Use this URL to cite or link to this record in EThOS:
Title: Analysis of Plasmodium falciparum var genes
Author: Ward, Christopher Patrick
Awarding Body: University of Edinburgh
Current Institution: University of Edinburgh
Date of Award: 2000
Availability of Full Text:
Access from EThOS:
Full text unavailable from EThOS. Please try the link below.
Access from Institution:
Plasmodium falciparum var genes encode the PfEMPI family of variant antigens expressed on the surface of infected erythrocytes. PfEMPlmediates the adhesion of the parasitized erythrocyte to the venular endothelium and to uninfected erythrocytes. PfEMP 1 variants use a range of different host molecules as receptors in these adhesive interactions. The expression of different PfEMPI variants may directly affect the clinical course of malaria infection by defining the distribution and intensity of parasite adhesion in the microvasculature of various organs within the host. PfEMPI is a major focus of the host immune response, and the slow onset of clinical immunity in endemic areas may be explained by the gradual accumulation of effective responses to a wide range of PfEMPI variants present in the local parasite population. It has been hypothesised that the immune response to PfEMPI may act to stratify the parasite population into co-circulating 'strains' defined by discrete, non-overlapping repertoires of var genes. Here, the DBL1 region of 56 var gene variants from 6 genetically distinct cocirculating Sudanese parasites have been cloned and sequenced. Sequence comparisons suggest that recombination and gene duplication are important mechanisms in the generation of new var variants. A model of the basic structural framework of DBL1 sequences is described and "sequence subtypes" identified within variable regions of sequence. Phylogenetic analysis of the Sudanese and other var sequences from GenBank fail to support the 'strain' model for Sudanese P. falciparum and suggests that the global pool of var genes is finite. 40 Sudanese variants have been expressed as GST-fusion proteins with yields of varying quantity and degree of degradation. 10 of the recombinant proteins have been tested against a cohort of sera in a pilot ELISA, and the role of anti-PfEMPI immune responses in the development of clinical immunity is discussed.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID:  DOI: Not available