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Diurnal rhythmicity of infant fecal microbiota and metabolites: A randomized controlled interventional trial with infant formula.

Authors :
Heppner N
Reitmeier S
Heddes M
Merino MV
Schwartz L
Dietrich A
List M
Gigl M
Meng C
van der Veen DR
Schirmer M
Kleigrewe K
Omer H
Kiessling S
Haller D
Source :
Cell host & microbe [Cell Host Microbe] 2024 Apr 10; Vol. 32 (4), pp. 573-587.e5. Date of Electronic Publication: 2024 Apr 02.
Publication Year :
2024

Abstract

Microbiota assembly in the infant gut is influenced by diet. Breastfeeding and human breastmilk oligosaccharides promote the colonization of beneficial bifidobacteria. Infant formulas are supplemented with bifidobacteria or complex oligosaccharides, notably galacto-oligosaccharides (GOS), to mimic breast milk. To compare microbiota development across feeding modes, this randomized controlled intervention study (German Clinical Trial DRKS00012313) longitudinally sampled infant stool during the first year of life, revealing similar fecal bacterial communities between formula- and breast-fed infants (N = 210) but differences across age. Infant formula containing GOS sustained high levels of bifidobacteria compared with formula containing B. longum and B. breve or placebo. Metabolite and bacterial profiling revealed 24-h oscillations and circadian networks. Rhythmicity in bacterial diversity, specific taxa, and functional pathways increased with age and was strongest following breastfeeding and GOS supplementation. Circadian rhythms in dominant taxa were further maintained ex vivo in a chemostat model. Hence, microbiota rhythmicity develops early in life and is impacted by diet.<br />Competing Interests: Declaration of interests The authors declare no competing interests.<br /> (Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1934-6069
Volume :
32
Issue :
4
Database :
MEDLINE
Journal :
Cell host & microbe
Publication Type :
Academic Journal
Accession number :
38569545
Full Text :
https://doi.org/10.1016/j.chom.2024.02.015