Evidence map›Paper›PMID 37624380›Full record

ArticleParasitology research2023

Plasmodium falciparum msp-1 and msp-2 genetic diversity and multiplicity of infection in isolates from Congolese patients in the Republic of Congo.

Marcel Tapsou Baina, Jean Claude Djontu, Abel Lissom, Naura Veil Assioro Doulamo, Dieu Merci Umuhoza, Jacque Dollon Mbama Ntabi, Christevy Jeanney Vouvoungui, Reauchelvy Kamal Boumpoutou, Jolivet Mayela, Steve Diafouka-Kietela and 2 more

Abstract read
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In one paragraph

Article in Parasitology research, 2023. 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
1.2field-weighted citation impact, top 21% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

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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

12 authors at 3 institutions in 3 countries.

Marcel Tapsou BainaFondation Congolaise pour la Recherche Médicale, Brazzaville, Republic of Congo.
Jean Claude DjontuFondation Congolaise pour la Recherche Médicale, Brazzaville, Republic of Congo. cdjontu@yahoo.fr.
Abel LissomFondation Congolaise pour la Recherche Médicale, Brazzaville, Republic of Congo.
Naura Veil Assioro DoulamoFondation Congolaise pour la Recherche Médicale, Brazzaville, Republic of Congo.
Dieu Merci UmuhozaFondation Congolaise pour la Recherche Médicale, Brazzaville, Republic of Congo.
Jacque Dollon Mbama NtabiFondation Congolaise pour la Recherche Médicale, Brazzaville, Republic of Congo.
Christevy Jeanney VouvounguiFondation Congolaise pour la Recherche Médicale, Brazzaville, Republic of Congo.
Reauchelvy Kamal BoumpoutouFondation Congolaise pour la Recherche Médicale, Brazzaville, Republic of Congo.
Jolivet MayelaFondation Congolaise pour la Recherche Médicale, Brazzaville, Republic of Congo.
Steve Diafouka-KietelaFondation Congolaise pour la Recherche Médicale, Brazzaville, Republic of Congo.
Etienne NguimbiFondation Congolaise pour la Recherche Médicale, Brazzaville, Republic of Congo.
Francine NtoumiFondation Congolaise pour la Recherche Médicale, Brazzaville, Republic of Congo. ffntoumi@hotmail.com.
Fondation Congolaise Pour La Recherche Médicale · CGMarien Ngouabi University · CGUniversity of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

With limited up to date data from the Republic of Congo, the aim of this study was to investigate allelic polymorphism of merozoite surface protein-1 (msp-1) and merozoite surface protein-2 (msp-2). This will help assess the genetic diversity and multiplicity of Plasmodium falciparum infection (MOI), from uncomplicated malaria individuals living in Brazzaville. Between March and October 2021, a cross-sectional study was carried out at a health center in Madibou District located in the south of Brazzaville. Plasmodium infection was diagnosed in human blood by microscopy and the block 2 of P. falciparum msp-1 and block 3 of msp-2 genes were genotyped by nested PCR. Overall, 57 genotypes with fragment sizes ranging from 110 to 410 bp were recorded for msp-1, among which 25, 21, and 11 genotypes identified for K1, MAD20, and RO33 allelic families respectively. RO33 (34.3%) and MAD20 (34.3%) allelic families were more frequent compared to K1 (31.4%) although the difference was not statistically significant. Also, 47 msp-2 genotypes were identified, including 26 FC27 genotypes type, and 21 genotypes belonging to the 3D7 allelic family. FC27 was more frequent (52.3%) compared to 3D7 (47.7%). The prevalence of the polyclonal infection was 90.0% while the MOI was 2.90 ± 1.0. The MOI and polyclonal infection were not significantly associated with the parasitaemia and anaemia. This study reveals a high genetic diversity and the trend of increasing MOI of P. falciparum isolates from the south of Brazzaville, compared to the reports from the same setting before the COVID-19 pandemic.

Indexed as

COVID-19Malaria, FalciparumAnimalsCongoCross-Sectional StudiesHumansMembrane ProteinsMerozoitesMerozoite Surface Protein 1PandemicsPlasmodium falciparumPolymorphism, GeneticMembrane ProteinsMerozoite Surface Protein 1Malariamsp-1msp-2Plasmodium falciparumRepublic of Congo

Identifiers

PMID37624380
OpenAlexW4386154080

What OpenQuestion holds

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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.