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Published on: January 27, 2019
Longitudinal Survey of Microbiota in Hospitalized Preterm Very-Low-Birth-Weight Infants
Aloka L Patel1, Ece A Mutlu, Yan Sun
1*Rush University Medical Center, Chicago, IL †Texas Department of State Health Services, Austin ‡Research and Testing Laboratory, Lubbock, TX §University of Illinois at Chicago, Chicago ||WakeMed Health and Hospitals, Raleigh, NC.
Insights
The gut bacteria of hospitalized preterm infants become less diverse and more uniform during the first month, with a rise in potentially pathogenic microbes. This study tracked infant gut microbiome changes in the neonatal intensive care unit.
Area of Science:
- Microbiology
- Neonatal Research
- Gut Microbiome Studies
Background:
- The gut microbiome plays a crucial role in infant health and development.
- Preterm infants often experience altered microbial colonization due to medical interventions and prolonged hospitalization.
- Understanding the early life microbiome is vital for developing targeted interventions.
Purpose of the Study:
- To investigate the dynamic changes in bacterial communities within hospitalized preterm infants during their first month of life.
- To characterize the composition and diversity of the infant gut microbiota from birth through neonatal intensive care unit (NICU) stay.
Main Methods:
- Daily rectal swabs collected from 12 preterm infants for 16S ribosomal DNA (rDNA) next-generation sequencing.
- Operational taxonomic unit (OTU) clustering and taxonomy assignment using Greengenes database and Quantitative Insights Into Microbial Ecology (QIIME).
- Quantitative polymerase chain reaction (qPCR) for Bifidobacterium spp. abundance and Phylogenetic Investigation of Communities by Reconstruction of Unobserved States (PICRUSt) for functional analysis.
Main Results:
- Microbial richness and Shannon diversity decreased significantly during NICU hospitalization, indicating a shift towards a more uniform microbiota.
- Enterobacteriaceae, Staphylococcaceae, and Enterococcaceae dominated the bacterial composition, while Bifidobacterium spp. were rarely detected.
- Functional analysis revealed enrichment of pathways related to peroxisome, PPAR signaling, and aminobenzoate degradation in early samples.
Conclusions:
- Hospitalized preterm infants exhibit individualized microbiota at birth, but this diversity diminishes during NICU stays.
- The developing gut microbiome in preterm infants shows an increasing prevalence of potentially pathogenic bacteria over time.
- These findings highlight the impact of the NICU environment on the preterm infant microbiome and suggest potential risks associated with dysbiosis.
Objectives:
The aim of the present study was to examine the changes in bacteria in hospitalized preterm infants during the first month of life.
Methods:
Rectal swabs were collected daily from 12 preterm infants. DNA was extracted from swabs from day of birth and weekly thereafter. Bacterial taxa were identified with next generation sequencing using universal bacterial primers targeted at the 16S ribosomal DNA on a 454 Roche titanium platform. Sequences were clustered into operational taxonomic units, and taxonomy was assigned against the Greengenes databank using Quantitative Insights Into Microbial Ecology version 1.4. Quantitative polymerase chain reaction was used to determine the abundance of Bifidobacterium spp. Functional assessment of the microbiome was performed with Phylogenetic Investigation of Communities by Reconstruction of Unobserved States (PICRUSt).
Results:
Average birth weight and gestational age were 1055 g and 28 weeks, respectively. There were 6 to 35 different bacterial families identified in the day-of-birth samples, unrelated to the mode of delivery. Richness decreased through hospitalization (week 1, 16.9 ± 7.7 vs weeks 3-5, 10.7 ± 3.4, P < 0.001). The Shannon diversity index demonstrated the lowest diversity at birth, an increase at week 2, followed by a rapid decline at weeks 3 to 5, suggesting the development of a more uniform microbiota composition after 2 weeks of stay at a neonatal intensive care unit. Enterobacteriaceae, Staphylococcaceae, and Enterococcaceae constituted the majority of the bacterial families. Bifidobacterium spp were infrequently detected at extremely low levels. PICRUSt analysis revealed the enhancement of peroxisome, PPAR, and adipocytokine signaling; plant-pathogen interaction; and aminobenzoate degradation pathways in week 1 samples.
Conclusions:
Our results suggest that although preterm infants have individualized microbiota that are detectable at birth, the differences decrease during the neonatal intensive care unit hospitalization with increasing prominence of pathogenic microbiota.
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