The isolation and characterisation of a Babesia bovis stock from outbreaks on a farm in the Swartberg region of KwaZulu-Natal, South Africa

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dc.contributor.advisor Latif, Abdalla A. en
dc.contributor.advisor Collins, Nicola E. en
dc.contributor.postgraduate Olds, Cassandra Leah en
dc.date.accessioned 2013-09-07T19:15:52Z
dc.date.available 2009-04-15 en
dc.date.available 2013-09-07T19:15:52Z
dc.date.created 2008-11-28 en
dc.date.issued 2009-04-15 en
dc.date.submitted 2009-02-20 en
dc.description Dissertation (MSc)--University of Pretoria, 2008. en
dc.description.abstract Babesia bovis outbreaks were reported in cattle alleged to be immunised with the commercially available live-blood vaccine in the Swartberg region of KwaZulu-Natal, South Africa and an investigation into the nature of parasites causing the outbreaks was carried out. The H isolate was obtained from a clinically ill animal on the Haistings farm and characterised using BvVA1 and Bv80 size analysis coupled with Bv80 and 18S rRNA V4 hypervariable region sequence analysis. In total, four South African B. bovis isolates were analysed: the vaccine stock (S) at passage 11 and 23 and field isolates H and F. The S23 strain used to infect vaccine donor animals could not be detected in the H isolate and could not be responsible for the severe disease symptoms observed in the field animals. Sequence profiles of the Bv80 and 18S rRNA V4 hypervariable regions for all detectable strains were compiled and now serve as a basis for the investigation of future babesiosis outbreaks. It was determined that the Bv80 PCR is not able to detect animals at the carrier stage of infection and that non-specific primer binding to Boophilus microplus and Boophilus decoloratus tick DNA occurs. For this reason, the Bv80 PCR is not suitable for investigating the nature of B. bovis infections in ticks. The BvVA1 PCR reaction required extensive optimisation and did not detect all strains present in the isolates and was therefore not used as a basis for strain discrimination. Microaerophilous stationary phase cultures of the vaccine strain at passage 24 (S24) and the H strain were initiated as a potential source of soluble parasite antigens. Continuous cultivation was not possible despite the alteration of a number of conditions. Currently there is no culture adapted B. bovis strain in South Africa and the availability of such a strain would form the basis of studies on the development of alternative vaccines. en
dc.description.availability unrestricted en
dc.description.department Veterinary Tropical Diseases en
dc.identifier.citation 2008 en
dc.identifier.other E1263/gm en
dc.identifier.upetdurl http://upetd.up.ac.za/thesis/available/etd-02202009-152422/ en
dc.identifier.uri http://hdl.handle.net/2263/30519
dc.language.iso en
dc.publisher University of Pretoria en_ZA
dc.rights ©University of Pretoria 2008 E1263/ en
dc.subject Swartberg region en
dc.subject Cattle en
dc.subject Babesia bovis en
dc.subject South Africa (SA) en
dc.subject KwaZulu-Natal (KZN) en
dc.subject UCTD en_US
dc.title The isolation and characterisation of a Babesia bovis stock from outbreaks on a farm in the Swartberg region of KwaZulu-Natal, South Africa en
dc.type Dissertation en


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