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 in | The Journal of pediatrics Vol. 156; no. 1; pp. 20 - 25 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Maryland Heights, MO
Mosby, Inc
2010
Elsevier |
Subjects | |
Online Access | Get full text |
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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. |
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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 |
BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22280648$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/19783002$$D View this record in MEDLINE/PubMed |
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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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