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Journal of Virology, May 2001, p. 4490-4498, Vol. 75, No. 10
Engelhardt Institute of Molecular Biology,
Moscow, Russia,1 and Department of Cell
and Virus Genetics2 and the Group of
Molecular Pathology,3 Heinrich Pette Institute
for Experimental Immunology and Virology at Hamburg
University, D-20251 Hamburg, Germany
Received 20 December 2000/Accepted 13 February 2001
Murine leukemia virus (MuLV) M813 was originally isolated from the
Southeast Asian rodent Mus cervicolor. As with the
ecotropic MuLVs derived from Mus musculus, its host
range is limited to rodent cells. Earlier studies have mapped its
receptor to chromosome 2, but it has not been established whether M813
shares a common receptor with any other MuLVs. In this study, we have
performed interference assays with M813 and viruses from four
interference groups of MuLV. The infection efficiency of M813 was not
compromised in cells expressing any one of the other MuLVs,
demonstrating that M813 must use a distinct receptor for cell entry.
The entire M813 env coding region was molecularly
cloned. Sequence analysis revealed high similarity with other MuLVs but
with a unique receptor-binding domain. Substitution of M813
env sequences in Moloney MuLV resulted in a
replication-competent virus with a host range and interference profile
similar to those of the biological clone M813. M813 thus defines a
novel receptor interference group of type C MuLVs.
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.10.4490-4498.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Mus cervicolor Murine Leukemia Virus
Isolate M813 Belongs to a Unique Receptor Interference
Group

*
Corresponding author. Mailing address:
Heinrich-Pette-Institut, Martinistr. 52, D-20251 Hamburg, Germany.
Phone: 49 40 480 51 273. Fax: 49 40 480 51 187. E-mail:
stocking{at}hpi.uni-hamburg.de.
Present address: The Salk Institute, Infectious Disease Laboratory,
La Jolla, CA 92037.
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