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Fecal microbiota and volatile metabolome pattern alterations precede late-onset meningitis in preterm neonates.
Frerichs, Nina M; Deianova, Nancy; El Manouni El Hassani, Sofia; Acharjee, Animesh; Quraishi, Mohammed Nabil; de Boode, Willem P; Cossey, Veerle; Hulzebos, Christian V; van Kaam, Anton H; Kramer, Boris W; d'Haens, Esther; de Jonge, Wouter J; Vijlbrief, Daniel C; van Weissenbruch, Mirjam M; Daulton, Emma; Wicaksono, Alfian N; Covington, James A; Benninga, Marc A; de Boer, Nanne K H; van Goudoever, Johannes B; Niemarkt, Hendrik J; de Meij, Tim G J.
Afiliação
  • Frerichs NM; Amsterdam UMC, University of Amsterdam, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Department of Pediatric Gastroenterology, Emma Children's Hospital.
  • Deianova N; Amsterdam UMC, University of Amsterdam, Amsterdam Reproduction and Development Research Institute, Amsterdam, 1105 AZ, The Netherlands.
  • El Manouni El Hassani S; Amsterdam UMC, University of Amsterdam, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Department of Pediatric Gastroenterology, Emma Children's Hospital.
  • Acharjee A; Amsterdam UMC, University of Amsterdam, Amsterdam Reproduction and Development Research Institute, Amsterdam, 1105 AZ, The Netherlands.
  • Quraishi MN; Amsterdam UMC, University of Amsterdam, Amsterdam Gastroenterology Endocrinology Metabolism Research Institute, Department of Pediatric Gastroenterology, Emma Children's Hospital.
  • de Boode WP; Amsterdam UMC, University of Amsterdam, Amsterdam Reproduction and Development Research Institute, Amsterdam, 1105 AZ, The Netherlands.
  • Cossey V; Institute of Cancer and Genomic Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham, B15 2TT, UK.
  • Hulzebos CV; Institute of Translational Medicine, University Hospitals Birmingham NHS Foundation Trust, Birmingham, B15 2TT, UK.
  • van Kaam AH; Health Data Research UK (HDR UK), London, NW1 2BE, UK.
  • Kramer BW; Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, B15 2TT, UK.
  • d'Haens E; Neonatal Intensive Care Unit, Radboud University Medical Centre, Radboud Institute for Health Sciences, Amalia Children's Hospital, Nijmegen, 6525 GA, The Netherlands.
  • de Jonge WJ; Neonatal Intensive Care Unit, University Hospitals Leuven, Leuven, 3000, Belgium.
  • Vijlbrief DC; Neonatal Intensive Care Unit, Beatrix Children's Hospital/University Medical Centre Groningen, Groningen, 9713 GZ, The Netherlands.
  • van Weissenbruch MM; Department of Neonatology, Emma Children's Hospital; Amsterdam Reproduction and Development Research Institute, Amsterdam, 1105 AZ, the Netherlands.
  • Daulton E; University of Western Australia, Crawley, Australia; Neuroplast BV, Maastricht, 6167 RD, The Netherlands.
  • Wicaksono AN; Neonatal Intensive Care Unit, Amalia Children's Centre, Isala, Zwolle, 8025 AB, The Netherlands.
  • Covington JA; Tytgat Institute for Liver and Intestinal Research, Amsterdam UMC, Location AMC, Amsterdam, 1105 AZ, The Netherlands.
  • Benninga MA; Department of Surgery, University of Bonn, Bonn, D-53113, Germany.
  • de Boer NKH; Neonatal Intensive Care Unit, Wilhelmina Children's Hospital, University Medical Centre Utrecht, Utrecht, 3584 CX, The Netherlands.
  • van Goudoever JB; Department of Neonatology, Emma Children's Hospital; Amsterdam Reproduction and Development Research Institute, Amsterdam, 1105 AZ, the Netherlands.
  • Niemarkt HJ; School of Engineering, University of Warwick, Coventry, CV4 7AL, United Kingdom.
  • de Meij TGJ; School of Engineering, University of Warwick, Coventry, CV4 7AL, United Kingdom.
J Infect Dis ; 2024 May 23.
Article em En | MEDLINE | ID: mdl-38781449
ABSTRACT

OBJECTIVE:

The fecal microbiota and metabolome are hypothesized to be altered before late-onset neonatal meningitis (LOM), in analogy to late-onset sepsis (LOS). The present study aimed to identify fecal microbiota composition and volatile metabolomics preceding LOM.

METHODS:

Cases and gestational age-matched controls were selected from a prospective, longitudinal preterm cohort study (born <30 weeks' gestation) at nine neonatal intensive care units. The microbial composition (16S rRNA sequencing) and volatile metabolome (gas chromatography-ion mobility spectrometry (GC-IMS) and GC-time-of-flight-mass spectrometry (GC-TOF-MS)), were analyzed in fecal samples 1-10 days pre-LOM.

RESULTS:

Of 1397 included infants, 21 were diagnosed with LOM (1.5%), and 19 with concomitant LOS (90%). Random Forest classification and MaAsLin2 analysis found similar microbiota features contribute to the discrimination of fecal pre-LOM samples versus controls. A Random Forest model based on six microbiota features accurately predicts LOM 1-3 days before diagnosis with an area under the curve (AUC) of 0.88 (n=147). Pattern recognition analysis by GC-IMS revealed an AUC of 0.70-0.76 (P<0.05) in the three days pre-LOM (n=92). No single discriminative metabolites were identified by GC-TOF-MS (n=66).

CONCLUSION:

Infants with LOM could be accurately discriminated from controls based on preclinical microbiota composition, while alterations in the volatile metabolome were moderately associated with preclinical LOM.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article