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Defining the human gut host-phage network through single-cell viral tagging.
Nat. Microbiol. 4, 2192-2203 (2019)
Viral discovery is accelerating at an unprecedented rate due to continuing advances in culture-independent sequence-based analyses. One important facet of this discovery is identification of the hosts of these recently characterized uncultured viruses. To this end, we have adapted the viral tagging approach, which bypasses the need for culture-based methods to identify host-phage pairings. Fluorescently labelled anonymous virions adsorb to unlabelled anonymous bacterial host cells, which are then individually sorted as host-phage pairs, followed by genome amplification and high-throughput sequencing to establish the identities of both the host and the attached virus(es). We demonstrate single-cell viral tagging using the faecal microbiome, including cross-tagging of viruses and bacteria between human subjects. A total of 363 unique host-phage pairings were predicted, most of which were subject-specific and involved previously uncharacterized viruses despite the majority of their bacterial hosts having known taxonomy. One-fifth of these pairs were confirmed by multiple individual tagged cells. Viruses targeting more than one bacterial species were conspicuously absent in the host-phage network, suggesting that phages are not major vectors of inter-species horizontal gene transfer in the human gut. A high level of cross-reactivity between phages and bacteria from different subjects was noted despite subject-specific viral profiles, which has implications for faecal micro-biota transplant therapy.
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Publication type
Article: Journal article
Document type
Scientific Article
Keywords
Microbial Genomes; Alignment; Sequence; Bacteria; Viruses; Virome; Populations
Language
Publication Year
2019
HGF-reported in Year
2019
ISSN (print) / ISBN
2058-5276
e-ISSN
2058-5276
Journal
Nature microbiology
Quellenangaben
Volume: 4,
Issue: 12,
Pages: 2192-2203
Publisher
Nature Publishing Group
Publishing Place
London
Reviewing status
Peer reviewed
Institute(s)
Institute of Virology (VIRO)
POF-Topic(s)
30203 - Molecular Targets and Therapies
Research field(s)
Immune Response and Infection
PSP Element(s)
G-554300-001
WOS ID
WOS:000499071100023
Scopus ID
85070203272
PubMed ID
31384000
Erfassungsdatum
2019-08-13