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Journal of Virology, June 2000, p. 5542-5547, Vol. 74, No. 12
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Adaptation and Selection of Prion Protein Strain
Conformations following Interspecies Transmission of Transmissible
Mink Encephalopathy
Jason C.
Bartz,1,
Richard A.
Bessen,2,*
Debbie
McKenzie,1
Richard F.
Marsh,1,
and
Judd M.
Aiken1,*
Animal Health and Biomedical Sciences,
University of Wisconsin, Madison, Wisconsin
53706,1 and Medical Microbiology and
Immunology, Creighton University, Omaha, Nebraska,
681782
Received 15 December 1999/Accepted 17 March 2000
Interspecies transmission of the transmissible spongiform
encephalopathies (TSEs), or prion diseases, can result in the
adaptation and selection of TSE strains with an expanded host range and
increased virulence such as in the case of bovine spongiform
encephalopathy and variant Creutzfeldt-Jakob disease. To investigate
TSE strain adaptation, we serially passaged a biological clone of
transmissible mink encephalopathy (TME) into Syrian golden hamsters and
examined the selection of distinct strain phenotypes and conformations of the disease-specific isoform of the prion protein
(PrPSc). The long-incubation-period drowsy (DY) TME strain
was the predominate strain, based on the presence of its
strain-specific PrPSc following interspecies passage.
Additional serial passages in hamsters resulted in the selection of the
hyper (HY) TME PrPSc strain-dependent conformation and its
short incubation period phenotype unless the passages were performed
with a low-dose inoculum (e.g., 10
5 dilution), in which
case the DY TME clinical phenotype continued to predominate. For both
TME strains, the PrPSc strain pattern preceded
stabilization of the TME strain phenotype. These findings demonstrate
that interspecies transmission of a single cloned TSE strain resulted
in adaptation of at least two strain-associated PrPSc
conformations that underwent selection until one type of
PrPSc conformation and strain phenotype became predominant.
To examine TME strain selection in the absence of host adaptation,
hamsters were coinfected with hamster-adapted HY and DY TME. DY TME was able to interfere with the selection of the short-incubation HY TME
phenotype. Coinfection could result in the DY TME phenotype and
PrPSc conformation on first passage, but on subsequent
passages, the disease pattern converted to HY TME. These findings
indicate that during TSE strain adaptation, there is selection of a
strain-specific PrPSc conformation that can determine the
TSE strain phenotype.
*
Corresponding author. Mailing address for Richard A. Bessen: Medical Microbiology & Immunology, Creighton University, 2500 California Plaza, Omaha, NE 68178. Phone: (402) 280-3072. Fax: (402)
280-1875. E-mail: rbessen{at}creighton.edu. Mailing address for
Judd M. Aiken: Animal Health & Biomedical Sciences, University of
Wisconsin, 1656 Linden Dr., Madison, WI 53706. Phone: (608) 262-7362. Fax: (608) 262-7420. E-mail:
aiken{at}ahabs.wisc.edu.

Present address: Medical Microbiology & Immunology, Creighton
University, Omaha, NE
68178.

Deceased.
Journal of Virology, June 2000, p. 5542-5547, Vol. 74, No. 12
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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