Journal of Virology, April 1999, p. 3511-3513, Vol. 73, No. 4
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.
0022-538X/99
Effectiveness of Polyene Antibiotics in Treatment
of Transmissible Spongiform Encephalopathy in Transgenic Mice
Expressing Syrian Hamster PrP Only in Neurons
*
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.
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