Variation in susceptibility to viral infection is well documented across mo
use strains. Specific combinations of viral strains and murine hosts may fa
vor viral infection and disease, and could potentially allow the unexpected
development of chronic, persistent, or latent infections. In some genetica
lly modified strains of mice, immune function and perhaps other physiologic
or metabolic systems may be substantially or marginally impaired. In the c
ase study reported here, we document the apparent persistent transmission o
f mouse hepatitis virus (MHV) over a two-year period by MHV-seropositive tr
ansgenic mice. Transmission occurred via direct contact with seropositive m
ice and exposure to contaminated bedding. However, MHV was not detected at
diagnostic laboratories by use of viral isolation or reverse transcriptase-
polymerase chain reaction (RT-PCR) analysis of tissues from MHV-seropositiv
e animals. Our observation, together with the constantly expanding varietie
s of immune-impaired or poorly characterized murine hosts and the burgeonin
g dissemination of these animals throughout the biomedical research communi
ty, indicate that unexpected pathophysiologic presentations of common murin
e viral diseases may present new challenges to the biomedical research comm
unity in the future.