Evidence map›Paper›PMID 38178249›Full record

ArticleParasites & vectors2024

Genomic surveillance of Anopheles mosquitoes on the Bijagós Archipelago using custom targeted amplicon sequencing identifies mutations associated with insecticide resistance.

Sophie Moss, Elizabeth Pretorius, Sainey Ceesay, Harry Hutchins, Eunice Teixeira da Silva, Mamadou Ousmane Ndiath, Robert T Jones, Hristina Vasileva, Jody Phelan, Holly Acford-Palmer and 6 more

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
4.3field-weighted citation impact, top 6% of its field
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

6 citing papers in PubMed, 8 citations in OpenAlex.

  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

16 authors at 4 institutions in 5 countries.

Sophie MossFaculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK. sophie.moss@lshtm.ac.uk.
Elizabeth PretoriusFaculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK.
Sainey CeesayMedical Research Council, The Gambia (MRCG), Fajara, Gambia.
Harry HutchinsFaculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK.
Eunice Teixeira da SilvaMinistério de Saúde Pública, Bissau, Guinea-Bissau.
Mamadou Ousmane NdiathMedical Research Council, The Gambia (MRCG), Fajara, Gambia.
Robert T JonesFaculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK.
Hristina VasilevaFaculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK.
Jody PhelanFaculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK.
Holly Acford-PalmerFaculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK.
Emma CollinsFaculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK.
Amabelia RodriguesProjecto de Saúde Bandim, Bissau, Guinea-Bissau.
Sanjeev KrishnaClinical Academic Group, Institute for Infection and Immunity, St. George's University Hospitals NHS Foundation Trust-St. George's University of London, London, UK.
Taane G Clark *Faculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK.
Anna Last *Faculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK.
Susana Campino *Faculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK.
London School of Hygiene & Tropical Medicine · GBBandim Health Project · GWMRC Unit the Gambia · GMSt George's, University of London · GB

Funding

Medical Research Council MR/N013638/1Medical Research Council MR/S005013/1Medical Research Council MR/X005895/1Medical Research Council PhD Studentship
6 · The paper itself

Abstract

backgroundInsecticide resistance is reducing the efficacy of vector control interventions, consequently threatening efforts to control vector-borne diseases, including malaria. Investigating the prevalence of molecular markers of resistance is a useful tool for monitoring the spread of insecticide resistance in disease vectors. The Bijagós Archipelago (Bijagós) in Guinea-Bissau is a region of stable malaria transmission where insecticide-treated nets are the mainstay for malaria control. However, the prevalence of molecular markers of insecticide resistance in malaria vectors is not well understood.

methodsA total of 214 Anopheles mosquitoes were analysed from 13 islands across the Bijagós. These mosquitoes were collected using CDC light traps in November 2019, during the peak malaria transmission season. High-throughput multiplex amplicon sequencing was used to investigate the prevalence of 17 different molecular markers associated with insecticide resistance in four genes: vgsc, rdl, ace1 and gste2.

resultsOf the 17 screened mutations, four were identified in mosquitoes from the Bijagós: vgsc L995F (12.2%), N1570Y (6.2%) and A1746S (0.7%) and rdl A269G (1.1%). This study is the first to report the L995F knock-down resistance (kdr)-west allele in Anopheles melas on the Archipelago. An additional eight non-synonymous single-nucleotide polymorphisms were identified across the four genes which have not been described previously. The prevalences of the vgsc L995F and N1570Y mutations were higher on Bubaque Island than on the other islands in this study; Bubaque is the most populous island in the archipelago, with the greatest population mobility and connection to continental Guinea-Bissau.

conclusionsThis study provides the first surveillance data for genetic markers present in malaria vectors from islands across the Bijagós Archipelago. Overall prevalence of insecticide resistance mutations was found to be low. However, the identification of the vgsc L995F and N1570Y mutations associated with pyrethroid resistance warrants further monitoring. This is particularly important as the mainstay of malaria control on the islands is the use of pyrethroid insecticide-treated nets.

Indexed as

AnophelesInsecticidesMalariaPyrethrinsAnimalsGenomicsInsecticide ResistanceMosquito VectorsMutationInsecticidesPyrethrinsAnopheles mosquitoesInsecticide resistanceMolecular monitoringVector control

Identifiers

PMID38178249
PMCPMC10768400
OpenAlexW4390579349

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.