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J Virol, February 1998, p. 1043-1051, Vol. 72, No. 2
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Resistance to Virus Infection Conferred by the Interferon-Induced Promyelocytic Leukemia Protein

Mounira K. Chelbi-Alix,* Frédérique Quignon, Luis Pelicano, Marcel H. M. Koken, and Hugues de Thé

CNRS UPR 9051, Centre Hayem, Hôpital St. Louis, 75475 Paris Cedex 10, France

Received 4 August 1997/Accepted 31 October 1997

The interferon (IFN)-induced promyelocytic leukemia (PML) protein is specifically associated with nuclear bodies (NBs) whose functions are yet unknown. Two of the NB-associated proteins, PML and Sp100, are induced by IFN. Here we show that overexpression of PML and not Sp100 induces resistance to infections by vesicular stomatitis virus (VSV) (a rhabdovirus) and influenza A virus (an orthomyxovirus) but not by encephalomyocarditis virus (a picornavirus). Inhibition of viral multiplication was dependent on both the level of PML expression and the multiplicity of infection and reached 100-fold. PML was shown to interfere with VSV mRNA and protein synthesis. Compared to the IFN mediator MxA protein, PML had less powerful antiviral activity. While nuclear body localization of PML did not seem to be required for the antiviral effect, deletion of the PML coiled-coil domain completely abolished it. Taken together, these results suggest that PML can contribute to the antiviral state induced in IFN-treated cells.

* Corresponding author. Mailing address: CNRS UPR 9051, Hôpital St. Louis, 1, Ave. Claude Vellefaux, 75475 Paris Cedex 10, France. Phone: 33-1-42-06-31-53. Fax: 33-1-53-72-40-90. E-mail: mchelbi{at}infobiogen.fr.




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