Modelling the in-human host and in-mosquito dynamics of malaria parasite and effect of therapy

dc.contributor.authorSelemani, Mohamed Abdallah
dc.date.accessioned2022-10-13T08:31:25Z
dc.date.available2022-10-13T08:31:25Z
dc.date.issued2017
dc.descriptionPhD-Thesisen_US
dc.description.abstractIn this study, a basic mathematical model for the in-human host and in-mosquito dynamics of malaria parasite is formulated. A positive invariant region of the model was established, and a basic reproduction number 7vo, of the model was computed. Conditions for existence and stability of two equilibrium points: malaria free equilibrium (MFE) and malaria infection equilibrium (MIE) were established. The impacts of model parameters on control of malaria infection were assessed through the sensitivity analysis of TZ q . Despite having lower sensitivity index compared to death rate of merozoites. and death rate of schizonts have greater impact on malaria control than that of merozoites. The model was extended to incorporate the effect of immune responses using nonlinear bounded Michaelis- Menten-Monod functions to describe how immune responses interact with infected cells and parasites. Our results revealed that immunity has significant influence on reducing malaria infection at erythrocytic and sporogonic stages, but not at exo-erythrocytic stage. We further extended the model to incorporate the antimalarial drug therapy, where four thera­ peutic classes of antimalarial drugs in various stages of entire life cycle of malaria parasite are included. In contrast to the immunity whose effect reduces infections on only two stages, drug therapy has the effect of reducing infection on all stages of the life cycle. Although its compo­ nents do not appear in the expression of reproduction number, tissue schizonticidal drugs reveal a substantial effect on reducing the infection at each stage of malaria life cycle. This study suggests that a combination therapy with all four classes of antimalaria! drugs should be developed because of its prolific effect on controlling malaria, and for such case, an artemisinin derivatives-primaquine combination therapy is proposed.en_US
dc.identifier.urihttp://www.suaire.sua.ac.tz/handle/123456789/4651
dc.language.isoenen_US
dc.publisherNelson Mandela African Institution of Science and Technologyen_US
dc.subjectMalaria parasiteen_US
dc.subjectMosquitoen_US
dc.subjectTherapyen_US
dc.titleModelling the in-human host and in-mosquito dynamics of malaria parasite and effect of therapyen_US
dc.typeThesisen_US

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