Equine herpesvirus type 1 (EHV-1) replication in primary murine neurons culture.
Abstract: Equine herpesvirus-1 (EHV-1) infections cause significant economic losses for equine industries worldwide as a result of abortion, respiratory illness, and neurologic disease in all breeds of horses. The occurrence of abortions caused by EHV-1 has repeatedly been confirmed in Poland, but neurological manifestations of the infection have not been described yet. Also it is unknown how the infection of neurons with non-neuropathogenic strains is regulated. To further understand the virus-neuron interaction we studied two strains of EHV-1 in murine primary neuron cell cultures. Both strains were isolated from aborted fetuses: Rac-H, a reference strain isolated by Woyciechowska in 1959 (Woyciechowska 1960) and Jan-E isolated by Bańbura et al. (Bańbura et al. 2000). Upon infection of primary murine neuronal cell cultures with Jan-E or Rac-H strains, a cytopathic effect was observed, manifested by a changed morphology and disintegration of the cell monolayer. Positive results of immunofluorescence, nPCR and real-time PCR tests indicated high virus concentration in neurons, meaning that both EHV-1 strains were likely to replicate in mouse neurons in vitro without the need for adaptation. Moreover, we demonstrated that some neurons may survive (limited) virus replication during primary infection, and these neurons (eight weeks p.i.) harbour EHV-1 and were still able to transmit infection to other cells.
Publication Date: 2010-01-01 PubMed ID: 21370750DOI: 10.2478/v10181-010-0022-3Google Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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This research investigates the replication of two strains of Equine herpesvirus type 1 (EHV-1) in primary murine neuron cell cultures. The study underlines that both EHV-1 strains, known for causing significant issues in horse industries, can multiply in mouse neurons without the need for adaptation, and some neurons can survive this process and transmit the infection further.
Study Background
- The research focuses on EHV-1, a virus that leads to significant economic losses within the global horse industries due to instances of abortion, respiratory disease, and neurological illness.
- Instances of abortion due to EHV-1 have been frequently confirmed in Poland, but there have been no detailed studies concerning the neurological symptoms arising from the infection.
- The purpose of this study is to analyze how the infection of neurons with non-neuropathogenic strains progresses and interacts with the neurons.
Approach and Methodology
- Two EHV-1 strains, namely Jan-E and Rac-H, were studied in the context of murine primary neuron cell cultures. Both these strains were collected from aborted fetuses.
- Rac-H is a reference strain first isolated in 1959 by Woyciechowska, while Jan-E was isolated by Bańbura and colleagues in the year 2000.
- These strains were used to infect primary murine neuronal cell cultures, and specific changes observed in the morphology and integrity of the cell monolayer, commonly labelled as a cytopathic effect, were tracked.
Outcomes & Findings
- Post the infection of the neuronal cell cultures with either Jan-E or Rac-H strains, positive results of immunofluorescence, nPCR, and real-time PCR tests were obtained, indicating a high virus concentration within the neurons.
- The study concludes that both strains of EHV-1 have shown potential to replicate within neurons of murine origin without needing adaptation in vitro.
- Remarkably, some neurons exhibited resilience against the virus replication during primary infection and lived through the process.
- These survivors (eight weeks post-infection) continued to harbor EHV-1 and demonstrated a capacity to transmit the infection to other cells.
Implications
- The discovery that these EHV-1 strains were able to replicate in murine neurons has significant implications for the understanding of EHV-1, including the virus’s potential ability to affect other species beyond equines.
- The survival and further infection capabilities of some neurons post-infection suggest alternative avenues for the virus’s propagation and persistence, which may need to be taken into account in the development of treatment methods and preventative measures in the future.
Cite This Article
APA
Cymerys J, Dzieciatkowski T, Słońska A, Bierla J, Tucholska A, Chmielewska A, Golke A, Bańbura MW.
(2010).
Equine herpesvirus type 1 (EHV-1) replication in primary murine neurons culture.
Pol J Vet Sci, 13(4), 701-708.
https://doi.org/10.2478/v10181-010-0022-3 Publication
Researcher Affiliations
- Division of Virology, Department of Preclinical Science, Faculty of Veterinary Medicine, Warsaw University of Life Science (SGGW), Ciszewskiego 8, 02-786 Warsaw, Poland. jcymerys@op.pl
MeSH Terms
- Animals
- Cells, Cultured
- DNA, Viral
- Herpesvirus 1, Equid / physiology
- Mice
- Neurons / virology
- Virus Replication / physiology
Citations
This article has been cited 5 times.- Chodkowski M, Słońska A, Gregorczyk-Zboroch K, Nowak-Zyczynska Z, Golke A, Krzyżowska M, Bańbura MW, Cymerys J. Equid Alphaherpesvirus 1 (EHV-1) Influences Morphology and Function of Neuronal Mitochondria In Vitro.. Pathogens 2022 Aug 3;11(8).
- Bartak M, Chodkowski M, Słońska A, Grodzik M, Szczepaniak J, Bańbura MW, Cymerys J. Equid Alphaherpesvirus 1 Modulates Actin Cytoskeleton and Inhibits Migration of Glioblastoma Multiforme Cell Line A172.. Pathogens 2022 Mar 25;11(4).
- Cymerys J, Kowalczyk A, Mikołajewicz K, Słońska A, Krzyżowska M. Nitric Oxide Influences HSV-1-Induced Neuroinflammation.. Oxid Med Cell Longev 2019;2019:2302835.
- Cymerys J, Słońska A, Tucholska A, Golke A, Chmielewska A, Bańbura MW. Influence of long-term equine herpesvirus type 1 (EHV-1) infection on primary murine neurons-the possible effects of the multiple passages of EHV-1 on its neurovirulence.. Folia Microbiol (Praha) 2018 Jan;63(1):1-11.
- Słońska A, Cymerys J, Godlewski MM, Dzieciątkowski T, Tucholska A, Chmielewska A, Golke A, Bańbura MW. Equine herpesvirus type 1 (EHV-1)-induced rearrangements of actin filaments in productively infected primary murine neurons.. Arch Virol 2014 Jun;159(6):1341-9.
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