Defining the human gut host–phage network through single-cell viral tagging
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...
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Published in | Nature microbiology Vol. 4; no. 12; pp. 2192 - 2203 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
01.12.2019
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
ISSN | 2058-5276 2058-5276 |
DOI | 10.1038/s41564-019-0526-2 |
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Abstract | 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 microbiota transplant therapy.
Single-cell viral tagging was used to identify uncharacterized bacterial host–phage pairs present in the human faecal microbiome, revealing a lack of phages targeting more than one host species and a high level of cross-reactivity between hosts and phages from different subjects, despite subject-specific pairings, which could have implications for faecal microbiota transplants. |
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AbstractList | 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 microbiota transplant therapy. 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 microbiota transplant therapy. Single-cell viral tagging was used to identify uncharacterized bacterial host–phage pairs present in the human faecal microbiome, revealing a lack of phages targeting more than one host species and a high level of cross-reactivity between hosts and phages from different subjects, despite subject-specific pairings, which could have implications for faecal microbiota transplants. 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 microbiota transplant therapy.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 microbiota transplant therapy. |
Author | Rinke, Christian Deng, Li Low, Soo Jen Daly, Joshua N. Hugenholtz, Philip Džunková, Mária |
Author_xml | – sequence: 1 givenname: Mária orcidid: 0000-0002-1765-0697 surname: Džunková fullname: Džunková, Mária email: dzunkovam@gmail.com organization: Australian Centre for Ecogenomics, School of Chemistry and Molecular Biosciences, The University of Queensland – sequence: 2 givenname: Soo Jen surname: Low fullname: Low, Soo Jen organization: Australian Centre for Ecogenomics, School of Chemistry and Molecular Biosciences, The University of Queensland – sequence: 3 givenname: Joshua N. surname: Daly fullname: Daly, Joshua N. organization: Australian Centre for Ecogenomics, School of Chemistry and Molecular Biosciences, The University of Queensland – sequence: 4 givenname: Li orcidid: 0000-0003-0225-0663 surname: Deng fullname: Deng, Li organization: Helmholtz Zentrum München-German Research Center for Environmental Health, Institute of Virology, Technical University Munich, Institute of Virology – sequence: 5 givenname: Christian orcidid: 0000-0003-4632-1187 surname: Rinke fullname: Rinke, Christian organization: Australian Centre for Ecogenomics, School of Chemistry and Molecular Biosciences, The University of Queensland – sequence: 6 givenname: Philip orcidid: 0000-0001-5386-7925 surname: Hugenholtz fullname: Hugenholtz, Philip email: p.hugenholtz@uq.edu.au organization: Australian Centre for Ecogenomics, School of Chemistry and Molecular Biosciences, The University of Queensland |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/31384000$$D View this record in MEDLINE/PubMed |
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Title | Defining the human gut host–phage network through single-cell viral tagging |
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