Cargando…

The virota and its transkingdom interactions in the healthy infant gut

Virome and 16/18S analyses were performed on 304 longitudinal fecal samples of eight infants. The gut virota—the collection of all viruses present in the gut—was dominated by bacteriophages, which were nearly absent at birth and emerged rapidly within the first weeks after birth. Over 85% of phage r...

Descripción completa

Detalles Bibliográficos
Autores principales: Beller, Leen, Deboutte, Ward, Vieira-Silva, Sara, Falony, Gwen, Yhossef Tito, Raul, Rymenans, Leen, Yinda, Claude Kwe, Vanmechelen, Bert, Van Espen, Lore, Jansen, Daan, Shi, Chenyan, Zeller, Mark, Maes, Piet, Faust, Karoline, Van Ranst, Marc, Raes, Jeroen, Matthijnssens, Jelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9060457/
https://www.ncbi.nlm.nih.gov/pubmed/35320047
http://dx.doi.org/10.1073/pnas.2114619119
_version_ 1784698506909319168
author Beller, Leen
Deboutte, Ward
Vieira-Silva, Sara
Falony, Gwen
Yhossef Tito, Raul
Rymenans, Leen
Yinda, Claude Kwe
Vanmechelen, Bert
Van Espen, Lore
Jansen, Daan
Shi, Chenyan
Zeller, Mark
Maes, Piet
Faust, Karoline
Van Ranst, Marc
Raes, Jeroen
Matthijnssens, Jelle
author_facet Beller, Leen
Deboutte, Ward
Vieira-Silva, Sara
Falony, Gwen
Yhossef Tito, Raul
Rymenans, Leen
Yinda, Claude Kwe
Vanmechelen, Bert
Van Espen, Lore
Jansen, Daan
Shi, Chenyan
Zeller, Mark
Maes, Piet
Faust, Karoline
Van Ranst, Marc
Raes, Jeroen
Matthijnssens, Jelle
author_sort Beller, Leen
collection PubMed
description Virome and 16/18S analyses were performed on 304 longitudinal fecal samples of eight infants. The gut virota—the collection of all viruses present in the gut—was dominated by bacteriophages, which were nearly absent at birth and emerged rapidly within the first weeks after birth. Over 85% of phage reads correspond to 305 near-complete genomes, most of which (70.5%) were individual infant–specific, including two crAssphages, whereas 7.8% of phages were present in at least 50% of infants. Bacterial hosts could be predicted for 80% of phages, mainly infecting Firmicutes. Strong temporal correlations between phages and their predicted bacterial hosts were identified for >40% of our phages, and together with the observation of a decreasing fraction of phages with a temperate lifestyle further suggest that phages are induced from early-colonizing bacteria. The vast majority (>86%) of identified eukaryotic viruses, known to cause gastroenteritis, occurred without clinical signs, and an increase in the rate of infection occurred after day-care entrance. On average, 112 genomic contigs of distinct anelloviruses could be identified per infant, some of which were shed at >1 y. The identified plant viruses reflected the infant diet. Finally, the sporadic identification of fungi and parasites argues against the presence of such stable communities in the study population. Overall, this work provides a very high temporal resolution on how the different members of the infant gut microbiota, and especially the virome, develop over time in the gut of healthy infants, and might serve as valuable baseline knowledge for further studies investigating the effect of perturbations in the infant gut microbiota.
format Online
Article
Text
id pubmed-9060457
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher National Academy of Sciences
record_format MEDLINE/PubMed
spelling pubmed-90604572022-05-03 The virota and its transkingdom interactions in the healthy infant gut Beller, Leen Deboutte, Ward Vieira-Silva, Sara Falony, Gwen Yhossef Tito, Raul Rymenans, Leen Yinda, Claude Kwe Vanmechelen, Bert Van Espen, Lore Jansen, Daan Shi, Chenyan Zeller, Mark Maes, Piet Faust, Karoline Van Ranst, Marc Raes, Jeroen Matthijnssens, Jelle Proc Natl Acad Sci U S A Biological Sciences Virome and 16/18S analyses were performed on 304 longitudinal fecal samples of eight infants. The gut virota—the collection of all viruses present in the gut—was dominated by bacteriophages, which were nearly absent at birth and emerged rapidly within the first weeks after birth. Over 85% of phage reads correspond to 305 near-complete genomes, most of which (70.5%) were individual infant–specific, including two crAssphages, whereas 7.8% of phages were present in at least 50% of infants. Bacterial hosts could be predicted for 80% of phages, mainly infecting Firmicutes. Strong temporal correlations between phages and their predicted bacterial hosts were identified for >40% of our phages, and together with the observation of a decreasing fraction of phages with a temperate lifestyle further suggest that phages are induced from early-colonizing bacteria. The vast majority (>86%) of identified eukaryotic viruses, known to cause gastroenteritis, occurred without clinical signs, and an increase in the rate of infection occurred after day-care entrance. On average, 112 genomic contigs of distinct anelloviruses could be identified per infant, some of which were shed at >1 y. The identified plant viruses reflected the infant diet. Finally, the sporadic identification of fungi and parasites argues against the presence of such stable communities in the study population. Overall, this work provides a very high temporal resolution on how the different members of the infant gut microbiota, and especially the virome, develop over time in the gut of healthy infants, and might serve as valuable baseline knowledge for further studies investigating the effect of perturbations in the infant gut microbiota. National Academy of Sciences 2022-03-23 2022-03-29 /pmc/articles/PMC9060457/ /pubmed/35320047 http://dx.doi.org/10.1073/pnas.2114619119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Beller, Leen
Deboutte, Ward
Vieira-Silva, Sara
Falony, Gwen
Yhossef Tito, Raul
Rymenans, Leen
Yinda, Claude Kwe
Vanmechelen, Bert
Van Espen, Lore
Jansen, Daan
Shi, Chenyan
Zeller, Mark
Maes, Piet
Faust, Karoline
Van Ranst, Marc
Raes, Jeroen
Matthijnssens, Jelle
The virota and its transkingdom interactions in the healthy infant gut
title The virota and its transkingdom interactions in the healthy infant gut
title_full The virota and its transkingdom interactions in the healthy infant gut
title_fullStr The virota and its transkingdom interactions in the healthy infant gut
title_full_unstemmed The virota and its transkingdom interactions in the healthy infant gut
title_short The virota and its transkingdom interactions in the healthy infant gut
title_sort virota and its transkingdom interactions in the healthy infant gut
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9060457/
https://www.ncbi.nlm.nih.gov/pubmed/35320047
http://dx.doi.org/10.1073/pnas.2114619119
work_keys_str_mv AT bellerleen thevirotaanditstranskingdominteractionsinthehealthyinfantgut
AT deboutteward thevirotaanditstranskingdominteractionsinthehealthyinfantgut
AT vieirasilvasara thevirotaanditstranskingdominteractionsinthehealthyinfantgut
AT falonygwen thevirotaanditstranskingdominteractionsinthehealthyinfantgut
AT yhosseftitoraul thevirotaanditstranskingdominteractionsinthehealthyinfantgut
AT rymenansleen thevirotaanditstranskingdominteractionsinthehealthyinfantgut
AT yindaclaudekwe thevirotaanditstranskingdominteractionsinthehealthyinfantgut
AT vanmechelenbert thevirotaanditstranskingdominteractionsinthehealthyinfantgut
AT vanespenlore thevirotaanditstranskingdominteractionsinthehealthyinfantgut
AT jansendaan thevirotaanditstranskingdominteractionsinthehealthyinfantgut
AT shichenyan thevirotaanditstranskingdominteractionsinthehealthyinfantgut
AT zellermark thevirotaanditstranskingdominteractionsinthehealthyinfantgut
AT maespiet thevirotaanditstranskingdominteractionsinthehealthyinfantgut
AT faustkaroline thevirotaanditstranskingdominteractionsinthehealthyinfantgut
AT vanranstmarc thevirotaanditstranskingdominteractionsinthehealthyinfantgut
AT raesjeroen thevirotaanditstranskingdominteractionsinthehealthyinfantgut
AT matthijnssensjelle thevirotaanditstranskingdominteractionsinthehealthyinfantgut
AT bellerleen virotaanditstranskingdominteractionsinthehealthyinfantgut
AT deboutteward virotaanditstranskingdominteractionsinthehealthyinfantgut
AT vieirasilvasara virotaanditstranskingdominteractionsinthehealthyinfantgut
AT falonygwen virotaanditstranskingdominteractionsinthehealthyinfantgut
AT yhosseftitoraul virotaanditstranskingdominteractionsinthehealthyinfantgut
AT rymenansleen virotaanditstranskingdominteractionsinthehealthyinfantgut
AT yindaclaudekwe virotaanditstranskingdominteractionsinthehealthyinfantgut
AT vanmechelenbert virotaanditstranskingdominteractionsinthehealthyinfantgut
AT vanespenlore virotaanditstranskingdominteractionsinthehealthyinfantgut
AT jansendaan virotaanditstranskingdominteractionsinthehealthyinfantgut
AT shichenyan virotaanditstranskingdominteractionsinthehealthyinfantgut
AT zellermark virotaanditstranskingdominteractionsinthehealthyinfantgut
AT maespiet virotaanditstranskingdominteractionsinthehealthyinfantgut
AT faustkaroline virotaanditstranskingdominteractionsinthehealthyinfantgut
AT vanranstmarc virotaanditstranskingdominteractionsinthehealthyinfantgut
AT raesjeroen virotaanditstranskingdominteractionsinthehealthyinfantgut
AT matthijnssensjelle virotaanditstranskingdominteractionsinthehealthyinfantgut