Author
Listed:
- Bo Xing
(University of Chinese Academy of Sciences, College of Life Sciences
BGI Research)
- Cong Liu
(BGI Research)
- Wantong Chen
(BGI Research
South China University of Technology, School of Biology and Biological Engineering)
- Zhuoran Li
(University of Chinese Academy of Sciences, College of Life Sciences
BGI Research)
- Xiaohuan Jing
(BGI Research)
- Chao Wu
(Shanghai Jiao Tong University School of Medicine, Department of Endocrine and Metabolic Diseases, Shanghai Institute of Endocrine and Metabolic Diseases, Ruijin Hospital
Shanghai Jiao Tong University School of Medicine, Shanghai National Clinical Research Center for Metabolic Diseases, Ruijin Hospital)
- Ruixin Liu
(Shanghai Jiao Tong University School of Medicine, Department of Endocrine and Metabolic Diseases, Shanghai Institute of Endocrine and Metabolic Diseases, Ruijin Hospital
Shanghai Jiao Tong University School of Medicine, Shanghai National Clinical Research Center for Metabolic Diseases, Ruijin Hospital)
- Xiuqing Zhang
(University of Chinese Academy of Sciences, College of Life Sciences
BGI Research)
- Xun Xu
(BGI Research
BGI Research, State Key Laboratory of Genome and Multi-omics Technologies)
- Junhua Li
(BGI Research, State Key Laboratory of Genome and Multi-omics Technologies
BGI Research
BGI Research, Shenzhen Key Laboratory of Unknown Pathogen Identification)
- Minfeng Xiao
(BGI Research
BGI Research, State Key Laboratory of Genome and Multi-omics Technologies
BGI College)
Abstract
The scarcity of cultivated gut bacteriophages hinders gut microbial research and application. Here we report the establishment and characterization of a Gut Phage Biobank (GPB) ( https://db.cngb.org/genomics/datasets/GDS0000055 ) through a systematic isolation workflow and containing 104 isolates that target abundant or disease-associated gut bacteria. Genomic analysis reveals high diversity among these phages, and key genes of phage-bacteria interactions. The infection matrix demonstrates high host-specificity and varying infectivity of these phages under different conditions, unveiling phage-bacteria interaction mechanisms. In-depth characterization of the phages targeting obligate anaerobes uncovers a previously undescribed family and four previously undescribed genera, one of which is more prevalent than the well-known crAss-like phages globally except in Eurafrica. Cohort analysis reveals a higher prevalence of Mediterraneibacter and Dorea and a lower prevalence of Mediterraneibacter phages in Asian disease population. In vitro and in vivo evidence of phage inhibiting Dorea highlight the potential of phages in disease intervention. This biobank represents a valuable resource for advancing gut microbial research and holds promise for manipulating microbiomes.
Suggested Citation
Bo Xing & Cong Liu & Wantong Chen & Zhuoran Li & Xiaohuan Jing & Chao Wu & Ruixin Liu & Xiuqing Zhang & Xun Xu & Junhua Li & Minfeng Xiao, 2025.
"Gut Phage Biobank: a collection of bacteriophages targeting human commensal bacteria,"
Nature Communications, Nature, vol. 16(1), pages 1-17, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-61946-0
DOI: 10.1038/s41467-025-61946-0
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