Affiliation:
1. Laboratory of Molecular Microbiology, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20892
Abstract
ABSTRACT
Laboratory mouse strains carry endogenous copies of the xenotropic mouse leukemia viruses (X-MLVs), named for their inability to infect cells of the laboratory mouse. This resistance to exogenous infection is due to a nonpermissive variant of the XPR1 gammaretrovirus receptor, a resistance that also limits
in vivo
expression of germ line X-MLV proviruses capable of producing infectious virus. Because laboratory mice vary widely in their proviral contents and in their virus expression patterns, we screened inbred strains for sequence and functional variants of the XPR1 receptor. We also typed inbred strains and wild mouse species for an endogenous provirus,
Bxv1
, that is capable of producing infectious X-MLV and that also contributes to the generation of pathogenic recombinant MLVs. We identified the active
Bxv1
provirus in many common inbred strains and in some Japanese
Mus molossinus
mice but in none of the other wild mouse species that carry X-MLVs. Our screening for
Xpr1
variants identified the permissive
Xpr1
sxv
allele in 7 strains of laboratory mice, including a
Bxv1
-positive strain, F/St, which is characterized by lifelong X-MLV viremia. Cells from three strains carrying
Xpr1
sxv
, namely, SWR, SJL, and SIM.R, were shown to be infectable by X-MLV and XMRV; these strains carry different alleles at
Fv1
and vary in their sensitivities to specific X/P-MLV isolates and XMRV. Several strains with
Xpr1
sxv
lack the active
Bxv1
provirus or other endogenous X-MLVs and may provide a useful model system to evaluate the
in vivo
spread of these gammaretroviruses and their disease potential in their natural host.
Publisher
American Society for Microbiology
Subject
Virology,Insect Science,Immunology,Microbiology
Cited by
25 articles.
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