Integrins alpha 2 beta 1 and alpha 4 beta 1 can mediate SA11 rotavirus attachment and entry into cells

Most mammalian rotaviruses contain tripeptide amino acid sequences in outer capsid proteins VP4 and VP7 which have been shown to act as ligands for in tegrins alpha 2 beta 1 and alpha 4 beta 1. Peptides containing these sequen ces and monoclonal antibodies directed to these integrins block rotavirus i nfection of cells. Here we report that SA11 rotavirus binding to and infect ion of K562 cells expressing alpha 2 beta 1 or alpha 4 beta 1 integrins via transfection is increased over virus binding to and infection of cells tra nsfected with alpha 3 integrin or parent cells. The increased binding and g rowth mere specifically blocked by a monoclonal antibody to the transfected integrin subunit hut not by irrelevant antibodies. In our experiments, int egrin activation with phorbol ester did not affect virus binding to cells. However, phorbol ester treatment of K562 parent and transfected cells induc ed endogenous gene expression of alpha 2 beta 1 integrin, which was detecta ble by flow cytometry 16 h after treatment and quantitatively correlated wi th the increased level of SA11 virus growth observed after this time. Virus binding to K562 cells treated with phorbol ester 24 h previously and expre ssing alpha 2 beta 1 was elevated over binding to control cells and was spe cifically blocked by the anti-alpha 2 monoclonal antibody AK7. Virus growth in alpha 4-transfected K562 cells which had also been induced to express a lpha 2 beta 1 integrin with phorbol ester occurred at a level approaching t hat in the permissive MA104 cell line. We therefore have demonstrated that two integrins, alpha 2 beta 1 and alpha 4 beta 1, are capable of acting as cellular receptors for SA11 rotavirus.