Modulation of the human gut microbiota by short chain ... · Modulation of the human gut microbiota...

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Modulation of the human gut microbiota by short chain Fructo-oligosaccharides Ashok Kumar Dubey, Ph.D. Tata Chemicals Ltd Innovation Centre ILSI Conference, 6th December 2018 1

Transcript of Modulation of the human gut microbiota by short chain ... · Modulation of the human gut microbiota...

Page 1: Modulation of the human gut microbiota by short chain ... · Modulation of the human gut microbiota by short chain Fructo-oligosaccharides Ashok Kumar Dubey, Ph.D. Tata Chemicals

Modulation of the human gut microbiota by short chain Fructo-oligosaccharides

Ashok Kumar Dubey, Ph.D. Tata Chemicals Ltd Innovation Centre

ILSI Conference, 6th December 2018

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Humans: More Microbes Than Human Cells?

100 trillion bacterial cells 100X more bacterial cells than host cells 1000X more bacterial genes than host genes

MICROBIAL ROOTS

SUPRA-ORGANISMS: CONGLOMERATES OF MAMMALIAN AND MICROBIAL CELLS

Archaea Bacteria Fungi Protozoans

THE INTESTINE (~100 trillion organisms)

SITE OF LARGEST COLLECTION

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Prebiotics: Beneficial Modulation of the Gut Microbiome

Gut Microbes Prebiotics Consume Producing

Metabolites (SCFAs)

Nutrient absorption and metabolism

Immune response

Cell-to-Cell signaling

Can be applied in

Metabolic Syndromes (Obesity, Type II Diabetes, Cardiovascular Diseases)

Cognitive Health (motor activity and memory retention)

Chronic Disorders (ulcerative colitis, IBS, and Crohn’s Disease)

Creation of acidic environment (decreased

pH) Increasing good bacteria

Reduce pathogenic microbial abundance

through

This influences

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TATA-Yale Collaborative Study: Design

Germ free Mice

Colonized with human gut microbiota

Fed customized diet with FOS

Fed customized diet without FOS

FOS Group

Control Group

-7d Gut microbiota

(Gavage)

0 d

7 d

14 d

21 d

28 d

Fecal Sample Collection

Mice euthanized

Intestinal content

collected

DNA sequencing on Illumina

Miseq

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FOS Supplementation response

Snapshot of microbial relative abundance

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FOS promoted the growth of Bifidobacterium , Faecalibacterium prausnitzii,

Blautia and bacteria belonging to Lachnospiraceae family

Bio-geographical and Spatial arrangement of gut bacteria play a role in

determining the impact of prebiotics

Utilization of FOS by good gut bacteria results in reduction of Sutterella, a

pathogenic bacteria

Consumption of FOS enhanced production of SCFAs

Summary

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Impact of Fructo-oligosaccharides (FOS) on human gut microbiota: A clinical trial

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71.5

18.7

3.8 0.6 5.4 Relative Abundance (%)

Bacteroidetes

Firmicutes

Proteobacteria

Actinobacteria

Others

95% of sequences were found to belong to microbes belonging to the four phyla

Remaining 5% belonged to 16 other phyla

More than 80% of sequences were assigned to 5 genera - Prevotella, Faecalibacterium, Alloprevotella, Roseburia, and Bacteroides

Two distinct clusters were obtained Cluster 1 was further divided into 2

subclusters subcluster 1a (core taxa): Bacteroides,

Faecalibacterium, and Roseburia Subcluster 1b (core taxa): Bacteroides,

Faecalibacterium, Bifidobacterium, Blautia, Dorea, Lachnospiraceaincertaesedis, and Streptococcus

Cluster 2 (core taxa): Prevotella and Faecalibacterium

Analysis of basal phase sample revealed uniqueness

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Prevotella, Faecalibacterium were predominantly present in the Western

Indian subjects

FOS consumption increased the relative abundance of OTUs belonging to

Bifidobacterium and Lactobacillus.

FOS at higher dosage appear to promote the selective proliferation of OTUs

belonging to Lactobacillus.

A significant change was also observed in certain butyrate-producing

microbes

Positive impact of FOS on butyrate-producing bacteria reinforces the role of

prebiotics in conferring beneficial functions to the host.

Summary

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Acknowledgement Noah Palm Deguang Song David Urbonas Gary Cline Sharmila Mande Anirban Bhaduri

Funding by Tata Chemicals as a part of TATA-YALE Collaboration

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Thank you