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A Murine Model of Group B Streptococcus Vaginal Colonization
Published on: November 16, 2016
Mode of Delivery Determines Neonatal Pharyngeal Bacterial Composition and Early Intestinal Colonization
David E Brumbaugh1, Jaime Arruda, Kristen Robbins
1*Department of Pediatrics †Department of Obstetrics and Gynecology ‡Department of Medicine, University of Colorado School of Medicine, Aurora §Department of Mathematical & Statistical Sciences, University of Colorado Denver ||Microbiome Research Consortium, Aurora, CO.
Insights
Cesarean delivery (CS) disrupts infant oral and gut bacteria, leading to altered microbial succession and a deficit in beneficial Bacteroidetes compared to vaginal delivery (VD). Early oral bacteria do not consistently colonize the infant gut.
Area of Science:
- Microbiology
- Immunology
- Neonatal Health
Background:
- Infant gut microbiome development influences immune function and allergy risk.
- Early bacterial colonization patterns and their determinants are not fully understood.
Purpose of the Study:
- Investigate the impact of delivery mode (cesarean vs. vaginal) on initial infant oropharyngeal (OP) bacterial inoculation.
- Determine the relationship between OP colonization and subsequent intestinal microbial succession.
Main Methods:
- Prospective cohort study of 23 mother/infant pairs.
- Collected maternal swabs, infant OP aspirates, and infant stool.
- Utilized 16S rRNA and shotgun DNA metagenomic sequencing.
Main Results:
- Vaginal delivery (VD) infants showed more maternal-like OP bacteria (Firmicutes), while cesarean (CS) infants had skin bacteria.
- CS infants had a different oral inoculum, chaotic bacterial succession, and fewer intestinal Bacteroidetes.
- Infant fecal microbiomes differed from maternal samples regardless of delivery mode.
Conclusions:
- Cesarean delivery alters the initial oral microbiome, impacting infant gut bacterial succession.
- Early oral bacteria may influence the intestinal environment, affecting microbial development.
- Delivery mode significantly shapes early infant gut microbial composition and function.
Objectives:
Bacterial colonization and succession of the human intestine shape development of immune function and risk for allergic disease, yet these processes remain poorly understood. We investigated the relations between delivery mode, initial bacterial inoculation of the infant oropharynx (OP), and intestinal colonization.
Methods:
We prospectively collected maternal rectal and vaginal swabs, infant OP aspirates, and infant stool from 23 healthy mother/infant pairs delivering by cesarean (CS) or vaginal delivery (VD) in an academic hospital. Bacterial abundance (16S rRNA sequencing) and community similarity between samples were compared by delivery mode. Shotgun DNA metagenomic sequencing of infant stool was performed.
Results:
VD infants had higher abundance of Firmicutes (mainly lactobacilli) in OP aspirates whereas CS OP aspirates were enriched in skin bacteria. OP aspirates were more similar to maternal vaginal and rectal microbiomes in VD compared with CS. Bacteroidetes were more abundant through 6 weeks in stool of VD infants. Infant fecal microbiomes in both delivery groups did not resemble maternal rectal or vaginal microbiomes. Differences in fecal bacterial gene potential between CS and VD at 6 weeks clustered in metabolic pathways and were mediated by abundance of Proteobacteria and Bacteroidetes.
Conclusions:
CS infants exhibited different microbiota in the oral inoculum, a chaotic pattern of bacterial succession, and a persistent deficit of intestinal Bacteroidetes. Pioneer OP bacteria transferred from maternal vaginal and intestinal communities were not prominent constituents of the early infant fecal microbiome. Oral inoculation at birth may impact the intestinal microenvironment, thereby modulating early succession of intestinal bacteria.
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