Abstract

Correct establishment of the gut microbiome is compromised in premature babies, with Bifidobacterium being one of the most affected genera. Prematurity often entails the inability to successfully breastfeed, therefore requiring the implementation of other feeding modes; breast milk expression from a donor mother is the recommended option when their own mother’s milk is not available. Some studies showed different gut microbial profiles in premature infants fed with breast milk and donor human milk, however, it is not known how this affects the species composition of the genus Bifidobacterium. The objective of this study was to assess the effect of donated human milk on shaping the gut bifidobacterial populations of premature babies during the first three months of life. We analyzed the gut bifidobacterial communities of 42 premature babies fed with human donor milk or own-mother milk by the 16S rRNA–23S rRNA internal transcriber spaces (ITS) region sequencing and q-PCR. Moreover, metabolic activity was assessed by gas chromatography. We observed a specific bifidobacterial profile based on feeding type, with higher bifidobacterial diversity in the human donor milk group. Differences in specific Bifidobacterium species composition may contribute to the development of specific new strategies or treatments aimed at mimicking the impact of own-mother milk feeding in neonatal units.

Highlights

  • In premature infants, the correct process of gut microbiota colonization is compromised due to several factors, such as their immature immune systems and gut mucosa, long stays in hospitals, various medications, antibiotics, etc. [1]

  • Twenty-eight infants were breastfed with own mother’s milk (OMM) during the first 10 days of life, whereas 13 premature received Donor human milk (DHM) from the Breast Milk HUCA Bank at the hospital

  • We focused our interest on Operational Taxonomic Units (OTUs) belonging to the 27 species most present in the babies (B. adolescentis; B. animalis spp. animalis; B. animalis spp. lactis; Bifidobacterium anseris; Bifidobacterium asteroides; Bifidobacterium biavatii; B. bifidum; B. breve; B. catenulatum; Bifidobacterium choerinum; Bifidobacterium crudilactis; B. dentium; Bifidobacterium italicum; B. longum spp. infantis; B. longum spp. longum; B. longum spp. suis; Bifidobacterium magnum; Bifidobacterium mongoliense; Bifidobacterium parmae; Bifidobacterium pseudocatenulatum; Bifidobacterium pseudolongum spp. globosum; Bifidobacterium pseudolongum spp. pseudolongum; Bifidobacterium reuteri; Bifidobacterium thermacidophilum spp. porcinum; Bifidobacterium thermacidophilum spp. thermacidophilum; Bifidobacterium thermophilum; Bifidobacterium vansinderenii)

Read more

Summary

Introduction

The correct process of gut microbiota colonization is compromised due to several factors, such as their immature immune systems and gut mucosa, long stays in hospitals, various medications, antibiotics, etc. [1]. The correct process of gut microbiota colonization is compromised due to several factors, such as their immature immune systems and gut mucosa, long stays in hospitals, various medications, antibiotics, etc. These factors result in increased gut permeability, reducing the gut barrier and increasing the risk of infections and disease, in addition to other complications associated with decreasing gestational age [2]. Bifidobacteria are some of the first colonizers of the gut microbiota and are dominant in fecal samples of healthy breastfed infants, associated with the consumption of human milk oligosaccharides (HMOs) [1,5]. Bifidobacteria are essential in maintaining gut homeostasis and exert an important role in human health maintenance from the early stages of life [6,7]

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call