The Minor Envelope Glycoproteins GP2a and GP4 of Porcine Reproductive and Respiratory Syndrome Virus Interact with the Receptor CD163

Authors

Phani B. Das, University of Nebraska-LincolnFollow
Phat X. Dinh, University of Nebraska-LincolnFollow
Israrul H. Ansari, University of Nebraska - LincolnFollow
Marcelo de Lima, University of Nebraska - Lincoln
Fernando A. Osorio, University of Nebraska - LincolnFollow
Asit K. Pattnaik, University of Nebraska-LincolnFollow

Document Type

Article

Date of this Version

2-2010

Citation

JOURNAL OF VIROLOGY, Feb. 2010, p. 1731–1740

Comments

Copyright © 2010, American Society for Microbiology. All Rights Reserved.

Abstract

Porcine reproductive and respiratory syndrome virus (PRRSV) contains the major glycoprotein, GP5, as well as three other minor glycoproteins, namely, GP2a, GP3, and GP4, on the virion envelope, all of which are required for generation of infectious virions. To study their interactions with each other and with the cellular receptor for PRRSV, we have cloned each of the viral glycoproteins and CD163 receptor in expression vectors and examined their expression and interaction with each other in transfected cells by coimmunoprecipitation (co-IP) assay using monospecific antibodies. Our results show that a strong interaction exists between the GP4 and GP5 proteins, although weak interactions among the other minor envelope glycoproteins and GP5 have been detected. Both GP2a and GP4 proteins were found to interact with all the other GPs, resulting in the formation of multiprotein complex. Our results further show that the GP2a and GP4 proteins also specifically interact with the CD163 molecule. The carboxy-terminal 223 residues of the CD163 molecule are not required for interactions with either the GP2a or the GP4 protein, although these residues are required for conferring susceptibility to PRRSV infection in BHK-21 cells. Overall, we conclude that the GP4 protein is critical for mediating interglycoprotein interactions and, along with GP2a, serves as the viral attachment protein that is responsible for mediating interactions with CD163 for virus entry into susceptible host cell.