This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Demaimay, R.
Right arrow Articles by Chesebro, B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Demaimay, R.
Right arrow Articles by Chesebro, B.

 Previous Article

Journal of Virology, April 1999, p. 3511-3513, Vol. 73, No. 4
0022-538X/99

Effectiveness of Polyene Antibiotics in Treatment of Transmissible Spongiform Encephalopathy in Transgenic Mice Expressing Syrian Hamster PrP Only in Neurons

Remi Demaimay, Richard Race, and Bruce Chesebro*

Laboratory of Persistent Viral Diseases, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana 59840

Received 25 September 1998/Accepted 11 January 1999

To date very few drugs have favorably influenced the course of transmissible spongiform encephalopathies. In previous studies, the polyene antibiotics amphotericin B (AmB) and MS-8209 prolonged the incubation time in Syrian hamsters of the 263K strain of scrapie, but AmB had no effect against other scrapie strains in Syrian hamsters. In the present experiments using transgenic mice expressing Syrian hamster PrP in neurons only, MS-8209 extended the life spans of animals infected with the 263K strain but not the DY strain. AmB was effective against both 263K and DY and prevented death in 18% of DY-infected animals. The AmB effect against strain 263K was more prominent in mice whose endogenous PrP gene had been inactivated by homologous recombination. It was unclear whether this difference was due to a change in the duration of the disease or to possible interactive effects between the mouse PrP gene and the drugs themselves. The effectiveness of treatment after intracerebral scrapie infection in transgenic mice expressing PrP only in neurons suggested that neurons are important sites of action for these drugs.


* Corresponding author. Mailing address: Laboratory of Persistent Viral Diseases, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 903 S. 4th St., Hamilton, MT 59840. Phone: (406) 363-9354. Fax: (406) 363-9286. E-mail: bchesebro{at}nih.gov.


Journal of Virology, April 1999, p. 3511-3513, Vol. 73, No. 4
0022-538X/99



This article has been cited by other articles:

  • Cronier, S., Beringue, V., Bellon, A., Peyrin, J.-M., Laude, H. (2007). Prion Strain- and Species-Dependent Effects of Antiprion Molecules in Primary Neuronal Cultures. J. Virol. 81: 13794-13800 [Abstract] [Full Text]  
  • Trevitt, C. R, Collinge, J. (2006). A systematic review of prion therapeutics in experimental models. Brain 129: 2241-2265 [Abstract] [Full Text]  
  • Kim, C.-L., Karino, A., Ishiguro, N., Shinagawa, M., Sato, M., Horiuchi, M. (2004). Cell-surface retention of PrPC by anti-PrP antibody prevents protease-resistant PrP formation. J. Gen. Virol. 85: 3473-3482 [Abstract] [Full Text]  
  • Kocisko, D. A., Baron, G. S., Rubenstein, R., Chen, J., Kuizon, S., Caughey, B. (2003). New Inhibitors of Scrapie-Associated Prion Protein Formation in a Library of 2,000 Drugs and Natural Products. J. Virol. 77: 10288-10294 [Abstract] [Full Text]  
  • Beringue, V., Adjou, K. T., Lamoury, F., Maignien, T., Deslys, J.-P., Race, R., Dormont, D. (2000). Opposite Effects of Dextran Sulfate 500, the Polyene Antibiotic MS-8209, and Congo Red on Accumulation of the Protease-Resistant Isoform of PrP in the Spleens of Mice Inoculated Intraperitoneally with the Scrapie Agent. J. Virol. 74: 5432-5440 [Abstract] [Full Text]  
  • Mangé, A., Nishida, N., Milhavet, O., McMahon, H. E. M., Casanova, D., Lehmann, S. (2000). Amphotericin B Inhibits the Generation of the Scrapie Isoform of the Prion Protein in Infected Cultures. J. Virol. 74: 3135-3140 [Abstract] [Full Text]