Establishment and characterization of stable, diverse, fecal-derived in vitro microbial communities that model the intestinal microbiota.
Autor: | Aranda-Díaz A; Department of Bioengineering, Stanford University, Stanford, CA 94305, USA., Ng KM; Department of Bioengineering, Stanford University, Stanford, CA 94305, USA., Thomsen T; Department of Bioengineering, Stanford University, Stanford, CA 94305, USA., Real-Ramírez I; Department of Bioengineering, Stanford University, Stanford, CA 94305, USA., Dahan D; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA., Dittmar S; Department of Bioengineering, Stanford University, Stanford, CA 94305, USA., Gonzalez CG; Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, CA 94305, USA., Chavez T; Department of Bioengineering, Stanford University, Stanford, CA 94305, USA., Vasquez KS; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA., Nguyen TH; Department of Bioengineering, Stanford University, Stanford, CA 94305, USA., Yu FB; Chan Zuckerberg Biohub, San Francisco, CA 94158, USA., Higginbottom SK; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA., Neff NF; Chan Zuckerberg Biohub, San Francisco, CA 94158, USA., Elias JE; Chan Zuckerberg Biohub, San Francisco, CA 94158, USA., Sonnenburg JL; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA; Chan Zuckerberg Biohub, San Francisco, CA 94158, USA., Huang KC; Department of Bioengineering, Stanford University, Stanford, CA 94305, USA; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA; Chan Zuckerberg Biohub, San Francisco, CA 94158, USA. Electronic address: kchuang@stanford.edu. |
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Jazyk: | angličtina |
Zdroj: | Cell host & microbe [Cell Host Microbe] 2022 Feb 09; Vol. 30 (2), pp. 260-272.e5. Date of Electronic Publication: 2022 Jan 19. |
DOI: | 10.1016/j.chom.2021.12.008 |
Abstrakt: | Efforts to probe the role of the gut microbiota in disease would benefit from a system in which patient-derived bacterial communities can be studied at scale. We addressed this by validating a strategy to propagate phylogenetically complex, diverse, stable, and highly reproducible stool-derived communities in vitro. We generated hundreds of in vitro communities cultured from diverse stool samples in various media; certain media generally preserved inoculum composition, and inocula from different subjects yielded source-specific community compositions. Upon colonization of germ-free mice, community composition was maintained, and the host proteome resembled the host from which the community was derived. Treatment with ciprofloxacin in vivo increased susceptibility to Salmonella invasion in vitro, and the in vitro response to ciprofloxacin was predictive of compositional changes observed in vivo, including the resilience and sensitivity of each Bacteroides species. These findings demonstrate that stool-derived in vitro communities can serve as a powerful system for microbiota research. Competing Interests: Declaration of interests The authors declare no competing interests. (Copyright © 2021. Published by Elsevier Inc.) |
Databáze: | MEDLINE |
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