'Trypanosomes' are a group of
kinetoplastid protozoa distinguished by having only a single
flagellum. All members are exclusively
parasitic, found primarily in
insects. A few genera have life-cycles involving a secondary host, which may be a
vertebrate or a
plant. These include several species that cause major diseases in humans.
The most notable trypanosomal diseases are
trypanosomiasis (African
Sleeping Sickness and South American
Chagas Disease); these are caused by species of ''
Trypanosoma''.
Leishmaniasis is a trypanosomal disease caused by species of ''
Leishmania''.
A variety of different forms appear in the life-cycles of trypanosomes, distinguished mainly by the position of the flagellum:
| Amastigote (leishmanial) | - reduced or absent |
| Promastigote (leptomonad) | - anterior of nucleus, free from cell body |
| Epimastigote (crithidial) | - anterior of nucleus, connected by a short undulating membrane |
| Opisthomastigote (herpetomonad) | - posterior of nucleus, passing through a long groove in the cell |
| Trypomastigote (trypanosomal) | - posterior of nucleus, connected by a long undulating membrane |
All trypanosomes have at least amastigote and promastigote stages. ''Trypanosoma'' appears in all five forms, with the trypanosomal stage occurring in the vertebrate host. ''Trypanosoma brucei'' sub-species have two forms in the bloodstream of a vertebrate host, the rapidly dividing long-slender form and the non-dividing short stumpy form. The short stumpy parasites are adapted for uptake into the tsetse fly vector, and are non-proliferative in comparison with the slender forms.
Unique to ''Trypansoma brucei'' is the expression of a variable surface glycoprotein (VSG) coat on the cell surface, which undergoes constant variation in order to evade the humoral immune system and host antibodies. It is thought that recombination from a repertoire of >1000 VSG genes is responsible for the vast diversity of the parasite, and its effectiveness in immune evasion.