Evidence map›Paper›PMID 42143087›Full record

ArticleScientific reports2026

Genetic polymorphism of Plasmodium falciparum MSP-2 (3D7/IC) and multiplicity of infection in N'Djamena, Chad.

Yamssi Cedric, Noukeu Diomède, Masra Mislengar Hervé, Tchuenkam Kom Pacome, Djobo Abel, Tordibaye Ngaryedji, Barka Saleh, Haibo Hu, Noumedem Anangmo Christelle Nadia

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Yamssi CedricDepartment of Biomedical Sciences, University of Bamenda, Bambili, Cameroon. cyamssi@yahoo.com.
Noukeu DiomèdeDepartment of Biomedical Sciences, University of Bamenda, Bambili, Cameroon.
Masra Mislengar HervéDepartment of Biomedical Sciences, University of Bamenda, Bambili, Cameroon.
Tchuenkam Kom PacomeDepartment of Biomedical Sciences, University of Bamenda, Bambili, Cameroon.
Djobo AbelDepartment of Biomedical Sciences, University of Bamenda, Bambili, Cameroon.
Tordibaye NgaryedjiDepartment of Biomedical Sciences, University of Bamenda, Bambili, Cameroon.
Barka SalehDepartment of Biomedical Sciences, University of Bamenda, Bambili, Cameroon.
Haibo HuDepartment of Biomedical Sciences, University of Bamenda, Bambili, Cameroon. hhb2017@gmu.edu.cn.
Noumedem Anangmo Christelle NadiaDepartment of Biomedical Sciences, University of Bamenda, Bambili, Cameroon. noums11@yahoo.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malaria remains one of the most widespread endemic diseases in Africa. Molecular epidemiological studies of Plasmodium falciparum genetic diversity are essential for understanding transmission dynamics and informing effective control strategies. This study aimed to assess the genetic polymorphism of the merozoite surface protein 2 (msp2) 3D7/IC allelic family and multiplicity of infection in malaria patients. A cross-sectional analytical study was conducted from July to September 2024. Blood samples were collected from 217 participants attending Our Lady of the Apostles Hospital in N'Djamena, Chad. Malaria infection and parasite density were determined using immunochromatographic tests and thick blood smears. Parasite DNA was extracted using the Chelex-100 method, and the msp2 3D7/IC allelic family was amplified by nested PCR. Phylogenetic analysis was performed using the Lower Left matrix with R software, and statistical analyses were conducted using Excel 2016 and SPSS version 23. The prevalence of Plasmodium falciparum infection was 23.5%, while the molecular frequency of the msp2 3D7/IC allelic family was 94.11%. Genetic polymorphism within this allelic family was observed, with a predominance of one genotype (18.46%) and low-frequency alleles ranging between 560 and 570 base pairs (3.07% and 1.53%, respectively). Single-clone infections were most frequent (64.65%), followed by double (33.33%) and triple infections (2.08%), with no quadruple infections detected. Phylogenetic analysis revealed eight clades, with clades 1, 4, and 7 showing a higher concentration of genetically related isolates. This study demonstrates substantial genetic diversity and multiplicity offalciparum infections within the msp-2 3D7/IC allelic family, reflecting ongoing malaria transmission in the study area. The findings underscore the importance of expanding molecular surveillance to include additional allelic families and multiple sites to generate more comprehensive data for national malaria control strategies.

Indexed as

Antigens, ProtozoanMalaria, FalciparumPlasmodium falciparumPolymorphism, GeneticProtozoan ProteinsAllelesChadCross-Sectional StudiesFemaleGenotypeHumansPhylogenyAntigens, Protozoanmerozoite surface protein 2, PlasmodiumProtozoan ProteinsGenetic polymorphismMalariaMSP-2 3D7/IC allelic familyMultiplicity of infectionPlasmodium falciparum

Identifiers

PMID42143087
PMCPMC13377077

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.