Evidence map›Paper›PMID 38620029›Full record

ArticlePLoS neglected tropical diseases2024

Extant interspecific hybridization among trematodes within the Schistosoma haematobium species complex in Nigeria.

Oluwaremilekun G Ajakaye, Elisha E Enabulele, Joshua B Balogun, Oyetunde T Oyeyemi, Michael E Grigg

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Molecular Identification ofTropical medicine and infectious disease · 2026
    Article
  2. Article
  3. Review
  4. Review
  5. Schistosoma bovis Infecting Humans in Nigeria.The American journal of tropical medicine and hygiene · 2025
    Article
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

5 authors at 3 institutions in 2 countries.

Oluwaremilekun G AjakayeMolecular Parasitology Section, Laboratory of Parasitic Diseases, NIAID, National Institutes of Health, Bethesda Maryland, United States of America.
Elisha E EnabuleleDisease Intervention and Prevention Program, Biomedical Research Institute, San Antonio, Texas, United States of America.
Joshua B BalogunDepartment of Biological Sciences Federal University, Dutse, Nigeria.
Oyetunde T OyeyemiDepartment of Biosciences and Biotechnology, University of Medical Sciences, Ondo, Nigeria.
Michael E GriggMolecular Parasitology Section, Laboratory of Parasitic Diseases, NIAID, National Institutes of Health, Bethesda Maryland, United States of America.ORCID 0000-0003-3465-3782
National Institutes of Health · USTexas Biomedical Research Institute · USUniversity of Medical Sciences, Ondo

Funding

Toxoplasma Population GeneticsZIAAI001018 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI GRIGG, MICHAEL · 2009 to 2025
$11.3M
Toxoplasma Population GeneticsZ01AI001018 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI GRIGG, MICHAEL · 2007 to 2008
$801k
Intramural NIH HHS Z01 AI001018Wellcome Trust
6 · The paper itself

Abstract

backgroundNatural interspecific hybridization between the human parasite (Schistosoma haematobium [Sh]) and bovine parasites (Schistosoma bovis [Sb], Schistosoma curassoni [Sc]) is increasingly reported in Africa. We developed a multi-locus PCR DNA-Seq strategy that amplifies two unlinked nuclear (transITS, BF) and two linked organellar genome markers (CO1, ND5) to genotype S. haematobium eggs collected from infected people in Ile Oluji/Oke Igbo, Ondo State (an agrarian community) and Kachi, Jigawa State (a pastoral community) in Southwestern and Northern Nigeria, respectively. PRINCIPAL

findingsOut of a total of 219 urine samples collected, 57 were positive for schistosomes. All patients from Jigawa state possessed an Sh mitochondrial genome and were infected with a genetic profile consistent with an Sh x Sb hybrid based on sequences obtained at CO1, ND5, transITS and BF nuclear markers. Whereas samples collected from Ondo state were more varied. Mitonuclear discordance was observed in all 17 patients, worms possessed an Sb mitochondrial genome but one of four different genetic profiles at the nuclear markers, either admixed (heterozygous between Sh x Sc or Sh x Sb) at both markers (n = 10), Sh at BF and admixed at transITS (Sh x Sc) (n = 5), admixed (Sh x Sc) at BF and homozygous Sc at transITS (n = 1) or homozygous Sh at BF and homozygous Sc at transITS (n = 1). SIGNIFICANCE: Previous work suggested that zoonotic transmission of S. bovis in pastoral communities, where humans and animals share a common water source, is a driving factor facilitating interspecific hybridization. However, our data showed that all samples were hybrids, with greater diversity identified in Southwestern Nigeria, a non-pastoral site. Further, one patient possessed an S. bovis mitochondrial genome but was homozygous for S. haematobium at BF and homozygous for S. curassoni at transITS supporting at least two separate backcrosses in its origin, suggesting that interspecific hybridization may be an ongoing process.

Indexed as

Hybridization, GeneticSchistosoma haematobiumSchistosomiasis haematobiaAdultAnimalsDNA, HelminthFemaleGenome, MitochondrialGenotypeHumansMaleNigeriaDNA, Helminth

Identifiers

PMID38620029
PMCPMC11045100
OpenAlexW4394805587

What OpenQuestion holds

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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.