Full Text Available

Note: Clicking the button above will open the full text document at the original institutional repository in a new window.

Genetic manipulation of Plasmodium falciparum for conditional knockdown of potassium channels

Dissertation (MSc (Biochemistry))--University of Pretoria, 2021.

Saved in:
Bibliographic Details
Other Authors: Niemand, Jandeli
Format: Thesis
Language:English
Published: University of Pretoria 2021
Subjects:
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1867613614594064384
access_status_str Open Access
author2 Niemand, Jandeli
author_browse Niemand, Jandeli
author_facet Niemand, Jandeli
collection Thesis
dc_rights_str_mv © 2019 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria.
description Dissertation (MSc (Biochemistry))--University of Pretoria, 2021.
format Thesis
id oai:repository.up.ac.za:2263/79963
institution University of Pretoria (South Africa)
language English
last_indexed 2026-06-10T12:38:57.201Z
license_str Other — see source repository
provenance_str_mv Harvested via OAI-PMH from UPSpace — University of Pretoria Institutional Repository
publishDate 2021
publishDateRange 2021
publishDateSort 2021
publisher University of Pretoria
publisherStr University of Pretoria
record_format dspace
source_str UPSpace — University of Pretoria Institutional Repository
spelling oai:repository.up.ac.za:2263/79963 Genetic manipulation of Plasmodium falciparum for conditional knockdown of potassium channels Niemand, Jandeli elsfiona@gmail.com Birkholtz, Lyn-Marie Els, Fiona Plasmodium falciparum Genetic manipulation UCTD Dissertation (MSc (Biochemistry))--University of Pretoria, 2021. Malaria is a devastating disease with the most severe cases caused by the Plasmodium falciparum parasite. Despite it being a preventable disease, mortality rates remain a concern due to emerging drug resistance. Ion channels have been recognized as important therapeutic targets for treating numerous illnesses, since the maintenance of the ion concentration gradient regulates a wide range of physiological processes. Studies on Na+ transporter PfATP4 have revealed its potential as an effective drug target, and disrupts the K+ gradient with an ionophore, such as salinomycin, kills the parasite throughout the intra-erythrocytic stages. K+ channels are essential to maintain the electrochemical gradient in a eukaryotic cell. In P. falciparum, two K+ channels, PF3D7_1227200 (K1) and PF3D7_1465500 (K2), have been identified. Both K+ channels are expressed throughout the asexual intra-erythrocytic stages, whereas only K2 is expressed in the sexual intra-erythrocytic stages. However, the essentiality and localisation of these channels throughout intra-erythrocytic development is unknown. In this study, it was attempted to genetically modify K1 and K2 by adding a green fluorescent protein tag and conditional knockdown mechanism to investigate localisation and prove their essentiality in P. falciparum in future studies. This was done by cloning C-terminal gene fragments into two plasmid systems that contain an inducible riboswitch which regulates the level of mRNA and ultimately leads to reduced levels of protein produced, thus knocking down the protein. An original glmS and a modified SLI glmS system was compared. The modified SLI glmS system use a double selection mechanism and thus produces modified parasites at a faster rate than the original glmS system. Recombinant parasite lines were produced for K2, but not for K1. The original glmS system proved to integrate faster into the genome compared to the modified SLI glmS system. The successful construction of these recombinant lines allows for subsequent studies to determine essentiality and localisation of K2 in P. falciparum during intra-erythrocytic development. This study provides the basis for future studies that may develop K+ homeostasis as an intra-erythrocytic drug target. UP ISMC NRF Biochemistry MSc (Biochemistry) Unrestricted 2021-05-19T08:12:22Z 2021-05-19T08:12:22Z 2021 2021-05-19 Dissertation Els, F 2021, Genetic manipulation of Plasmodium falciparum for conditional knockdown of potassium channels, MSc dissertation, University of Pretoria, Pretoria, viewed yymmdd http://hdl.handle.net/2263/79963 S2021 http://hdl.handle.net/2263/79963 en © 2019 University of Pretoria. All rights reserved. The copyright in this work vests in the University of Pretoria. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of the University of Pretoria. application/pdf University of Pretoria
spellingShingle Plasmodium falciparum
Genetic manipulation
UCTD
Genetic manipulation of Plasmodium falciparum for conditional knockdown of potassium channels
title Genetic manipulation of Plasmodium falciparum for conditional knockdown of potassium channels
title_full Genetic manipulation of Plasmodium falciparum for conditional knockdown of potassium channels
title_fullStr Genetic manipulation of Plasmodium falciparum for conditional knockdown of potassium channels
title_full_unstemmed Genetic manipulation of Plasmodium falciparum for conditional knockdown of potassium channels
title_short Genetic manipulation of Plasmodium falciparum for conditional knockdown of potassium channels
title_sort genetic manipulation of plasmodium falciparum for conditional knockdown of potassium channels
topic Plasmodium falciparum
Genetic manipulation
UCTD
url http://hdl.handle.net/2263/79963