Evidence map›Paper›PMID 37542265›Full record

ArticleParasites & vectors2023

Genetic profiles of Schistosoma haematobium parasites from Malian transmission hotspot areas.

Privat Agniwo, Jérôme Boissier, Bakary Sidibé, Laurent Dembélé, Assitan Diakité, Doumbo Safiatou Niaré, Ahristode Akplogan, Hassim Guindo, Manon Blin, Sarah Dametto and 3 more

Erratum issuedAbstract read
In one paragraph

Article in Parasites & vectors, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–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

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  4. Review
  5. Article
  6. Schistosoma bovis Infecting Humans in Nigeria.The American journal of tropical medicine and hygiene · 2025
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Privat AgniwoDepartment of Epidemiology of Infectious Diseases, Faculty of Pharmacy, Malaria Research and Training Center (MRTC), University of Sciences, Techniques and Technologies of Bamako, Environnement, Santé, Sociétés (USTTB/UCAD/UGB/CNRST/CNRS), BP 1805, IRL 3189, Bamako, Mali.
Jérôme BoissierIHPE, University Montpellier, CNRS, Ifremer, University Perpignan Via Domitia, Perpignan, France.
Bakary SidibéDepartment of Epidemiology of Infectious Diseases, Faculty of Pharmacy, Malaria Research and Training Center (MRTC), University of Sciences, Techniques and Technologies of Bamako, Environnement, Santé, Sociétés (USTTB/UCAD/UGB/CNRST/CNRS), BP 1805, IRL 3189, Bamako, Mali.
Laurent DembéléDepartment of Epidemiology of Infectious Diseases, Faculty of Pharmacy, Malaria Research and Training Center (MRTC), University of Sciences, Techniques and Technologies of Bamako, Environnement, Santé, Sociétés (USTTB/UCAD/UGB/CNRST/CNRS), BP 1805, IRL 3189, Bamako, Mali.
Assitan DiakitéDepartment of Epidemiology of Infectious Diseases, Faculty of Pharmacy, Malaria Research and Training Center (MRTC), University of Sciences, Techniques and Technologies of Bamako, Environnement, Santé, Sociétés (USTTB/UCAD/UGB/CNRST/CNRS), BP 1805, IRL 3189, Bamako, Mali.
Doumbo Safiatou NiaréIHPE, University Montpellier, CNRS, Ifremer, University Perpignan Via Domitia, Perpignan, France.
Ahristode AkploganDepartment of Epidemiology of Infectious Diseases, Faculty of Pharmacy, Malaria Research and Training Center (MRTC), University of Sciences, Techniques and Technologies of Bamako, Environnement, Santé, Sociétés (USTTB/UCAD/UGB/CNRST/CNRS), BP 1805, IRL 3189, Bamako, Mali.
Hassim GuindoDepartment of Epidemiology of Infectious Diseases, Faculty of Pharmacy, Malaria Research and Training Center (MRTC), University of Sciences, Techniques and Technologies of Bamako, Environnement, Santé, Sociétés (USTTB/UCAD/UGB/CNRST/CNRS), BP 1805, IRL 3189, Bamako, Mali.
Manon BlinIHPE, University Montpellier, CNRS, Ifremer, University Perpignan Via Domitia, Perpignan, France.
Sarah DamettoIHPE, University Montpellier, CNRS, Ifremer, University Perpignan Via Domitia, Perpignan, France.
Moudachirou IbikounléCentre de Recherche pour la lutte contre les Maladies Infectieuses Tropicales (CReMIT/TIDRC), Université d'Abomey-Calavi, Abomey-Calavi, Bénin.
Thomas SpangenbergGlobal Health Institute of Merck, Ares Trading S.A., a subsidiary of Merck KGaA, Darmstadt, Route de Crassier 1, 1262, Eysins, Switzerland.
Abdoulaye DaboDepartment of Epidemiology of Infectious Diseases, Faculty of Pharmacy, Malaria Research and Training Center (MRTC), University of Sciences, Techniques and Technologies of Bamako, Environnement, Santé, Sociétés (USTTB/UCAD/UGB/CNRST/CNRS), BP 1805, IRL 3189, Bamako, Mali. daboabdoulaye17@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough schistosomiasis is a public health issue in Mali, little is known about the parasite genetic profile. The purpose of this study was to analyze the genetic profile of the schistosomes of Schistosoma haematobium group in school-aged children in various sites in Mali.

methodsUrine samples were collected from 7 to 21 November 2021 and subjected to a filtration method for the presence S. haematobium eggs. The study took place in two schistosomiasis endemic villages (Fangouné Bamanan and Diakalèl), qualified as hotspots according to the World Health Organization (WHO) definition. Molecular genotyping on both Cox1 and ITS2/18S was used for eggs' taxonomic assignation.

resultsA total of 970 miracidia were individually collected from 63 school-aged children and stored on Whatman FTA cards for molecular analysis. After genotyping 42.0% (353/840) and 58.0% (487/840) of miracidia revealed Schistosoma bovis and S. haematobium Cox1 profiles, respectively; 95.7 (885/925) and 4.3% (40/925) revealed S. haematobium and S. haematobium/S. curassoni profiles for ITS/18S genes, respectively. There was a significant difference in the Cox1 and ITS2/18S profile distribution according to the village (P < 0.0001). Overall, 45.6% (360/789) were hybrids, of which 72.0% (322/447) were from Diakalèl. Three hybrids' profiles (Sb/Sc_ShxSc with 2.3%; Sb/Sc_ShxSh with 40.5%; Sh_ShxSc with 2.8%) and one pure profile (Sh_ShxSh with 54.4%) were identified.

conclusionOur findings show, for the first time to our knowledge, high prevalence of hybrid schistosomes in Mali. More studies are needed on population genetics of schistosomes at the human and animal interface to evaluate the parasite's gene flow and its consequences on epidemiology of the disease as well as the transmission to humans.

Indexed as

ParasitesSchistosomiasisSchistosomiasis haematobiaAnimalsChildDisease HotspotGenetic ProfileHumansSchistosomaSchistosoma haematobiumCox1HybridizationITS/18SMaliSchistosoma bovisSchistosoma curassoniSchistosoma haematobium

Identifiers

PMID37542265
PMCPMC10403946

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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.