Adsorptive Endocytosis of California Encephalitis Virus into Mosquito and Mammalian Cells: A Role for G1

• Published in: Virology (New York, N.Y.) N.Y.), 1997-08, Vol.235 (1), p.40-47
• Main Authors: Hacker, Jill K., Hardy, James L.
• Format: Article
• Language: English
• Subjects: Adsorption; Aedes - virology; Aedes albopictus; Ammonium Chloride - pharmacology; Animals; Antibodies, Monoclonal - pharmacology; Cell Line; cell lines; Cricetinae; Encephalitis Virus, California - drug effects; Encephalitis Virus, California - physiology; Endocytosis; Endopeptidases - metabolism; Giant Cells; hamsters; Hydrogen-Ion Concentration; Kidney; Kinetics; Mammals; Viral Proteins - biosynthesis; Viral Proteins - isolation & purification
• ISSN: 0042-6822; 1096-0341
• DOI: 10.1006/viro.1997.8675

The G1 glycoprotein of California encephalitis (CE) virus plays a critical role in the infection of mosquito and mammalian cells. We found that CE virus enters baby hamster kidney (BHK-21) andAedes albopictus(C6/36) cells by the endocytic pathway. Ammonium chloride, a lysosomotropic amine that prevents release of virus from endosomes, inhibited infection of both cell types when added within 10 min after viral adsorption. In addition, infected cells formed polykaryons when the extracellular pH was lowered to 6.3; optimal fusion occurred at pH 5.8 and 6.0 (C6/36 and BHK-21 cells, respectively). Two neutralizing G1 MAbs, 6D5.5 and 7D4.5, inhibited low pH-induced syncytia formation without affecting viral attachment, suggesting a role for G1 in viral entry. Since viral fusion proteins have been demonstrated to undergo conformational changes at low pH, acid-induced changes in G1 and G2 were assessed. While both G1 and G2 demonstrated low pH-induced alterations in detergent binding, only G1 displayed an altered protease cleavage pattern at the fusion pH. These results indicate that the G1 protein of CE virus undergoes conformational changes necessary for low pH-mediated entry into both mosquito and mammalian cells.