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Publication Details
AFRICAN RESEARCH NEXUS
SHINING A SPOTLIGHT ON AFRICAN RESEARCH
Trypanosoma brucei rhodesiense transmitted by a single tsetse fly bite in vervet monkeys as a model of human African trypanosomiasis
PLoS Neglected Tropical Diseases, Volume 2, No. 5, Article e238, Year 2008
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Description
We have investigated the pathogenicity of tsetse (Glossina pollidipes)-transmitted cloned strains of Trypanosoma brucei rhodesiense in velvet monkeys. Tsetse files were confirmed to have mature trypanosome infections by xenodiagnosis, after which nine monkeys were infected via the bite of a single infected fly. Chancres developed in five of the nine (55.6%) monkeys within 4 to 8 days post infection (dpi). All nine individuals were successfully infected, with a median pre-patent period of 4 (range = 4-10) days, indicating that trypanosomes migrated from the site of fly bite to the systemic circulation rapidly and independently of the development of the chancre. The time lag to detection of parasites in cerebrospinal fluid (CSF) was a median 16 (range=8-40) days, making the onset of central nervous system (CNS, late) stage disease. Subsequently. CSF white cell numbers increased above the pre-infection median count of 2 (range=0-9) cells/μl, with a positive linear association between their numbers and that of CSF trypanosomes. Haematological changes showed that the monkeys experienced an early microcytic-hypochromic anaemia and severe progressive thrombocytopaenia. Despite a 3-monkeys fold increase in granulocyte numbers by 4 dpi, leucopaenia occured early (8 dpi) in the monkey infection, determined mainly by reductions in lymphocyte numbers. Terminally, leucocytosis was observed in three of nine (33%) individuls. The duration of infection was a median of 68 (range = 22-120) days. Strain and individual differences were observed in the severity of the clinical and clinical pathology findings, with two strains (KETRI 3741 and 3801) producing a more cute disease than the other two (KETRI 3804 and 3928). The study shows that the fly-transmitted model accurately mimics the human disease and is therefore a suitable gateway to understanding human African trypanosomiasis (HAT; sleeping sickness).© 2008 Thuita et al.
Authors & Co-Authors
Thuita, John Kibuthu
Unknown Affiliation
Kagira, John Maina
Unknown Affiliation
Mwangangi, David Mumo
Unknown Affiliation
Matovu, Enock
Unknown Affiliation
Turner, Charles Michael R.
Unknown Affiliation
Masiga, Daniel K.
Unknown Affiliation
Statistics
Citations: 53
Authors: 6
Affiliations: 6
Identifiers
Doi:
10.1371/journal.pntd.0000238