Gut dysbiosis: Ecological causes and causative effects on human disease

The gut microbiota plays a role in many human diseases, but high-throughput sequence analysis does not provide a straightforward path for defining healthy microbial communities. Therefore, understanding mechanisms that drive compositional changes during disease (gut dysbiosis) continues to be a cent...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 2023-12, Vol.120 (50), p.e2316579120-e2316579120
Hauptverfasser: Winter, Sebastian E, Bäumler, Andreas J
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description The gut microbiota plays a role in many human diseases, but high-throughput sequence analysis does not provide a straightforward path for defining healthy microbial communities. Therefore, understanding mechanisms that drive compositional changes during disease (gut dysbiosis) continues to be a central goal in microbiome research. Insights from the microbial pathogenesis field show that an ecological cause for gut dysbiosis is an increased availability of host-derived respiratory electron acceptors, which are dominant drivers of microbial community composition. Similar changes in the host environment also drive gut dysbiosis in several chronic human illnesses, and a better understanding of the underlying mechanisms informs approaches to causatively link compositional changes in the gut microbiota to an exacerbation of symptoms. The emerging picture suggests that homeostasis is maintained by host functions that control the availability of resources governing microbial growth. Defining dysbiosis as a weakening of these host functions directs attention to the underlying cause and identifies potential targets for therapeutic intervention.
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subjects Availability
Community composition
Dysbacteriosis
Dysbiosis
Ecological effects
Gastrointestinal Microbiome
Homeostasis
Humans
Intestinal microflora
Microbial activity
Microbiomes
Microbiota
Microorganisms
Pathogenesis
Resource availability
Sequence analysis
Signs and symptoms
title Gut dysbiosis: Ecological causes and causative effects on human disease
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