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Genetic Manipulation of Francisella Tularensis

Francisella tularensis is a facultative intracellular pathogen that causes the disease tularemia. F. tularensis subsp. tularensis causes the most severe disease in humans and has been classified as a Category A select agent and potential bioweapon. There is currently no vaccine approved for human us...

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Detalles Bibliográficos
Autores principales: Zogaj, Xhavit, Klose, Karl E.
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3095392/
https://www.ncbi.nlm.nih.gov/pubmed/21607086
http://dx.doi.org/10.3389/fmicb.2010.00142
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author Zogaj, Xhavit
Klose, Karl E.
author_facet Zogaj, Xhavit
Klose, Karl E.
author_sort Zogaj, Xhavit
collection PubMed
description Francisella tularensis is a facultative intracellular pathogen that causes the disease tularemia. F. tularensis subsp. tularensis causes the most severe disease in humans and has been classified as a Category A select agent and potential bioweapon. There is currently no vaccine approved for human use, making genetic manipulation of this organism critical to unraveling the genetic basis of pathogenesis and developing countermeasures against tularemia. The development of genetic techniques applicable to F. tularensis have lagged behind those routinely used for other bacteria, primarily due to lack of research and the restricted nature of the biocontainment required for studying this pathogen. However, in recent years, genetic techniques, such as transposon mutagenesis and targeted gene disruption, have been developed, that have had a dramatic impact on our understanding of the genetic basis of F. tularensis virulence. In this review, we describe some of the methods developed for genetic manipulation of F. tularensis.
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spelling pubmed-30953922011-05-23 Genetic Manipulation of Francisella Tularensis Zogaj, Xhavit Klose, Karl E. Front Microbiol Microbiology Francisella tularensis is a facultative intracellular pathogen that causes the disease tularemia. F. tularensis subsp. tularensis causes the most severe disease in humans and has been classified as a Category A select agent and potential bioweapon. There is currently no vaccine approved for human use, making genetic manipulation of this organism critical to unraveling the genetic basis of pathogenesis and developing countermeasures against tularemia. The development of genetic techniques applicable to F. tularensis have lagged behind those routinely used for other bacteria, primarily due to lack of research and the restricted nature of the biocontainment required for studying this pathogen. However, in recent years, genetic techniques, such as transposon mutagenesis and targeted gene disruption, have been developed, that have had a dramatic impact on our understanding of the genetic basis of F. tularensis virulence. In this review, we describe some of the methods developed for genetic manipulation of F. tularensis. Frontiers Research Foundation 2011-01-05 /pmc/articles/PMC3095392/ /pubmed/21607086 http://dx.doi.org/10.3389/fmicb.2010.00142 Text en Copyright © 2011 Zogaj and Klose. http://www.frontiersin.org/licenseagreement This is an open-access article subject to an exclusive license agreement between the authors and the Frontiers Research Foundation, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.
spellingShingle Microbiology
Zogaj, Xhavit
Klose, Karl E.
Genetic Manipulation of Francisella Tularensis
title Genetic Manipulation of Francisella Tularensis
title_full Genetic Manipulation of Francisella Tularensis
title_fullStr Genetic Manipulation of Francisella Tularensis
title_full_unstemmed Genetic Manipulation of Francisella Tularensis
title_short Genetic Manipulation of Francisella Tularensis
title_sort genetic manipulation of francisella tularensis
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3095392/
https://www.ncbi.nlm.nih.gov/pubmed/21607086
http://dx.doi.org/10.3389/fmicb.2010.00142
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