Recombinant inbred BXH-2 mice spontaneously produce a B-tropic murine
leukemia virus (MuLV) beginning early in life and have a high incidenc
e of spontaneous myeloid leukemia. These traits are not characteristic
of the progenitor strains (C57BL/6J and C3H/HeJ) or of 11 other recom
binant inbred BXH strains. Genetic analysis has shown that the virus i
s not transmitted through the germ line, suggesting that the virus is
passed from one generation to the next by horizontal transmission. An
additional ecotropic proviral locus was detected in some mice of this
strain after several generations of inbreeding. We show that BXH ecotr
opic virus was transmitted to other strains when fostered on viremic B
XH-2 mice and that these mice go on to develop tumors of hematopoietic
origin. Our earlier finding that virus is expressed early in gestatio
n suggested that the ecotropic MuLV is also transmitted in utero. In o
rder to determine the stage at which the ecotropic MuLV is transmitted
in utero, preimplantation stage embryos were transferred to the uteri
of recipient ecotropic virus-negative mice. These mice were found to
be negative for the presence of the ecotropic MuLV, suggesting that tr
ansplacental transmission of the ecotropic virus readily occurs in BXH
-2 mice. Although other viruses, including human lentiviruses, are tra
nsmitted across the placental barrier, transplacental transmission of
MuLV is a rare event. Thus, the BXH-2 mouse strain may contribute to o
ur understanding of the mechanism of transplacental transmission and p
athogenesis and offers a potential new model for use in drug therapy o
f exogenously transmitted viruses related to lentiviruses.