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Journal of Virology, May 1999, p. 4493-4497, Vol. 73, No. 5
Department of Microbiology-Immunology,
Northwestern University Medical School, Chicago, Illinois
60611,1 and Department of Microbiology,
Columbia University College of Physicians and Surgeons, New York, New
York 100322
Received 8 December 1998/Accepted 12 February 1999
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.
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
The Murine Homolog (Mph) of Human Herpesvirus Entry
Protein B (HveB) Mediates Entry of Pseudorabies Virus but Not
Herpes Simplex Virus Types 1 and 2
*
Corresponding author. Mailing address: Department of
Microbiology-Immunology, Northwestern University Medical School,
Chicago, IL 60611. Phone: (312) 503-8230. Fax: (312) 503-1339. E-mail: p-spear{at}nwu.edu.
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