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Editing the microbiome the CRISPR way

Our bodies are colonized by a complex ecosystem of bacteria, unicellular eukaryotes and their viruses that together play a major role in our health. Over the past few years tools derived from the prokaryotic immune system known as CRISPR-Cas have empowered researchers to modify and study organisms w...

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Detalles Bibliográficos
Autores principales: Ramachandran, Gayetri, Bikard, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6452265/
https://www.ncbi.nlm.nih.gov/pubmed/30905295
http://dx.doi.org/10.1098/rstb.2018.0103
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author Ramachandran, Gayetri
Bikard, David
author_facet Ramachandran, Gayetri
Bikard, David
author_sort Ramachandran, Gayetri
collection PubMed
description Our bodies are colonized by a complex ecosystem of bacteria, unicellular eukaryotes and their viruses that together play a major role in our health. Over the past few years tools derived from the prokaryotic immune system known as CRISPR-Cas have empowered researchers to modify and study organisms with unprecedented ease and efficiency. Here we discuss how various types of CRISPR-Cas systems can be used to modify the genome of gut microorganisms and bacteriophages. CRISPR-Cas systems can also be delivered to bacterial population and programmed to specifically eliminate members of the microbiome. Finally, engineered CRISPR-Cas systems can be used to control gene expression and modulate the production of metabolites and proteins. Together these tools provide exciting opportunities to investigate the complex interplay between members of the microbiome and our bodies, and present new avenues for the development of drugs that target the microbiome. This article is part of a discussion meeting issue ‘The ecology and evolution of prokaryotic CRISPR-Cas adaptive immune systems’.
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spelling pubmed-64522652019-04-18 Editing the microbiome the CRISPR way Ramachandran, Gayetri Bikard, David Philos Trans R Soc Lond B Biol Sci Articles Our bodies are colonized by a complex ecosystem of bacteria, unicellular eukaryotes and their viruses that together play a major role in our health. Over the past few years tools derived from the prokaryotic immune system known as CRISPR-Cas have empowered researchers to modify and study organisms with unprecedented ease and efficiency. Here we discuss how various types of CRISPR-Cas systems can be used to modify the genome of gut microorganisms and bacteriophages. CRISPR-Cas systems can also be delivered to bacterial population and programmed to specifically eliminate members of the microbiome. Finally, engineered CRISPR-Cas systems can be used to control gene expression and modulate the production of metabolites and proteins. Together these tools provide exciting opportunities to investigate the complex interplay between members of the microbiome and our bodies, and present new avenues for the development of drugs that target the microbiome. This article is part of a discussion meeting issue ‘The ecology and evolution of prokaryotic CRISPR-Cas adaptive immune systems’. The Royal Society 2019-05-13 2019-03-25 /pmc/articles/PMC6452265/ /pubmed/30905295 http://dx.doi.org/10.1098/rstb.2018.0103 Text en © 2019 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Articles
Ramachandran, Gayetri
Bikard, David
Editing the microbiome the CRISPR way
title Editing the microbiome the CRISPR way
title_full Editing the microbiome the CRISPR way
title_fullStr Editing the microbiome the CRISPR way
title_full_unstemmed Editing the microbiome the CRISPR way
title_short Editing the microbiome the CRISPR way
title_sort editing the microbiome the crispr way
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6452265/
https://www.ncbi.nlm.nih.gov/pubmed/30905295
http://dx.doi.org/10.1098/rstb.2018.0103
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