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Caspase-dependent apoptosis during infection with Cryptosporidium parvum

  • David M. Ojcius*
  • , Jean Luc Perfettini
  • , Alain Bonnin
  • , Fabrice Laurent
  • *Corresponding author for this work
  • CNRS
  • Hôpital du Bocage, CHU Dijon Bourgogne
  • Université de Bourgogne
  • INRAE

Research output: Contribution to journalJournal Article peer-review

63 Scopus citations

Abstract

The protozoan parasite Cryptosporidium parvum causes persistent diarrhea and malnutrition in children and the diarrhea-wasting syndrome in AIDS. No therapy exists for eliminating the parasite in the absence of a healthy immune response. Although it had been reported that infection of intestinal cell lines with C. parvum leads to host cell death, the mechanisms of cytolysis have not been characterized. We show here that infection with C. parvum leads to typical apoptotic nuclear condensation and DNA fragmentation in host cells. Both nuclear condensation and DNA fragmentation are inhibited by a caspase inhibitor, showing that caspases are involved in this type of apoptosis. Finally, blocking apoptosis with the caspase inhibitor increases the percentage of infected cells, suggesting that parasites may use apoptosis to exit from the infected cell or that the infected cells may eliminate the parasite through apoptosis. These results suggest that apoptosis could be involved in the pathogenesis of C. parvum infections in vivo, and raise the possibility that therapeutic interference with host cell death could alter the course of the pathology in vivo.

Original languageEnglish
Pages (from-to)1163-1168
Number of pages6
JournalMicrobes and Infection
Volume1
Issue number14
DOIs
StatePublished - 12 1999
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 2 - Zero Hunger
    SDG 2 Zero Hunger
  2. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Apoptosis
  • Infectious immunity-parasites
  • Protozoan parasites

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