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Department of Biochemistry and Cell Biology, Faculty of Veterinary Medicine, Utrecht University, 3584 CM Utrecht, The Netherlands; Department of Parasitology, Unit of Entomology, Institute of Tropical Medicine Antwerp, B-2000 Antwerp, Belgium; Department of Animal Health, Institute of Tropical Medicine Antwerp, B-2000 Antwerp, Belgium; Department of Veterinary Tropical Diseases, Faculty of Veterinary Science, Onderstepoort, South Africa; and Department of Medical Microbiology & Infectious Diseases, ErasmusMC University Medical Center, 3015 GD Rotterdam, The Netherlands
* To whom correspondence should be addressed. Email:
a.tielens{at}erasmusmc.nl.
Procyclic forms of Trypanosoma brucei isolated from midguts of infected tsetse flies, or freshly transformed from a strain that is close to field isolates, do not use a complete Krebs cycle. Furthermore, short-stumpy bloodstream forms produce acetate and are apparently metabolically pre-adapted to adequate functioning in the tsetse fly.
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Adaptations in the glucose metabolism of procyclic Trypanosoma brucei isolated from tsetse flies and during differentiation of bloodstream forms
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