Actively replicating gut bacteria identified by 5-ethynyl-2'-deoxyuridine (EdU) click chemistry and cell sorting

被引:4
作者
Beauchemin, Eve T. T. [1 ]
Hunter, Claire [1 ]
Maurice, Corinne F. F. [1 ,2 ]
机构
[1] McGill Univ, Fac Med & Hlth Sci, Dept Microbiol & Immunol, Montreal, PQ, Canada
[2] McGill Univ, McGill Ctr Microbiome Res, Montreal, PQ, Canada
基金
加拿大健康研究院;
关键词
Click chemistry; gut microbiota; bacterial physiology; bacterial replication; EdU; 5-ethynyl-2'-deoxyuridine; flow cytometry; cell sorting; THYMIDINE UPTAKE; GROWTH DYNAMICS; DNA-SYNTHESIS; MICROBIOME; RESISTANCE;
D O I
10.1080/19490976.2023.2180317
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The composition of the intestinal bacterial community is well described, but recent research suggests that the metabolism of these bacteria plays a larger role in health than which species are present. One fundamental aspect of gut bacterial metabolism that remains understudied is bacterial replication. Indeed, there exist few techniques which can identify actively replicating gut bacteria. In this study, we aimed to address this gap by adapting 5-ethynyl-2'-deoxyuridine (EdU) click chemistry (EdU-click), a metabolic labeling method, coupled with fluorescence-activated cell sorting and sequencing (FACS-Seq) to characterize replicating gut bacteria. We first used EdU-click with human gut bacterial isolates and show that many of them are amenable to this technique. We then optimized EdU-click and FACS-Seq for murine fecal bacteria and reveal that Prevotella UCG-001 and Ileibacterium are enriched in the replicating fraction. Finally, we labeled the actively replicating murine gut bacteria during exposure to cell wall-specific antibiotics in vitro. We show that regardless of the antibiotic used, the actively replicating bacteria largely consist of Ileibacterium, suggesting the resistance of this taxon to perturbations. Overall, we demonstrate how combining EdU-click and FACSeq can identify the actively replicating gut bacteria and their link with the composition of the whole community in both homeostatic and perturbed conditions. This technique will be instrumental in elucidating in situ bacterial replication dynamics in a variety of other ecological states, including colonization and species invasion, as well as for investigating the relationship between the replication and abundance of bacteria in complex communities. Plain Language Summary The bacteria that live in our guts are known to influence our intestinal and overall health. Though we know a lot about which kinds of bacteria are in our guts, we still don't know much about which bacteria are actually alive and growing. This is important to know, because bacteria that are growing, or replicating, are more likely to impact our health than bacteria which are not replicating. Our research group aimed to address this issue by developing a new technique that can identify which gut bacteria are actively replicating. We first tested this technique on specific gut bacteria, and then we made sure the technique worked when it was used on the gut bacteria of mice. By using this technique, we identified several types of mouse gut bacteria that were actively replicating. We also demonstrated one possible application of this technique by using it to identify mouse gut bacteria that were able to replicate after they were grown with antibiotics. Overall, we have introduced a new technique to identify replicating gut bacteria and show how it can be used to increase our knowledge on which bacteria are growing in the gut. This technique will help us identify which bacteria may be more important to our health due to their active growth.
引用
收藏
页数:23
相关论文
共 64 条
[11]   Cell cycle synchronization of Escherichia coli using the stringent response, with fluorescence labeling assays for DNA content and replication [J].
Ferullo, Daniel J. ;
Cooper, Deani L. ;
Moore, Hayley R. ;
Lovett, Susan T. .
METHODS, 2009, 48 (01) :8-13
[12]   Gut microbiome structure and metabolic activity in inflammatory bowel disease [J].
Franzosa, Eric A. ;
Sirota-Madi, Alexandra ;
Avila-Pacheco, Julian ;
Fornelos, Nadine ;
Haiser, Henryj ;
Reinker, Stefan ;
Vatanen, Tommi ;
Hall, A. Brantley ;
Mallick, Himel ;
Mclver, Lauren J. ;
Sauk, Jenny S. ;
Wilson, Robin G. ;
Stevens, Betsy W. ;
Scott, Justin M. ;
Pierce, Kerry ;
Deik, Amy A. ;
Bullock, Kevin ;
Imhann, Floris ;
Porter, Jeffrey A. ;
Zhernakova, Alexandra ;
Fu, Jingyuan ;
Weersma, Rinse K. ;
Wijmenga, Cisca ;
Clish, Clary B. ;
Vlamakis, Hera ;
Huttenhower, Curtis ;
Xavier, Ramnik J. .
NATURE MICROBIOLOGY, 2019, 4 (02) :293-305
[13]   Relating the metatranscriptome and metagenome of the human gut [J].
Franzosa, Eric A. ;
Morgan, Xochitl C. ;
Segata, Nicola ;
Waldron, Levi ;
Reyes, Joshua ;
Earl, Ashlee M. ;
Giannoukos, Georgia ;
Boylan, Matthew R. ;
Ciulla, Dawn ;
Gevers, Dirk ;
Izard, Jacques ;
Garrett, Wendy S. ;
Chan, Andrew T. ;
Huttenhower, Curtis .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2014, 111 (22) :E2329-E2338
[14]   Metagenomic analysis of the human distal gut microbiome [J].
Gill, Steven R. ;
Pop, Mihai ;
DeBoy, Robert T. ;
Eckburg, Paul B. ;
Turnbaugh, Peter J. ;
Samuel, Buck S. ;
Gordon, Jeffrey I. ;
Relman, David A. ;
Fraser-Liggett, Claire M. ;
Nelson, Karen E. .
SCIENCE, 2006, 312 (5778) :1355-1359
[15]   Stem and progenitor cell division kinetics during postnatal mouse mammary gland development [J].
Giraddi, Rajshekhar R. ;
Shehata, Mona ;
Gallardo, Mercedes ;
Blasco, Maria A. ;
Simons, Benjamin D. ;
Stingl, John .
NATURE COMMUNICATIONS, 2015, 6
[16]   Evaluating the Genotoxic and Cytotoxic Effects of Thymidine Analogs, 5-Ethynyl-2′-Deoxyuridine and 5-Bromo-2′-Deoxyurdine to Mammalian Cells [J].
Haskins, Jeremy S. ;
Su, Cathy ;
Maeda, Junko ;
Walsh, Kade D. ;
Haskins, Alexis H. ;
Allum, Allison J. ;
Froning, Coral E. ;
Kato, Takamitsu A. .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2020, 21 (18) :1-17
[17]   Next-generation physiology approaches to study microbiome function at single cell level [J].
Hatzenpichler, Roland ;
Krukenberg, Viola ;
Spietz, Rachel L. ;
Jay, Zackary J. .
NATURE REVIEWS MICROBIOLOGY, 2020, 18 (04) :241-256
[18]   Illuminating vital surface molecules of symbionts in health and disease [J].
Hudak, Jason E. ;
Alvarez, David ;
Skelly, Ashwin ;
von Andrian, Ulrich H. ;
Kasper, Dennis L. .
NATURE MICROBIOLOGY, 2017, 2 (09)
[19]   THYMIDINE UPTAKE, THYMIDINE INCORPORATION, AND THYMIDINE KINASE-ACTIVITY IN MARINE BACTERIUM ISOLATES [J].
JEFFREY, WH ;
PAUL, JH .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1990, 56 (05) :1367-1372
[20]   Accurate and robust inference of microbial growth dynamics from metagenomic sequencing reveals personalized growth rates [J].
Joseph, Tyler A. ;
Chlenski, Philippe ;
Litman, Aviya ;
Korem, Tal ;
Pe'er, Itsik .
GENOME RESEARCH, 2022, 32 (03) :558-568