Metagenomic Analysis of the Human Distal Gut Microbiome

Author:

Gill Steven R.12345,Pop Mihai12345,DeBoy Robert T.12345,Eckburg Paul B.12345,Turnbaugh Peter J.12345,Samuel Buck S.12345,Gordon Jeffrey I.12345,Relman David A.12345,Fraser-Liggett Claire M.12345,Nelson Karen E.12345

Affiliation:

1. The Institute for Genomic Research, 9712 Medical Center Drive, Rockville, MD 20850, USA.

2. Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.

3. Department of Microbiology and Immunology, 299 Campus Drive, Stanford University, Stanford, CA 94305, USA.

4. Veterans Affairs Palo Alto Health Care System, Palo Alto, CA 94304, USA.

5. Center for Genome Sciences, Washington University School of Medicine, St. Louis, MO 63108, USA.

Abstract

The human intestinal microbiota is composed of 10 13 to 10 14 microorganisms whose collective genome (“microbiome”) contains at least 100 times as many genes as our own genome. We analyzed ∼78 million base pairs of unique DNA sequence and 2062 polymerase chain reaction–amplified 16 S ribosomal DNA sequences obtained from the fecal DNAs of two healthy adults. Using metabolic function analyses of identified genes, we compared our human genome with the average content of previously sequenced microbial genomes. Our microbiome has significantly enriched metabolism of glycans, amino acids, and xenobiotics; methanogenesis; and 2-methyl- d -erythritol 4-phosphate pathway–mediated biosynthesis of vitamins and isoprenoids. Thus, humans are superorganisms whose metabolism represents an amalgamation of microbial and human attributes.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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