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Infection and Immunity, June 1999, p. 2797-2803, Vol. 67, No. 6
Department of Veterinary and Animal Sciences,
University of Massachusetts, Amherst, Massachusetts
01003,1 and International
Livestock Research Institute, Nairobi,
Kenya2
Received 16 November 1998/Returned for modification 8 January
1999/Accepted 12 March 1999
Clearance of trypanosomes from the blood of infected Cape buffalo
was associated with the development of two responses: (i) complement-dependent and clone-specific lytic activity and (ii) complement-independent trypanocidal activity that was not
restricted by trypanosome clone or species. This latter activity was
mediated by H2O2 and required the presence of
xanthine oxidase in serum but not the addition of purine
substrates. Expression of the xanthine oxidase-dependent
trypanocidal activity in Cape buffalo serum was coincident with,
and required, a decline in its H2O2
catabolic activity. The H2O2 catabolic activity
of Cape buffalo serum was due solely to catalase and declined by
eightfold around the time that trypanosomes were cleared from the
blood, accompanied by a fivefold drop in erythrocyte-associated
catalase activity. The Cape buffalo did not develop
subsequent parasitemic waves. Clearance of parasitemia in
similarly infected cattle was also associated with
development of trypanosome clone-specific lytic activity, but
not with the acquisition of H2O2-dependent
trypanocidal activity in serum, and the cattle supported recurring
parasitemia. The lack of trypanocidal activity in pre- and
postinfection cattle sera was due to their low content of xanthine
oxidase and sustained catalase activity. These data strongly suggest
that an infection-induced serum oxidative response, the efficacy of
which is amplified by a decline in blood catalase, contributes
to suppression of recurring parasitemia in Cape buffalo.
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Infection-Associated Decline of Cape Buffalo Blood
Catalase Augments Serum Trypanocidal Activity
*
Corresponding author. Mailing address: University of
Massachusetts, Department of Veterinary and Animal Sciences, Paige
Laboratory, Amherst, MA 01003. Phone: (413) 545-2573. Fax: (413)
545-6326. E-mail: sblack{at}vasci.umass.edu.
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