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Bacterial and Host Determinants of Group B Streptococcal Vaginal Colonization and Ascending Infection in Pregnancy

Journal

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fcimb.2021.720789

Keywords

group B streptococcus; bacteria; pregnancy; colonization; vagina; placenta; fetus; preterm birth

Funding

  1. National Institutes of Health [R01AI133976, R01AI145890, R01HD098713, R01AI152268, T32AI055396, T32AI007509]
  2. Seattle Childrens Research Institute
  3. Washington National Primate Research Center [P51OD010425]
  4. [U42OD011123]

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Group B streptococcus colonization during pregnancy can lead to adverse outcomes, but there is currently no approved vaccine to prevent GBS infections. Understanding the pathogenesis of GBS disease may help in finding targeted therapeutic strategies to reduce the global burden of GBS infections.
Group B streptococcus (GBS) is a gram-positive bacteria that asymptomatically colonizes the vaginal tract. However, during pregnancy maternal GBS colonization greatly predisposes the mother and baby to a wide range of adverse outcomes, including preterm birth (PTB), stillbirth, and neonatal infection. Although many mechanisms involved in GBS pathogenesis are partially elucidated, there is currently no approved GBS vaccine. The development of a safe and effective vaccine that can be administered during or prior to pregnancy remains a principal objective in the field, because current antibiotic-based therapeutic strategies do not eliminate all cases of invasive GBS infections. Herein, we review our understanding of GBS disease pathogenesis at the maternal-fetal interface with a focus on the bacterial virulence factors and host defenses that modulate the outcome of infection. We follow GBS along its path from an asymptomatic colonizer of the vagina to an invasive pathogen at the maternal-fetal interface, noting factors critical for vaginal colonization, ascending infection, and vertical transmission to the fetus. Finally, at each stage of infection we emphasize important host-pathogen interactions, which, if targeted therapeutically, may help to reduce the global burden of GBS.

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