B. Koudela et al., THE SEVERE COMBINED IMMUNODEFICIENT MOUSE AS A MODEL FOR ENCEPHALITOZOON-CUNICULI MICROSPORIDIOSIS, Folia parasitologica, 40(4), 1993, pp. 279-286
Microsporidia have been recently recognized as opportunistic pathogens
in AIDS patients. In attempt to develop an animal model with features
similar to the infections observed in the immunodeficient patients, t
he adult severe combined immunodeficient mice (SCID) were administered
both intraperitoneally and perorally by 2x10(7) spores of the murine
isolate of E. cuniculi. The experimental inoculation caused a severe,
fatal disease characterized by the dissemination of microsporidia into
the host tissues. The dominant route of E. cuniculi dissemination in
the SCID mice was continual direct extension from the site of inoculat
ion to adjacent tissues and organs, terminating in hematogenous spread
of infection in the host. The different courses of microsporidiosis i
n SCID mice relative to the mode of inoculation (i.p. vs. p. o.) was o
bserved. The survival time of i.p. infected SCID mice was 3 weeks - vs
. 5 weeks in p.o. infected SCID mice. Experimental microsporidiosis in
SCID mice should provide a useful model for studies in microsporidial
pathogenesis, mechanisms of resistance, immunotherapy, and in evaluat
ing potential antimicrosporidial agents.