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A Protocol to Engineer Bacteriophages for Live-Cell Imaging of Bacterial Prophage Induction Inside Mammalian Cells

The gut microbiome is dominated by lysogens, bacteria that carry bacterial viruses (phages). Uncovering the function of phages in the microbiome and observing interactions between phages, bacteria, and mammalian cells in real time in specific cell types are limited by the difficulty of engineering f...

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Detalles Bibliográficos
Autores principales: Bodner, Katie, Melkonian, Arin L., Covert, Markus W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7580223/
https://www.ncbi.nlm.nih.gov/pubmed/33111117
http://dx.doi.org/10.1016/j.xpro.2020.100084
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author Bodner, Katie
Melkonian, Arin L.
Covert, Markus W.
author_facet Bodner, Katie
Melkonian, Arin L.
Covert, Markus W.
author_sort Bodner, Katie
collection PubMed
description The gut microbiome is dominated by lysogens, bacteria that carry bacterial viruses (phages). Uncovering the function of phages in the microbiome and observing interactions between phages, bacteria, and mammalian cells in real time in specific cell types are limited by the difficulty of engineering fluorescent markers into large, lysogenic phage genomes. Here, we present a method to multiplex the engineering of life-cycle reporters into lysogenic phages and how to infect macrophages with engineered lysogens to study these interactions at the single-cell level. For complete details on the use and execution of this protocol, please refer to Bodner et al. (2020).
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spelling pubmed-75802232020-10-26 A Protocol to Engineer Bacteriophages for Live-Cell Imaging of Bacterial Prophage Induction Inside Mammalian Cells Bodner, Katie Melkonian, Arin L. Covert, Markus W. STAR Protoc Protocol The gut microbiome is dominated by lysogens, bacteria that carry bacterial viruses (phages). Uncovering the function of phages in the microbiome and observing interactions between phages, bacteria, and mammalian cells in real time in specific cell types are limited by the difficulty of engineering fluorescent markers into large, lysogenic phage genomes. Here, we present a method to multiplex the engineering of life-cycle reporters into lysogenic phages and how to infect macrophages with engineered lysogens to study these interactions at the single-cell level. For complete details on the use and execution of this protocol, please refer to Bodner et al. (2020). Elsevier 2020-08-07 /pmc/articles/PMC7580223/ /pubmed/33111117 http://dx.doi.org/10.1016/j.xpro.2020.100084 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Protocol
Bodner, Katie
Melkonian, Arin L.
Covert, Markus W.
A Protocol to Engineer Bacteriophages for Live-Cell Imaging of Bacterial Prophage Induction Inside Mammalian Cells
title A Protocol to Engineer Bacteriophages for Live-Cell Imaging of Bacterial Prophage Induction Inside Mammalian Cells
title_full A Protocol to Engineer Bacteriophages for Live-Cell Imaging of Bacterial Prophage Induction Inside Mammalian Cells
title_fullStr A Protocol to Engineer Bacteriophages for Live-Cell Imaging of Bacterial Prophage Induction Inside Mammalian Cells
title_full_unstemmed A Protocol to Engineer Bacteriophages for Live-Cell Imaging of Bacterial Prophage Induction Inside Mammalian Cells
title_short A Protocol to Engineer Bacteriophages for Live-Cell Imaging of Bacterial Prophage Induction Inside Mammalian Cells
title_sort protocol to engineer bacteriophages for live-cell imaging of bacterial prophage induction inside mammalian cells
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7580223/
https://www.ncbi.nlm.nih.gov/pubmed/33111117
http://dx.doi.org/10.1016/j.xpro.2020.100084
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