Evidence map›Paper›PMID 41204395›Full record

ArticleTropical diseases, travel medicine and vaccines2025

Genetic polymorphism of MSP2 and its implications for Plasmodium falciparum resistance in N'Djamena, Chad.

Djobo Abel, Noumedem Anangmo Christelle Nadia, Yamssi Cedric, Tchuenkam Kom Pacome, Nganji Bismarck, Tordibaye Ngaryedji, Toumko Towa Merveille, Masra Mislengar Hervé, Darkaou Kidedji Deborah, Haibo Hu and 1 more

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Article in Tropical diseases, travel medicine and vaccines, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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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.

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2 · The registry

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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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Genetic Diversity and Allelic Distribution ofJournal of parasitology research · 2026
    Article
4 · The record

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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

11 authors.

Djobo AbelDepartment of Microbiology, Haematology and Immunology, Faculty of Medicine and Pharmaceutical Sciences, University of Dschang, Dschang, Cameroon.
Noumedem Anangmo Christelle NadiaDepartment of Microbiology, Haematology and Immunology, Faculty of Medicine and Pharmaceutical Sciences, University of Dschang, Dschang, Cameroon. noums11@yahoo.fr.
Yamssi CedricLaboratory of Tropical and Emerging Infectious Diseases, Dschang, Cameroon. cyamssi@yahoo.com.
Tchuenkam Kom PacomeLaboratory of Tropical and Emerging Infectious Diseases, Dschang, Cameroon.
Nganji BismarckLaboratory of Tropical and Emerging Infectious Diseases, Dschang, Cameroon.
Tordibaye NgaryedjiDepartment of Microbiology, Haematology and Immunology, Faculty of Medicine and Pharmaceutical Sciences, University of Dschang, Dschang, Cameroon.
Toumko Towa MerveilleDepartment of Microbiology, Haematology and Immunology, Faculty of Medicine and Pharmaceutical Sciences, University of Dschang, Dschang, Cameroon.
Masra Mislengar HervéDepartment of Microbiology, Haematology and Immunology, Faculty of Medicine and Pharmaceutical Sciences, University of Dschang, Dschang, Cameroon.
Darkaou Kidedji DeborahDepartment of Microbiology, Haematology and Immunology, Faculty of Medicine and Pharmaceutical Sciences, University of Dschang, Dschang, Cameroon.
Haibo HuLaboratory of Tropical and Emerging Infectious Diseases, Dschang, Cameroon. hhb2017@gmu.edu.cn.
Noubom MichelDepartment of Microbiology, Haematology and Immunology, Faculty of Medicine and Pharmaceutical Sciences, University of Dschang, Dschang, Cameroon.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMalaria control is a major challenge for countries in endemic areas, and Chad is one of them. The objective of this study was to determine the genetic diversity of the merozoite surface protein 2 (MSP-2) of Plasmodium falciparum in four health facilities in N’Djamena in order to better understand the variability of circulating strains and its epidemiological implications for malaria control.

methodsBlood samples were collected from 302 patients for both parasitological and molecular analyses. Positive samples were spotted on Whatman paper for molecular analyses. The parasite DNA was extracted by the chelex-100 method. The MSP2 gene was amplified by nested PCR and the revelation of this gene was done on a 1.3% agarose gel. The diversity parameters were calculated from the fragments and the number of alleles obtained. The data obtained were analyzed using SPSS 23 software. The phylogenetic tree of the Pf population was carried out using R software.

resultsThe prevalence of P. falciparum infection was 40.72% with a higher parasite intensity in women (317.81±109.93). Of the samples analyzed, 101 carried the MSP-2 gene (78.21%) on which 12 different alleles were obtained, thus a genetic diversity of 9.37%. A multiplicity of infections of 1.26 was determined with a percentage of 73.26; 25.74 and 1% respectively for monoclonal, double clonal and triple clonal infections. The phylogenetic tree showed 11 clades in four health structures of N’Djamena with parasites that are more or less genetically related.

conclusionA significantly high genetic diversity thus indicates a high intensity of malaria transmission of P. falciparum. in N’Djamena. The multiplicity of infections and the high allelic diversity obtained allow us to understand that the malaria transmission situation in this area is critical and should guide studies of resistance to other antimalarial.

Indexed as

ChadGenetic diversityMSP-2N’DjamenaPlasmodium falciparumResistance

Identifiers

PMID41204395
PMCPMC12595742

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