Essential or redundant? Disentangling the (GR)ESAG families of Trypanosoma brucei

Chamberlain, James W. (2018) Essential or redundant? Disentangling the (GR)ESAG families of Trypanosoma brucei. PhD thesis, University of Nottingham.

[img] PDF (Thesis - as examined) - Repository staff only - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader
Download (32MB)


The protozoan parasite Trypanosoma brucei escapes its mammalian host’s immune response by switching expression of its major surface antigen, variant surface glycoprotein (VSG), which forms a protective coat around the cell. The actively expressed VSG is transcribed from one of 14 bloodstream expression sites (BESs), which also encode variable repertoires of expression site associated genes (ESAGs), most of which localise to the parasite surface. These genes form distinct families, are co-transcribed with VSG, and the repertoire expressed changes upon in situ switch. Specific ESAGs are known to protect the parasite from human serum lytic effects, modulate the host’s innate immune response, mediate uptake of essential nutrients, and may adapt the parasite to the serum of different mammalian hosts. In addition to BES-linked ESAGs, these families also encompass non-BES encoded genes related to ESAGs (GRESAGs), some of which, unlike the ESAGs, are expressed in both mammalian and insect lifecycle stages.

To investigate the functional relationship between BES and non-BES (GR)ESAGs, I established a system to specifically ablate only BES-derived transcript or multiple (GR)ESAG family members. The former was carried out by tagging BES-linked ESAGs with GFP, and then targeting the GFP ORF by RNAi. The latter involved pan-family RNAi constructs, designed using regions with high identity across individual (GR)ESAG families. Pan-family, but not BES-specific, knockdown induced growth defects, showing that transcript from the active BES itself is not essential for parasite survival in vitro. To investigate this further, a strategy based on Cre recombinase genome engineering was developed to specifically reduce the ESAG repertoire contained within the active BES. Stable cell lines ready for recombination were obtained, and will be used for analysis of modified BESs.

Together, the results achieved show that (GR)ESAG families, as opposed to the actively-expressed ESAG copy, are important for parasite survival in vitro, and there is redundancy between BES-linked and non-BES transcripts. Therefore, the often-overlooked GRESAGs may play more significant roles than originally thought.

Item Type: Thesis (University of Nottingham only) (PhD)
Supervisors: Gadelha, Catarina
Wickstead, W.
Subjects: Q Science > QH Natural history. Biology > QH426 Genetics
Q Science > QL Zoology > QL360 Invertebrates
Faculties/Schools: UK Campuses > Faculty of Medicine and Health Sciences > School of Life Sciences
Item ID: 49921
Depositing User: Chamberlain, James
Date Deposited: 27 Sep 2021 11:48
Last Modified: 27 Sep 2021 11:51

Actions (Archive Staff Only)

Edit View Edit View