Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.782577
Title: Investigating the molecular mechanisms of pathogenic Group B Streptococcus interactions with fungus Candida albicans
Author: Pidwill, Grace
ISNI:       0000 0004 7968 1821
Awarding Body: University of Bristol
Current Institution: University of Bristol
Date of Award: 2019
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Abstract:
Group B Streptococcus (GBS) is the leading cause of neonatal sepsis and meningitis in developed countries. In the majority of cases, GBS is vertically transmitted from the mother during or preceding birth. Candida albicans is an opportunistic fungal pathogen of the female GU tract, causing vaginal thrush, for which pregnancy is a risk factor. As C. albicans is known to synergistically interact with Streptococcus bacteria within the oral cavity, it was hypothesised that C. albicans and GBS may interact within the vaginal tract. Using a vaginal epithelial cell association assay, it was shown that C. albicans significantly promoted GBS association with vaginal epithelial cells (VECs) and, likewise, GBS significantly promoted C. albicans. The AgI/II family surface-expressed adhesins of GBS, designated Bsp proteins, were found to contribute to GBS interactions with VECs and with C. albicans, while the C. albicans cell surface protein Als3 was pivotal for the coassociation between these species. Investigations into the VEC response to GBS and C. albicans implied that coassociation may reduce neutrophil chemotaxis, despite enhanced transcription of proinflammatory cytokine genes. Proteomics studies revealed that extracellular matrix (ECM) components, or proteins that modulate ECM components, were significantly elevated in dual-species-infected VECs, while apoptosis related proteins and proteins involved in MAPK signalling were largely downregulated. Taken together, these data suggest that GBS and C. albicans synergistically interact in a manner that could promote GU tract colonisation and persistence, and that this coassociation is dependent on C. albicans Als3 and partially dependent on GBS Bsp proteins.
Supervisor: Nobbs, Angela Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.782577  DOI: Not available
Keywords: Microbiology ; Polymicrobial ; Co-association ; Group B Streptococcus ; Candida albicans
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