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Bacterial variability in the mammalian gut captured by a single-cell synthetic oscillator

Synthetic gene oscillators have the potential to control timed functions and periodic gene expression in engineered cells. Such oscillators have been refined in bacteria in vitro, however, these systems have lacked the robustness and precision necessary for applications in complex in vivo environmen...

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Autores principales: Riglar, David T., Richmond, David L., Potvin-Trottier, Laurent, Verdegaal, Andrew A., Naydich, Alexander D., Bakshi, Somenath, Leoncini, Emanuele, Lyon, Lorena G., Paulsson, Johan, Silver, Pamela A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6789134/
https://www.ncbi.nlm.nih.gov/pubmed/31604953
http://dx.doi.org/10.1038/s41467-019-12638-z
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author Riglar, David T.
Richmond, David L.
Potvin-Trottier, Laurent
Verdegaal, Andrew A.
Naydich, Alexander D.
Bakshi, Somenath
Leoncini, Emanuele
Lyon, Lorena G.
Paulsson, Johan
Silver, Pamela A.
author_facet Riglar, David T.
Richmond, David L.
Potvin-Trottier, Laurent
Verdegaal, Andrew A.
Naydich, Alexander D.
Bakshi, Somenath
Leoncini, Emanuele
Lyon, Lorena G.
Paulsson, Johan
Silver, Pamela A.
author_sort Riglar, David T.
collection PubMed
description Synthetic gene oscillators have the potential to control timed functions and periodic gene expression in engineered cells. Such oscillators have been refined in bacteria in vitro, however, these systems have lacked the robustness and precision necessary for applications in complex in vivo environments, such as the mammalian gut. Here, we demonstrate the implementation of a synthetic oscillator capable of keeping robust time in the mouse gut over periods of days. The oscillations provide a marker of bacterial growth at a single-cell level enabling quantification of bacterial dynamics in response to inflammation and underlying variations in the gut microbiota. Our work directly detects increased bacterial growth heterogeneity during disease and differences between spatial niches in the gut, demonstrating the deployment of a precise engineered genetic oscillator in real-life settings.
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spelling pubmed-67891342019-10-15 Bacterial variability in the mammalian gut captured by a single-cell synthetic oscillator Riglar, David T. Richmond, David L. Potvin-Trottier, Laurent Verdegaal, Andrew A. Naydich, Alexander D. Bakshi, Somenath Leoncini, Emanuele Lyon, Lorena G. Paulsson, Johan Silver, Pamela A. Nat Commun Article Synthetic gene oscillators have the potential to control timed functions and periodic gene expression in engineered cells. Such oscillators have been refined in bacteria in vitro, however, these systems have lacked the robustness and precision necessary for applications in complex in vivo environments, such as the mammalian gut. Here, we demonstrate the implementation of a synthetic oscillator capable of keeping robust time in the mouse gut over periods of days. The oscillations provide a marker of bacterial growth at a single-cell level enabling quantification of bacterial dynamics in response to inflammation and underlying variations in the gut microbiota. Our work directly detects increased bacterial growth heterogeneity during disease and differences between spatial niches in the gut, demonstrating the deployment of a precise engineered genetic oscillator in real-life settings. Nature Publishing Group UK 2019-10-11 /pmc/articles/PMC6789134/ /pubmed/31604953 http://dx.doi.org/10.1038/s41467-019-12638-z Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Riglar, David T.
Richmond, David L.
Potvin-Trottier, Laurent
Verdegaal, Andrew A.
Naydich, Alexander D.
Bakshi, Somenath
Leoncini, Emanuele
Lyon, Lorena G.
Paulsson, Johan
Silver, Pamela A.
Bacterial variability in the mammalian gut captured by a single-cell synthetic oscillator
title Bacterial variability in the mammalian gut captured by a single-cell synthetic oscillator
title_full Bacterial variability in the mammalian gut captured by a single-cell synthetic oscillator
title_fullStr Bacterial variability in the mammalian gut captured by a single-cell synthetic oscillator
title_full_unstemmed Bacterial variability in the mammalian gut captured by a single-cell synthetic oscillator
title_short Bacterial variability in the mammalian gut captured by a single-cell synthetic oscillator
title_sort bacterial variability in the mammalian gut captured by a single-cell synthetic oscillator
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6789134/
https://www.ncbi.nlm.nih.gov/pubmed/31604953
http://dx.doi.org/10.1038/s41467-019-12638-z
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