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dc.contributor.authorOpiyo, EA
dc.date.accessioned2013-05-27T11:39:05Z
dc.date.available2013-05-27T11:39:05Z
dc.date.issued1984
dc.identifier.citationA Thesis submitted in fulfilment of the requirements for the Degree of Doctor of Philosophy in the University of Nairobi.en
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/26196
dc.description.abstractThis thesis is primarily a study of factors which influence the virulence of T. (N). simiae for pigs. The factors investigated include the species of tsetse vectors, size of inocula of trypanosomes injected into pigs and the method of maintenance of the trypanosomes. The rate of development of T. (N). simiae in different species of tsetse and its relationship to the resulting infection in pigs was also investigated. In addition, an attempt was made to adapt T. (N). simiae to laboratory rodents. In this study three stocks of I. ().simiae were cyclically transmitted through tsetse. Transmitting the isolates through Glossina morsitans and Q. pallidipes resulted in a disease less severe than did syringe inoculations. Pigs infected through tsetse bites survived much longer than had previously been reported, with some pigs exhibiting self-cure after running infection for varying lengths of time. The response of pigs to experimental infection with I. (~).simiae varied from one animal to another and pigs appear to fall into three categories. Pigs in the first group were the very susceptible and died during th0 first peak of parasitaemia. The parasitaemia built up fast and Lhe pigs died soon after the first appearance of trypanosomes ill the peripheral blood circulation. VI The second group developed parasitaem{a, and survived more than one parasitaemia peak but eventually succumbed to the infection. The third group became parasitaemic, apparently controlled the parasitaemia for some weeks at very low levels and eventually threw off the infection. Grouping the pigs according to their place of origin shows that those which experienced chronic, self-limiting infections were from the same farm. The less susceptible pigs came from this farm. This suggest that the course of infection observed might have been determined by the ability of the individual pig to control the infection rather than by the vector. No clear evidence was obtained to show whether or not the species of the vector influenced the virulence of T. (N). simiae. Teneral tsetse flies became infected with T. (N). simiae when they were fed on pigs carrying predominantly stumpy trypanosomes in their blood, but the number of trypanosomes circulating in blood did not appear to influence the infection rate in tsetse. At 2SoC G. morsitans developed mature T. (N). simiae infections in 19 days and ~. pallidipes in 23 days. G. morsitans was more frequently infected than Q. pallidipes. In pigs neither the prepatent period nor the period of patency appeared not to be related to the rate of development or the infection rate in the tsetse fly. VII One isolate of T. (N). simiae (EATRO 1786) has been successfully adapted to rats. The parasite has been maintained in rats through 20 passages without pig serum and 14 passages with pig serum. The infection first became lethal to rats in the seventh passage. Abnormal trypanosomes were observed during the initial stages of adaptation. The rat adapted I. (~).simiae were shorter than trypanosomes from the original strain. Trypanosomes from the original isolate had a mean length of range 13.5 pm to 17. 43 ~m.',.Ln.rats the trypanosomes measured a mean of 12.59 ~m (range 8.8 and 14.4 ~m). In pigs the rat adapted T. (N). simiae measured a mean of 12.35 um (range 9.9 - 14.38 ~m). The rat adapted T. (N). simiae strain has remained infective to tsetse and to pigs. It infects mice readily.en
dc.language.isoenen
dc.titleStudies on the biology of trypanosoma (nannomonas) simiaeen
dc.typeThesisen
local.publisherDepartment of Biologyen


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