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Džunková, M.* ; Low, S.J.* ; Daly, J.N.* ; Deng, L. ; Rinke, C.* ; Hugenholtz, P.*

Defining the human gut host-phage network through single-cell viral tagging.

Nat. Microbiol. 4, 2192-2203 (2019)
DOI PMC
Open Access Green as soon as Postprint is submitted to ZB.
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
Quellenangaben Volume: 4, Issue: 12, Pages: 2192-2203 Article Number: , Supplement: ,
Publisher Nature Publishing Group
Publishing Place London
Reviewing status Peer reviewed
POF-Topic(s) 30203 - Molecular Targets and Therapies
Research field(s) Immune Response and Infection
PSP Element(s) G-554300-001
Scopus ID 85070203272
PubMed ID 31384000
Erfassungsdatum 2019-08-13