Characterization of experimental Cryptosporidium parvum infection in IFN-gamma knockout mice

• Published in: Parasitology Vol. 117 ( Pt 6); p. 525
• Main Authors: You, X, Mead, J R
• Format: Journal Article
• Language: English
• Published: England 01-12-1998
• Subjects: Animals; CD4 Antigens - analysis; CD8 Antigens - analysis; Cryptosporidiosis - immunology; Cryptosporidium parvum - pathogenicity; Disease Models, Animal; Feces - parasitology; Interferon-gamma - deficiency; Interferon-gamma - genetics; Intestinal Mucosa - parasitology; Lymph Nodes - parasitology; Lymphocyte Count; Mesentery - immunology; Mice; Mice, Inbred C57BL; Mice, Knockout; Parasite Egg Count; Specific Pathogen-Free Organisms; Spleen - immunology; Spleen - parasitology; Time Factors
• ISSN: 0031-1820
• DOI: 10.1017/S0031182098003424

Severe cryptosporidial infections were produced in gamma interferon (IFN-gamma) knockout mice. Mean oocyst shedding increased from 332 to 30,717 oocysts/100 microliters of faecal suspension between day 4 and 9 after administration of 1 x 10(5) oocysts/mouse. No significant differences in oocyst shedding were observed in mice after being inoculated with 1 x 10(5), 1 x 10(4) or 1 x 10(3) oocysts/mouse (P > 0.05). Infected mouse weights decreased an average 3-4 g before death or euthanization. Histological studies revealed heavy parasite colonization in small intestinal epithelium (approximately 250 organisms/high-power field at x 400). Mesenteric lymph nodes in infected mice were markedly enlarged compared to controls (P < 0.05). Both CD4+ and CD8+ T cell populations increased in spleens of infected mice while the B cell population increased in mesenteric lymph nodes from infected mice. No significant proliferation was observed when pooled lymphocytes from infected mice were exposed to C. parvum antigens in vitro. Addition of recombinant mouse IFN-gamma did not restore antigen responsiveness. While lymphoproliferative responses to specific antigen were not significant in the short period following infection, this mouse model provides unique features to study the characteristics of acute infection and the immune response against C. parvum.