
Naming
''T. brucei'' comprises a species complex that includes:⤷ ''T. brucei gambiense'' – Causes slow onset chronic trypanosomiasis in humans. Most common in central and western Africa, where humans are thought to be the primary reservoir.
⤷ ''T. brucei rhodesiense'' – Causes fast onset acute trypanosomiasis in humans. Most common in southern and eastern Africa, where game animals and livestock are thought to be the primary reservoir.
⤷ ''T. brucei brucei'' – Causes animal trypanosomiasis, along with several other species of ''Trypanosoma''. ''T. b. brucei'' is not infective to humans due to its susceptibility to lysis by trypanosome lytic factor-1 . However, it is closely related to, and shares fundamental features with the human-infective subspecies.
Distribution
''T. brucei'' is only found in the blue areas''T. brucei'' is found where its tsetse fly vectors are prevalent in continental Africa. That is to say, tropical rainforest , tropical monsoon , and tropical savannah areas of continental Africa. Hence, the equatorial region of Africa is called the "sleeping sickness" belt. However, the specific type of the trypanosome differs according to geography. ''T. b. rhodesiense'' is found primarily in East Africa , while ''T. b. gambiense'' is found in Central and West Africa.
Behavior
''T. brucei'' completes its life cycle between tsetse fly and mammalian hosts, including humans, cattle, horses, and wild animals.Evolution
''Trypanosoma brucei gambiense'' evolved from a single progenitor ~10,000 years ago. It is evolving asexually and its genome shows the Meselson effect.References:
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