Brief early antibiotic exposure (≤2 days) is not associated with disruption of gut microbiome in very low birth weight infants

TL;DR

Short antibiotic use (≤2 days) in very low birth weight infants does not disrupt gut microbiome development, unlike longer courses.

Contribution

Shows that brief antibiotic exposure in preterm infants does not harm gut microbiome development.

Findings

Short-course antibiotic exposure (≤2 days) did not disrupt gut microbiome composition or diversity in VLBW infants.

Prolonged antibiotic exposure (≥3 days) caused temporary dysbiosis with reduced Bifidobacterium and lower diversity.

Microbial recovery was observed by discharge in infants with prolonged antibiotic exposure.

Abstract

Early empirical antibiotic therapy is common in preterm and very low birth weight (VLBW) infants but may disrupt the developing gut microbiome. However, the effects of brief antibiotic courses remain unclear, particularly in the most immature infants. In this prospective multicenter cohort study, we examined gut microbiome trajectories in VLBW infants (many of whom were extremely preterm) receiving no antibiotics, a short course (≤2 days), or prolonged exposure (≥3 days). Serial stool samples were analyzed using 16S rRNA gene sequencing. Microbiome composition and diversity in the short-course group were similar to those in unexposed infants at all timepoints, indicating that brief antibiotic exposure did not disrupt microbial development. In contrast, prolonged exposure was associated with transient dysbiosis characterized by reduced Bifidobacterium abundance and lower alpha diversity, with partial recovery by discharge. These findings suggest that limiting empirical antibiotic therapy to ≤2 days (48 h) when infection is unconfirmed may not disrupt microbiome development even in highly immature preterm VLBW infants, supporting evidence-based antibiotic stewardship in neonatal intensive care.

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