Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.726664
Title: Identification of multigene cysteine protease gene families in Haemonchus contortus and analysis of gut gene expression
Author: Johnston, Stephanie Lauren
Awarding Body: University of Glasgow
Current Institution: University of Glasgow
Date of Award: 2012
Availability of Full Text:
Access from EThOS:
Access from Institution:
Abstract:
Haemonchus contortus is a blood-feeding Strongylid parasite that is economically significant worldwide. Due to the increasing problem of anthelmintic resistance, alternative approaches are urgently required for parasitic nematode control. H. contortus cathepsin B gut cysteine proteases have received attention as potential vaccine candidates because of their proposed role in blood feeding. The increasing amount of H. contortus genome information has now enabled detailed identification and annotation of cathepsin B protease gene families. In this study H. contortus BAC 18f22 was annotated and found to encode eight tandemly arranged cysteine proteases related to the previously identified AC family, but with six novel genes identified. Annotation of supercontig and scaffold sequence identified many more members of the HmCP and GCP-7 cathepsin B families. In total this work has shown that the H. contortus genome encodes at least 41 cathepsin B protease genes, more than in other nematodes, to date. In contrast, Hc-cpr-6 is present as a single copy gene that is highly conserved in a number of species, suggesting an important conserved function. Further work examined regulation of gut gene expression in H. contortus, in particular the H. contortus ELT-2 GATA transcription factor (TF), as it has been shown to be the major TF in C. elegans controlling gut gene expression. A high throughput assay was developed and used to screen an integrated C. elegans worm strain expressing GFP in the gut and hypodermis (Ce-cpl-1::gfp) against 594 chemical compounds. Compounds were identified that specifically cause a decrease in gut GFP expression, affect larval development and show a degree of lethality. Further work on two of the compounds identified an embryonic effect, with a significant decrease in number of progeny. To conclude, this thesis identified a number of novel cathepsin B genes as well as two compounds potentially interfering with TF activity and gut gene expression which may be of use as novel anthelmintics.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.726664  DOI: Not available
Keywords: SF600 Veterinary Medicine ; QH301 Biology
Share: