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First published online 28 February 2006
doi: 10.1242/jcs.02809

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Bloodstream form Trypanosoma brucei depend upon multiple metacaspases associated with RAB11-positive endosomes

Matthew J. Helms^1,*, Audrey Ambit^1,*, Paul Appleton², Laurence Tetley², Graham H. Coombs² and Jeremy C. Mottram^1,

¹ Wellcome Centre for Molecular Parasitology, The Anderson College, University of Glasgow, Glasgow G11 6NU, UK
² Division of Infection and Immunity, Institute of Biomedical and Life Sciences, Joseph Black Building, University of Glasgow, Glasgow G12 8QQ, UK

Author for correspondence (e-mail: j.mottram{at}udcf.gla.ac.uk)

Accepted 24 November 2005

Trypanosoma brucei possesses five metacaspase genes. Of these, MCA2 and MCA3 are expressed only in the mammalian bloodstream form of the parasite, whereas MCA5 is expressed also in the insect procyclic form. Triple RNAi analysis showed MCA2, MCA3 and MCA5 to be essential in the bloodstream form, with parasites accumulating pre-cytokinesis. Nevertheless, triple null mutants (mca2/3mca5) could be isolated after sequential gene deletion. Thereafter, mca2/3mca5 mutants were found to grow well both in vitro in culture and in vivo in mice. We hypothesise that metacaspases are essential for bloodstream form parasites, but they have overlapping functions and their progressive loss can be compensated for by activation of alternative biochemical pathways. Analysis of mca2/3mca5 revealed no greater or lesser susceptibility to stresses reported to initiate programmed cell death, such as treatment with prostaglandin D₂. The metacaspases were found to colocalise with RAB11, a marker for recycling endosomes. However, variant surface glycoprotein (VSG) recycling processes and the degradation of internalised anti-VSG antibody were found to occur similarly in wild type, mca2/3mca5 and triple RNAi induced parasites. Thus, the data provide no support for the direct involvement of T. brucei metacaspases in programmed cell death and suggest that the proteins have a function associated with RAB11 vesicles that is independent of known recycling processes of RAB11-positive endosomes.

Key words: Metacaspase, Endosomes, Recycling, Trypanosoma, Programmed cell death, RNAi

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