Center Variation in Intestinal Microbiota Prior to Late-Onset Sepsis in Preterm Infants

Late onset sepsis (LOS) contributes to mortality and morbidity in preterm infants. We tested the hypotheses that microbes causing LOS originate from the gut, and that distortions in the gut microbial community increases subsequent risk of LOS. We examined the gut microbial community in prospectively...

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Veröffentlicht in:PloS one 2015-06, Vol.10 (6), p.e0130604
Hauptverfasser: Taft, Diana H, Ambalavanan, Namasivayam, Schibler, Kurt R, Yu, Zhuoteng, Newburg, David S, Deshmukh, Hitesh, Ward, Doyle V, Morrow, Ardythe L
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creator Taft, Diana H
Ambalavanan, Namasivayam
Schibler, Kurt R
Yu, Zhuoteng
Newburg, David S
Deshmukh, Hitesh
Ward, Doyle V
Morrow, Ardythe L
description Late onset sepsis (LOS) contributes to mortality and morbidity in preterm infants. We tested the hypotheses that microbes causing LOS originate from the gut, and that distortions in the gut microbial community increases subsequent risk of LOS. We examined the gut microbial community in prospectively collected stool samples from preterm infants with LOS and an equal number of age-matched controls at two sites (Cincinnati, OH and Birmingham, AL), by sequencing the bacterial 16S rDNA. We confirmed our findings in a subset of infants by whole genome shotgun sequencing, and analyzed the data using R and LEfSe. Infants with LOS in Cincinnati, as compared to controls, had less abundant Actinobacteria in the first samples after birth (median 18 days before sepsis onset), and less abundant Pseudomonadales in the last samples collected prior to LOS (median 8 days before sepsis onset). Infants with LOS in Birmingham, as compared to controls, had no differences identified in the first sample microbial communities, but Lactobacillales was less abundant in the last samples prior to LOS (median 4 days before sepsis onset). Sequencing identified detectable levels of the sepsis-causative organism in stool samples prior to disease onset for 82% of LOS cases. Translocation of gut microbes may account for the majority of LOS cases. Distortions in the fecal microbiota occur prior to LOS, but the form of distortion depends on timing and site. The microbial composition of fecal samples does not predict LOS onset in a generalizable fashion.
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We tested the hypotheses that microbes causing LOS originate from the gut, and that distortions in the gut microbial community increases subsequent risk of LOS. We examined the gut microbial community in prospectively collected stool samples from preterm infants with LOS and an equal number of age-matched controls at two sites (Cincinnati, OH and Birmingham, AL), by sequencing the bacterial 16S rDNA. We confirmed our findings in a subset of infants by whole genome shotgun sequencing, and analyzed the data using R and LEfSe. Infants with LOS in Cincinnati, as compared to controls, had less abundant Actinobacteria in the first samples after birth (median 18 days before sepsis onset), and less abundant Pseudomonadales in the last samples collected prior to LOS (median 8 days before sepsis onset). Infants with LOS in Birmingham, as compared to controls, had no differences identified in the first sample microbial communities, but Lactobacillales was less abundant in the last samples prior to LOS (median 4 days before sepsis onset). Sequencing identified detectable levels of the sepsis-causative organism in stool samples prior to disease onset for 82% of LOS cases. Translocation of gut microbes may account for the majority of LOS cases. Distortions in the fecal microbiota occur prior to LOS, but the form of distortion depends on timing and site. 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Infants with LOS in Birmingham, as compared to controls, had no differences identified in the first sample microbial communities, but Lactobacillales was less abundant in the last samples prior to LOS (median 4 days before sepsis onset). Sequencing identified detectable levels of the sepsis-causative organism in stool samples prior to disease onset for 82% of LOS cases. Translocation of gut microbes may account for the majority of LOS cases. Distortions in the fecal microbiota occur prior to LOS, but the form of distortion depends on timing and site. The microbial composition of fecal samples does not predict LOS onset in a generalizable fashion.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>26110908</pmid><doi>10.1371/journal.pone.0130604</doi><oa>free_for_read</oa></addata></record>
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subjects Analysis
Antibiotics
Babies
Biology
Biomarkers
Birth weight
Breastfeeding & lactation
Children & youth
Communities
Data processing
Digestive system
Digestive tract
Distortion
Fecal microflora
Feces - microbiology
Female
Gastrointestinal Microbiome - physiology
Gastrointestinal tract
Gene sequencing
Genomes
Genomics
Health aspects
Humans
Infant
Infant, Newborn
Infant, Premature
Infant, Premature, Diseases - microbiology
Infants
Infection
Infections
Intestinal microflora
Intestine
Male
Microbial activity
Microbiota
Microbiota (Symbiotic organisms)
Microorganisms
Morbidity
Mortality
Newborn babies
Organisms
Pediatrics
Physiology
Premature babies
Premature infants
rRNA 16S
Sepsis
Sepsis - microbiology
Staphylococcus
Translocation
title Center Variation in Intestinal Microbiota Prior to Late-Onset Sepsis in Preterm Infants
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