Abstract
A mouse member of the immunoglobulin superfamily, originally designated the murine poliovirus receptor homolog (Mph), was found to be a receptor for the porcine alphaherpesvirus pseudorabies virus (PRV). This mouse protein, designated here murine herpesvirus entry protein B (mHveB), is most similar to one of three related human alphaherpesvirus receptors, the one designated HveB and also known as poliovirus receptor-related protein 2. Hamster cells resistant to PRV entry became susceptible upon expression of a cDNA encoding mHveB. Anti-mHveB antibody and a soluble protein composed of the mHveB ectodomain inhibited mHveB-dependent PRV entry. Expression of mHveB mRNA was detected in a variety of mouse cell lines, but anti-mHveB antibody inhibited PRV infection in only a subset of these cell lines, indicating that mHveB is the principal mediator of PRV entry into some mouse cell types but not others. Coexpression of mHveB with PRV gD, but not herpes simplex virus type 1 (HSV-1) gD, inhibited entry activity, suggesting that PRV gD may interact directly with mHveB as a ligand that can cause interference. By analogy with HSV-1, envelope-associated PRV gD probably also interacts directly with mHveB during viral entry.
MeSH Terms
3T3 Cells
Animals
Antibodies, Monoclonal/metabolism
CHO Cells
Cell Line
Cricetinae
Gene Expression
Herpesvirus 1, Human/metabolism,physiology
Herpesvirus 1, Suid/metabolism,physiology
Herpesvirus 2, Human/metabolism,physiology
Humans
Melanoma
Mice
Receptors, Tumor Necrosis Factor
Receptors, Tumor Necrosis Factor, Member 14
Receptors, Virus/genetics,metabolism
Tumor Cells, Cultured
Viral Envelope Proteins/metabolism
Chemicals
Antibodies, Monoclonal
Receptors, Tumor Necrosis Factor
Receptors, Tumor Necrosis Factor, Member 14
Receptors, Virus
TNFRSF14 protein, human
Tnfrsf14 protein, mouse
Viral Envelope Proteins
glycoprotein D, Human herpesvirus 1
glycoprotein D, pseudorabies virus
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Shukla D
Department of Microbiology-Immunology, Northwestern University Medical School, Chicago, Illinois 60611, USA.
Rowe C L
Dong Y
Racaniello V R
Spear P G
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