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Phenotypic changes in group B streptococci grown in the presence of the polyols, erythritol, sorbitol and mannitol
Maram Hulbah1,2, Matthew A Croxen1,3, Gregory J Tyrrell4,5
1Division of Diagnostic and Applied Microbiology, Department of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Canada.
Insights
Polyols like erythritol can increase Group B streptococci (GBS) virulence factors, enhancing bacterial survival and biofilm formation. This study reveals how sugar alcohols impact GBS, a key neonatal pathogen.
Area of Science:
- Microbiology
- Neonatal Pathogens
- Bacterial Virulence
Background:
- Group B streptococci (GBS) are significant neonatal pathogens.
- GBS can cause invasive disease in newborns, potentially through vaginal ascent to the uterus.
- Polyols (sugar alcohols) like erythritol, sorbitol, and mannitol are present in the amniotic fluid environment.
Purpose of the Study:
- To investigate the effects of polyols on GBS growth and virulence.
- To determine how erythritol, sorbitol, and mannitol influence GBS phenotype.
Main Methods:
- GBS were incubated in media with varying concentrations of erythritol, sorbitol, and mannitol.
- Bacterial growth, surface protein expression (GBS-PGK), blood survival, cell invasion (HeLa cells), hemolytic activity, and biofilm formation were assessed.
Main Results:
- Polyols did not significantly affect GBS growth rates.
- Erythritol significantly increased GBS surface expression of GBS-PGK (1.25-1.5x) and enhanced survival in human blood (3-18x).
- Erythritol modulated HeLa cell invasion (increased at 1%, decreased at 2-4%), increased hemolytic activity, and enhanced biofilm formation (1.4-3.3x).
Conclusions:
- Polyols, particularly erythritol, alter GBS phenotype.
- These alterations are associated with increased GBS virulence, including enhanced survival, invasion modulation, and biofilm formation.
Background:
Group B streptococci (GBS) are important neonatal bacterial pathogens that can cause severe invasive disease in the newborn. It is thought that in many cases of invasive neonatal GBS disease, the bacteria ascend the vagina into the uterus and infect the amniotic fluid surrounding the fetus. Important constituents of this environment include the polyols or sugar alcohols of which erythritol, sorbitol and mannitol are examples. The aim of our study was to investigate the effect of polyols on GBS grown in media containing these sugar alcohols.
Results:
GBS incubated in varying concentrations of polyols (erythritol, sorbitol or mannitol) did not display any significant enhancement or inhibition of bacterial growth. However, growth of GBS in the presence of erythritol significantly increased the surface expression of GBS-PGK (a plasminogen binding protein) 1.25 to 1.5-fold depending on the erythritol concentration and significantly enhanced the survival in human blood 3X to 18X depending on the concentration of polyol used. Interestingly, GBS grown in 1% erythritol significantly increased invasion by the bacteria of HeLa cells (epithelial cell line) (150% vs 100%) however, at higher concentrations (2% or 4% of polyol) the number of CFUs was significantly reduced (55-75% vs 100%) suggesting higher concentrations of polyols may inhibit invasion. Erythritol also increased GBS hemolytic activity as well as enhancing biofilm formation 1.4X to 3.3X depending on the concentration of polyol used.
Conclusions:
GBS grown in the presence of polyols alters the bacteria's phenotype resulting in changes associated with GBS virulence. This effect was greatest for the polyol erythritol.
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