Synergy and oxygen adaptation for development of next-generation probiotics
The human gut microbiota has gained interest as an environmental factor that may contribute to health or disease 1 . The development of next-generation probiotics is a promising strategy to modulate the gut microbiota and improve human health; however, several key candidate next-generation probiotic...
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Veröffentlicht in: | Nature (London) 2023-08, Vol.620 (7973), p.381-385 |
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Zusammenfassung: | The human gut microbiota has gained interest as an environmental factor that may contribute to health or disease
1
. The development of next-generation probiotics is a promising strategy to modulate the gut microbiota and improve human health; however, several key candidate next-generation probiotics are strictly anaerobic
2
and may require synergy with other bacteria for optimal growth.
Faecalibacterium prausnitzii
is a highly prevalent and abundant human gut bacterium associated with human health, but it has not yet been developed into probiotic formulations
2
. Here we describe the co-isolation of
F. prausnitzii
and
Desulfovibrio piger
, a sulfate-reducing bacterium, and their cross-feeding for growth and butyrate production. To produce a next-generation probiotic formulation, we adapted
F. prausnitzii
to tolerate oxygen exposure, and, in proof-of-concept studies, we demonstrate that the symbiotic product is tolerated by mice and humans (ClinicalTrials.gov identifier:
NCT03728868
) and is detected in the human gut in a subset of study participants. Our study describes a technology for the production of next-generation probiotics based on the adaptation of strictly anaerobic bacteria to tolerate oxygen exposures without a reduction in potential beneficial properties. Our technology may be used for the development of other strictly anaerobic strains as next-generation probiotics.
The anaerobic gut bacterium
Faecalibacterium prausnitzii
was isolated and adapted for oxygen tolerance to develop a next-generation probiotic for the treatment of conditions such as inflammatory bowel disease and type 2 diabetes. |
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ISSN: | 0028-0836 1476-4687 1476-4687 |
DOI: | 10.1038/s41586-023-06378-w |