Evidence map›Paper›PMID 41026115›Full record

ArticleVeterinary medicine and science2025

Serological and Molecular Detection of Toxoplasma gondii Among Slaughtered Domestic Ruminants in Gondar Town, Northwest Ethiopia.

Tsedalu Yirsa, Zewdu Seyoum, Mequanente Dagnaw, Nega Berhane

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Article in Veterinary medicine and science, 2025. 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 3 papers.

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3citing papers 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

3 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Tsedalu YirsaDepartment of Veterinary Medicine, College of Agriculture, Woldia University, Woldia, Ethiopia.ORCID https://orcid.org/0000-0002-6100-1598
Zewdu SeyoumDepartment of Veterinary Paraclinical Studies, College of Veterinary Medicine and Animal Sciences, University of Gondar, Gondar, Ethiopia.
Mequanente DagnawDepartment of Epidemiology and Biostatistics, Department of Medical Biotechnology, Institute of Public Health, Institute of Biotechnology, University of Gondar, Gondar, Ethiopia.
Nega BerhaneDepartment of Epidemiology and Biostatistics, Department of Medical Biotechnology, Institute of Public Health, Institute of Biotechnology, University of Gondar, Gondar, Ethiopia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundToxoplasma gondii is a globally prevalent zoonotic protozoan parasite that forms cysts and infects both animals and humans. Although there are reports on its seroprevalence, no comparative studies have validated the presence of this parasite in Ethiopian food animals.

objectivesThis study assessed and compared serological and molecular techniques for the detection of T. gondii in slaughtered domestic ruminants in the study area.

methodsA cross-sectional study was conducted from September 2019 to October 2020 by collecting 320 blood and corresponding tissue samples from purposively selected animals. The presence of this disease was identified using the latex agglutination test (LAT) and nested polymerase chain reaction (nPCR). SPSS version 25 with chi-square and logistic regression analyses was used to determine the relationship between associated risk factors and seropositivity of this disease.

findingsThe overall findings on the presence of this infection among slaughtered animals showed positivity rates of 180 (56.2%) through latex ATs, 68 (21.2%) in the first PCR run and 34 (10.6%) in the second PCR run. In latex ATs, positivity rates were recorded as 62% (62/100) in sheep, 52.7% (58/110) in goats and 54.5% (60/110) in cattle. The first PCR amplification detected positive cases in 34% (34/100) of sheep, 21.8% (24/110) of goats and 9.1% (10/110) of cattle. The second PCR amplification identified positivity in 20% (20/100) of sheep and 12.5% (14/110) of goats, whereas no positive cases were found in cattle. Seropositivity showed a significant association with sex and age in sheep and goats, origin in goats and breed and age in cattle (p value ≤ 0.05). A slight level of agreement was observed between latex agglutination and the first PCR test (Kappa = 0.230), whereas a fair agreement was noted between first PCR and nPCR (K = 0.338). Overall, nPCR demonstrated higher specificity (83.9%) compared to first PCR and the latex AT for detecting this disease.

conclusionsThus, comparative detection confirms its presence in slaughtered food animals, aiding in early effective prevention and control for food consumption. Further research on pathogen genotyping is strongly recommended.

Indexed as

Cattle DiseasesGoat DiseasesSheep DiseasesToxoplasmaToxoplasmosis, AnimalAbattoirsAnimalsCattleCross-Sectional StudiesEthiopiaFemaleGoatsLatex Fixation TestsMalePolymerase Chain ReactionPrevalenceGondarlatex agglutinationpolymerase chain reaction (PCR)slaughtered animalsToxoplasma gondii

Identifiers

PMID41026115
PMCPMC12482520

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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.