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Originally published as MBC in Press, 10.1091/mbc.01-12-0592 on February 28, 2002
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Vol. 13, Issue 5, 1750-1764, May 2002

Inhibitors of COP-mediated Transport and Cholera Toxin Action Inhibit Simian Virus 40 Infection

Ayanthi A. Richards,* Espen Stang,dagger Rainer Pepperkok,Dagger and Robert G. Parton*§

 *Institute for Molecular Bioscience, Center for Microscopy and Microanalysis, and Department of Physiology and Pharmacology, School of Biomedical Sciences, University of Queensland, Queensland 4072, Australia; and  Dagger European Molecular Biology Laboratory, 69117 Heidelberg, Germany

Simian virus 40 (SV40) is a nonenveloped virus that has been shown to pass from surface caveolae to the endoplasmic reticulum in an apparently novel infectious entry pathway. We now show that the initial entry step is blocked by brefeldin A and by incubation at 20°C. Subsequent to the entry step, the virus reaches a domain of the rough endoplasmic reticulum by an unknown pathway. This intracellular trafficking pathway is also brefeldin A sensitive. Infection is strongly inhibited by expression of GTP-restricted ADP-ribosylation factor 1 (Arf1) and Sar1 mutants and by microinjection of antibodies to beta COP. In addition, we demonstrate a potent inhibition of SV40 infection by the dipeptide N-benzoyl-oxycarbonyl-Gly-Phe-amide, which also inhibits late events in cholera toxin action. Our results identify novel inhibitors of SV40 infection and show that SV40 requires COPI- and COPII-dependent transport steps for successful infection.


dagger Present address: Institute of Pathology, University of Oslo, The National Hospital, 0027 Oslo, Norway.

§ Corresponding author. E-mail address: r.parton{at}imb.uq.edu.au.


Molecular Biology of the Cell
Vol. 13, 1750-1764, May 2002
Copyright © 2002 by The American Society for Cell Biology



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