Evidence map›Paper›PMID 40936274›Full record

ArticleJournal of veterinary science2025

Ivermectin inhibits replication of porcine deltacoronavirus

Duri Lee, Sungrae Kim, Phyo Wai Win, Guehwan Jang, Changhee Lee

Abstract read
In one paragraph

Article in Journal of veterinary science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Computational design of an ultrapotent deltacoronavirus miniprotein inhibitor.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
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

5 authors.

Duri Lee *College of Veterinary Medicine and Virus Vaccine Research Center, Gyeongsang National University, Jinju 52828, Korea.ORCID https://orcid.org/0000-0002-4311-2526
Sungrae Kim *College of Veterinary Medicine and Virus Vaccine Research Center, Gyeongsang National University, Jinju 52828, Korea.ORCID https://orcid.org/0009-0009-6177-6551
Phyo Wai WinCollege of Veterinary Medicine and Virus Vaccine Research Center, Gyeongsang National University, Jinju 52828, Korea.ORCID https://orcid.org/0000-0002-2672-2584
Guehwan JangCollege of Veterinary Medicine and Virus Vaccine Research Center, Gyeongsang National University, Jinju 52828, Korea. wayyonim12@naver.com.ORCID https://orcid.org/0000-0003-3108-8087
Changhee LeeCollege of Veterinary Medicine and Virus Vaccine Research Center, Gyeongsang National University, Jinju 52828, Korea. changhee@gnu.ac.kr.ORCID https://orcid.org/0000-0002-5930-5461

Funding

National Research Foundation of Korea RS-2023-00251145
6 · The paper itself

Abstract

importancePorcine deltacoronavirus (PDCoV) is an emerging swine enteric coronavirus that threatens the pig industry and acts as a viral spillover, infecting other farm animals and potentially humans. The recent emergence of highly pathogenic PDCoV in South Korea, causing severe neonatal piglet mortality, underscores the urgent need for effective countermeasures to mitigate economic and public health risks. Thus, discovering new therapeutic methods through drug repurposing is crucial for controlling PDCoV.

objectiveThis study investigated ivermectin (IVM) for its antiviral effect on PDCoV

methodsThe antiviral effects and mechanism of action of IVM against PDCoV were evaluated using various virological assays.

resultsIVM markedly impaired the replication of PDCoV in a dose-dependent manner. Time-of-addition assays showed that the anti-PDCoV activity of IVM was most potent when administered before infection, simultaneously with infection, or immediately after infection. Further mode of action experiments revealed that IVM targeted the replication stage of PDCoV infection at post-entry steps. CONCLUSIONS AND RELEVANCE: Our results indicated that IVM interfered with PDCoV genome replication by impairing viral RNA synthesis. These findings suggest the potential of IVM for inhibiting PDCoV RNA polymerase and provide an invaluable therapeutic strategy to combat PDCoV infection with IVM, offering a viable alternative in the absence of commercial vaccines.

Indexed as

Antiviral AgentsCoronavirus InfectionsDeltacoronavirusIvermectinVirus ReplicationAnimalsSwineSwine DiseasesAntiviral AgentsIvermectinanti-PDCoV activityivermectinPDCoVtherapeutic strategyviral RNA

Identifiers

PMID40936274
PMCPMC12511896

What OpenQuestion holds

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LicenceCC BY-NC
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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.