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      The double life of Group B Streptococcus: Asymptomatic colonizer and potent pathogen

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          Abstract

          Group B Streptococcus (GBS) is a β-hemolytic Gram-positive bacterium that colonizes the lower genital tract of approximately 18% of women globally as an asymptomatic member of the gastrointestinal and/or vaginal flora. If established in other host niches, however, GBS is highly pathogenic. During pregnancy, ascending GBS infection from the vagina to the intrauterine space is associated with preterm birth, stillbirth, and fetal injury. In addition, vertical transmission of GBS during or after birth results in life-threatening neonatal infections, including pneumonia, sepsis, and meningitis. Although the mechanisms by which GBS traffics from the lower genital tract to vulnerable host niches are not well understood, recent advances have revealed that many of the same bacterial factors that promote asymptomatic vaginal carriage also facilitate dissemination and virulence. Further, highly pathogenic GBS strains have acquired unique factors that enhance survival in invasive niches. Several host factors also exist that either subdue GBS upon vaginal colonization or alternatively permit invasive infection. This review summarizes the GBS and host factors involved in GBS’s state as both an asymptomatic colonizer and invasive pathogen. Gaining a better understanding of these mechanisms is key to overcoming the challenges associated with vaccine development and identification of novel strategies to mitigate GBS virulence.

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          Author and article information

          Journal
          2985088R
          4967
          J Mol Biol
          J. Mol. Biol.
          Journal of molecular biology
          0022-2836
          1089-8638
          19 February 2019
          31 January 2019
          26 July 2019
          26 July 2020
          : 431
          : 16
          : 2914-2931
          Affiliations
          [1 ]Department of Global Health, University of Washington, Seattle, WA, United States of America
          [2 ]Center for Global Infectious Disease Research, Seattle Children’s Research Institute, Seattle, WA, United States of America
          [3 ]Department of Obstetrics and Gynecology, University of Washington School of Medicine, Seattle, WA, United States of America
          [4 ]Center for Innate Immunity and Immune Disease, University of Washington, Seattle, Washington, United States of America
          [5 ]Sahlgrenska Academy, Gothenburg University, Gothenburg, Sweden
          [6 ]Department of Pediatrics, University of Washington School of Medicine, Seattle, WA, United States of America
          Author notes
          [* ]Corresponding Author: Dr. Lakshmi Rajagopal, Ph.D., Department of Pediatrics, University of Washington, Seattle Children’s Research Institute, 1900 Ninth Avenue, Seattle, WA 98101-1304. Phone: (206) 884-7336. Fax: (206) 884-7311 lakshmi.rajagopal@ 123456seattlechildrens.org
          Article
          PMC6646060 PMC6646060 6646060 nihpa1521909
          10.1016/j.jmb.2019.01.035
          6646060
          30711542
          fb1604a9-99dc-4a6e-a15a-82581b3d45a3
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