Evidence map›Paper›PMID 42907751›Full record

ArticleBMC infectious diseases2026

Utility of recombinant Schistosoma bovis 22.6 kDa antigen for diagnosis of human urogenital schistosomiasis by ELISA: a cross-sectional study in Yewa North LGA, Ogun State, Nigeria.

Chiaka Anumudu, Abiola Ola, Maureen Efenovwe, Oluwayemisi Awobode, Rachael Ebuh, Cephas Akpabio, Christopher Anthony, Taiwo Banjo, Henrietta Awobode, Maria Trelis and 2 more

Abstract readEvaluation Study
In one paragraph

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

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

12 authors.

Chiaka AnumuduCellular Parasitology Programme, Department of Zoology, University of Ibadan, Ibadan, Nigeria. cianumudu@yahoo.com.
Abiola OlaCellular Parasitology Programme, Department of Zoology, University of Ibadan, Ibadan, Nigeria.
Maureen EfenovweParasitology Unit, Department of Zoology, University of Ibadan, Ibadan, Nigeria.
Oluwayemisi AwobodeCellular Parasitology Programme, Department of Zoology, University of Ibadan, Ibadan, Nigeria.
Rachael EbuhCellular Parasitology Programme, Department of Zoology, University of Ibadan, Ibadan, Nigeria.
Cephas AkpabioCellular Parasitology Programme, Department of Zoology, University of Ibadan, Ibadan, Nigeria.
Christopher AnthonyCellular Parasitology Programme, Department of Zoology, University of Ibadan, Ibadan, Nigeria.
Taiwo BanjoParasitology Unit, Department of Zoology, University of Ibadan, Ibadan, Nigeria.
Henrietta AwobodeParasitology Unit, Department of Zoology, University of Ibadan, Ibadan, Nigeria.
Maria TrelisParasites and Health Research Group, Department of Pharmacy and Pharmaceutical Technology and Parasitology, Faculty of Pharmacy, Universitat de València, València, Spain.
Antonio MarcillaParasites and Health Research Group, Department of Pharmacy and Pharmaceutical Technology and Parasitology, Faculty of Pharmacy, Universitat de València, València, Spain.
Ana OleagaAnimal Parasitology, Institute of Natural Resources and Agrobiology, Spanish National Research Council (IRNASA, CSIC), Salamanca, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn many endemic regions, accurately diagnosing urogenital schistosomiasis remains challenging, particularly in cases of low-intensity infection and limited laboratory capacity. Exploring antigens that cross-react between related schistosome species provides a promising alternative to conventional diagnostic approaches. Schistosoma bovis-an animal parasite closely related to S. haematobium and sharing the same Bulinus snail hosts in overlapping habitats- is a strong candidate for such studies. This work therefore assessed whether the recombinant S. bovis 22.6 kDa antigen (rSb22.6 kDa) could detect anti-schistosome antibodies in urine samples from individuals living in S. haematobium-endemic communities in Nigeria.

methodsUrine samples from 559 individuals (290 adults and 269 children; 235 males and 313 females) from four communities and schools in Yewa North Local Government Area, Ogun State, Nigeria, were collected. Samples were examined for S. haematobium eggs by microscopy, screened for anti-schistosomal antibodies using rSb 22.6 kDa ELISA, and analyzed for haematuria, leukocyturia, and proteinuria using reagent strips.

resultsPrevalence by microscopy was 13.9% (78/558), while 54.1% (299/553) of samples were seropositive by ELISA. Among ELISA-positive individuals, 29.8% had haematuria, 47.9% had leukocyturia, and 37.1% had proteinuria. Of 480 microscopy-negative individuals, 221 (46.0%) were ELISA-positive. When microscopy was used as the reference standard, the rSb 22.6 kDa-ELISA showed 46.2% sensitivity and 45.8% specificity. However, ELISA positivity correlated significantly with clinical markers of urogenital pathology (P < 0.05).

conclusionThe rSb 22.6 kDa antigen demonstrated cross-reactivity with antibodies in urine from individuals in S. haematobium-endemic communities. The high seropositivity compared to microscopy prevalence may reflect detection of low-intensity infections, past exposure with persistent antibodies, or ongoing transmission intensity in these communities. While the current performance of the assay does not support its use for individual diagnosis, it shows potential for sero-epidemiological surveillance in endemic areas. Further validation studies incorporating molecular diagnostics and longitudinal follow-up will clarify the significance of antibody positivity in the absence of detectable eggs. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

Antibodies, HelminthAntigens, HelminthSchistosomaSchistosomiasis haematobiaAdolescentAdultAnimalsChildChild, PreschoolCross-Sectional StudiesEnzyme-Linked Immunosorbent AssayFemaleHumansMaleMiddle AgedNigeriaAntibodies, HelminthAntigens, HelminthRecombinant ProteinsAntibody detectionCross-reactivityELISARecombinant S. bovis 22.6 kDa antigenSerodiagnosisUrogenital schistosomiasis

Identifiers

PMID42907751
PMCPMC13689337

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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.