Anti‐biofilm Activity of Human Milk Oligosaccharides in Clinical Strains of Streptococcus agalactiae with Diverse Capsular and Sequence Types

Author:

Moore Rebecca E.12,Spicer Sabrina K.3,Talbert Julie A.3,Manning Shannon D.4,Townsend Steven D.3,Gaddy Jennifer A.1256ORCID

Affiliation:

1. Division of Infectious Diseases, Department of Medicine Vanderbilt University Medical Center A22010 Medical Center North 1161 21st Avenue South Nashville TN 37232 USA

2. Tennessee Valley Healthcare Systems Department of Veterans Affairs 1310 24th Avenue South Nashville TN 37212 USA

3. Department of Chemistry Vanderbilt University 7330 Stevenson Center Station B 351822 Nashville TN 37235 USA

4. Department of Microbiology and Molecular Genetics Michigan State University East Lansing MI 48824 USA

5. Department of Pathology, Microbiology, and Immunology Vanderbilt University School of Medicine Nashville TN 37232 USA

6. Center for Medicine Health and Society Vanderbilt University Nashville TN 37232 USA

Abstract

AbstractGroup B Streptococcus (GBS) is an encapsulated Gram‐positive bacterial pathogen that causes severe perinatal infections. Human milk oligosaccharides (HMOs) are short‐chain sugars that have recently been shown to possess antimicrobial and anti‐biofilm activity against a variety of bacterial pathogens, including GBS. We have expanded these studies to demonstrate that HMOs can inhibit and dismantle biofilm in both invasive and colonizing strains of GBS. A cohort of 30 diverse strains of GBS were analyzed for susceptibility to HMO‐dependent biofilm inhibition or destruction. HMOs were significantly effective at inhibiting biofilm in capsular‐type‐ and sequence‐type‐specific fashion, with significant efficacy in CpsIb, CpsII, CpsIII, CpsV, and CpsVI strains as well as ST‐1, ST‐12, ST‐19, and ST‐23 strains. Interestingly, CpsIa as well as ST‐7 and ST‐17 were not susceptible to the anti‐biofilm activity of HMOs, underscoring the strain‐specific effects of these important antimicrobial molecules against the perinatal pathogen Streptococcus agalactiae.

Funder

National Science Foundation

National Center for Research Resources

National Center for Advancing Translational Sciences

Publisher

Wiley

Subject

Organic Chemistry,Molecular Biology,Molecular Medicine,Biochemistry

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