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Updated: Apr 9, 2026

Probiotic Studies in Neonatal Mice Using Gavage
Published on: January 27, 2019
Preterm infant gut colonization in the neonatal ICU and complete restoration 2 years later
Insights
Preterm infants in neonatal intensive care units (NICUs) can acquire antibiotic-resistant bacteria. These high-risk bacterial clones were not detected in infant faeces two years later.
Area of Science:
- Microbiology
- Neonatalogy
- Infectious Diseases
Background:
- Neonatal intensive care units (NICUs) pose a risk for preterm infants acquiring multidrug-resistant bacteria.
- Understanding the colonization patterns of these bacteria is crucial for infant health.
Purpose of the Study:
- To characterize antibiotic-resistant bacterial lineages colonizing preterm infants in the NICU.
- To investigate the persistence of these clones in faeces up to two years after NICU discharge.
Main Methods:
- Collected faecal and milk samples from preterm infants and mothers.
- Identified bacterial isolates using 16S rDNA sequencing and MALDI-TOF.
- Determined antibiotic susceptibility, genetic diversity (RAPD, PFGE, MLST), and virulence factors via PCR.
Main Results:
- High prevalence of antibiotic-resistant, high-risk clones (e.g., Enterococcus faecalis ST64, Enterococcus faecium ST18) in NICU infants' faeces and maternal milk.
- Greater genetic diversity observed in Gram-negative isolates.
- These multidrug-resistant clones were absent in faecal samples at the 2-year follow-up.
Conclusions:
- Preterm infants' guts can be initially colonized by virulent, antibiotic-resistant lineages in the NICU.
- These high-risk clones are subsequently replaced by antibiotic-susceptible, community-acquired bacteria.
Abstract:
Preterm infants in a neonatal intensive care unit (NICU) are exposed to multidrug-resistant bacteria previously adapted to the hospital environment. The aim of the present study was to characterize the bacterial antibiotic-resistant high-risk lineages colonizing preterm infants during their NICU stay and their persistence in faeces after 2 years. A total of 26 preterm neonates were recruited between October 2009 and June 2010 and provided 144 faecal samples. Milk samples (86 mother's milk, 35 human donor milk and 15 formula milk) were collected at the same time as faecal samples. An additional faecal sample was recovered in 16 infants at the age of 2 years. Samples were plated onto different selective media, and one colony per morphology was selected. Isolates were identified by 16S rDNA nucleotide sequence and MALDI-TOF. Antibiotic susceptibility (agar dilution), genetic diversity (RAPD, PFGE and MLST) and virulence factors (only in enterococcal and staphylococcal isolates) were determined by PCR. A high proportion of antibiotic-resistant high-risk clones was detected in both faecal and milk samples during the NICU admittance. Almost all infants were colonized by Enterococcus faecalis ST64 and Enterococcus faecium ST18 clones, while a wider genetic diversity was observed for the Gram-negative isolates. Multidrug-resistant high-risk clones were not recovered from the faecal samples of the 2-year-olds. In conclusion, the gut of preterm infants admitted to the NICU might be initially colonized by antibiotic-resistant and virulent high-risk lineages, which are later replaced by antibiotic-susceptible community ones.
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