Abstract

Primary infection and pathogenesis of equine herpesvirus type 1 (EHV-1) require an intricate interaction of virus with the mucosal epithelium, mononuclear cells and the vascular endothelium. Studies on EHV-1 have been facilitated by the development of different in vitro models that recapitulate the in vivo tissue complexity. The available in vitro assays can be categorized into (i) models mimicking the epithelium-peripheral blood mononuclear cell (PBMC) interaction, which include ex vivo mucosal (nasal and vaginal) explants and equine respiratory epithelial cells (EREC) cultures; and (ii) PBMC-endothelium mimicking models, including flow chamber and contact assays. These in vitro models have proven their worth in attempts to recapitulate the in vivo architecture and complexity, produce data relevant to natural host infection, and reduce animal use due to in vivo experiments. Although horse models are still needed for certain experiments, e.g., EHV-1 myeloencephalopathy or vaccination studies, available in vitro models can be used to obtain highly valuable data on virus-host tissue interactions. Microfluidic based 3D culture system (e.g., horse-on-a-chip) could be a potential upgraded version of these in vitro models for future research.

Highlights

  • Alphaherpesviruses are a heterogeneous group of morphologically similar DNA viruses that includes important pathogen of humans and animals

  • In mononuclear cells and dendritic cells (DC), virus is captured from the primary site of replication, and infected cells rapidly migrate to lymphoid tissues associated with the upper respiratory tract and infect other mononuclear cells that enter the blood stream

  • In the contact model and under static conditions, equine herpesvirus type 1 (EHV-1)-infected peripheral blood mononuclear cell (PBMC) were co-cultured with endothelial cells (EC) monolayers in the presence of neutralizing antibodies, and virus transfer from PBMC to EC was reported

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Summary

INTRODUCTION

Alphaherpesviruses are a heterogeneous group of morphologically similar DNA viruses that includes important pathogen of humans and animals. In mononuclear cells and dendritic cells (DC), virus is captured from the primary site of replication (respiratory epithelia), and infected cells rapidly migrate to lymphoid tissues associated with the upper respiratory tract and infect other mononuclear cells that enter the blood stream (cell-associated viremia). (i) Epithelium-PBMC mimicking models, which include ex vivo nasal explants and equine respiratory epithelial cells (EREC) culture; (ii) PBMC-EC mimicking models, which include flow chamber assay and contact assay. These models are widely used to recapitulate in vivo architecture and investigate the host-pathogen interaction

EX VIVO NASAL EXPLANTS
CONTACT ASSAYS
EREC CULTURE
CONCLUSION AND FUTURE PERSPECTIVES
Merits Demerits
Incorporate analytical biosensors into the culture platform
AUTHOR CONTRIBUTIONS
Full Text
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