Group B Streptococcus cpsE Is Required for Serotype V Capsule Production and Aids in Biofilm Formation and Ascending Infection of the Reproductive Tract during Pregnancy.
Kristen NobleJacky LuMiriam A GuevaraRyan S DosterSchuyler A ChambersLisa M RogersRebecca E MooreSabrina K SpicerAlison J EastmanJamisha D FrancisShannon D ManningLakshmi RajagopalDavid M AronoffSteven D TownsendJennifer A GaddyPublished in: ACS infectious diseases (2021)
Group B Streptococcus (GBS) is an encapsulated Gram-positive pathogen that causes ascending infections of the reproductive tract during pregnancy. The capsule of this organism is a critical virulence factor that has been implicated in a variety of cellular processes to promote pathogenesis. Primarily comprised of carbohydrates, the GBS capsule and its synthesis is driven by the capsule polysaccharide synthesis (cps) operon. The cpsE gene within this operon encodes a putative glycosyltransferase that is responsible for the transfer of a Glc-1-P from UDP-Glc to an undecaprenyl lipid molecule. We hypothesized that the cpsE gene product is important for GBS virulence and ascending infection during pregnancy. Our work demonstrates that a GBS cpsE mutant secretes fewer carbohydrates, has a reduced capsule, and forms less biofilm than the wild-type parental strain. We show that, compared to the parental strain, the ΔcpsE deletion mutant is more readily taken up by human placental macrophages and has a significantly attenuated ability to invade and proliferate in the mouse reproductive tract. Taken together, these results demonstrate that the cpsE gene product is an important virulence factor that aids in GBS colonization and invasion of the gravid reproductive tract.
Keyphrases
- biofilm formation
- candida albicans
- pseudomonas aeruginosa
- staphylococcus aureus
- wild type
- escherichia coli
- genome wide
- copy number
- pulmonary artery
- cystic fibrosis
- endothelial cells
- genome wide identification
- gram negative
- multidrug resistant
- aortic dissection
- klebsiella pneumoniae
- gene expression
- pulmonary arterial hypertension
- genome wide analysis
- coronary artery