Role of the cytoplasmic domain of the beta-subunit of integrin alpha(v)beta6 in infection by foot-and-mouth disease virus.

Abstract

Field isolates of foot-and-mouth disease virus (FMDV) are believed to use RGD-dependent integrins as cellular receptors in vivo. Using SW480 cell transfectants, we have recently established that one such integrin, alpha(v)beta6, functions as a receptor for FMDV. This integrin was shown to function as a receptor for virus attachment. However, it was not known if the alpha(v)beta6 receptor itself participated in the events that follow virus binding to the host cell. In the present study, we investigated the effects of various deletion mutations in the beta6 cytoplasmic domain on infection. Our results show that although loss of the beta6 cytoplasmic domain has little effect on virus binding, this domain is essential for infection, indicating a critical role in postattachment events. The importance of endosomal acidification in alpha(v)beta6-mediated infection was confirmed by experiments showing that infection could be blocked by concanamycin A, a specific inhibitor of the vacuolar ATPase.

• Authors: L C Miller, W Blakemore, D Sheppard, A Atakilit, A M King, T Jackson
• Journal: Journal of virology (J Virol) Vol. 75 Issue 9 Pg. 4158-64 (May 2001) ISSN: 0022-538X [Print] United States
• PMID: 11287565 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Acids
• Antigens, Neoplasm
• Integrins
• Receptors, Virus
• integrin alphavbeta6

Topics

• Acids
• Animals
• Antigens, Neoplasm
• Aphthovirus (metabolism, physiology)
• Binding Sites
• Cell Line
• Cricetinae
• Cytoplasm (metabolism)
• Endosomes (metabolism)
• Integrins (genetics, physiology)
• Receptors, Virus (genetics, physiology)