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Article: Systematically investigating and identifying bacteriocins in the human gut microbiome

TitleSystematically investigating and identifying bacteriocins in the human gut microbiome
Authors
Keywordsantimicrobial activity
antimicrobial peptides
bacteriocin
genome mining
human microbiome
metagenomics
natural products
omics analysis
Issue Date12-Nov-2025
PublisherCell Press
Citation
Cell Genomics, 2025, v. 5, n. 11 How to Cite?
Abstract

Human gut microbiota produces unmodified bacteriocins, natural antimicrobial peptides that protect against pathogens and regulate host physiology. However, current bioinformatic tools limit the comprehensive investigation of bacteriocins’ biosynthesis, obstructing research into their biological functions. Here, we introduce IIBacFinder, a superior analysis pipeline for identifying unmodified class II bacteriocins. Through large-scale bioinformatic analysis and experimental validation, we demonstrate their widespread distribution across the bacterial kingdom, with most being habitat specific. Analyzing over 280,000 bacterial genomes, we reveal the diverse potential of human gut bacteria to produce these bacteriocins. Guided by meta-omics analysis, we synthesized 26 hypothetical bacteriocins from gut commensal species, with 16 showing antibacterial activities. Further ex vivo tests show minimal impact of narrow-spectrum bacteriocins on human fecal microbiota. Our study highlights the huge biosynthetic potential of unmodified bacteriocins in the human gut, paving the way for understanding their biological functions and health implications.


Persistent Identifierhttp://hdl.handle.net/10722/369765
ISSN
2023 Impact Factor: 11.1
2023 SCImago Journal Rankings: 8.807

 

DC FieldValueLanguage
dc.contributor.authorZhang, Dengwei-
dc.contributor.authorZou, Yinai-
dc.contributor.authorShi, Yuqi-
dc.contributor.authorZhang, Junliang-
dc.contributor.authorLiu, Jing-
dc.contributor.authorWu, Gengfan-
dc.contributor.authorZhang, Jian-
dc.contributor.authorGao, Ying-
dc.contributor.authorChen, Muxuan-
dc.contributor.authorLi, Yong Xin-
dc.date.accessioned2026-01-31T00:35:44Z-
dc.date.available2026-01-31T00:35:44Z-
dc.date.issued2025-11-12-
dc.identifier.citationCell Genomics, 2025, v. 5, n. 11-
dc.identifier.issn2666-979X-
dc.identifier.urihttp://hdl.handle.net/10722/369765-
dc.description.abstract<p>Human gut microbiota produces unmodified bacteriocins, natural antimicrobial peptides that protect against pathogens and regulate host physiology. However, current bioinformatic tools limit the comprehensive investigation of bacteriocins’ biosynthesis, obstructing research into their biological functions. Here, we introduce IIBacFinder, a superior analysis pipeline for identifying unmodified class II bacteriocins. Through large-scale bioinformatic analysis and experimental validation, we demonstrate their widespread distribution across the bacterial kingdom, with most being habitat specific. Analyzing over 280,000 bacterial genomes, we reveal the diverse potential of human gut bacteria to produce these bacteriocins. Guided by meta-omics analysis, we synthesized 26 hypothetical bacteriocins from gut commensal species, with 16 showing antibacterial activities. Further ex vivo tests show minimal impact of narrow-spectrum bacteriocins on human fecal microbiota. Our study highlights the huge biosynthetic potential of unmodified bacteriocins in the human gut, paving the way for understanding their biological functions and health implications.</p>-
dc.languageeng-
dc.publisherCell Press-
dc.relation.ispartofCell Genomics-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectantimicrobial activity-
dc.subjectantimicrobial peptides-
dc.subjectbacteriocin-
dc.subjectgenome mining-
dc.subjecthuman microbiome-
dc.subjectmetagenomics-
dc.subjectnatural products-
dc.subjectomics analysis-
dc.titleSystematically investigating and identifying bacteriocins in the human gut microbiome-
dc.typeArticle-
dc.identifier.doi10.1016/j.xgen.2025.100983-
dc.identifier.scopuseid_2-s2.0-105016849968-
dc.identifier.volume5-
dc.identifier.issue11-
dc.identifier.eissn2666-979X-
dc.identifier.issnl2666-979X-

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