dc.contributor.author |
Ndondo, A.M.
|
|
dc.contributor.author |
Munganga, J.M.W.
|
|
dc.contributor.author |
Mwambakana, Jeanine
|
|
dc.contributor.author |
Saad-Roy, C.M.
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|
dc.contributor.author |
Van den Driessche, P.
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|
dc.contributor.author |
Walo, R.O.
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|
dc.date.accessioned |
2017-03-01T11:30:24Z |
|
dc.date.available |
2017-03-01T11:30:24Z |
|
dc.date.issued |
2016-01 |
|
dc.description.abstract |
Human African Trypanosomiasis (HAT) and Nagana in cattle, commonly called sleeping sickness, is caused by trypanosome protozoa transmitted by bites of infected tsetse flies. We present a deterministic model for the transmission of HAT caused by Trypanosoma brucei gambiense between human hosts, cattle hosts and tsetse flies. The model takes into account the growth of the tsetse fly, from its larval stage to the adult stage. Disease in the tsetse fly population is modeled by three compartments, and both the human and cattle populations are modeled by four compartments incorporating the two stages of HAT. We provide a rigorous derivation of the basic reproduction number R0. For R0 < 1, the disease free equilibrium is globally asymptotically stable, thus HAT dies out; whereas (assuming no return to susceptibility) for R0 >1, HAT persists. Elasticity indices for R0 with respect to different parameters are calculated with baseline parameter values appropriate for HAT in West Africa; indicating parameters that are important for control strategies to bring R0 below 1. Numerical simulations with R0 > 1 show values for the infected populations at the endemic equilibrium, and indicate that with certain parameter values, HAT could not persist in the human population in the absence of cattle |
en_ZA |
dc.description.department |
Science, Mathematics and Technology Education |
en_ZA |
dc.description.librarian |
hb2017 |
en_ZA |
dc.description.sponsorship |
The authors are grateful to the office of Prof. Mamokgethi Phakeng, Vice-Principal: Research and
Innovation, UNISA and DST/NRF SARChI Chair in Mathematical Models and Methods in Bioengineering and Biosciences, University of Pretoria; for the funding and sponsoring of the 1st Joint Unisa — UPWorkshop on Theoretical and Mathematical Epidemiology, Science Campus, Florida,South Africa, 2–8 March 2014, where the work was initiated. |
en_ZA |
dc.description.uri |
http://www.tandfonline.com/loi/tjbd20 |
en_ZA |
dc.identifier.citation |
Ndondo, AM, Munganga, JMW, Mwambakana, JN, Saad-Roy, CM, Van den Driessche, P & Walo, RO 2016, 'Analysis of a model of gambiense sleeping sickness in humans and cattle', Journal of Biological Dynamics, vol. 10, no. 1, pp. 347-365. |
en_ZA |
dc.identifier.issn |
1751-3758 (print) |
|
dc.identifier.issn |
1751-3766 (online) |
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dc.identifier.other |
10.1080/17513758.2016.1190873 |
|
dc.identifier.uri |
http://hdl.handle.net/2263/59223 |
|
dc.language.iso |
en |
en_ZA |
dc.publisher |
Taylor and Francis (open access) |
en_ZA |
dc.rights |
© 2016 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/). |
en_ZA |
dc.subject |
34D23 |
en_ZA |
dc.subject |
92D30 |
en_ZA |
dc.subject |
Trypanosoma brucei gambiense |
en_ZA |
dc.subject |
Elasticity |
en_ZA |
dc.subject |
Global stability |
en_ZA |
dc.subject |
Sleeping sickness |
en_ZA |
dc.subject |
Vector-borne disease |
en_ZA |
dc.subject |
Human African Trypanosomiasis (HAT) |
en_ZA |
dc.subject |
Nagana |
en_ZA |
dc.title |
Analysis of a model of gambiense sleeping sickness in humans and cattle |
en_ZA |
dc.type |
Article |
en_ZA |