Abstract
The role of bacteriophages in influencing the structure and function of the healthy human gut microbiome is unknown. With few exceptions, previous studies have found a high level of heterogeneity in bacteriophages from healthy individuals. To better estimate and identify the shared phageome of humans, we analyzed a deep DNA sequence dataset of active bacteriophages and available metagenomic datasets of the gut bacteriophage community from healthy individuals. We found 23 shared bacteriophages in more than one-half of 64 healthy individuals from around the world. These shared bacteriophages were found in a significantly smaller percentage of individuals with gastrointestinal/irritable bowel disease. A network analysis identified 44 bacteriophage groups of which 9 (20%) were shared in more than one-half of all 64 individuals. These results provide strong evidence of a healthy gut phageome (HGP) in humans. The bacteriophage community in the human gut is a mixture of three classes: a set of core bacteriophages shared among more than one-half of all people, a common set of bacteriophages found in 20-50% of individuals, and a set of bacteriophages that are either rarely shared or unique to a person. We propose that the core and common bacteriophage communities are globally distributed and comprise the HGP, which plays an important role in maintaining gut microbiome structure/function and thereby contributes significantly to human health.
Keywords
gut microbiome bacteriophage
gut microbiome viruses
human gut viral metagenome
shared microbiome viruses
MeSH Terms
Bacteriophages/classification,genetics,isolation & purification
Computational Biology
Feces/microbiology
Gastrointestinal Microbiome/genetics
Gastrointestinal Tract/microbiology
Humans
Inflammatory Bowel Diseases/genetics,microbiology
Metagenomics
Microbiota/genetics
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Manrique Pilar
Department of Microbiology and Immunology, Montana State University, Bozeman, MT 59717;
Bolduc Benjamin
Department of Chemistry and Biochemistry Research, Montana State University, Bozeman, MT 59717;
Walk Seth T
Department of Microbiology and Immunology, Montana State University, Bozeman, MT 59717;
van der Oost John
Laboratory of Microbiology, Wageningen University, Stippeneng 4, 6708 WE, Wageningen, The Netherlands;
de Vos Willem M
Laboratory of Microbiology, Wageningen University, Stippeneng 4, 6708 WE, Wageningen, The Netherlands; Department of Bacteriology & Immunology, University of Helsinki, Haartmaninkatu 3, 00290, Finland;
Young Mark J
Department of Plant Sciences and Plant Pathology, Montana State University, Bozeman, MT 59717 myoung@montana.edu.
Conflict of Interest
The authors declare no conflict of interest.
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