C3H/HeJ mice were inoculated intraperitoneally with 10(7) uncloned Bor
relia burgdorferi at 4 weeks of age and examined on days 30,90,180, an
d 360. Spirochetes were isolated from multiple tissues at all interval
s. Joint and heart disease were present in all mice at 30 days and res
olved after 90 days. At 180 and 360 days, some mice had mild recurrent
joint and heart disease, and most bad peripheral segmental periarteri
tis. The protein electrophoretic migration of 360-day isolates differe
d from the original inoculum. The experiment was repeated with C3H/HeN
and BALB/cByJ mice inoculated intradermally with 10(4) cloned B. burg
dorferi Characterization of infection and disease at 180 and 360 days
were similar to those of the first experiment, but spirochetal protein
s of isolates from both intervals displayed no protein variation in el
ectrophoretic mobilities. Spirochetes isolated at 360 days were fully
pathogenic in naive mice. Sera from infected mice showed an initial im
munoglobulin M response, followed by a sustained immunoglobulin G resp
onse, involving IgG1, IgG2a, IgG2b and IgG3, with expanding reactivity
against multiple antigens over time. These results indicate that immu
nocompetent mice sustain persistent infections and develop early acute
joint and heart lesions that resolve and then recur intermittent