Characterisation of Biofilm-Forming Ability and Haemolytic Activity of Clinical Group B Streptococcus (GBS) Isolates From the Urinary Tract
File version
Author(s)
Primary Supervisor
Ulett, Glen C
Other Supervisors
Goh, Kelvin G
Editor(s)
Date
Size
File type(s)
Location
License
Abstract
Urinary tract infections (UTIs) are among the most common infections caused by both Gram-negative and Gram-positive bacteria, acquired in the community and hospitals. There are three main groups of UTIs: (i) lower UTIs that affect the urethra or the bladder, (ii) upper UTIs that affect the kidneys, or (iii) asymptomatic bacteriuria (ABU).
Group B Streptococcus (GBS) is a Gram-positive bacteria known to cause a variety of infections in neonates, pregnant women, the elderly or immunocompromised individuals. GBS has been estimated to cause 1-2% of all single organism UTIs. GBS has been shown to form biofilms, on abiotic and biotic surfaces, protecting it from killing by antibiotics or host immune cells and promotes host colonisation. Various factors have been shown to affect the biofilm forming ability of GBS. Here we determined that LB supplemented with glucose was the optimal media for biofilm formation by a strong biofilm forming strain. We then investigated the biofilm forming phenotype of 292 clinical GBS isolates that presented with asymptomatic, acute, or recurrent infection. We found that there was no significant difference in the biofilm forming ability across the clinical presentations. We also showed a significant reduction in the biofilm forming ability of a strong biofilm forming strain and its isogenic maeK and maeE mutants in LB supplemented with 1% glucose. A multiplex PCR screen for genes encoding bsaB, pil1, pil2a, and pil2b found that there was no significant difference in the number of strains that had the right sized fragments for all four genes across the three clinical presentations. We also found that there was a significant difference in the proportion of strains that had the right sized fragments for the pil genes across the three different levels of biofilm activity under shaking conditions. High biofilm forming strains had the lowest proportion of strains that possessed all four genes, compared to low and medium biofilm formers. Lastly, we assessed the haemolytic activity of the strains by growing them on tryptic soy agar plates supplemented with 5% horse blood and found that asymptomatic strains had a significantly higher number of strains with high haemolytic activity compared to acute and recurrent strains.
Journal Title
Conference Title
Book Title
Edition
Volume
Issue
Thesis Type
Thesis (Masters)
Degree Program
Master of Medical Research (MMedRes)
School
School of Medical Science
Publisher link
Patent number
Funder(s)
Grant identifier(s)
Rights Statement
Rights Statement
The author owns the copyright in this thesis, unless stated otherwise.
Item Access Status
Note
Access the data
Related item(s)
Subject
Biofilm-Forming Ability
Haemolytic Activity
Clinical Group B Streptococcus (GBS)
Urinary tract infections (UTIs)
Gram-negative bacteria
Gram-positive bacteria