Abstract
dc:description.abstractStaphylococcus aureus is an important human pathogen and crucial part of its pathogenesis depends on its ability to acquire purines to cause disease. In this study, I screened a library of individual mutants under purine import-dependent conditions by inhibiting the purine biosynthesis using the pharmacological agents methotrexate and 6-mercaptopurine and supplementing inosine monophosphate and/or guanine as an exogenous purine source. I identified an ATP-Binding Cassette transporter mutant that failed to grow under the selective purine transport conditions. Further growth characterization of the mutant revealed that the growth defect was not due to an inability to transport purines but rather to downstream effects related to the toxicity of the purine biosynthesis inhibitors. A thorough understanding of S. aureus purine acquisition will allow for development of antimicrobials with prolonged effectiveness.
Degree
thesis:*- Name thesis:degree_name
- M Sc
- Discipline thesis:degree_discipline
- Microbiology and Immunology
- Grantor dc:publisher
- The University of Western Ontario
- Year dc:date.issued
- 2022
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
-
- Sonpaveerawong, Tothong
- Advisor dc:contributor.advisor
-
- David Heinrichs
Subjects
dc:subject × 7Rights
- Language dc:language.iso
- en_ca
Identifiers
dc:identifier.*- Handle dc:identifier.uri
- https://hdl.handle.net/20.500.14721/32085
- OAI identifier oai:identifier
- oai:uwo.scholaris.ca:20.500.14721/32085