Evidence map›Paper›PMID 39201398›Full record

ArticleInternational journal of molecular sciences2024

Targeting Peptidylarginine Deiminase 3 to Efficiently Suppress Herpes Simplex Virus Type 2 Infection.

Selina Pasquero, Francesca Gugliesi, Matteo Biolatti, Camilla Albano, Greta Bajetto, Linda Trifirò, Stefano Raviola, Valentina Dell'Oste, Marco De Andrea

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

9 authors.

Selina PasqueroDepartment of Public Health and Pediatric Sciences, Medical School, University of Turin, 10124 Turin, Italy.ORCID 0000-0002-3815-2494
Francesca GugliesiDepartment of Public Health and Pediatric Sciences, Medical School, University of Turin, 10124 Turin, Italy.ORCID 0000-0001-6389-5129
Matteo BiolattiDepartment of Public Health and Pediatric Sciences, Medical School, University of Turin, 10124 Turin, Italy.ORCID 0000-0001-7675-0762
Camilla AlbanoDepartment of Public Health and Pediatric Sciences, Medical School, University of Turin, 10124 Turin, Italy.ORCID 0000-0002-0847-6332
Greta BajettoDepartment of Public Health and Pediatric Sciences, Medical School, University of Turin, 10124 Turin, Italy.ORCID 0000-0002-2339-2479
Linda TrifiròDepartment of Public Health and Pediatric Sciences, Medical School, University of Turin, 10124 Turin, Italy.ORCID 0009-0008-3441-6561
Stefano RaviolaCAAD Center for Translational Research on Autoimmune and Allergic Disease, University of Piemonte Orientale, Novara Medical School, 28100 Novara, Italy.ORCID 0000-0002-7626-2934
Valentina Dell'OsteDepartment of Public Health and Pediatric Sciences, Medical School, University of Turin, 10124 Turin, Italy.ORCID 0000-0002-9336-7906
Marco De AndreaDepartment of Public Health and Pediatric Sciences, Medical School, University of Turin, 10124 Turin, Italy.ORCID 0000-0002-3188-5783

Funding

Cassa di Risparmio of Turin Foundation RF=2021.1745EU funding within the MUR PNRR Extended Partnership initiative on Emerging Infectious Dis-eases Project no. PE00000007, INF-ACTIstituto di Ricerca Virologica Oretta Bartolomei Corsi", Florence, Italy 2023/2024Ministry of Education, University and Research - MUR PRIN Project 2022 ALPCMUniversity of Turin RILO2021, RILO2022 and RILO2023
6 · The paper itself

Abstract

Protein expression is regulated through multiple mechanisms, including post-translational modifications (PTMs), which can alter protein structure, stability, localization, and function. Among these, citrullination stands out due to its ability to convert arginine residues into citrulline, altering protein charge and mass. This modification is catalyzed by calcium-dependent protein arginine deiminases (PADs), enzymes implicated in various inflammatory diseases. We have recently shown that human cytomegalovirus (HCMV) and herpes simplex virus type 1 (HSV-1) exploit these enzymes to enhance their replication capabilities. Although the role of PADs in HCMV and HSV-1 infections is well documented, their involvement in HSV-2 infection has not yet been thoroughly investigated. Here, we demonstrate that HSV-2 manipulates the overall protein citrullination profile by activating three PAD isoforms: PAD2, PAD3, and PAD4. However, as previously observed during HSV-1 infection, PAD3 is the most significantly upregulated isoform, both at the mRNA and protein levels. Consistently, we demonstrate that inhibiting PAD3, either through the specific inhibitor CAY10727 or via CRISPR/Cas9-mediated gene silencing, markedly reduces HSV-2 replication and viral protein expression. Lastly, we show that CAY10727 displays an IC50 value of 0.3 μM, which is extremely close to what was previously observed for HSV-1. Overall, our findings highlight the crucial role of PAD3 in the life cycle of HSV-2 and suggest that the targeted inhibition of PAD3 may represent a promising approach for treating HSV-2 infections, especially in cases resistant to existing antiviral therapies.

Indexed as

Herpesvirus 2, HumanProtein-Arginine Deiminase Type 3AnimalsAntiviral AgentsCitrullinationHerpes GenitalisHerpes SimplexHumansProtein-Arginine Deiminase Type 2Virus ReplicationAntiviral AgentsPADI2 protein, humanProtein-Arginine Deiminase Type 2Protein-Arginine Deiminase Type 3citrullinationherpes simplex virus type 2 (HSV-2)host-targeting antivirals (HTAs)protein arginine deiminase type 3 (PAD3, PADI3)

Identifiers

PMID39201398
PMCPMC11354815

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.