Evidence map›Paper›PMID 41872927›Full record

ArticleParasites & vectors2026

Improved serological testing for bovine schistosomiasis in Eastern Africa.

Veronika Tóth, Thomas A Gasan, Bethany Crooks, Jahashi Nzalawahe, Alexandra Juhász, James E LaCourse, J Russell Stothard, Shaali M Ame, Wei Hu, Geoffrey N Gobert

Abstract read
In one paragraph

Article in Parasites & vectors, 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

10 authors.

Veronika Tóth *School of Biological Sciences, Queen's University Belfast, Belfast, UK.
Thomas A Gasan *School of Biological Sciences, Queen's University Belfast, Belfast, UK.
Bethany CrooksSchool of Biological Sciences, Queen's University Belfast, Belfast, UK.
Jahashi NzalawaheSokoine University of Agriculture, Morogoro, Tanzania.
Alexandra JuhászDepartment of Tropical Disease Biology, Liverpool School of Tropical Medicine, Liverpool, L3 5QA, UK.
James E LaCourseDepartment of Tropical Disease Biology, Liverpool School of Tropical Medicine, Liverpool, L3 5QA, UK.
J Russell StothardDepartment of Tropical Disease Biology, Liverpool School of Tropical Medicine, Liverpool, L3 5QA, UK.
Shaali M AmePublic Health Laboratory, Ivo de Carneri, Pemba, United Republic of Tanzania.
Wei HuNational Institute of Parasitic Diseases, Chinese Centre for Disease Control and Prevention (Chinese Centre for Tropical Diseases Research), National Health Commission Key Laboratory of Parasite and Vector Biology, WHO Collaborating Centre for Tropical Diseases, National Centre for International Research on Tropical Diseases, Shanghai, China.
Geoffrey N GobertSchool of Biological Sciences, Queen's University Belfast, Belfast, UK. G.Gobert@qub.ac.uk.

Funding

Royal Academy of Engineering, UK FF\1920\1\10
6 · The paper itself

Abstract

backgroundIn East Africa, bovine schistosomiasis, although common, is poorly appreciated and managed, detrimentally impacting upon livestock health. In certain settings, bovine schistosomiasis may be involved in zoonotic transmission of human schistosomiasis. Better disease management and more effective control of bovine schistosomiasis require the development of sensitive and specific serological screening and rapid diagnostic tools.

methodsWe developed an enzyme-linked immunosorbent assay (ELISA) for Schistosoma bovis detection in cattle, utilizing nine shortlisted potential diagnostic protein targets. These shortlisted candidates, STI, IPP, OP, PGK1, COG, PDZ, and Sbp80 (as three fragments), were identified from Schistosoma japonicum homologs already reported with the highest diagnostic potential. In S. bovis, these proteins participate in various biological processes, including metabolic pathways, transcriptional regulation, glycolysis, phosphorylation, and cell signalling, although their real diagnostic potential has not been explored until now.

resultsThe ELISA was optimized using bovine blood serum samples from regions in Tanzania and validated for sensitivity and specificity. Two targets of specific focus, Conserved Oligomerix Golgi complex subunit 4 (COG) and a domain of the cysteine protease calpain (Sbp80), achieved the highest specificity and sensitivity among the recombinant proteins, with 92% and 88% sensitivity and 100% and 80% specificity, respectively. We further evaluated the COG-based and calpain-based ELISA on further "real-world" bovine serum samples from abattoir sites in Zanzibar, detecting S. bovis in 59.1% of tested animals.

conclusionsBoth COG and calpain are promising candidates for serological screening and later inclusion in portable diagnostic tests for S. bovis infection in cattle. Such future diagnostic assays will enable better point-of-detection monitoring, and once scalable, aid in the control of disease in cattle.

Indexed as

Cattle DiseasesSchistosomaSchistosomiasisSerologic TestsAfrica, EasternAnimalsAntibodies, HelminthAntigens, HelminthCattleEnzyme-Linked Immunosorbent AssaySensitivity and SpecificityAntibodies, HelminthAntigens, HelminthAfricaBovineCattleDiagnosticELISAOne HealthSchistosomaSchistosoma bovisSchistosomiasisSerum

Identifiers

PMID41872927
PMCPMC13130579

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.