Dual infections of equine herpesvirus 1 and equine arteritis virus in equine respiratory mucosa explants.
Abstract: Equine herpesvirus 1 (EHV-1) and equine arteritis virus (EAV) induce respiratory problems and abortion in horses and are considered as two serious threats to equine industry. Both EHV-1 and EAV misuse patrolling leukocytes in the upper respiratory tract to breach the basement membrane (BM) and to migrate to blood vessels. So far, the behavior and impact of a double infection in the respiratory mucosa of a horse are unknown. In the present study, the outcome of double infections with EHV-1 and the low virulent EAV strain 08P187 (superinfection with an interval of 12h or co-infection) were compared with single infections in fully susceptible RK-13 cells and equine upper respiratory mucosa explants. When RK-13 cells were inoculated with either EHV-1 or EAV 12h prior to the subsequent EAV or EHV-1 inoculation, the latter EAV or EHV-1 infection was clearly suppressed at 24hpi or 36hpi, respectively, without EHV-1 and EAV co-infecting the same RK-13 cells. After simultaneous infection with EHV-1 and EAV, higher numbers of EAV infected cells but similar numbers of EHV-1 infected cells were found compared to the single infections, with a low number of EHV-1 and EAV co-infected RK-13 cells at 48hpi and 72hpi. In the upper respiratory mucosa exposed to EAV 12h prior to EHV-1, the number and size of the EHV-1-induced plaques were similar to those of the EHV-1 single infected mucosa explants. In nasal and nasopharyngeal mucosae, EAV and EHV-1 pre-infections slightly reduced the number of EHV-1 and EAV infected leukocytes compared to the single infections and co-infection. In double EAV and EHV-1 infected explants, no co-infected leukocytes were detected. From these results, it can be concluded that EAV and EHV-1 are only slightly influencing each other's infection and that they do not infect the same mucosal leukocytes.
Copyright © 2016 Elsevier B.V. All rights reserved.
Publication Date: 2016-04-23 PubMed ID: 27117322DOI: 10.1016/j.virusres.2016.04.013Google Scholar: Lookup
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- Journal Article
Summary
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The research investigates the impact of dual infections of Equine Herpesvirus 1 (EHV-1) and Equine Arteritis Virus (EAV) in horses, with their results suggesting these infections don’t significantly influence each other and do not infect the same mucosal leukocytes.
Objectives and Methodology
- The researchers embarked on this study to ascertain the effect and behavior of both EHV-1 and EAV – responsible for respiratory issues and abortion in horses – when there is a dual infection in the respiratory mucosa of a horse.
- The investigation included comparing the consequences of dual infections and single infections in RK-13 cells (which are fully susceptible to these viruses) and equine upper respiratory mucosa explants.
- The process of superinfection involved infecting the cells with one virus, waiting 12 hours, and then infecting the same cells with the other virus. In co-infection, both viruses were introduced at the same time.
Findings
- Results showed that when RK-13 cells were initially infected with either EHV-1 or EAV, followed by an infection of the other virus after 12 hours, the subsequent virus infection was suppressed at 24 hours post-infection or 36 hours post-infection respectively.
- In the case of simultaneous infection, there was an increase in the numbers of EAV-infected cells while EHV-1 infected cell numbers remained the same when compared to single virus infections.
- No co-infection of EHV-1 and EAV was observed in any of the RK-13 cells, indicating that both viruses do not infect the same cells.
- In the respiratory mucosa that was exposed to EAV 12 hours prior to EHV-1, EHV-1-induced plaques (damage caused by the virus) were similar in size and number to those found in single virus infections.
- Pre-infections and co-infections of both viruses resulted in a slight reduction in the number of virus-infected leukocytes in the nasal and nasopharyngeal mucosae compared to single infections.
Conclusions
- The study concluded that dual infections of EHV-1 and EAV do not significantly affect each other’s propagation and do not co-infect the same mucosal leukocytes within the horse’s respiratory system.
- This research provides critical insights into the dynamics of these dual infections, which can help develop effective strategies to manage and treat these conditions.
Cite This Article
APA
Zhao J, Negussie H, Laval K, Poelaert KC, Nauwynck HJ.
(2016).
Dual infections of equine herpesvirus 1 and equine arteritis virus in equine respiratory mucosa explants.
Virus Res, 220, 104-111.
https://doi.org/10.1016/j.virusres.2016.04.013 Publication
Researcher Affiliations
- Laboratory of Virology, Department of Virology, Parasitology and Immunology, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium.
- Laboratory of Virology, Department of Virology, Parasitology and Immunology, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium.
- Laboratory of Virology, Department of Virology, Parasitology and Immunology, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium.
- Laboratory of Virology, Department of Virology, Parasitology and Immunology, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium.
- Laboratory of Virology, Department of Virology, Parasitology and Immunology, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium. Electronic address: Hans.Nauwynck@UGent.be.
MeSH Terms
- Animals
- Arterivirus Infections / veterinary
- Arterivirus Infections / virology
- Cell Line
- Coinfection
- Epithelial Cells / virology
- Equartevirus / pathogenicity
- Equartevirus / physiology
- Herpesviridae Infections / veterinary
- Herpesviridae Infections / virology
- Herpesvirus 1, Equid / pathogenicity
- Herpesvirus 1, Equid / physiology
- Horse Diseases / virology
- Horses
- Leukocytes / virology
- Respiratory Mucosa / virology
- Tissue Culture Techniques
- Viral Load
- Virus Replication
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