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An efficient and versatile CRISPR-Cas9 system for genetic manipulation of multi-drug resistant Klebsiella pneumoniae

Multi-drug resistant (MDR) Klebsiella pneumoniae remains an urgent public health threat. While whole-genome sequencing has helped identify genetic changes underlying resistance, functional validation remains difficult due to a lack of genetic manipulation systems for MDR K. pneumoniae. CRISPR-Cas9 h...

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Detalles Bibliográficos
Autores principales: McConville, Thomas H., Giddins, Marla J., Uhlemann, Anne-Catrin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7941085/
https://www.ncbi.nlm.nih.gov/pubmed/33733242
http://dx.doi.org/10.1016/j.xpro.2021.100373
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author McConville, Thomas H.
Giddins, Marla J.
Uhlemann, Anne-Catrin
author_facet McConville, Thomas H.
Giddins, Marla J.
Uhlemann, Anne-Catrin
author_sort McConville, Thomas H.
collection PubMed
description Multi-drug resistant (MDR) Klebsiella pneumoniae remains an urgent public health threat. While whole-genome sequencing has helped identify genetic changes underlying resistance, functional validation remains difficult due to a lack of genetic manipulation systems for MDR K. pneumoniae. CRISPR-Cas9 has revolutionized molecular biology, but its use was only recently adapted in bacteria by overcoming the lack of genetic repair systems. We describe a CRISPR-Cas9/lambda recombineering system utilizing a zeocin resistance cassette allowing efficient and versatile genetic manipulation of K. pneumoniae. For complete details on the use and execution of this protocol, please refer to McConville et al. (2020).
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spelling pubmed-79410852021-03-16 An efficient and versatile CRISPR-Cas9 system for genetic manipulation of multi-drug resistant Klebsiella pneumoniae McConville, Thomas H. Giddins, Marla J. Uhlemann, Anne-Catrin STAR Protoc Protocol Multi-drug resistant (MDR) Klebsiella pneumoniae remains an urgent public health threat. While whole-genome sequencing has helped identify genetic changes underlying resistance, functional validation remains difficult due to a lack of genetic manipulation systems for MDR K. pneumoniae. CRISPR-Cas9 has revolutionized molecular biology, but its use was only recently adapted in bacteria by overcoming the lack of genetic repair systems. We describe a CRISPR-Cas9/lambda recombineering system utilizing a zeocin resistance cassette allowing efficient and versatile genetic manipulation of K. pneumoniae. For complete details on the use and execution of this protocol, please refer to McConville et al. (2020). Elsevier 2021-03-06 /pmc/articles/PMC7941085/ /pubmed/33733242 http://dx.doi.org/10.1016/j.xpro.2021.100373 Text en © 2021 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
McConville, Thomas H.
Giddins, Marla J.
Uhlemann, Anne-Catrin
An efficient and versatile CRISPR-Cas9 system for genetic manipulation of multi-drug resistant Klebsiella pneumoniae
title An efficient and versatile CRISPR-Cas9 system for genetic manipulation of multi-drug resistant Klebsiella pneumoniae
title_full An efficient and versatile CRISPR-Cas9 system for genetic manipulation of multi-drug resistant Klebsiella pneumoniae
title_fullStr An efficient and versatile CRISPR-Cas9 system for genetic manipulation of multi-drug resistant Klebsiella pneumoniae
title_full_unstemmed An efficient and versatile CRISPR-Cas9 system for genetic manipulation of multi-drug resistant Klebsiella pneumoniae
title_short An efficient and versatile CRISPR-Cas9 system for genetic manipulation of multi-drug resistant Klebsiella pneumoniae
title_sort efficient and versatile crispr-cas9 system for genetic manipulation of multi-drug resistant klebsiella pneumoniae
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7941085/
https://www.ncbi.nlm.nih.gov/pubmed/33733242
http://dx.doi.org/10.1016/j.xpro.2021.100373
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