Evidence map›Paper›PMID 41681341›Full record

ArticleAnimals : an open access journal from MDPI2026

Surveillance of Swine Coronaviruses in Hungarian Herds with a Newly Established Pan-Coronavirus RT-PCR System.

Dóra Máté, Renáta Varga-Kugler, Eszter Kaszab, Henrik Fülöp Károlyi, Tamás Görföl, Gábor Kemenesi, Barbara Igriczi, Gyula Balka, Marianna Domán, Ádám Bálint and 2 more

Abstract read
In one paragraph

Article in Animals : an open access journal from MDPI, 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

12 authors.

Dóra MátéDepartment of Microbiology and Infectious Diseases, University of Veterinary Medicine Budapest, Hungária krt. 23-25, H-1143 Budapest, Hungary.ORCID 0009-0001-7200-4823
Renáta Varga-KuglerCeva-Phylaxia Ltd., Szállás utca 5, H-1107 Budapest, Hungary.ORCID 0000-0002-0093-5418
Eszter KaszabDepartment of Microbiology and Infectious Diseases, University of Veterinary Medicine Budapest, Hungária krt. 23-25, H-1143 Budapest, Hungary.ORCID 0000-0002-5750-1872
Henrik Fülöp KárolyiNational Laboratory of Virology, Szentágothai Research Centre, University of Pécs, Ifjúság útja 20, H-7624 Pécs, Hungary.ORCID 0009-0007-5035-7701
Tamás GörfölNational Laboratory of Virology, Szentágothai Research Centre, University of Pécs, Ifjúság útja 20, H-7624 Pécs, Hungary.ORCID 0000-0002-1910-4024
Gábor KemenesiNational Laboratory of Virology, Szentágothai Research Centre, University of Pécs, Ifjúság útja 20, H-7624 Pécs, Hungary.ORCID 0000-0001-9775-3065
Barbara IgricziNational Laboratory for Infectious Animal Diseases, Antimicrobial Resistance, Veterinary Public Health and Food Chain Safety, István utca 2, H-1078 Budapest, Hungary.ORCID 0000-0001-7372-3144
Gyula BalkaNational Laboratory for Infectious Animal Diseases, Antimicrobial Resistance, Veterinary Public Health and Food Chain Safety, István utca 2, H-1078 Budapest, Hungary.ORCID 0000-0003-2742-173X
Marianna DománHUN-REN Veterinary Medical Research Institute, Hungária krt. 21, H-1143 Budapest, Hungary.ORCID 0000-0002-1823-9971
Ádám BálintVetcontrol Ltd., Déli-Bekötő út 8, H-1211 Budapest, Hungary.
Zoltán ZádoriHUN-REN Veterinary Medical Research Institute, Hungária krt. 21, H-1143 Budapest, Hungary.ORCID 0000-0001-7312-618X
Enikő FehérDepartment of Microbiology and Infectious Diseases, University of Veterinary Medicine Budapest, Hungária krt. 23-25, H-1143 Budapest, Hungary.ORCID 0000-0001-7778-9116

Funding

Ministry of Culture and Innovation of Hungary 2024-2.1.1-EKÖP-2024-00018National Research, Development and Innovation Office FK137778National Research, Development and Innovation Office FK154149National Research, Development and Innovation Office RRF-2.3.1-21-2022-00001, National Laboratory for Infectious Animal Diseases, Antimicrobial Resistance, Veterinary Public Health and Food Chain Safety
6 · The paper itself

Abstract

The rapid evolution of coronaviruses (CoVs) requires researchers to develop specific yet broad-spectrum detection methods to monitor their constant genomic changes. The goal of the present study was to establish a current pan-coronavirus RT-PCR system capable of detecting a wide variety of CoVs and useful for the investigation of virus diversity and host spectrum. For optimization, one-step and two-step nested RT-PCRs with three RT enzymes were examined, amplifying a ~600 bp long product of the RNA-dependent RNA polymerase. As templates, the in vitro transcribed RNA of ten pathogenic CoVs (SARS-CoV, SARS-CoV-2, NL-63, OC43, feline CoV, porcine epidemic diarrhea virus or PEDV, transmissible gastroenteritis virus or TGEV, canine CoV, bat CoV, and infectious bronchitis virus) were applied instead of the often-used DNA standards. A limit of detection of 5-50 copies/reaction was achieved with a random hexamer-primed two-step RT-PCR and a touchdown cycling profile, representing a lower detection limit and higher specificity compared to previously published primer sets. Swine origin pooled samples (

Indexed as

avianhumanmammalianpan-coronavirusPCRswine

Identifiers

PMID41681341
PMCPMC12896397

What OpenQuestion holds

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LicenceCC BY
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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.