Citrobacter and Acinetobacter are respectively involved in feeding intolerance in preterm infants of different

Chunyan Fu1,2, Jinglin Xu1,2, He Wang1,2

  • 1The Graduate School of Fujian Medical University, Fuzhou, 35000, Fujian, China.

PubMed

Insights

Feeding intolerance in preterm infants is linked to specific gut bacteria. Citrobacter and Acinetobacter were elevated in infants with feeding intolerance, while Clostridium XI may play a role in gut health for some preterm infants.

Area of Science:

  • Microbiology
  • Neonatology
  • Gastroenterology

Background:

  • Feeding intolerance (FI) is a prevalent issue in preterm infants, significantly influenced by gut microbiota composition.
  • Understanding these microbial differences is crucial for managing FI and guiding therapeutic interventions like probiotics.

Purpose of the Study:

  • To investigate the distinct gut microbiota profiles in preterm infants experiencing feeding intolerance (FI) across different gestational ages.
  • To establish a foundation for targeted probiotic interventions based on specific microbial findings.

Main Methods:

  • A prospective case-control study involving 80 preterm infants (<34 weeks gestational age) divided into four groups based on gestational age and feeding tolerance.
  • 16S rDNA high-throughput sequencing was used to analyze fecal microbiota, with statistical analyses to explore associations between gut microbiota, FI, and gestational age.

Main Results:

  • Elevated Citrobacter abundance was observed in early preterm infants with FI (<32 weeks) compared to those with feeding tolerance.
  • Increased Acinetobacter was found in moderate preterm infants with FI (≥32 weeks) versus those with feeding tolerance.
  • Lower abundance of Clostridium XI was noted in moderate preterm infants with feeding tolerance.

Conclusions:

  • Citrobacter and Acinetobacter are implicated in feeding intolerance in preterm infants across different gestational age categories.
  • Clostridium XI may contribute to maintaining intestinal homeostasis in moderate preterm infants (≥32 weeks).
Abstract