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Original Article |
6 Nucleocapsid
iusb,c,
Päivi M. Ojalaa,b,
Michael W. Hessa, and
Dennis H. Bamforda,b
Correspondence to: Dennis H. Bamford, Viikki Biocenter, P.O. Box 56 (Viikinkaari 5), FIN-00014, University of Helsinki, Finland. Tel:358-9-191 59100 Fax:358-9-191 59098 E-mail:gen_phag{at}cc.helsinki.fi.
Studies on the viruscell interactions have proven valuable in elucidating vital cellular processes. Interestingly, certain virushost membrane interactions found in eukaryotic systems seem also to operate in prokaryotes (Bamford, D.H., M. Romantschuk, and P.J. Somerharju, 1987. EMBO (Eur. Mol. Biol. Organ.) J. 6:14671473; Romantschuk, M., V.M. Olkkonen, and D.H. Bamford. 1988. EMBO (Eur. Mol. Biol. Organ.) J. 7:18211829).
6 is an enveloped double-stranded RNA virus infecting a gram-negative bacterium. The viral entry is initiated by fusion between the virus membrane and host outer membrane, followed by delivery of the viral nucleocapsid (RNA polymerase complex covered with a protein shell) into the host cytosol via an endocytic-like route. In this study, we analyze the interaction of the nucleocapsid with the host plasma membrane and demonstrate a novel approach for dissecting the early events of the nucleocapsid entry process. The initial binding of the nucleocapsid to the plasma membrane is independent of membrane voltage (
) and the K+ and H+ gradients. However, the following internalization is dependent on plasma membrane voltage (
), but does not require a high ATP level or K+ and H+ gradients. Moreover, the nucleocapsid shell protein, P8, is the viral component mediating the membranenucleocapsid interaction.
Key Words: endocytosis, cell energetics, dsRNA virus entry, prokaryote, phi6
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