Abstract
The well-described herpesvirus entry receptors HveA (TNFRSF14), HveB (nectin 2), and HveC (nectin 1) have been shown to mediate the entry of alphaherpesviruses. Our findings showed that the alphaherpesvirus equine herpesvirus 1 (EHV-1) efficiently entered and replicated in CHO-K1 cells that lack the entry receptors HveA, HveB, and HveC, demonstrating that EHV-1 utilizes a unique entry receptor. As with other alphaherpesviruses, efficient EHV-1 entry was dependent on glycoprotein D and cell surface glycosaminoglycans.
Publication types
-
Research Support, U.S. Gov't, P.H.S.
MeSH terms
-
Animals
-
CHO Cells
-
Chlorocebus aethiops
-
Cricetinae
-
Glycosaminoglycans / physiology
-
Herpesviridae Infections / etiology
-
Herpesviridae Infections / veterinary
-
Herpesviridae Infections / virology
-
Herpesvirus 1, Equid / pathogenicity*
-
Herpesvirus 1, Equid / physiology*
-
Horse Diseases / etiology
-
Horse Diseases / virology
-
Horses
-
Receptors, Virus / physiology*
-
Vero Cells
-
Viral Envelope Proteins / physiology
Substances
-
Glycosaminoglycans
-
Receptors, Virus
-
Viral Envelope Proteins
-
glycoprotein D, Equid herpesvirus 1