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Human milk oligosaccharides inhibit growth of group B Streptococcus.
Lin, Ann E; Autran, Chloe A; Szyszka, Alexandra; Escajadillo, Tamara; Huang, Mia; Godula, Kamil; Prudden, Anthony R; Boons, Geert-Jan; Lewis, Amanda L; Doran, Kelly S; Nizet, Victor; Bode, Lars.
Afiliação
  • Lin AE; From the Divisions of Host-Microbe Systems and Therapeutics.
  • Autran CA; Neonatology, and.
  • Szyszka A; Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics.
  • Escajadillo T; Neonatology, and.
  • Huang M; Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics.
  • Godula K; From the Divisions of Host-Microbe Systems and Therapeutics.
  • Prudden AR; Department of Chemistry and Biochemistry.
  • Boons GJ; Department of Chemistry and Biochemistry.
  • Lewis AL; the Complex Carbohydrate Research Center, University of Georgia, Athens, Georgia 30602.
  • Doran KS; the Complex Carbohydrate Research Center, University of Georgia, Athens, Georgia 30602.
  • Nizet V; the Department of Molecular Microbiology and Center for Women's Infectious Disease Research, Washington University School of Medicine, St. Louis, Missouri 63110, and.
  • Bode L; From the Divisions of Host-Microbe Systems and Therapeutics.
J Biol Chem ; 292(27): 11243-11249, 2017 07 07.
Article em En | MEDLINE | ID: mdl-28416607
Streptococcus agalactiae (group B Streptococcus, GBS) is a leading cause of invasive bacterial infections in newborns, typically acquired vertically during childbirth secondary to maternal vaginal colonization. Human milk oligosaccharides (HMOs) have important nutritional and biological activities that guide the development of the immune system of the infant and shape the composition of normal gut microbiota. In this manner, HMOs help protect against pathogen colonization and reduce the risk of infection. In the course of our studies of HMO-microbial interactions, we unexpectedly uncovered a novel HMO property to directly inhibit the growth of GBS independent of host immunity. By separating different HMO fractions through multidimensional chromatography, we found the bacteriostatic activity to be confined to specific non-sialylated HMOs and synergistic with a number of conventional antibiotic agents. Phenotypic screening of a GBS transposon insertion library identified a mutation within a GBS-specific gene encoding a putative glycosyltransferase that confers resistance to HMOs, suggesting that HMOs may function as an alternative substrate to modify a GBS component in a manner that impairs growth kinetics. Our study uncovers a unique antibacterial role for HMOs against a leading neonatal pathogen and expands the potential therapeutic utility of these versatile molecules.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oligossacarídeos / Streptococcus agalactiae / Leite Humano / Antibacterianos Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oligossacarídeos / Streptococcus agalactiae / Leite Humano / Antibacterianos Idioma: En Ano de publicação: 2017 Tipo de documento: Article