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Structural analysis of capsular polysaccharides produced by some emerging Klebsiella pneumoniae serotypes

Klebsiella pneumoniae (K. pneumoniae), a Gram-negative pathogenic bacterium, is a leading cause of neonatal sepsis in low- and middle-income countries (LMICs). Due to rapidly increasing anti-microbial resistance (AMR), it has been ranked among the “critical-priority 1” pathogens to human health by t...

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Main Author: Mfana, Siwaphiwe
Other Authors: Ravenscroft, Neil
Format: Thesis
Language:Eng
Published: Department of Chemistry 2025
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access_status_str Open Access
author Mfana, Siwaphiwe
author2 Ravenscroft, Neil
author_browse Mfana, Siwaphiwe
Ravenscroft, Neil
author_facet Ravenscroft, Neil
Mfana, Siwaphiwe
author_sort Mfana, Siwaphiwe
collection Thesis
description Klebsiella pneumoniae (K. pneumoniae), a Gram-negative pathogenic bacterium, is a leading cause of neonatal sepsis in low- and middle-income countries (LMICs). Due to rapidly increasing anti-microbial resistance (AMR), it has been ranked among the “critical-priority 1” pathogens to human health by the World Health Organisation (WHO). K. pneumoniae produces a capsular polysaccharide (CPS or Kantigen), which constitutes an important virulence factor and a potential vaccine antigen. To date, there are up to 77 known distinct K. pneumoniae K-antigen serotypes, that have been classified through serotyping. Furthermore, there are additional K-locus (KL) serotypes that have been recently identified using genotyping. This project involved the characterisation and structural elucidation of the CPS repeating unit (RU) structures, known as chemotyping, of four emerging clinically significant strains of K. pneumoniae, which were identified through genotyping as novel serotypes: KL102; KL112; KL122; and KL107. NMR spectroscopy provides a non-destructive method for the structural elucidation of polysaccharides on relatively small amounts of samples. A combination of 1D and 2D homo and heteronuclear NMR experiments can be used to determine the monosaccharide composition, anomeric configurations ( or ), linkage positions and sequence of residues in the polysaccharide RU. NMR can also identify the presence and positions of non-carbohydrate substituents including O-acetyl and pyruvate groups. Complete NMR characterisation and structural elucidation was successfully achieved for all four capsular polysaccharides investigated. Their proposed RU structures were compared to those of known K. pneumoniae K-antigens, using a database that was constructed during this investigation, to confirm if they were novel serotypes. KL102 CPS has a novel hexasaccharide RU, made up of a trisaccharide backbone, and is doubly-branched with a disaccharide and a single terminal residue side chains, this can be categorised as a 3 + 2 + 1 RU type. KL112 CPS has a novel and unusual pentasaccharide RU, consisting of a disaccharide backbone chain and a trisaccharide side chain, categorised as a 2 + 3 RU type. KL122 CPS also has a novel hexasaccharide RU containing three uronic acids and is made up of a tetrasaccharide backbone chain with two terminal monosaccharide residues, thus a 4 + 1 + 1 RU type. In contrast, KL107 CPS was found to be identical to serotype K2, having a tetrasaccharide RU, with a trisaccharide backbone chain and a single terminal residue with Oacetylation on the branched backbone residues. The diagnostic NMR data acquired for these CPSs can be used for serotype identity testing, and to monitor the structures of K-antigens during the process of glycoconjugate vaccine development
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language Eng
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license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2025
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source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/41117 Structural analysis of capsular polysaccharides produced by some emerging Klebsiella pneumoniae serotypes Mfana, Siwaphiwe Ravenscroft, Neil Edmonds-Smith Cesarina Chemistry Klebsiella pneumoniae (K. pneumoniae), a Gram-negative pathogenic bacterium, is a leading cause of neonatal sepsis in low- and middle-income countries (LMICs). Due to rapidly increasing anti-microbial resistance (AMR), it has been ranked among the “critical-priority 1” pathogens to human health by the World Health Organisation (WHO). K. pneumoniae produces a capsular polysaccharide (CPS or Kantigen), which constitutes an important virulence factor and a potential vaccine antigen. To date, there are up to 77 known distinct K. pneumoniae K-antigen serotypes, that have been classified through serotyping. Furthermore, there are additional K-locus (KL) serotypes that have been recently identified using genotyping. This project involved the characterisation and structural elucidation of the CPS repeating unit (RU) structures, known as chemotyping, of four emerging clinically significant strains of K. pneumoniae, which were identified through genotyping as novel serotypes: KL102; KL112; KL122; and KL107. NMR spectroscopy provides a non-destructive method for the structural elucidation of polysaccharides on relatively small amounts of samples. A combination of 1D and 2D homo and heteronuclear NMR experiments can be used to determine the monosaccharide composition, anomeric configurations ( or ), linkage positions and sequence of residues in the polysaccharide RU. NMR can also identify the presence and positions of non-carbohydrate substituents including O-acetyl and pyruvate groups. Complete NMR characterisation and structural elucidation was successfully achieved for all four capsular polysaccharides investigated. Their proposed RU structures were compared to those of known K. pneumoniae K-antigens, using a database that was constructed during this investigation, to confirm if they were novel serotypes. KL102 CPS has a novel hexasaccharide RU, made up of a trisaccharide backbone, and is doubly-branched with a disaccharide and a single terminal residue side chains, this can be categorised as a 3 + 2 + 1 RU type. KL112 CPS has a novel and unusual pentasaccharide RU, consisting of a disaccharide backbone chain and a trisaccharide side chain, categorised as a 2 + 3 RU type. KL122 CPS also has a novel hexasaccharide RU containing three uronic acids and is made up of a tetrasaccharide backbone chain with two terminal monosaccharide residues, thus a 4 + 1 + 1 RU type. In contrast, KL107 CPS was found to be identical to serotype K2, having a tetrasaccharide RU, with a trisaccharide backbone chain and a single terminal residue with Oacetylation on the branched backbone residues. The diagnostic NMR data acquired for these CPSs can be used for serotype identity testing, and to monitor the structures of K-antigens during the process of glycoconjugate vaccine development 2025-03-05T13:17:05Z 2025-03-05T13:17:05Z 2024 2025-03-05T13:11:38Z Thesis / Dissertation Masters MSc http://hdl.handle.net/11427/41117 Eng application/pdf Department of Chemistry Faculty of Science University of Cape town
spellingShingle Chemistry
Mfana, Siwaphiwe
Structural analysis of capsular polysaccharides produced by some emerging Klebsiella pneumoniae serotypes
thesis_degree_str Master's
title Structural analysis of capsular polysaccharides produced by some emerging Klebsiella pneumoniae serotypes
title_full Structural analysis of capsular polysaccharides produced by some emerging Klebsiella pneumoniae serotypes
title_fullStr Structural analysis of capsular polysaccharides produced by some emerging Klebsiella pneumoniae serotypes
title_full_unstemmed Structural analysis of capsular polysaccharides produced by some emerging Klebsiella pneumoniae serotypes
title_short Structural analysis of capsular polysaccharides produced by some emerging Klebsiella pneumoniae serotypes
title_sort structural analysis of capsular polysaccharides produced by some emerging klebsiella pneumoniae serotypes
topic Chemistry
url http://hdl.handle.net/11427/41117
work_keys_str_mv AT mfanasiwaphiwe structuralanalysisofcapsularpolysaccharidesproducedbysomeemergingklebsiellapneumoniaeserotypes