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Equine Arteritis Virus Uses Equine CXCL16 as an Entry Receptor.

Sanjay SarkarLakshman ChelvarajanYun Young GoFrank CookSergey ArtiushinShankar MondalKelsi AndersonJohn EberthPeter J TimoneyTheodore S KalbfleischErnest BaileyUdeni B R Balasuriya
Published in: Journal of virology (2016)
Outbreaks of EVA can be a source of significant economic loss for the equine industry from high rates of abortion in pregnant mares, death in young foals, establishment of the carrier state in stallions, and trade restrictions imposed by various countries. Similar to other arteriviruses, EAV primarily targets cells of the monocyte/macrophage lineage, which, when infected, are believed to play a critical role in EVA pathogenesis. To this point, however, the host-specified molecules involved in EAV binding and entry into monocytes/macrophages have not been identified. Identification of the cellular receptors for EAV may provide insights to design antivirals and better prophylactic reagents. In this study, we have demonstrated that EqCXCL16 acts as an EAV entry receptor in EAV-susceptible cells, equine monocytes. These findings represent a significant advance in our understanding of the fundamental mechanisms associated with the entry of EAV into susceptible cells.
Keyphrases
  • induced apoptosis
  • cell cycle arrest
  • dendritic cells
  • signaling pathway
  • cell death
  • oxidative stress
  • pregnant women
  • immune response
  • binding protein