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Article: Large-scale phage cultivation for commensal human gut bacteria

TitleLarge-scale phage cultivation for commensal human gut bacteria
Authors
Keywordshost specificity
human gut bacteria
microbiota modulation
phage cultivation
phage susceptibility
Issue Date12-Apr-2023
PublisherCell Press
Citation
Cell Host & Microbe, 2023, v. 31, n. 4, p. 665-677 How to Cite?
AbstractPhages are highly abundant in the human gut, yet most of them remain uncultured. Here, we present a gut phage isolate collection (GPIC) containing 209 phages for 42 commensal human gut bacterial species. Genome analysis of the phages identified 34 undescribed genera. We discovered 22 phages from the Salasmaviridae family that have small genomes (∼10–20 kbp) and infect Gram-positive bacteria. Two phages from a candidate family, Paboviridae, with high prevalence in the human gut were also identified. Infection assays showed that Bacteroides and Parabacteroides phages are specific to a bacterial species, and strains of the same species also exhibit substantial variations in phage susceptibility. A cocktail of 8 phages with a broad host range for Bacteroides fragilis strains effectively reduced their abundance in complex host-derived communities in vitro. Our study expands the diversity of cultured human gut bacterial phages and provides a valuable resource for human microbiome engineering.
Persistent Identifierhttp://hdl.handle.net/10722/367342
ISSN
2023 Impact Factor: 20.6
2023 SCImago Journal Rankings: 7.760
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorShen, Juntao-
dc.contributor.authorZhang, Jieqiong-
dc.contributor.authorMo, Luofei-
dc.contributor.authorLi, Yanchen-
dc.contributor.authorLi, Yake-
dc.contributor.authorLi, Cun-
dc.contributor.authorKuang, Xiaoxian-
dc.contributor.authorTao, Zining-
dc.contributor.authorQu, Zepeng-
dc.contributor.authorWu, Lu-
dc.contributor.authorChen, Junyu-
dc.contributor.authorLiu, Shiying-
dc.contributor.authorZeng, Linfang-
dc.contributor.authorHe, Zexi-
dc.contributor.authorChen, Zuohong-
dc.contributor.authorDeng, Yu-
dc.contributor.authorZhang, Tong-
dc.contributor.authorLi, Bing-
dc.contributor.authorDai, Lei-
dc.contributor.authorMa, Yingfei-
dc.date.accessioned2025-12-10T08:06:38Z-
dc.date.available2025-12-10T08:06:38Z-
dc.date.issued2023-04-12-
dc.identifier.citationCell Host & Microbe, 2023, v. 31, n. 4, p. 665-677-
dc.identifier.issn1931-3128-
dc.identifier.urihttp://hdl.handle.net/10722/367342-
dc.description.abstractPhages are highly abundant in the human gut, yet most of them remain uncultured. Here, we present a gut phage isolate collection (GPIC) containing 209 phages for 42 commensal human gut bacterial species. Genome analysis of the phages identified 34 undescribed genera. We discovered 22 phages from the Salasmaviridae family that have small genomes (∼10–20 kbp) and infect Gram-positive bacteria. Two phages from a candidate family, Paboviridae, with high prevalence in the human gut were also identified. Infection assays showed that Bacteroides and Parabacteroides phages are specific to a bacterial species, and strains of the same species also exhibit substantial variations in phage susceptibility. A cocktail of 8 phages with a broad host range for Bacteroides fragilis strains effectively reduced their abundance in complex host-derived communities in vitro. Our study expands the diversity of cultured human gut bacterial phages and provides a valuable resource for human microbiome engineering.-
dc.languageeng-
dc.publisherCell Press-
dc.relation.ispartofCell Host & Microbe-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjecthost specificity-
dc.subjecthuman gut bacteria-
dc.subjectmicrobiota modulation-
dc.subjectphage cultivation-
dc.subjectphage susceptibility-
dc.titleLarge-scale phage cultivation for commensal human gut bacteria-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1016/j.chom.2023.03.013-
dc.identifier.pmid37054680-
dc.identifier.scopuseid_2-s2.0-85151657028-
dc.identifier.volume31-
dc.identifier.issue4-
dc.identifier.spage665-
dc.identifier.epage677-
dc.identifier.eissn1934-6069-
dc.identifier.isiWOS:000982882500001-
dc.identifier.issnl1931-3128-

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