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Infection and Immunity, August 2008, p. 3657-3663, Vol. 76, No. 8
0019-9567/08/$08.00+0 doi:10.1128/IAI.00112-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Department of Internal Medicine, The University of Texas Medical Branch, Galveston, Texas 77555
Received 25 January 2008/ Returned for modification 28 February 2008/ Accepted 22 May 2008
Severe experimental infections with Cryptosporidium parvum have been reported in immunocompromised animals such as SCID mice (mice without functional T cells and B cells). In a C. parvum infection with 1 x 106 oocysts/mouse in SCID beige (SCIDbg) mice (SCID mice lacking functional NK cells), oocyst shedding was first demonstrated 18 days after infection. However, shedding was shown as early as 3 days after the same infection in SCIDbgMN mice. All of the SCIDbgMN mice died within 16 days of C. parvum infection, while 100% of the SCIDbg mice exposed to the parasite survived. SCIDbgMN mice are SCIDbg mice depleted of functional macrophages (M
) and neutrophils (PMN), suggesting that the severity early after C. parvum infection is strongly influenced by the functions of M
and PMN. All SCIDbgMN mice orally infected with a lethal dose of C. parvum survived after they were inoculated with M
from SCIDbg mice exposed to C. parvum (CP-M
) or resident M
previously cultured with PMN from C. parvum-infected SCIDbg mice (CP-PMN). However, all SCIDbgMN mice inoculated with CP-PMN alone or resident M
alone died after C. parvum infection. CP-M
were identified as classically activated M
(M1M
), and CP-PMN were characterized as PMN-I. In in vitro studies, resident M
converted to M1M
after transwell cultivation with CP-PMN. These results indicate that the resistance of SCIDbg mice early after C. parvum infection is displayed through the function of M1M
which are converted from resident M
influenced by CP-PMN (PMN-I).
Published ahead of print on 2 June 2008.
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