Hostname: page-component-cd9895bd7-jn8rn Total loading time: 0 Render date: 2024-12-26T05:08:02.960Z Has data issue: false hasContentIssue false

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

Published online by Cambridge University Press:  01 December 1998

XIANGDONG YOU
Affiliation:
Department of Pediatrics, Emory University School of Medicine, Atlanta, GA 30322, USA
J. R. MEAD
Affiliation:
Department of Pediatrics, Emory University School of Medicine, Atlanta, GA 30322, USA Georgia VA Research Center on AIDS and HIV Infection, Veterans Affairs Medical Center, Decatur, GA 30033, USA

Abstract

Severe cryptosporidial infections were produced in gamma interferon (IFN-γ) knockout mice. Mean oocyst shedding increased from 332 to 30717 oocysts/100 μl of faecal suspension between day 4 and 9 after administration of 1×105 oocysts/mouse. No significant differences in oocyst shedding were observed in mice after being inoculated with 1×105, 1×104 or 1×103 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 ×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-γ 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.

Type
Research Article
Copyright
1998 Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)