Evidence map›Paper›PMID 41432793›Full record

ArticleTropical animal health and production2025

Screening for SARS-CoV-2 in different sheep and goat breeds in Türkiye using in-house ELISAs and real-time PCR.

Mervenur Güvendi, Hüseyin Can, Çağrı Kandemir, Ecem Su Koçkaya, Ecem Sürgeç, Sedef Erkunt Alak, Özge Dülek, Turgay Taşkın, Muhammet Karakavuk, Aysu Değirmenci Döşkaya and 8 more

Abstract read
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Article in Tropical animal health and production, 2025. 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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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

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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

18 authors.

Mervenur GüvendiDepartment of Biology Molecular Biology Section, Faculty of Science, Ege University, İzmir, Türkiye.
Hüseyin CanDepartment of Biology Molecular Biology Section, Faculty of Science, Ege University, İzmir, Türkiye.
Çağrı KandemirDepartment of Animal Science, Faculty of Agriculture, Ege University, İzmir, Türkiye.
Ecem Su KoçkayaDepartment of Biology Molecular Biology Section, Faculty of Science, Ege University, İzmir, Türkiye.
Ecem SürgeçDepartment of Biology Molecular Biology Section, Faculty of Science, Ege University, İzmir, Türkiye.
Sedef Erkunt AlakDepartment of Biology Molecular Biology Section, Faculty of Science, Ege University, İzmir, Türkiye.
Özge DülekDepartment of Biology Molecular Biology Section, Faculty of Science, Ege University, İzmir, Türkiye.
Turgay TaşkınDepartment of Animal Science, Faculty of Agriculture, Ege University, İzmir, Türkiye.
Muhammet KarakavukVaccine Development Application and Research Center, Ege University, İzmir, Türkiye.
Aysu Değirmenci DöşkayaVaccine Development Application and Research Center, Ege University, İzmir, Türkiye.
Erkan PehlivanDepartment of Animal Science, Faculty of Agriculture, Ankara University, Ankara, Türkiye.
Halit Deniz ŞireliDepartment of Animal Science, Faculty of Agriculture, Dicle University, Diyarbakır, Türkiye.
Serdar KoçakDepartment of Animal Science, Faculty of Veterinary Medicine, Afyon Kocatepe University, Afyonkarahisar, Türkiye.
Ömer Faruk YılmazDepartment of Animal Science, Faculty of Agriculture, Ondokuz Mayıs University, Samsun, Türkiye.
Rana YılmazDepartment of Biology Molecular Biology Section, Faculty of Science, Ege University, İzmir, Türkiye.
Mert DöşkayaVaccine Development Application and Research Center, Ege University, İzmir, Türkiye.
Adnan Yüksel GürüzVaccine Development Application and Research Center, Ege University, İzmir, Türkiye.
Cemal ÜnDepartment of Biology Molecular Biology Section, Faculty of Science, Ege University, İzmir, Türkiye. cemaluen@gmail.com.

Funding

Türkiye Bilimsel ve Teknolojik Araştırma Kurumu 122O549
6 · The paper itself

Abstract

SARS-CoV-2, a type of coronavirus that infects humans, uses its spike protein to bind to the ACE-2 receptor during cell entry, which is highly conserved among vertebrates. Therefore, various animal species are thought to be susceptible to SARS-CoV-2 infection. In this study, we aimed to investigate the presence of SARS-CoV-2 RNA in swab samples using real-time PCR and anti-S1 IgG antibodies in serum samples using an in-house ELISA using recombinant S1 protein. Swab and serum samples were collected from different sheep and goat breeds living in different locations of Türkiye. In order to eliminate false seropositivity due to possible cross-reactions between bovine coronavirus (BCoV) and SARS-CoV-2 spike proteins, seropositive samples were further investigated by another ELISA using a SARS-CoV-2 spike specific peptide. According to the results of ELISA detecting anti-S1 IgG antibodies, 23 sheep serum samples (6.74%; 23/341) and 17 goat serum samples (22.07%; 17/77) were seropositive. After the analysis of these seropositive samples by peptide-ELISA, seroprevalence rates decreased to 3.81% (13/341) in sheep and 3.89% (3/77) in goats. According to the real-time PCR results, no SARS-CoV-2 RNA was detected in swab samples of sheep and goats. In conclusion, although SARS-CoV-2 specific antibodies were detected in sheep and goats, SARS-CoV-2 RNA was not detected and this does not suggest an important role for sheep or goats in the transmission of SARS-CoV-2 to other hosts, including humans.

Indexed as

COVID-19Goat DiseasesSARS-CoV-2Sheep DiseasesAnimalsAntibodies, ViralEnzyme-Linked Immunosorbent AssayGoatsImmunoglobulin GReal-Time Polymerase Chain ReactionRNA, ViralSeroepidemiologic StudiesSheepSpike Glycoprotein, CoronavirusTurkeyAntibodies, ViralImmunoglobulin GRNA, ViralSpike Glycoprotein, CoronavirusELISAPrevalenceReal-time PCRSARS-CoV-2Türkiye

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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.