Evidence map›Paper›PMID 40508063›Full record

ArticleInternational journal of molecular sciences2025

Inhibiting Infectious Bronchitis Virus PLpro Using Ubiquitin Variants.

Vera J E van Vliet, Olivia Roscow, Kihun Kim, Brian L Mark, Marjolein Kikkert, Christine Tait-Burkard

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. 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

6 authors.

Vera J E van VlietMolecular Virology Laboratory, Leiden University Center for Infectious Diseases (LUCID), Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.ORCID 0000-0003-0401-3055
Olivia RoscowDepartment of Biology, Faculty of Science, University of Waterloo, Waterloo, ON N2L 3G1, Canada.
Kihun KimDepartment of Microbiology, University of Manitoba, Winnipeg, MB R3T 2N2, Canada.ORCID 0000-0002-2379-4654
Brian L MarkDepartment of Microbiology, University of Manitoba, Winnipeg, MB R3T 2N2, Canada.
Marjolein KikkertMolecular Virology Laboratory, Leiden University Center for Infectious Diseases (LUCID), Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.ORCID 0000-0002-5779-7386
Christine Tait-BurkardThe Roslin Institute, Royal (Dick) School of Veterinary Studies, University of Edinburgh, Easter Bush, Midlothian EH25 9RG, UK.ORCID 0000-0002-0471-3230

Funding

Biotechnology and Biological Sciences Research Council BBS/E/D/20241866, BBS/E/D/20002172, and BBS/E/D/20002174Federation of European Microbiological Societies #1812Leiden University Fund W232015-2-1Natural Sciences and Engineering Research Council RGPIN-2020-05682
6 · The paper itself

Abstract

Infectious bronchitis virus (IBV) is a coronavirus first isolated in the 1930s infecting chickens. IBV causes great economic losses to the global poultry industry, as it affects egg production and causes mortality by leaving the host susceptible to secondary bacterial infections. Even though vaccines are available, they are poorly cross-protective against new variants of the virus, which are always on the cusp of emerging. Effective antiviral therapies, or possibly the production of transgenic animals immune to IBV infection, are therefore sorely needed. As the papain-like protease (PLpro) of IBV has deubiquitinating activity besides its crucial ability to cleave the viral polyprotein, we have applied a novel strategy of selecting ubiquitin variants (UbVs) from a phage-displayed library that have high affinity to this viral protease. These UbVs were found to inhibit the deubiquitinating activity of PLpro and consequently obstruct the virus's ability to evade the innate immune response in the host cell. By obstructing the proteolytic activity of PLpro, these UbVs were seemingly able to inhibit viral infection as assessed using immunofluorescence microscopy. Whilst virus infection was detected in around 5% of UbV-expressing cells, the virus was present in around 30-40% of GFP (control)-expressing cells. This suggests that the expression of UbVs indeed seems to inhibit IBV infection, making UbVs a potentially potent and innovative antiviral strategy in the quest for control of IBV infections.

Indexed as

Coronavirus InfectionsCoronavirus Papain-Like ProteasesInfectious bronchitis virusUbiquitinViral ProteinsAnimalsAntiviral AgentsCell LineChickensHumansImmunity, InnateAntiviral AgentsCoronavirus Papain-Like ProteasesUbiquitinViral Proteinsantiviralsavian infectious bronchitis viruscoronavirusesinnate immunityubiquitin variants

Identifiers

PMID40508063
PMCPMC12155308

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Registered trials

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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.