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Meconium Microbiome of Very Preterm Infants across Germany.
Klopp, Jonas; Ferretti, Pamela; Meyer, Claudius U; Hilbert, Katja; Haiß, Annette; Marißen, Janina; Henneke, Philipp; Hudalla, Hannes; Pirr, Sabine; Viemann, Dorothee; Zemlin, Michael; Forslund, Sofia Kirke; Härtel, Christoph; Bork, Peer; Gehring, Stephan; Van Rossum, Thea.
Afiliação
  • Klopp J; University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.
  • Ferretti P; Structural and Computational Biology Unit, European Molecular Biology Laboratorygrid.4709.a (EMBL), Heidelberg, Germany.
  • Meyer CU; University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.
  • Hilbert K; University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.
  • Haiß A; Department of Pediatrics, University of Lübeck, Lübeck, Germany.
  • Marißen J; Department of Pediatrics, University of Würzburg, Würzburg, Germany.
  • Henneke P; Center for Pediatrics and Adolescent Medicine Pediatrics, Medical Center and Faculty of Medicine, University of Freiburg, Freiburg, Germany.
  • Hudalla H; Institute for Immunodeficiency, Medical Center and Faculty of Medicine, University of Freiburg, Freiburg, Germany.
  • Pirr S; Center for Chronic Immunodeficiency (CCI) Medical Center and Faculty of Medicine, University of Freiburg, Freiburg, Germany.
  • Viemann D; Department of Neonatology, University of Heidelberg, Heidelberg, Germany.
  • Zemlin M; Hanover Medical School, Department of Pediatric Pneumology, Allergology and Neonatology, Hanover, Germany.
  • Forslund SK; Department of Pediatrics, University of Würzburg, Würzburg, Germany.
  • Härtel C; Hanover Medical School, Department of Pediatric Pneumology, Allergology and Neonatology, Hanover, Germany.
  • Bork P; Department of Pediatrics, Saar University Homburg, Homburg, Germany.
  • Gehring S; Structural and Computational Biology Unit, European Molecular Biology Laboratorygrid.4709.a (EMBL), Heidelberg, Germany.
  • Van Rossum T; Experimental and Clinical Research Center, a cooperation of Charité-Universitätsmedizin and the Max-Delbrück Center, Berlin, Germany.
mSphere ; 7(1): e0080821, 2022 02 23.
Article em En | MEDLINE | ID: mdl-35019670
Meconium constitutes infants' first bowel movements postnatally. The consistency and microbial load of meconium are different from infant and adult stool. While recent evidence suggests that meconium is sterile in utero, rapid colonization occurs after birth. The meconium microbiome has been associated with negative health outcomes, but its composition is not well described, especially in preterm infants. Here, we characterized the meconium microbiomes from 330 very preterm infants (gestational ages 28 to 32 weeks) from 15 hospitals in Germany and in fecal samples from a subset of their mothers (N = 217). Microbiome profiles were compiled using 16S rRNA gene sequencing with negative and positive controls. The meconium microbiome was dominated by Bifidobacterium, Staphylococcus, and Enterococcus spp. and was associated with gestational age at birth and age at sample collection. Bifidobacterial abundance was negatively correlated with potentially pathogenic genera. The amount of bacterial DNA in meconium samples varied greatly across samples and was associated with the time since birth but not with gestational age or hospital site. In samples with low bacterial load, human mitochondrial sequences were highly amplified using commonly used, bacterial-targeted 16S rRNA primers. Only half of the meconium samples contained sufficient bacterial material to study the microbiome using a standard approach. To facilitate future meconium studies, we present a five-level scoring system ("MecBac") that predicts the success of 16S rRNA bacterial sequencing for meconium samples. These findings provide a foundational characterization of an understudied portion of the human microbiome and will aid the design of future meconium microbiome studies. IMPORTANCE Meconium is present in the intestines of infants before and after birth and constitutes their first bowel movements postnatally. The consistency, composition and microbial load of meconium is largely different from infant and adult stool. While recent evidence suggests that meconium is sterile in utero, rapid colonization occurs after birth. The meconium microbiome has been associated with short-term and long-term negative health outcomes, but its composition is not yet well described, especially in preterm infants. We provide a characterization of the microbiome structure and composition of infant meconium and maternal feces from a large study cohort and propose a method to evaluate meconium samples for bacterial sequencing suitability. These findings provide a foundational characterization of an understudied portion of the human microbiome and will aid the design of future meconium microbiome studies.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Microbiota / Mecônio Tipo de estudo: Prognostic_studies Limite: Adult / Humans / Infant / Newborn País/Região como assunto: Europa Idioma: En Revista: MSphere Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Microbiota / Mecônio Tipo de estudo: Prognostic_studies Limite: Adult / Humans / Infant / Newborn País/Região como assunto: Europa Idioma: En Revista: MSphere Ano de publicação: 2022 Tipo de documento: Article