Literature DB >> 35318524

Gut Bifidobacterium responses to probiotic Lactobacillus casei Zhang administration vary between subjects from different geographic regions.

Feiyan Zhao1, Xiaoye Bai1,2, Juntao Zhang1, Lai-Yu Kwok1, Lingling Shen1, Hao Jin1, Tiansong Sun1, Zhihong Sun1, Heping Zhang3.   

Abstract

Bifidobacteria are health-promoting human gut inhabitants, but accurate species-level composition of the gut bifidobacteria and their responses to probiotic intervention have not been fully explored. This was a follow-up work of our previous study, in which 104 volunteers from six different Asiatic regions (Singapore, Indonesia, Xinjiang, Gansu, Inner Mongolia, Mongolia) were recruited. The gut microbiota and their responses towards Lactobacillus casei Zhang (LCZ) intervention were characterized (at days 0, 7, and 14; 14 days after stopping probiotic intake), and region-based differential responses were observed after LCZ intervention. This study further investigated changes in the species-level gut bifidobacteria by PacBio small-molecule real-time sequencing (SMRT) using bifidobacteria-specific primers. Firstly, this study found that Bifidobacterium adolescentis (42.58%) and Bifidobacterium breve (26.34%) were the core species across the six Asiatic regions. Secondly, principal coordinate analysis of probiotic-induced changes in the gut bifidobacterial microbiota (represented by weighted UniFrac distances) grouped the six regions into two clusters, namely northern (Xinjiang, Gansu, Inner Mongolia, and Mongolia) and southern (Singapore, Indonesia) regions. Thirdly, LCZ intervention induced region-based differential responses of gut bifidobacterial microbiota. The relative abundance of Bifidobacterium animalis in subjects from northern but not southern region substantially increased after LCZ intervention. Moreover, LCZ intervention significantly increased the weighted UniFrac distances in the southern but not northern subjects 7 days after LCZ intervention. The gut B. adolescentis correlated significantly and negatively with the weighted UniFrac distances of the baseline gut bifidobacterial microbiota in subjects of northern but not southern region, suggesting a possible homeostatic effect of LCZ on the gut bifidobacterial population of northern but not southern subjects. Collectively, our study found that probiotic-induced responses of the gut bifidobacterial microbiota varied with subjects' geographic origins, and B. adolescentis might play a role in maintaining the overall stability of the gut bifidobacterial population. KEY POINTS: • The core species in the six Asiatic regions are Bifidobacterium adolescentis and Bifidobacterium breve. • The gut bifidobacterial microbiota in people from various geographic origins showed different responses on probiotic administration.
© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Asian regions; Bifidobacterium; Gut microbiota; Lactobacillus casei Zhang

Mesh:

Year:  2022        PMID: 35318524     DOI: 10.1007/s00253-022-11868-4

Source DB:  PubMed          Journal:  Appl Microbiol Biotechnol        ISSN: 0175-7598            Impact factor:   4.813


  24 in total

1.  Quantification of human fecal bifidobacterium species by use of quantitative real-time PCR analysis targeting the groEL gene.

Authors:  Jana Junick; Michael Blaut
Journal:  Appl Environ Microbiol       Date:  2012-02-03       Impact factor: 4.792

2.  Two routes of metabolic cross-feeding between Bifidobacterium adolescentis and butyrate-producing anaerobes from the human gut.

Authors:  Alvaro Belenguer; Sylvia H Duncan; A Graham Calder; Grietje Holtrop; Petra Louis; Gerald E Lobley; Harry J Flint
Journal:  Appl Environ Microbiol       Date:  2006-05       Impact factor: 4.792

Review 3.  Genomic insights into bifidobacteria.

Authors:  Ju-Hoon Lee; Daniel J O'Sullivan
Journal:  Microbiol Mol Biol Rev       Date:  2010-09       Impact factor: 11.056

4.  Quantitative PCR with 16S rRNA-gene-targeted species-specific primers for analysis of human intestinal bifidobacteria.

Authors:  Takahiro Matsuki; Koichi Watanabe; Junji Fujimoto; Yukiko Kado; Toshihiko Takada; Kazumasa Matsumoto; Ryuichiro Tanaka
Journal:  Appl Environ Microbiol       Date:  2004-01       Impact factor: 4.792

5.  QIIME allows analysis of high-throughput community sequencing data.

Authors:  J Gregory Caporaso; Justin Kuczynski; Jesse Stombaugh; Kyle Bittinger; Frederic D Bushman; Elizabeth K Costello; Noah Fierer; Antonio Gonzalez Peña; Julia K Goodrich; Jeffrey I Gordon; Gavin A Huttley; Scott T Kelley; Dan Knights; Jeremy E Koenig; Ruth E Ley; Catherine A Lozupone; Daniel McDonald; Brian D Muegge; Meg Pirrung; Jens Reeder; Joel R Sevinsky; Peter J Turnbaugh; William A Walters; Jeremy Widmann; Tanya Yatsunenko; Jesse Zaneveld; Rob Knight
Journal:  Nat Methods       Date:  2010-04-11       Impact factor: 28.547

6.  Microbiota-derived acetate activates intestinal innate immunity via the Tip60 histone acetyltransferase complex.

Authors:  Bat-Erdene Jugder; Layla Kamareddine; Paula I Watnick
Journal:  Immunity       Date:  2021-06-08       Impact factor: 43.474

7.  Breast milk-derived human milk oligosaccharides promote Bifidobacterium interactions within a single ecosystem.

Authors:  Melissa A E Lawson; Ian J O'Neill; Magdalena Kujawska; Sree Gowrinadh Javvadi; Anisha Wijeyesekera; Zak Flegg; Lisa Chalklen; Lindsay J Hall
Journal:  ISME J       Date:  2019-11-18       Impact factor: 10.302

8.  Evaluation of the Anti-Aging Effects of a Probiotic Combination Isolated From Centenarians in a SAMP8 Mouse Model.

Authors:  Xin Fang; Mengyun Yue; Jing Wei; Yun Wang; Daojun Hong; Bo Wang; Xiaoting Zhou; Tingtao Chen
Journal:  Front Immunol       Date:  2021-12-02       Impact factor: 7.561

9.  Bifidobacteria-mediated immune system imprinting early in life.

Authors:  Bethany M Henrick; Lucie Rodriguez; Tadepally Lakshmikanth; Christian Pou; Ewa Henckel; Aron Arzoomand; Axel Olin; Jun Wang; Jaromir Mikes; Ziyang Tan; Yang Chen; Amy M Ehrlich; Anna Karin Bernhardsson; Constantin Habimana Mugabo; Ylva Ambrosiani; Anna Gustafsson; Stephanie Chew; Heather K Brown; Johann Prambs; Kajsa Bohlin; Ryan D Mitchell; Mark A Underwood; Jennifer T Smilowitz; J Bruce German; Steven A Frese; Petter Brodin
Journal:  Cell       Date:  2021-06-17       Impact factor: 41.582

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.