Differential susceptibility of equine and mouse brain microvascular endothelial cells to equine herpesvirus 1 infection.
Abstract: Equine herpesvirus 1 (EHV-1) shows endotheliotropism in the central nervous system (CNS) of infected horses. However, infection of endothelial cells has not been observed in the CNS of infected mice. To explore the basis for this difference in endotheliotropism, we compared the susceptibility of equine brain microvascular endothelial cells (EBMECs) and mouse brain microvascular endothelial cells (MBMECs) to EHV-1 infection. The kinetics of viral growth in EBMECs was typical of a fully productive infection whereas viral infection in MBMECs seemed to be nonproductive. Immunofluorescence microscopy using anti-EHV-1 polyclonal antibody demonstrated viral antigen in infected EBMECs, but not infected MBMECs. EHV-1 immediate early (IE), early (ICP0), and late (gB, gD and gK) transcripts were expressed in infected EBMECs. However, none of these genes was detected in infected MBMECs by reverse transcription-polymerase chain reaction. Electron microscopic examination at the stage of viral entry showed that viral particles were present within uncoated vesicles in the cytoplasm of EBMECs, but absent from those of MBMECs. These results suggest that viral entry is an important determinant of the susceptibility of EBMECs and MBMECs to EHV-1 infection.
Publication Date: 2005-11-17 PubMed ID: 16328147DOI: 10.1007/s00705-005-0653-3Google Scholar: Lookup
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- Comparative Study
- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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This research paper investigates why equine herpesvirus 1 (EHV-1) affects the central nervous system (CNS) of horses but not mice, by comparing the virus’s impact on endothelial cells from both species. The study found that the virus enters and behaves differently in these cells, suggesting that the method of viral entry plays a significant role in species susceptibility to EHV-1 infection.
Key Research Findings
- The researchers investigated EHV-1, a virus that displays endotheliotropism – a predilection for attacking the endothelial cells – in horses’ central nervous system (CNS).
- However, EHV-1 does not infect endothelial cells in mice’s CNS, a divergence the researchers sought to understand.
- The team compared EHV-1 infection in equine brain microvascular endothelial cells (EBMECs) and mouse brain microvascular endothelial cells (MBMECs).
Viral Growth and Detection
- The scientists observed that the rate of viral growth in EBMECs reflected a fully productive infection, exhibiting the usual progression.
- However, the virus’s presence in the MBMECs seemed to be nonproductive, lacking signs of active viral reproduction.
- Immunofluorescence microscopy – a technique used to visualize antigens in cells – was employed, showing EHV-1 in infected EBMECs but not in MBMECs.
Gene Expression
- The researchers found that EHV-1 immediate early (IE), early (ICP0) and late (gB, gD and gK) genes were expressed in infected EBMECs, indicating the active reproduction and progression of the virus.
- However, these genes were not detected in infected MBMECs, pointing towards the absence of productive EHV-1 replication in these cells.
Viral Entry Stage
- Upon examining the cells using electron microscopy at the viral entry stage, the scientists discovered that viral particles were present within uncoated vesicles (tiny spherical structures) in the cytoplasm of EBMECs.
- In contrast, these viral particles were absent from the MBMECs.
- This observation led to the conclusion that the way a virus enters a cell – in this case, the presence or absence of uncoated vesicles – is a significant factor in determining whether it can establish an infection.
Cite This Article
APA
Hasebe R, Kimura T, Nakamura K, Ochiai K, Okazaki K, Wada R, Umemura T.
(2005).
Differential susceptibility of equine and mouse brain microvascular endothelial cells to equine herpesvirus 1 infection.
Arch Virol, 151(4), 775-786.
https://doi.org/10.1007/s00705-005-0653-3 Publication
Researcher Affiliations
- Laboratory of Comparative Pathology, Hokkaido University, Sapporo, Japan.
MeSH Terms
- Animals
- Brain / blood supply
- Cells, Cultured
- Cytoplasm / virology
- Endothelium, Vascular / virology
- Herpesviridae Infections / veterinary
- Herpesviridae Infections / virology
- Herpesvirus 1, Equid / growth & development
- Herpesvirus 1, Equid / metabolism
- Herpesvirus 1, Equid / physiology
- Horse Diseases / virology
- Horses
- Immediate-Early Proteins / genetics
- Immediate-Early Proteins / metabolism
- Mice
- Microcirculation
- Polymerase Chain Reaction
- RNA, Messenger / genetics
- RNA, Viral / genetics
- Species Specificity
- Viral Proteins / genetics
- Viral Proteins / metabolism
- Virus Replication
Citations
This article has been cited 5 times.- Di Carlo P, Trizzino M, Titone L, Capra G, Colletti P, Mazzola G, Pistoia D, Sarno C. Unusual MRI findings in an immunocompetent patient with EBV encephalitis: a case report.. BMC Med Imaging 2011 Mar 24;11:6.
- Sasaki M, Hasebe R, Makino Y, Suzuki T, Fukushi H, Okamoto M, Matsuda K, Taniyama H, Sawa H, Kimura T. Equine major histocompatibility complex class I molecules act as entry receptors that bind to equine herpesvirus-1 glycoprotein D.. Genes Cells 2011 Apr;16(4):343-57.
- Hasebe R, Sasaki M, Sawa H, Wada R, Umemura T, Kimura T. Infectious entry of equine herpesvirus-1 into host cells through different endocytic pathways.. Virology 2009 Oct 25;393(2):198-209.
- Van de Walle GR, Peters ST, VanderVen BC, O'Callaghan DJ, Osterrieder N. Equine herpesvirus 1 entry via endocytosis is facilitated by alphaV integrins and an RSD motif in glycoprotein D.. J Virol 2008 Dec;82(23):11859-68.
- Goodman LB, Loregian A, Perkins GA, Nugent J, Buckles EL, Mercorelli B, Kydd JH, Palù G, Smith KC, Osterrieder N, Davis-Poynter N. A point mutation in a herpesvirus polymerase determines neuropathogenicity.. PLoS Pathog 2007 Nov;3(11):e160.
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