Intestinal Microbial Ecology in Premature Infants Assessed with Non–Culture-Based Techniques

To use high throughput techniques to analyze intestinal microbial ecology in premature neonates, who are highly susceptible to perturbations of the luminal environment associated with necrotizing enterocolitis (NEC) and late-onset sepsis. With non–culture-based techniques, we evaluated intestinal mi...

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Published inThe Journal of pediatrics Vol. 156; no. 1; pp. 20 - 25
Main Authors Mshvildadze, Maka, Neu, Josef, Shuster, Jonathan, Theriaque, Douglas, Li, Nan, Mai, Volker
Format Journal Article
LanguageEnglish
Published Maryland Heights, MO Mosby, Inc 2010
Elsevier
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Abstract To use high throughput techniques to analyze intestinal microbial ecology in premature neonates, who are highly susceptible to perturbations of the luminal environment associated with necrotizing enterocolitis (NEC) and late-onset sepsis. With non–culture-based techniques, we evaluated intestinal microbiota shortly after birth and during hospitalization in 23 neonates born at 23 to 32 weeks gestational age. Microbiota compositions were compared in 6 preterm infants in whom NEC, signs of systemic inflammation, or both developed with matched control subjects by using 16S ribosomal RNA pyrosequencing. Microbial DNA was detected in meconium, suggesting an intrauterine origin. Differences in diversity were detected in infants whose mothers intended to breast feed ( P = .03), babies born to mothers with chorioamnionitis ( P = .06), and in babies born at <30 weeks gestation ( P = .03). A 16S ribosomal RNA sequence analysis detected Citrobacter-like sequences only in cases with NEC (3 of 4) and an increased frequency of Enterococcus-like sequences in cases and Klebsiella in control subjects ( P = .06). The overall microbiota profiles in cases with NEC were not distinguishable from that in control subjects. Microbial DNA in meconium of premature infants suggests prenatal influences.
AbstractList To use high throughput techniques to analyze intestinal microbial ecology in premature neonates, who are highly susceptible to perturbations of the luminal environment associated with necrotizing enterocolitis (NEC) and late-onset sepsis. With non-culture-based techniques, we evaluated intestinal microbiota shortly after birth and during hospitalization in 23 neonates born at 23 to 32 weeks gestational age. Microbiota compositions were compared in 6 preterm infants in whom NEC, signs of systemic inflammation, or both developed with matched control subjects by using 16S ribosomal RNA pyrosequencing. Microbial DNA was detected in meconium, suggesting an intrauterine origin. Differences in diversity were detected in infants whose mothers intended to breast feed (P = .03), babies born to mothers with chorioamnionitis (P = .06), and in babies born at <30 weeks gestation (P = .03). A 16S ribosomal RNA sequence analysis detected Citrobacter-like sequences only in cases with NEC (3 of 4) and an increased frequency of Enterococcus-like sequences in cases and Klebsiella in control subjects (P = .06). The overall microbiota profiles in cases with NEC were not distinguishable from that in control subjects. Microbial DNA in meconium of premature infants suggests prenatal influences.
To use high throughput techniques to analyze intestinal microbial ecology in premature neonates, who are highly susceptible to perturbations of the luminal environment associated with necrotizing enterocolitis (NEC) and late-onset sepsis. With non–culture-based techniques, we evaluated intestinal microbiota shortly after birth and during hospitalization in 23 neonates born at 23 to 32 weeks gestational age. Microbiota compositions were compared in 6 preterm infants in whom NEC, signs of systemic inflammation, or both developed with matched control subjects by using 16S ribosomal RNA pyrosequencing. Microbial DNA was detected in meconium, suggesting an intrauterine origin. Differences in diversity were detected in infants whose mothers intended to breast feed ( P = .03), babies born to mothers with chorioamnionitis ( P = .06), and in babies born at <30 weeks gestation ( P = .03). A 16S ribosomal RNA sequence analysis detected Citrobacter-like sequences only in cases with NEC (3 of 4) and an increased frequency of Enterococcus-like sequences in cases and Klebsiella in control subjects ( P = .06). The overall microbiota profiles in cases with NEC were not distinguishable from that in control subjects. Microbial DNA in meconium of premature infants suggests prenatal influences.
Objectives - To use high throughput techniques to analyze intestinal microbial ecology in premature neonates, who are highly susceptible to perturbations of the luminal environment associated with necrotizing enterocolitis (NEC) and late-onset sepsis. Study design - With non-culture-based techniques, we evaluated intestinal microbiota shortly after birth and during hospitalization in 23 neonates born at 23 to 32 weeks gestational age. Microbiota compositions were compared in 6 preterm infants in whom NEC, signs of systemic inflammation, or both developed with matched control subjects by using 16S ribosomalA pyrosequencing. Results - Microbial DNA was detected in meconium, suggesting an intrauterine origin. Differences in diversity were detected in infants whose mothers intended to breast feed (P = .03), babies born to mothers with chorioamnionitis (P = .06), and in babies born at <30 weeks gestation (P = .03). A 16S ribosomalA sequence analysis detected Citrobacter-like sequences only in cases with NEC (3 of 4) and an increased frequency of Enterococcus-like sequences in cases and Klebsiella in control subjects (P = .06). The overall microbiota profiles in cases with NEC were not distinguishable from that in control subjects. Conclusions - Microbial DNA in meconium of premature infants suggests prenatal influences.
Objectives To use high throughput techniques to analyze intestinal microbial ecology in premature neonates, who are highly susceptible to perturbations of the luminal environment associated with necrotizing enterocolitis (NEC) and late-onset sepsis. Study design With non–culture-based techniques, we evaluated intestinal microbiota shortly after birth and during hospitalization in 23 neonates born at 23 to 32 weeks gestational age. Microbiota compositions were compared in 6 preterm infants in whom NEC, signs of systemic inflammation, or both developed with matched control subjects by using 16S ribosomal RNA pyrosequencing. Results Microbial DNA was detected in meconium, suggesting an intrauterine origin. Differences in diversity were detected in infants whose mothers intended to breast feed ( P = .03), babies born to mothers with chorioamnionitis ( P  = .06), and in babies born at <30 weeks gestation ( P = .03). A 16S ribosomal RNA sequence analysis detected Citrobacter-like sequences only in cases with NEC (3 of 4) and an increased frequency of Enterococcus-like sequences in cases and Klebsiella in control subjects ( P = .06). The overall microbiota profiles in cases with NEC were not distinguishable from that in control subjects. Conclusions Microbial DNA in meconium of premature infants suggests prenatal influences.
To use high throughput techniques to analyze intestinal microbial ecology in premature neonates, who are highly susceptible to perturbations of the luminal environment associated with necrotizing enterocolitis (NEC) and late-onset sepsis.OBJECTIVESTo use high throughput techniques to analyze intestinal microbial ecology in premature neonates, who are highly susceptible to perturbations of the luminal environment associated with necrotizing enterocolitis (NEC) and late-onset sepsis.With non-culture-based techniques, we evaluated intestinal microbiota shortly after birth and during hospitalization in 23 neonates born at 23 to 32 weeks gestational age. Microbiota compositions were compared in 6 preterm infants in whom NEC, signs of systemic inflammation, or both developed with matched control subjects by using 16S ribosomal RNA pyrosequencing.STUDY DESIGNWith non-culture-based techniques, we evaluated intestinal microbiota shortly after birth and during hospitalization in 23 neonates born at 23 to 32 weeks gestational age. Microbiota compositions were compared in 6 preterm infants in whom NEC, signs of systemic inflammation, or both developed with matched control subjects by using 16S ribosomal RNA pyrosequencing.Microbial DNA was detected in meconium, suggesting an intrauterine origin. Differences in diversity were detected in infants whose mothers intended to breast feed (P = .03), babies born to mothers with chorioamnionitis (P = .06), and in babies born at <30 weeks gestation (P = .03). A 16S ribosomal RNA sequence analysis detected Citrobacter-like sequences only in cases with NEC (3 of 4) and an increased frequency of Enterococcus-like sequences in cases and Klebsiella in control subjects (P = .06). The overall microbiota profiles in cases with NEC were not distinguishable from that in control subjects.RESULTSMicrobial DNA was detected in meconium, suggesting an intrauterine origin. Differences in diversity were detected in infants whose mothers intended to breast feed (P = .03), babies born to mothers with chorioamnionitis (P = .06), and in babies born at <30 weeks gestation (P = .03). A 16S ribosomal RNA sequence analysis detected Citrobacter-like sequences only in cases with NEC (3 of 4) and an increased frequency of Enterococcus-like sequences in cases and Klebsiella in control subjects (P = .06). The overall microbiota profiles in cases with NEC were not distinguishable from that in control subjects.Microbial DNA in meconium of premature infants suggests prenatal influences.CONCLUSIONSMicrobial DNA in meconium of premature infants suggests prenatal influences.
Author Li, Nan
Theriaque, Douglas
Neu, Josef
Mshvildadze, Maka
Shuster, Jonathan
Mai, Volker
Author_xml – sequence: 1
  givenname: Maka
  surname: Mshvildadze
  fullname: Mshvildadze, Maka
  organization: Chachava Scientific-Research Institute of Perinatal Medicine Obstetrics and Gynecology, Tbilisi, Georgia
– sequence: 2
  givenname: Josef
  surname: Neu
  fullname: Neu, Josef
  email: neuj@peds.ufl.edu
  organization: Department of Pediatrics, University of Florida, Gainesville, FL
– sequence: 3
  givenname: Jonathan
  surname: Shuster
  fullname: Shuster, Jonathan
  organization: Departments of Epidemiology and Health Policy Research, University of Florida, Gainesville, FL
– sequence: 4
  givenname: Douglas
  surname: Theriaque
  fullname: Theriaque, Douglas
  organization: General Clinical Research Center, University of Florida, Gainesville, FL
– sequence: 5
  givenname: Nan
  surname: Li
  fullname: Li, Nan
  organization: Department of Pediatrics, University of Florida, Gainesville, FL
– sequence: 6
  givenname: Volker
  surname: Mai
  fullname: Mai, Volker
  organization: Microbiology and Cell Sciences and Emerging Pathogens Institute, University of Florida, Gainesville, FL
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https://www.ncbi.nlm.nih.gov/pubmed/19783002$$D View this record in MEDLINE/PubMed
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Issue 1
Keywords OTU
GI
rRNA
SDI
NEC
DGGE
PCR
Simpson diversity index
Denaturing gradient gel electrophoresis
Gastrointestinal
Polymerase chain reaction
Ribosomal RNA
Necrotizing entercolitis
Operational taxonomic unit
Human
Premature
Pediatrics
Digestive system
Gut
Infant
Ecology
Cultural aspect
Technique
Culture
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Snippet To use high throughput techniques to analyze intestinal microbial ecology in premature neonates, who are highly susceptible to perturbations of the luminal...
Objectives To use high throughput techniques to analyze intestinal microbial ecology in premature neonates, who are highly susceptible to perturbations of the...
Objectives - To use high throughput techniques to analyze intestinal microbial ecology in premature neonates, who are highly susceptible to perturbations of...
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SubjectTerms Biological and medical sciences
DNA, Bacterial - analysis
Enterocolitis, Necrotizing - microbiology
Feces - microbiology
Female
General aspects
Humans
Infant, Newborn
Infant, Premature
Infant, Premature, Diseases - microbiology
Klebsiella
Male
Meconium - microbiology
Medical sciences
Pediatrics
Polymerase Chain Reaction - methods
RNA, Ribosomal, 16S
Title Intestinal Microbial Ecology in Premature Infants Assessed with Non–Culture-Based Techniques
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https://dx.doi.org/10.1016/j.jpeds.2009.06.063
https://www.ncbi.nlm.nih.gov/pubmed/19783002
https://www.proquest.com/docview/21261315
https://www.proquest.com/docview/733342359
Volume 156
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