Encephalitozoonosis is an opportunistic infection in animals and humans. It
s clinical form is observed in immunosuppressed hosts. We studied the occur
rence of the manifest form of rabbit microsporidiosis under cyclophosphamid
e immunomodulation in 40 New Zealand rabbits. The experimental animals were
intraperitoneally infected with 5 x 10(7) Encephalitozoon cuniculi spores.
Two weeks after infection the animals were treated intraperitoneally with
cyclophosphamide, first with 50 mg/kg and then with 15 mg/kg weekly during
the 12-week experimental period. Positive controls were either E. cuniculi-
infected or cyclophosphamide-immunosuppressed animals. The negative control
rabbits remained untreated. Both clinical signs of encephalitozoonosis and
depression of peripheral blood cell count developed between weeks 4 and 6
in the experimental animals which died during week 6 of the experiment. No
clinical signs compatible with encephalitozoonosis were observed in any of
the controls. The results suggest that immunosuppression induced by cycloph
osphamide can give rise to a lethal form of encephalitozoonosis.