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Frontiers in veterinary science2023; 10; 1165917; doi: 10.3389/fvets.2023.1165917

Anti-inflammatory compounds reduce equine herpesvirus type 1 replication and cell-to-cell spread.

Abstract: Equine herpesvirus type 1 (EHV-1) is a highly transmissible pathogen that leads to a variety of clinical disease outcomes in infected horses. A major sequela that can occur after an EHV-1 infection is a neurological disease termed equine herpesvirus myeloencephalopathy (EHM). Clinical manifestations of EHM include fever, ataxia, incontinence, and partial to full paralysis, which may ultimately lead to the euthanization of the infected horse. To develop an effective treatment strategy for EHM, it is critical that the specific virus-host interactions that lead to EHM be investigated so that safe and effective therapeutic interventions can be developed and delivered. In this study, we examined the ability of four non-steroidal anti-inflammatory drugs (NSAIDs), a steroidal anti-inflammatory drug (dexamethasone), a Rho-kinase (ROCK) inhibitor, and a JAK/STAT inhibitor (AG490) to reduce EHV-1 virus yields and cell-to-cell spread. We show that the NSAID, flunixin meglumine (FM), and the JAK/STAT inhibitor, AG490, significantly reduced virus yields in endothelial and epithelial cell lines, and this inhibition was similar for two neurologic and two non-neurologic EHV-1 strains. In addition to reducing virus yields, AG490 and FM also significantly reduced the ability of EHV-1 to spread laterally from cell to cell.
Publication Date: 2023-05-19 PubMed ID: 37275614PubMed Central: PMC10235532DOI: 10.3389/fvets.2023.1165917Google Scholar: Lookup
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  • Journal Article

Summary

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This study investigates the use of certain anti-inflammatory compounds to reduce the replication and spread of equine herpesvirus type 1 (EHV-1), a virus that can lead to severe neurological illnesses in horses.

Objective of the research

  • The main goal of the study was to evaluate the impact of different anti-inflammatory compounds on the replication and cell-to-cell spread of EHV-1. This was done with the aim of identifying potential therapeutic interventions for equine herpesvirus myeloencephalopathy (EHM), a serious neurological condition that can result from EHV-1 infection and could force euthanization of the infected horse.

Research Methods and Compounds Tested

  • The study specifically looked at four non-steroidal anti-inflammatory drugs (NSAIDs), a steroidal anti-inflammatory drug (dexamethasone), a Rho-kinase inhibitor, and a JAK/STAT inhibitor (AG490), and their effect on EHV-1 virus yields and spread.

Results of the study

  • The results of the study showed that flunixin meglumine (FM) – an NSAID, and AG490 – a JAK/STAT inhibitor, significantly reduced virus yields in endothelial and epithelial cell lines. This level of inhibition was similar for both neurologic and non-neurologic EHV-1 strains, indicating that these compounds could be effective against different forms of the virus.
  • Notably, AG490 and FM also notably reduced the ability of the EHV-1 to spread laterally from cell-to-cell. This is highly significant as it could potentially prevent the spread of the virus within the host, thus curtailing the progress and severity of the infection.

Implication of the Research

  • The findings of this research could pave the way for the development of a new therapeutic approach for EHM, by controlling and reducing the spread of EHV-1 using the compounds tested. This could potentially save many horses from being euthanized due to severe neurological illness resulting from EHV-1 infection.

Cite This Article

APA
Black JB, Frampton AR. (2023). Anti-inflammatory compounds reduce equine herpesvirus type 1 replication and cell-to-cell spread. Front Vet Sci, 10, 1165917. https://doi.org/10.3389/fvets.2023.1165917

Publication

ISSN: 2297-1769
NlmUniqueID: 101666658
Country: Switzerland
Language: English
Volume: 10
Pages: 1165917

Researcher Affiliations

Black, Jeanette B
  • Department of Biology and Marine Biology, University of North Carolina Wilmington, Wilmington, NC, United States.
Frampton, Arthur R
  • Department of Biology and Marine Biology, University of North Carolina Wilmington, Wilmington, NC, United States.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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