Biological and Biochemical Characteristics of Prion Strains Conserved in Persistently Infected Cell Cultures

Author:

Arima Kazuhiko1,Nishida Noriyuki1,Sakaguchi Suehiro12,Shigematsu Kazuto3,Atarashi Ryuichiro1,Yamaguchi Naohiro1,Yoshikawa Daisuke1,Yoon Jaewoo1,Watanabe Ken1,Kobayashi Nobuyuki1,Mouillet-Richard Sophie4,Lehmann Sylvain5,Katamine Shigeru1

Affiliation:

1. Department of Molecular Microbiology and Immunology

2. PRESTO, Japan Science and Technology Agency, 4-1-8 Honcho Kawaguchi, Saitama, Japan

3. Department of Pathology 2, Nagasaki University Graduate School of Biomedical Sciences, Sakamoto 1-12-4, Nagasaki 852-8523, Japan

4. Institut André Lwoff, CNRS UPR 1983-BP8, 94801 Villejuif Cedex, France

5. Institut de Genetique Humaine, CNRS UPR 1142, 34396 Montpellier Cedex 5, France

Abstract

ABSTRACT Abnormal prion protein (PrP Sc ) plays a central role in the transmission of prion diseases, but the molecular basis of prion strains with distinct biological characteristics remains to be elucidated. We analyzed the characteristics of prion disease by using mice inoculated with the Chandler and Fukuoka-1 strains propagated in a cultured mouse neuronal cell line, GT1-7, which is highly permissive to replication of the infectious agents. Strain-specific biological characteristics, including clinical manifestations, incubation period as related to the infectious unit, and pathological profiles, remained unchanged after passages in the cell cultures. We noted some differences in the biochemical aspects of PrP Sc between brain tissues and GT1-7 cells which were unlikely to affect the strain phenotypes. On the other hand, the proteinase K-resistant PrP core fragments derived from Fukuoka-1-infected tissues and cells were slightly larger than those from Chandler-infected versions. Moreover, Fukuoka-1 infection, but not Chandler infection, gave an extra fragment with a low molecular weight, ∼13 kDa, in both brain tissues and GT1-7 cells. This cell culture model persistently infected with different strains will provide a new insight into the understanding of the molecular basis of prion diversity.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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