Molecular pathological investigation of the pathophysiology of fatal malaria

<p>Malaria remains one of the world's major health problems, especially in developing countries. A better understanding of the pathology and pathophysiology of severe malaria is key to develop new treatments. Different approaches have been used in malaria research including the in vitro c...

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Autor Principal: Prapansilp, P
Outros autores: Day, N
Formato: Thesis
Idioma:English
Publicado: 2012
Subjects:
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author Prapansilp, P
author2 Day, N
author_facet Day, N
Prapansilp, P
author_sort Prapansilp, P
collection OXFORD
description <p>Malaria remains one of the world's major health problems, especially in developing countries. A better understanding of the pathology and pathophysiology of severe malaria is key to develop new treatments. Different approaches have been used in malaria research including the in vitro co-culture models with endothelial cells and both murine and simian animal models. However these are open to controversy due to disagreement on their representativeness of human disease. Using human post-mortem tissue in malaria research is another important approach but is practically challenging, limiting the availability of post mortem samples from malaria patients.</p> <p>The work in this thesis had two main themes. First I examined the role of the endothelial signalling Angiopoetin-Tie-2 receptor pathway in malaria. Ang-2 has been shown to be a significant biomarker of severe and fatal malaria. I examined the tissue specific expression of proteins from this pathway in post-mortem brain tissues from fatal malaria cases, but found no difference between cerebral malaria and non-cerebral malaria cases. Ang-2 correlated with the severity of malaria in these patients. An attempt to examine the interaction of hypoxia and the Ang-Tie-2 pathway in vitro using a co-culture model of human brain endothelial cells was unsuccessful due to contamination of the cell line.</p> <p>The second part of the thesis aimed to utilise molecular pathology techniques including miRNA and whole-genome microarrays. I have shown for the first time that these can be successfully applied to human post-mortem tissue in malaria. First I used archival tissues to examine the microRNA signature in the kidney of patients with malaria associated renal failure. Second I optimised a protocol to preserve post mortem tissue for molecular pathology, from an autopsy study in Mozambique. Using the subsequent total mRNA transcriptomic data and bioinformatics analysis this work has expanded our knowledge of differential gene expression and the families of genes which are dysregulated in the brain in response to malaria infection.</p>
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spelling oxford-uuid:e966a2f2-a37d-4586-b09e-2bb616e5dce22022-03-27T10:53:59ZMolecular pathological investigation of the pathophysiology of fatal malariaThesishttp://purl.org/coar/resource_type/c_db06uuid:e966a2f2-a37d-4586-b09e-2bb616e5dce2Infectious diseasesCerebral malariaPathologyTropical medicineMalariaEnglishOxford University Research Archive - Valet2012Prapansilp, PDay, NTurner, G<p>Malaria remains one of the world's major health problems, especially in developing countries. A better understanding of the pathology and pathophysiology of severe malaria is key to develop new treatments. Different approaches have been used in malaria research including the in vitro co-culture models with endothelial cells and both murine and simian animal models. However these are open to controversy due to disagreement on their representativeness of human disease. Using human post-mortem tissue in malaria research is another important approach but is practically challenging, limiting the availability of post mortem samples from malaria patients.</p> <p>The work in this thesis had two main themes. First I examined the role of the endothelial signalling Angiopoetin-Tie-2 receptor pathway in malaria. Ang-2 has been shown to be a significant biomarker of severe and fatal malaria. I examined the tissue specific expression of proteins from this pathway in post-mortem brain tissues from fatal malaria cases, but found no difference between cerebral malaria and non-cerebral malaria cases. Ang-2 correlated with the severity of malaria in these patients. An attempt to examine the interaction of hypoxia and the Ang-Tie-2 pathway in vitro using a co-culture model of human brain endothelial cells was unsuccessful due to contamination of the cell line.</p> <p>The second part of the thesis aimed to utilise molecular pathology techniques including miRNA and whole-genome microarrays. I have shown for the first time that these can be successfully applied to human post-mortem tissue in malaria. First I used archival tissues to examine the microRNA signature in the kidney of patients with malaria associated renal failure. Second I optimised a protocol to preserve post mortem tissue for molecular pathology, from an autopsy study in Mozambique. Using the subsequent total mRNA transcriptomic data and bioinformatics analysis this work has expanded our knowledge of differential gene expression and the families of genes which are dysregulated in the brain in response to malaria infection.</p>
spellingShingle Infectious diseases
Cerebral malaria
Pathology
Tropical medicine
Malaria
Prapansilp, P
Molecular pathological investigation of the pathophysiology of fatal malaria
title Molecular pathological investigation of the pathophysiology of fatal malaria
title_full Molecular pathological investigation of the pathophysiology of fatal malaria
title_fullStr Molecular pathological investigation of the pathophysiology of fatal malaria
title_full_unstemmed Molecular pathological investigation of the pathophysiology of fatal malaria
title_short Molecular pathological investigation of the pathophysiology of fatal malaria
title_sort molecular pathological investigation of the pathophysiology of fatal malaria
topic Infectious diseases
Cerebral malaria
Pathology
Tropical medicine
Malaria
work_keys_str_mv AT prapansilpp molecularpathologicalinvestigationofthepathophysiologyoffatalmalaria