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Development of a synbiotic that protects against ovariectomy-induced trabecular bone loss.

Authors :
Lawenius L
Gustafsson KL
Wu J
Nilsson KH
Movérare-Skrtic S
Schott EM
Soto-Girón MJ
Toledo GV
Sjögren K
Ohlsson C
Source :
American journal of physiology. Endocrinology and metabolism [Am J Physiol Endocrinol Metab] 2022 Apr 01; Vol. 322 (4), pp. E344-E354. Date of Electronic Publication: 2022 Feb 14.
Publication Year :
2022

Abstract

The gut microbiome has the capacity to regulate bone mass. The aim of this study was to develop a nutritional synbiotic dietary assemblage at an optimal dose to maintain bone mass in ovariectomized (Ovx) mice. We performed genomic analyses and in vitro experiments in a large collection of bacterial and fungal strains (>4,000) derived from fresh fruit and vegetables to identify candidates with the synergistic capacity to produce bone-protective short-chain fatty acids (SCFA) and vitamin K2. The candidate SBD111-A, composed of Lactiplantibacillus plantarum , Levilactobacillus brevis , Leuconostoc mesenteroides , Pseudomonas fluorescens , and Pichia kudriavzevii together with prebiotic dietary fibers, produced high levels of SCFA in vitro and protected against Ovx-induced trabecular bone loss in a dose-dependent manner in mice. Metagenomic sequencing revealed that SBD111-A changed the taxonomic composition and enriched specific pathways for synthesis of bone-protective SCFA, vitamin K2, and branched-chain amino acids in the gut microbiome. NEW & NOTEWORTHY We performed genomic analyses and in vitro experiments in a collection of bacterial and fungal strains. We identified a combination (SBD111-A) that produced high levels of SCFA in vitro and protected against ovariectomy-induced bone loss in a dose-dependent manner in mice. Metagenomic sequencing revealed that SBD111-A changed the taxonomic composition and function of the gut microbiome and enriched pathways for synthesis of bone-protective SCFA, vitamin K2, and branched-chain amino acids.

Details

Language :
English
ISSN :
1522-1555
Volume :
322
Issue :
4
Database :
MEDLINE
Journal :
American journal of physiology. Endocrinology and metabolism
Publication Type :
Academic Journal
Accession number :
35156423
Full Text :
https://doi.org/10.1152/ajpendo.00366.2021