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Isolation and Characterization of Human Umbilical Cord-derived Mesenchymal Stem Cells from Preterm and Term Infants
Published on: January 26, 2019
Early-life skin microbiota in hospitalized preterm and full-term infants
Noelle E Younge1, Félix Araújo-Pérez2, Debra Brandon1,3
1Department of Pediatrics, Duke University, Durham, NC, USA.
Insights
The infant skin microbiota varies by body site and infant maturity. Preterm infants show lower diversity and higher pathogen presence, with significant exchange between body sites and the hospital environment.
Area of Science:
- Microbiology
- Neonatal Health
- Immunology
Background:
- Infant skin microbiota can harbor bacteria linked to neonatal infections.
- Microbiota plays a crucial role in immune system development.
Purpose of the Study:
- Characterize skin microbiota in preterm and full-term infants.
- Examine relationships between infant body sites, hospital environment, and microbiota.
Main Methods:
- Cross-sectional study of 129 infants (40 preterm, 89 full-term).
- Sampled skin (upper/lower body), oral cavity, environment, and stool.
- Utilized source tracking to analyze microbial exchange.
Main Results:
- Staphylococcus, Streptococcus, Enterococcus, and enteric Gram-negatives dominated skin microbiota.
- Preterm infants had lower alpha diversity and higher Staphylococcus/Escherichia enrichment.
- Microbiota varied significantly by body site, postnatal age, and gestational age.
Conclusions:
- Infant skin microbiota is dynamic, varying by individual, body site, and developmental stage.
- Skin harbors potential pathogens relevant to hospitalized infants.
- Microbiota is exchanged across body sites and the hospital environment during infancy.
Background:
The infant skin microbiota may serve as a reservoir of bacteria that contribute to neonatal infections and stimulate local and systemic immune development. The objectives of our study were to characterize the skin microbiota of preterm and full-term infants during their birth hospitalization and describe its relationship to the microbiota of other body sites and the hospital environment.
Results:
We conducted a cross-sectional study of 129 infants, including 40 preterm and 89 full-term infants. Samples were collected from five sites: the forehead and posterior auricular scalp (skin upper body); the periumbilical region, inguinal folds, and upper thighs (skin lower body); the oral cavity; the infant's immediate environment; and stool. Staphylococcus, Streptococcus, Enterococcus, and enteric Gram-negative bacteria including Escherichia and Enterobacter dominated the skin microbiota. The preterm infant microbiota at multiple sites had lower alpha diversity and greater enrichment with Staphylococcus and Escherichia than the microbiota of comparable sites in full-term infants. The community structure was highly variable among individuals but differed significantly by body site, postnatal age, and gestational age. Source tracking indicated that each body site both contributed to and received microbiota from other body sites and the hospital environment.
Conclusion:
The skin microbiota of preterm and full-term infants varied across individuals, by body site, and by the infant's developmental stage. The skin harbored many organisms that are common pathogens in hospitalized infants. Bacterial source tracking suggests that microbiota are commonly exchanged across body sites and the hospital environment as microbial communities mature in infancy.
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