polymorphisms

Identifiers

PMID40730828
PMCPMC12307749

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