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http://hdl.handle.net/11375/26789
Title: | Prediction of Antimicrobial Resistance Phenotypes from Genotype |
Authors: | Tsang, Kara K. |
Advisor: | McArthur, Andrew G. |
Department: | Biochemistry and Biomedical Sciences |
Keywords: | antimicrobial resistance;phenotype;genomics;genotype;microbiology;bacteria;bioinformatics |
Publication Date: | 2021 |
Abstract: | Antimicrobial resistance (AMR) is a threat to global health, food security, and economic productivity. Infections caused by drug resistant Gram-negative pathogens, such as Escherichia coli, Pseudomonas aeruginosa, and Neisseria gonorrhoeae, are continuously becoming harder to treat due to limited treatment options and long turnaround times for culture-based phenotypic diagnosis. Alternatively, genotypic approaches that exploit whole genome sequencing have the potential to be faster and more accurate. Genotypic approaches rely on using bacterial genomes to predict AMR phenotypes. I generated a rules-based algorithm and machine learning models using known resistance determinants from bacterial genomes to predict resistance or susceptibility. I showed that machine learning was superior to a rules-based algorithm and achieved an average accuracy of 94% and 89% for E. coli and P. aeruginosa, respectively. These machine learning models identified novel AMR genotype-phenotype relationships between known resistance determinants and resistance phenotypes, which were experimentally validated. To identify the parameters that can improve machine learning models, I tested a variety of genetic features, algorithms, and evaluation metrics. I observed an intricate dependency between parameters for AMR prediction performance, illustrating that careful selection of parameters is required to generate accurate AMR prediction models. A limitation of this work was its prediction of resistance and susceptibility categories, as these are interpretations of minimum inhibitory concentrations defined by clinical breakpoint guidelines. Since multiple guidelines exist, these prediction models are not generalizable, so prediction of MIC values was explored. The average accuracy of my MIC prediction models was 86%, 41%, and 98% for E. coli, P. aeruginosa, and N. gonorrhoea, respectively. Despite the multifactorial and intricate nature of the resistome, I was able to accurately predict AMR phenotypes for many antibiotics for these pathogens. This is a step towards advanced diagnostic microbiology methods driven by genomics. |
URI: | http://hdl.handle.net/11375/26789 |
Appears in Collections: | Open Access Dissertations and Theses |
Files in This Item:
File | Description | Size | Format | |
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TSANG_KARA_K_finalsubmission_202107_PhD.pdf | 21.89 MB | Adobe PDF | View/Open |
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