Identification of target cells of a European equine arteritis virus strain in experimentally infected ponies.
Abstract: Currently, little is known on the cellular pathogenesis of equine arteritis virus (EAV). The purpose of the present study was to identify the target cells in ponies experimentally inoculated with EAV 08P178 (EU, clade-1). EAV-target organs (respiratory tissues with associated lymphoid tissues and large intestines), collected at 3 and 7 days post inoculation (dpi) and with virus titers≥10(5.0) TCID50/g, were processed with double immunofluorescence staining for the simultaneous detection of EAV N-protein and one of the following cell markers: CD172a (myeloid cells), CD3 (T lymphocytes), IgM (B lymphocytes) and von Willebrand factor (endothelial cells). In the different analyzed organs, 31-58% and 47-63% of the EAV-positive cells were mononuclear leukocytes (mainly CD172a(+) followed by CD3(+)) at 3 and 7 dpi, respectively. EAV-positive endothelial cells were not detected in 3.200 large blood vessels (≥3 endothelial cells/vessel cross section). However, in terminal capillaries (1-2 endothelial cells/vessel cross section) of the different organs, 15-51% of the endothelial cells were EAV-positive. In conclusion, the present study demonstrates that EAV 08P178 (i) has a main tropism for CD172a(+) and CD3(+) mononuclear leukocytes and (ii) infects a large number of endothelial cells in terminal capillaries. EAV 08P178 infection in capillaries is most probably the cause of an increased vascular permeability leading to leakage of fluid (edema-serous exudate) but not to severe vasculitis and hemorrhages.
Copyright © 2013 Elsevier B.V. All rights reserved.
Publication Date: 2013-08-07 PubMed ID: 23993255DOI: 10.1016/j.vetmic.2013.07.020Google Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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This research paper focuses on identifying the target cells in ponies infected experimentally with a specific strain of Equine arteritis virus (EAV). The research reveals that the virus has a primary attraction towards CD172a(+) and CD3(+) mononuclear leukocytes, and also affects a significant number of endothelial cells in terminal capillaries. This infection likely results in an elevation of vascular permeability, potentially leading to fluid leakage, but does not lead directly to severe vasculitis and hemorrhages.
Objective and Methodology
- The researchers aim to understand the cellular pathogenesis of the equine arteritis virus (EAV). They focus on a specific strain, EAV 08P178, from the European clade-1.
- The research’s objective is to identify which cells the virus primarily targets in ponies experimentally infected with the virus.
- The researchers notably focus on the organs typically targeted by EAV: respiratory tissues with related lymphoid tissues and large intestines. The organs are collected at two different time frames after inoculating the ponies with the virus: 3 and 7 days post infection.
- To identify which cells the virus targets, researchers use a technique called double immunofluorescence staining. This method helps detect the presence of EAV N-protein and one of four cell markers: CD172a for myeloid cells, CD3 for T lymphocytes, IgM for B lymphocytes, and von Willebrand factor for endothelial cells.
Findings
- Based on their analysis of different organs, the researchers observe that around 31-58% and 47-63% of EAV-positive cells were mononuclear leukocytes (mostly CD172a(+) followed by CD3(+)) at 3 and 7 days post infection.
- The study reveals that the virus did not affect endothelial cells present in large blood vessels. However, within terminal capillaries (those with 1-2 endothelial cells per cross section) of the organs studied, about 15-51% of the endothelial cells were EAV-positive.
Conclusions
- The study concludes that the EAV 08P178 strain mainly targets CD172a(+) and CD3(+) mononuclear leukocytes and also affects a large number of endothelial cells present in terminal capillaries.
- The infection of the virus in terminal capillaries could lead to increased vascular permeability. This can cause leakage of fluid, resulting in edema-serous exudate, but it doesn’t lead to severe vasculitis and hemorrhages.
Cite This Article
APA
Vairo S, Favoreel H, Scagliarini A, Nauwynck H.
(2013).
Identification of target cells of a European equine arteritis virus strain in experimentally infected ponies.
Vet Microbiol, 167(3-4), 235-241.
https://doi.org/10.1016/j.vetmic.2013.07.020 Publication
Researcher Affiliations
- Laboratory of Virology, Department of Virology, Parasitology and Immunology, Faculty of Veterinary Medicine, Ghent University, B-9820 Merelbeke, Belgium.
MeSH Terms
- Animals
- Arterivirus Infections / immunology
- Arterivirus Infections / pathology
- Arterivirus Infections / veterinary
- CD3 Complex / metabolism
- Equartevirus / immunology
- Female
- Horse Diseases / immunology
- Horse Diseases / pathology
- Horses
- Immunoglobulin M / metabolism
- Leukocytes, Mononuclear / immunology
- Leukocytes, Mononuclear / virology
- Male
- Receptors, Immunologic / metabolism
- T-Lymphocytes / immunology
- T-Lymphocytes / virology
- Viral Proteins / metabolism
- von Willebrand Factor / metabolism
Citations
This article has been cited 2 times.- Maloney SM, Shaw TM, Nennig KM, Larsen MS, Shah A, Kumar A, Marcotrigiano J, Grove J, Snijder EJ, Kirchdoerfer RN, Bailey AL. CD81 is a receptor for equine arteritis virus (family: Arteriviridae). mBio 2025 Jul 9;16(7):e0062325.
- Carossino M, Loynachan AT, Canisso IF, Cook RF, Campos JR, Nam B, Go YY, Squires EL, Troedsson MHT, Swerczek T, Del Piero F, Bailey E, Timoney PJ, Balasuriya UBR. Equine Arteritis Virus Has Specific Tropism for Stromal Cells and CD8(+) T and CD21(+) B Lymphocytes but Not for Glandular Epithelium at the Primary Site of Persistent Infection in the Stallion Reproductive Tract. J Virol 2017 Jul 1;91(13).
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