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Molecular epidemiology of Klebsiella pneumoniae isolates causing invasive disease from a private laboratory in South Africa

Dissertation (MSc (Medical Microbiology))--University of Pretoria, 2024.

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Other Authors: Kock, Marleen
Format: Thesis
Language:English
Published: University of Pretoria 2024
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access_status_str Open Access
author2 Kock, Marleen
author_browse Kock, Marleen
author_facet Kock, Marleen
collection Thesis
dc_rights_str_mv © 2023 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 (Medical Microbiology))--University of Pretoria, 2024.
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institution University of Pretoria (South Africa)
language English
last_indexed 2026-06-10T12:36:49.219Z
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provenance_str_mv Harvested via OAI-PMH from UPSpace — University of Pretoria Institutional Repository
publishDate 2024
publishDateRange 2024
publishDateSort 2024
publisher University of Pretoria
publisherStr University of Pretoria
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spelling oai:repository.up.ac.za:2263/97378 Molecular epidemiology of Klebsiella pneumoniae isolates causing invasive disease from a private laboratory in South Africa Kock, Marleen sarah.abro@gmail.com Pitout, Johann Dreyer, Andries Liknaitzky, Sarah UCTD Klebsiella pneumoniae South Africa Molecular epidemiology Antibiotic resistance ST307 Sustainable Development Goals (SDGs) SDG-03: Good health and well-being Health Sciences theses SDG-03 Dissertation (MSc (Medical Microbiology))--University of Pretoria, 2024. Klebsiella pneumoniae (K. pneumoniae) is the most clinically significant species within the Klebsiella genus. The main burden of K. pneumoniae infections are healthcare-associated infections (HAIs), generally caused by the classical multidrug resistant (MDR) strains that can resist the activity of multiple antibiotics. The most clinically significant antibiotic resistance in K. pneumoniae is toward the beta-lactam antibiotics mediated by beta-lactam hydrolysing enzymes, specifically the extended-spectrum beta-lactamases (ESBLs), AmpC beta-lactamases and carbapenemases. Resistance is constantly spreading and evolving, predominantly attributed to several high-risk clonal lineages. High-risk clonal lineages are those with an enhanced ability to disseminate and survive in multiple settings and cause antibiotic resistant infection. The aim of this study was to characterise and investigate the molecular epidemiology and beta-lactam resistance of invasive K. pneumoniae isolates from a private laboratory in Gauteng, South Africa. A total of 154 K. pneumoniae isolates isolated from invasive specimens including blood, tissue and fluid were collected between 2021 and 2022 from a private laboratory in Pretoria. Specimens originated from patients in hospitals in Johannesburg, Pretoria and Emalahleni. Antibiotic susceptibility profiles for isolates were obtained using Vitek 2. Disc xv diffusion tests phenotypically confirmed the production of ESBLs, AmpCs and carbapenemases by K. pneumoniae isolates. Phenotypically confirmed isolates underwent polymerase chain reaction (PCR) assays for the detection of specific resistance genes. All K. pneumoniae isolates were genotyped by pulsed field gel electrophoresis (PFGE) and subsequently a dendrogram was constructed using the PFGE profile of each isolate. Major and minor PFGE clusters were identified, and one representative isolate per cluster was chosen from six of the clusters to undergo whole genome sequencing (WGS). The majority of the K. pneumoniae isolates originated from specimens taken from patients in intensive care unit hospital wards, predominantly representing bloodstream infections. High levels of resistance toward multiple antibiotic classes were observed, with 107 (70%) isolates classified as MDR. Amongst all K. pneumoniae isolates, 99 (64%) were phenotypically confirmed ESBL producers, 18 (12%) AmpC producers and 55 (36%) carbapenemase producers. Resistance genes detected included beta-lactamase (bla) sulfhydryl variant (SHV) in 95 isolates (49%), Temoneira (blaTEM) in 60 isolates (39%), the ESBL cefotaximase-Munich (blaCTX-M-15) in 68 isolates (44%), Dhahran (blaDHA) AmpC in seven isolates (5%), and the carbapenemases, oxacillinase-48-like (blaOXA-48-like) in 65 isolates (42%), New Delhi metallo beta-lactamase (blaNDM) in 21 isolates (14%) and K. pneumoniae carbapenemase (blaKPC) in seven isolates (5%). A rare genotype of triple carbapenemase production was detected in two isolates. Within the dendrogram, nine minor PFGE clusters were identified. The six representative isolates from clusters Minor A, Minor C, Minor F, Minor G, Minor H and Minor I that underwent WGS belonged to sequence types (ST) 307 (n = 3), ST2497 (n = 2) and ST3559 (n = 1). The ST307 isolates carried the blaOXA-181 variant. The ST2497 isolates were positive for yersiniabactin, as well as MDR, characterised by the blaOXA-232 variant. The ST3559 isolate was unique in carrying the blaDHA-1 AmpC. The high-risk clones detected in this study are evidence to the local epidemiology of K. pneumoniae in the private healthcare sector of South Africa and represent a major healthcare crisis. Surveillance and molecular epidemiological studies allow insight into current state of affairs regarding HAIs, and are vital in implementing measures to curb spread and outbreaks, as well as developing effective treatment models for highly resistant strains. National Research Foundation Medical Microbiology MSc (Medical Microbiology) Restricted Faculty of Health Sciences 2024-07-31T13:46:06Z 2024-07-31T13:46:06Z 2024-09-06 2024-06-07 Dissertation * S2024 http://hdl.handle.net/2263/97378 DOI: https://doi.org/10.25403/UPresearchdata.26412847.v1 https://doi.org/10.25403/UPresearchdata.26412349 en © 2023 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 UCTD
Klebsiella pneumoniae
South Africa
Molecular epidemiology
Antibiotic resistance
ST307
Sustainable Development Goals (SDGs)
SDG-03: Good health and well-being
Health Sciences theses SDG-03
Molecular epidemiology of Klebsiella pneumoniae isolates causing invasive disease from a private laboratory in South Africa
title Molecular epidemiology of Klebsiella pneumoniae isolates causing invasive disease from a private laboratory in South Africa
title_full Molecular epidemiology of Klebsiella pneumoniae isolates causing invasive disease from a private laboratory in South Africa
title_fullStr Molecular epidemiology of Klebsiella pneumoniae isolates causing invasive disease from a private laboratory in South Africa
title_full_unstemmed Molecular epidemiology of Klebsiella pneumoniae isolates causing invasive disease from a private laboratory in South Africa
title_short Molecular epidemiology of Klebsiella pneumoniae isolates causing invasive disease from a private laboratory in South Africa
title_sort molecular epidemiology of klebsiella pneumoniae isolates causing invasive disease from a private laboratory in south africa
topic UCTD
Klebsiella pneumoniae
South Africa
Molecular epidemiology
Antibiotic resistance
ST307
Sustainable Development Goals (SDGs)
SDG-03: Good health and well-being
Health Sciences theses SDG-03
url http://hdl.handle.net/2263/97378
https://doi.org/10.25403/UPresearchdata.26412349