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1 Biology Division, Oak Ridge National Laboratory, P.O. Box Y, Oak Ridge, Tennessee 37830, U.S.A.
2 Biology Department, Virginia Polytechnic Institute and State University, Blacksburg, Virginia 24061, U.S.A.
and3 University of Tennessee-Oak Ridge Graduate School of Biomedical Sciences, Oak Ridge, Tennessee 37830, U.S.A.
Two antigenically indistinguishable strains, 171 and 308, of Kilham rat virus (KRV) have distinct host ranges and contain capsid proteins of identical size, but with different isoelectric points. The single-stranded DNA genomes of the viruses are also the same size but appear to have different secondary and tertiary structures. The genomes of the two strains have nearly identical cleavage maps for 11 restriction endonucleases, except for differences in five restriction sites in the region bracketed by 0.63 to 0.90 map units (from the 3' ends of the virus strands). However, there is a lack of extended heterology in the nucleotide sequence of the two virus genomes, as judged by electron microscopic analysis of the heteroduplex of the two virus DNAs. This suggests that very subtle differences in the sequences of the genome, and possibly of the capsid proteins, may play a role in the host specificity without affecting the antigenic similarity of KRV strains.
Keywords: KRV, isoelectric focusing, restriction endonuclease mapping
Present address: Department of Microbiology, University of Alabama at Birmingham, Birmingham, Alabama 35294, U.S.A.
Received 20 November 1981;
accepted 25 February 1982.
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