Evidence map›Paper›PMID 35183684›Full record

ArticleGene2022

Xeno-monitoring of molecular drivers of artemisinin and partner drug resistance in P. falciparum populations in malaria vectors across Cameroon.

Francis N Nkemngo, Leon M J Mugenzi, Magellan Tchouakui, Daniel Nguiffo-Nguete, Murielle J Wondji, Bertrand Mbakam, Micareme Tchoupo, Cyrille Ndo, Samuel Wanji, Charles S Wondji

Open access · hybridAbstract read
In one paragraph

Article in Gene, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

17 citing papers in PubMed, 27 citations in OpenAlex.

  1. Trial
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  8. NovelAntimicrobial agents and chemotherapy · 2025
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  15. Sampling for malaria molecular surveillance.Trends in parasitology · 2023
    Review
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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

10 authors at 3 institutions in 2 countries.

Francis N NkemngoCentre for Research in Infectious Diseases (CRID), P.O. Box 13591, Yaoundé, Cameroon; Department of Microbiology and Parasitology, Faculty of Science, University of Buea, P.O. Box 63, Buea, Cameroon. Electronic address: francis.nkemngo@crid-cam.net.
Leon M J MugenziCentre for Research in Infectious Diseases (CRID), P.O. Box 13591, Yaoundé, Cameroon. Electronic address: leon.mugenzi@crid-cam.net.
Magellan TchouakuiCentre for Research in Infectious Diseases (CRID), P.O. Box 13591, Yaoundé, Cameroon. Electronic address: magellan.tchouakui@crid-cam.net.
Daniel Nguiffo-NgueteCentre for Research in Infectious Diseases (CRID), P.O. Box 13591, Yaoundé, Cameroon. Electronic address: daniel.nguiffo@crid-cam.net.
Murielle J WondjiCentre for Research in Infectious Diseases (CRID), P.O. Box 13591, Yaoundé, Cameroon; Vector Biology Department, Liverpool School of Tropical Medicine, Pembroke Place, Liverpool L3 5QA, United Kingdom. Electronic address: murielle.wondji@lstmed.ac.uk.
Bertrand MbakamCentre for Research in Infectious Diseases (CRID), P.O. Box 13591, Yaoundé, Cameroon. Electronic address: bertrand.mbakam@crid-cam.net.
Micareme TchoupoCentre for Research in Infectious Diseases (CRID), P.O. Box 13591, Yaoundé, Cameroon. Electronic address: micareme.tchoupo@crid-cam.net.
Cyrille NdoCentre for Research in Infectious Diseases (CRID), P.O. Box 13591, Yaoundé, Cameroon; Department of Biological Sciences, Faculty of Medicine and Pharmaceutical Sciences, University of Douala, Douala, Cameroon. Electronic address: cyrille.ndo@crid-cam.net.
Samuel WanjiDepartment of Microbiology and Parasitology, Faculty of Science, University of Buea, P.O. Box 63, Buea, Cameroon; Research Foundation in Tropical Diseases and Environment, Buea, Cameroon. Electronic address: swanji@yahoo.fr.
Charles S WondjiCentre for Research in Infectious Diseases (CRID), P.O. Box 13591, Yaoundé, Cameroon; Vector Biology Department, Liverpool School of Tropical Medicine, Pembroke Place, Liverpool L3 5QA, United Kingdom. Electronic address: charles.wondji@lstmed.ac.uk.
Ministry of Scientific Research and Innovation · CMUniversity of Buea · CMUniversity of Douala · CM

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMonitoring of drug resistance in Plasmodium populations is crucial for malaria control. This has primarily been performed in humans and rarely in mosquitoes where parasites genetic recombination occurs. Here, we characterized the Plasmodium spp populations in wild Anopheles vectors by analyzing the genetic diversity of the P. falciparum kelch13 and mdr1 gene fragments implicated in artemisinin and partner drug resistance across Cameroon in three major malaria vectors.

methodsAnopheles mosquitoes were collected across nine localities in Cameroon and dissected into the head/thorax (H/T) and abdomen (Abd) after species identification. A TaqMan assay was performed to detect Plasmodium infection. Fragments of the Kelch 13 and mdr1 genes were amplified in P. falciparum positive samples and directly sequenced to assess their drug resistance polymorphisms and genetic diversity profile.

resultsThe study revealed a high Plasmodium infection rate in the major Anopheles vectors across Cameroon. Notably, An. funestus vector recorded the highest sporozoite (8.0%) and oocyst (14.4%) infection rates. A high P. falciparum sporozoite rate (80.08%) alongside epidemiological signatures of significant P. malariae (15.9%) circulation were recorded in these vectors. Low genetic diversity with six (A578S, R575I, G450R, L663L, G453D, N458D) and eight (H53H, V62L, V77E, N86Y, G102G, L132I, H143H, Y184F) point mutations were observed in the k13 and mdr1 backbones respectively. Remarkably, the R575I (4.4%) k13 and Y184F (64.2%) mdr1 mutations were the predominant variants in the P. falciparum populations.

conclusionThe emerging signal of the R575I polymorphism in the Pfk13 propeller backbone entails the regular surveillance of molecular markers to inform evidence-based policy decisions. Moreover, the high frequency of the

Indexed as

Drug ResistanceAnimalsAnophelesArtemisininsATP-Binding Cassette, Sub-Family C ProteinsCameroonFemaleGene FrequencyMalaria, FalciparumOocytesPlasmodium falciparumPoint MutationProtozoan ProteinsSequence Analysis, DNASporozoitesArtemisininsATP-Binding Cassette, Sub-Family C ProteinsMdr1 protein, Plasmodium falciparumProtozoan ProteinsAnopheles vectorsCameroonDrug resistanceK13 & mdr1MalariaP. falciparum

Identifiers

PMID35183684
PMCPMC8942117
OpenAlexW4226025175

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.