Cloning and manipulation of the Corynebacterium pseudotuberculosis recA gene for live vaccine vector development

Corynebacterium pseudotuberculosis is an intracellular bacterial pathogen causing a chronic abscessing disease in sheep and goats called caseous lymphadenitis. We are developing this bacterial species as a live vector system to deliver vaccine antigens to the animal immune system. Foreign genes expr...

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Autor principal: Simmons, Cameron
Formato: Journal Article
Lenguaje:inglés
Publicado: 2018
Acceso en línea:https://demo7.dspace.org/handle/123456789/81
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author Simmons, Cameron
author_browse Simmons, Cameron
author_facet Simmons, Cameron
author_sort Simmons, Cameron
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description Corynebacterium pseudotuberculosis is an intracellular bacterial pathogen causing a chronic abscessing disease in sheep and goats called caseous lymphadenitis. We are developing this bacterial species as a live vector system to deliver vaccine antigens to the animal immune system. Foreign genes expressed in bacterial hosts can be unstable so we undertook to delete the C. pseudotuberculosis chromosomal recA gene to determine whether a recA- background would reduce the frequency of recombination in cloned DNA. Homologous DNA recombination within an isogenic recA- C. pseudotuberculosis was 10-12-fold lower than that in the recA+ parental strain. Importantly, the recA mutation had no detectable affect upon the virulence of C. pseudotuberculosis in a mouse model. Taken together these results suggest that a recA- background may be useful in the further development of C. pseudotuberculosis as a vaccine vector.
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spelling oai:localhost:123456789-812021-04-07T16:30:07Z Cloning and manipulation of the Corynebacterium pseudotuberculosis recA gene for live vaccine vector development Simmons, Cameron Corynebacterium pseudotuberculosis is an intracellular bacterial pathogen causing a chronic abscessing disease in sheep and goats called caseous lymphadenitis. We are developing this bacterial species as a live vector system to deliver vaccine antigens to the animal immune system. Foreign genes expressed in bacterial hosts can be unstable so we undertook to delete the C. pseudotuberculosis chromosomal recA gene to determine whether a recA- background would reduce the frequency of recombination in cloned DNA. Homologous DNA recombination within an isogenic recA- C. pseudotuberculosis was 10-12-fold lower than that in the recA+ parental strain. Importantly, the recA mutation had no detectable affect upon the virulence of C. pseudotuberculosis in a mouse model. Taken together these results suggest that a recA- background may be useful in the further development of C. pseudotuberculosis as a vaccine vector. 2018-09-14T11:14:52Z 2017-07-05T02:20:43Z 2018-09-14T11:14:52Z 1996-09-01 Journal Article https://demo7.dspace.org/handle/123456789/81 English
spellingShingle Simmons, Cameron
Cloning and manipulation of the Corynebacterium pseudotuberculosis recA gene for live vaccine vector development
title Cloning and manipulation of the Corynebacterium pseudotuberculosis recA gene for live vaccine vector development
title_full Cloning and manipulation of the Corynebacterium pseudotuberculosis recA gene for live vaccine vector development
title_fullStr Cloning and manipulation of the Corynebacterium pseudotuberculosis recA gene for live vaccine vector development
title_full_unstemmed Cloning and manipulation of the Corynebacterium pseudotuberculosis recA gene for live vaccine vector development
title_short Cloning and manipulation of the Corynebacterium pseudotuberculosis recA gene for live vaccine vector development
title_sort cloning and manipulation of the corynebacterium pseudotuberculosis reca gene for live vaccine vector development
url https://demo7.dspace.org/handle/123456789/81
work_keys_str_mv AT simmonscameron cloningandmanipulationofthecorynebacteriumpseudotuberculosisrecageneforlivevaccinevectordevelopment