Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.662050
Title: Molecular definition of paratuberculosis pathologies by functional genomics
Author: Smeed, J.
Awarding Body: University of Edinburgh
Current Institution: University of Edinburgh
Date of Award: 2008
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Abstract:
Paratuberculosis (Johne’s disease) is a chronic intestinal disease of ruminants caused by Mycobacterium avium subspecies paratuberculosis (MAP). Three forms have been described in sheep – multibacillary, paucibacillary and asymptomatic. Real-time RT-PCR (qPCR) and microarray analyses were used to compare gene expression in ileal tissue from sheep with the three forms of the disease to try to understand the immune responses underpinning these three defined pathologies. All animals from the infected flocks were IS900 positive by qPCR and therefore infected with MAP. Asymptomatic sheep had no clinical signs of disease, showed no evidence of acid-fast bacteria (ZN-), exhibited normal histology of the terminal ileum and were seronegative. Paucibacillary sheep were ZN- and showed lymphocyte/eosinophil infiltrate into the lamina propria. 2/6 of the paucibacillary animals were seropositive. Multibacillary sheep had high numbers of ZN+ bacteria associated with infiltrating sheets of epithelioid macrophages and were seropositive. Control sheep were IS900 negative and thus uninfected with MAP. qPCR experiments confirmed that pauci- and multibacillary forms are linked to the differential expression of IFNγ and IL-10 respectively. Increased levels of the proinflammatory cytokines IL-1β, IL-8, IL-18, TNFα and TRAF-1, indicative of persistent inflammatory lesions, were observed in clinical tissues. IL-3 was detected at low levels in all infected animals but never in uninfected control samples. IGFBP-6 was upregulated and CXCR4 downregulated in paucibacillary samples compared to multibacillary samples. Microarray experiments discovered 64 differentially expressed genes. Ten genes were found to be differentially expressed in infected tissue compared to uninfected controls, and a further eight in clinical tissues compared to uninfected controls. Fifteen genes were differentially expressed in clinical tissue compared to asymptomatic tissue. Six genes were quantified by qPCR and validated in microarray data well. Pathway analysis of the microarray data identified several immune pathways that are involved in pathogenesis. Infected tissues displayed upregulation of the genes involved in TCR signalling and complement activation, and downregulation of MHC class II genes. In addition, clinical tissues displayed upregulation of genes involved in the JAK-STAT and TLR2 signalling pathways, NK cell cytotoxicity and antibody production. Multibacillary tissues also displayed upregulation of genes involved in leukocyte migration. Overall, these data confirm that multibacillary pathology is linked to type 2 and paucibacillary pathology is linked to type 1 immune responses and identify novel genes and gene pathways for future analyses.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.662050  DOI: Not available
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