Genomic and functional diversity of cultivated Bifidobacterium from human gut microbiota

Research output: Contribution to journalJournal articleResearchpeer-review

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Genomic and functional diversity of cultivated Bifidobacterium from human gut microbiota. / Li, Wenxi; Liang, Hewei; He, Wenxin; Gao, Xiaowei; Wu, Zhinan; Hu, Tongyuan; Lin, Xiaoqian; Wang, Mengmeng; Zhong, Yiyi; Zhang, Haifeng; Ge, Lan; Jin, Xin; Xiao, Liang; Zou, Yuanqiang.

In: Heliyon, Vol. 10, No. 5, e27270, 2024.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Li, W, Liang, H, He, W, Gao, X, Wu, Z, Hu, T, Lin, X, Wang, M, Zhong, Y, Zhang, H, Ge, L, Jin, X, Xiao, L & Zou, Y 2024, 'Genomic and functional diversity of cultivated Bifidobacterium from human gut microbiota', Heliyon, vol. 10, no. 5, e27270. https://doi.org/10.1016/j.heliyon.2024.e27270

APA

Li, W., Liang, H., He, W., Gao, X., Wu, Z., Hu, T., Lin, X., Wang, M., Zhong, Y., Zhang, H., Ge, L., Jin, X., Xiao, L., & Zou, Y. (2024). Genomic and functional diversity of cultivated Bifidobacterium from human gut microbiota. Heliyon, 10(5), [e27270]. https://doi.org/10.1016/j.heliyon.2024.e27270

Vancouver

Li W, Liang H, He W, Gao X, Wu Z, Hu T et al. Genomic and functional diversity of cultivated Bifidobacterium from human gut microbiota. Heliyon. 2024;10(5). e27270. https://doi.org/10.1016/j.heliyon.2024.e27270

Author

Li, Wenxi ; Liang, Hewei ; He, Wenxin ; Gao, Xiaowei ; Wu, Zhinan ; Hu, Tongyuan ; Lin, Xiaoqian ; Wang, Mengmeng ; Zhong, Yiyi ; Zhang, Haifeng ; Ge, Lan ; Jin, Xin ; Xiao, Liang ; Zou, Yuanqiang. / Genomic and functional diversity of cultivated Bifidobacterium from human gut microbiota. In: Heliyon. 2024 ; Vol. 10, No. 5.

Bibtex

@article{464ce58d755e435e9f8d57ee94985029,
title = "Genomic and functional diversity of cultivated Bifidobacterium from human gut microbiota",
abstract = "The genus Bifidobacterium widely exists in human gut and has been increasingly used as the adjuvant probiotics for the prevention and treatment of diseases. However, the functional differences of Bifidobacterium genomes from different regions of the world remain unclear. We here describe an extensive study on the genomic characteristics and function annotations of 1512 genomes (clustered to 849 non-redundant genomes) of Bifidobacterium cultured from human gut. The distribution of some carbohydrate-active enzymes varied among different Bifidobacterium species and continents. More than 36% of the genomes of B. pseudocatenulatum harbored biosynthetic gene clusters of lanthipeptide-class-iv. 99.76% of the cultivated genomes of Bifidobacterium harbored genes of bile salt hydrolase. Most genomes of B. adolescentis, and all genomes of B. dentium harbored genes involved in gamma-aminobutyric acid synthesis. B. longum subsp. infantis were characterized harboring most genes related to human milk oligosaccharide utilization. Significant differences between the distribution of antibiotic resistance genes among different species and continents revealed the importance to use antibiotics precisely in the clinical treatment. Phages infecting Bifidobacterium and horizontal gene transfers occurring in genomes of Bifidobacterium were dependent on species and region sources, and might help Bifidobacterium adapt to the environment. In addition, the distribution of Bifidobacterium in human gut was found varied from different regions of the world. This study represents a comprehensive view of characteristics and functions of genomes of cultivated Bifidobacterium from human gut, and enables clinical advances in the future.",
keywords = "Bifidobacterium, Bile salt hydrolase, Gut microbiome, Horizontal gene transfers, Phages",
author = "Wenxi Li and Hewei Liang and Wenxin He and Xiaowei Gao and Zhinan Wu and Tongyuan Hu and Xiaoqian Lin and Mengmeng Wang and Yiyi Zhong and Haifeng Zhang and Lan Ge and Xin Jin and Liang Xiao and Yuanqiang Zou",
note = "Publisher Copyright: {\textcopyright} 2024 The Authors",
year = "2024",
doi = "10.1016/j.heliyon.2024.e27270",
language = "English",
volume = "10",
journal = "Heliyon",
issn = "2405-8440",
publisher = "Elsevier",
number = "5",

}

RIS

TY - JOUR

T1 - Genomic and functional diversity of cultivated Bifidobacterium from human gut microbiota

AU - Li, Wenxi

AU - Liang, Hewei

AU - He, Wenxin

AU - Gao, Xiaowei

AU - Wu, Zhinan

AU - Hu, Tongyuan

AU - Lin, Xiaoqian

AU - Wang, Mengmeng

AU - Zhong, Yiyi

AU - Zhang, Haifeng

AU - Ge, Lan

AU - Jin, Xin

AU - Xiao, Liang

AU - Zou, Yuanqiang

N1 - Publisher Copyright: © 2024 The Authors

PY - 2024

Y1 - 2024

N2 - The genus Bifidobacterium widely exists in human gut and has been increasingly used as the adjuvant probiotics for the prevention and treatment of diseases. However, the functional differences of Bifidobacterium genomes from different regions of the world remain unclear. We here describe an extensive study on the genomic characteristics and function annotations of 1512 genomes (clustered to 849 non-redundant genomes) of Bifidobacterium cultured from human gut. The distribution of some carbohydrate-active enzymes varied among different Bifidobacterium species and continents. More than 36% of the genomes of B. pseudocatenulatum harbored biosynthetic gene clusters of lanthipeptide-class-iv. 99.76% of the cultivated genomes of Bifidobacterium harbored genes of bile salt hydrolase. Most genomes of B. adolescentis, and all genomes of B. dentium harbored genes involved in gamma-aminobutyric acid synthesis. B. longum subsp. infantis were characterized harboring most genes related to human milk oligosaccharide utilization. Significant differences between the distribution of antibiotic resistance genes among different species and continents revealed the importance to use antibiotics precisely in the clinical treatment. Phages infecting Bifidobacterium and horizontal gene transfers occurring in genomes of Bifidobacterium were dependent on species and region sources, and might help Bifidobacterium adapt to the environment. In addition, the distribution of Bifidobacterium in human gut was found varied from different regions of the world. This study represents a comprehensive view of characteristics and functions of genomes of cultivated Bifidobacterium from human gut, and enables clinical advances in the future.

AB - The genus Bifidobacterium widely exists in human gut and has been increasingly used as the adjuvant probiotics for the prevention and treatment of diseases. However, the functional differences of Bifidobacterium genomes from different regions of the world remain unclear. We here describe an extensive study on the genomic characteristics and function annotations of 1512 genomes (clustered to 849 non-redundant genomes) of Bifidobacterium cultured from human gut. The distribution of some carbohydrate-active enzymes varied among different Bifidobacterium species and continents. More than 36% of the genomes of B. pseudocatenulatum harbored biosynthetic gene clusters of lanthipeptide-class-iv. 99.76% of the cultivated genomes of Bifidobacterium harbored genes of bile salt hydrolase. Most genomes of B. adolescentis, and all genomes of B. dentium harbored genes involved in gamma-aminobutyric acid synthesis. B. longum subsp. infantis were characterized harboring most genes related to human milk oligosaccharide utilization. Significant differences between the distribution of antibiotic resistance genes among different species and continents revealed the importance to use antibiotics precisely in the clinical treatment. Phages infecting Bifidobacterium and horizontal gene transfers occurring in genomes of Bifidobacterium were dependent on species and region sources, and might help Bifidobacterium adapt to the environment. In addition, the distribution of Bifidobacterium in human gut was found varied from different regions of the world. This study represents a comprehensive view of characteristics and functions of genomes of cultivated Bifidobacterium from human gut, and enables clinical advances in the future.

KW - Bifidobacterium

KW - Bile salt hydrolase

KW - Gut microbiome

KW - Horizontal gene transfers

KW - Phages

U2 - 10.1016/j.heliyon.2024.e27270

DO - 10.1016/j.heliyon.2024.e27270

M3 - Journal article

C2 - 38463766

AN - SCOPUS:85186716167

VL - 10

JO - Heliyon

JF - Heliyon

SN - 2405-8440

IS - 5

M1 - e27270

ER -

ID: 385123679