Electron microscopy of equine respiratory viruses in organ cultures of equine fetal respiratory tract epithelium.
Abstract: Organ cultures of equine fetal tracheal and nasal turbinate epithelium were inoculated with equine influenza virus-A1 (EIV-A1), equine herpesvirus-1 (EHV-1), or equine rhinovirus-1 (ERV-1). Infected organ cultures were processed for scanning and transmission electron microscopy at various intervals and were compared with noninfected controls. Organ cultures inoculated with ERV-1 appeared normal with the exception of rare island-like lesions in infected nasal turbinate. Virus particles were not seen in thin sections of organ cultures infected with ERV-1. The EHV-1 caused extensive loss of the epithelial layer in tracheal and nasal turbinate organ cultures. The classic stages of herpesvirus morphogenesis were seen in thin sections of organ cultures infected with EHV-1. The EIV-A1 caused a scattered loss of cilia that was only apparent in infected tracheal organ cultures. Cilia were also seen bound in bundles. In thin sections, EIV-A1 particles were seen budding from the bases of microvilli.
Publication Date: 1984-10-01 PubMed ID: 6093639
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- Journal Article
Summary
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This study examines the effects of various equine respiratory viruses on organ cultures of horse fetal tracheal and nasal tissues. The researchers observed how the structure of these tissues changed upon infection with equine influenza virus-A1, equine herpesvirus-1, and equine rhinovirus-1 using advanced electron microscopy tools.
Experimental Methodology
- The scientists grew organ cultures of equine fetal tracheal and nasal tissues in a controlled lab setting.
- These cultures were then exposed to three different equine respiratory viruses: equine influenza virus-A1 (EIV-A1), equine herpesvirus-1 (EHV-1), and equine rhinovirus-1 (ERV-1).
- Both inoculated and control (non-inoculated) cultures were examined under scanning and transmission electron microscopes at different time points to view the conditions of cells.
Observations and Findings
- Organ cultures exposed to ERV-1 showed minimal changes, with only occasional island-like lesions in the nasal turbinate. No virus particles were visible in the thin sections of these infected cultures.
- Tissues exposed to EHV-1 had a significant reduction in the epithelial layer. The various stages of herpesvirus morphogenesis (the progression of the virus’ life cycle) were visible in these cultures.
- Exposure to EIV-A1 resulted in the sporadic loss of cilia, filament-like structures responsible for the movement of particles over cell surfaces. This effect was primarily seen in tracheal organ cultures. The virus particles were visible, budding from the base of microvilli (small, finger-like extensions from the cell surface).
Conclusion
- This study offers valuable information on how equine respiratory viruses affect the morphological structure of equine fetal tracheal and nasal tissues.
- The results depict the varying degrees of tissue damage and virus particle visibility across different virus types. ERV-1 led to minor visible changes, while EHV-1 and EIV-A1 caused more significant structural changes, including cell layer loss and cilia disruption.
- This research could serve as a basis for further studies to understand the pathogenicity and virulence of these viruses and may contribute to the development of more effective treatments and prevention strategies.
Cite This Article
APA
O'Niell FD, Issel CJ, Henk WG.
(1984).
Electron microscopy of equine respiratory viruses in organ cultures of equine fetal respiratory tract epithelium.
Am J Vet Res, 45(10), 1953-1960.
Publication
Researcher Affiliations
MeSH Terms
- Animals
- Cytopathogenic Effect, Viral
- Epithelium / microbiology
- Epithelium / pathology
- Herpesviridae / growth & development
- Herpesvirus 1, Equid / growth & development
- Herpesvirus 1, Equid / ultrastructure
- Horses
- Influenza A virus / growth & development
- Influenza A virus / ultrastructure
- Microscopy, Electron
- Microscopy, Electron, Scanning
- Morphogenesis
- Organ Culture Techniques
- Picornaviridae / growth & development
- Rhinovirus / growth & development
- Trachea
- Turbinates
- Virus Replication
Citations
This article has been cited 4 times.- Shan L, Noritake S, Fujiwara M, Asano S, Yoshida-Noro C, Noro N, Yamashita K, Kawakami T. Sec14l3 is specifically expressed in mouse airway ciliated cells. Inflammation 2012 Apr;35(2):702-12.
- Sutton GA, Viel L, Carman PS, Boag BL. Study of the duration and distribution of equine influenza virus subtype 2 (H3N8) antigens in experimentally infected ponies in vivo. Can J Vet Res 1997 Apr;61(2):113-20.
- Jönsson L, Beck-Friis J, Renström LH, Nikkilä T, Thebo P, Sundquist B. Equine herpes virus 1 (EHV-1) in liver, spleen, and lung as demonstrated by immunohistology and electron microscopy. Acta Vet Scand 1989;30(2):141-6.
- Chambers TM. Equine Influenza. Cold Spring Harb Perspect Med 2022 Jan 4;12(1).
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