Cargando…
Isolation of the Bacteriophage DinoHI from Dichelobacter nodosus and its Interactions with other Integrated Genetic Elements
The Gram-negative anaerobic pathogen Dichelobacter nodosus carries several genetic elements that integrate into the chromosome. These include the intA, intB, intC and intD elements, which integrate adjacent to csrA and pnpA, two putative global regulators of virulence and the virulence-related locus...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Bentham Science Publishers Ltd
2008
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2593044/ https://www.ncbi.nlm.nih.gov/pubmed/19088904 http://dx.doi.org/10.2174/1874285800802010001 |
_version_ | 1782161608503459840 |
---|---|
author | Cheetham, Brian F Parker, Dane Bloomfield, Garry A Shaw, Bruce E Sutherland, Megan Hyman, Jessica A Druitt, Jenifer Kennan, Ruth M Rood, Julian I Katz, Margaret E |
author_facet | Cheetham, Brian F Parker, Dane Bloomfield, Garry A Shaw, Bruce E Sutherland, Megan Hyman, Jessica A Druitt, Jenifer Kennan, Ruth M Rood, Julian I Katz, Margaret E |
author_sort | Cheetham, Brian F |
collection | PubMed |
description | The Gram-negative anaerobic pathogen Dichelobacter nodosus carries several genetic elements that integrate into the chromosome. These include the intA, intB, intC and intD elements, which integrate adjacent to csrA and pnpA, two putative global regulators of virulence and the virulence-related locus, vrl, which integrates into ssrA. Treatment of D. nodosus strains with ultraviolet light resulted in the isolation of DinoHI, a member of the Siphoviridae and the first bacteriophage to be identified in D. nodosus. Part of the DinoHI genome containing the packaging site is found in all D. nodosus strains tested and is located at the end of the vrl, suggesting a role for DinoHI in the transfer of the vrl by transduction. Like the intB element, the DinoHI genome contains a copy of regA which has similarity to the repressors of lambdoid bacteriophages, suggesting that the maintenance of DinoHI and the intB element may be co-ordinately controlled. |
format | Text |
id | pubmed-2593044 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Bentham Science Publishers Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-25930442008-12-16 Isolation of the Bacteriophage DinoHI from Dichelobacter nodosus and its Interactions with other Integrated Genetic Elements Cheetham, Brian F Parker, Dane Bloomfield, Garry A Shaw, Bruce E Sutherland, Megan Hyman, Jessica A Druitt, Jenifer Kennan, Ruth M Rood, Julian I Katz, Margaret E Open Microbiol J Article The Gram-negative anaerobic pathogen Dichelobacter nodosus carries several genetic elements that integrate into the chromosome. These include the intA, intB, intC and intD elements, which integrate adjacent to csrA and pnpA, two putative global regulators of virulence and the virulence-related locus, vrl, which integrates into ssrA. Treatment of D. nodosus strains with ultraviolet light resulted in the isolation of DinoHI, a member of the Siphoviridae and the first bacteriophage to be identified in D. nodosus. Part of the DinoHI genome containing the packaging site is found in all D. nodosus strains tested and is located at the end of the vrl, suggesting a role for DinoHI in the transfer of the vrl by transduction. Like the intB element, the DinoHI genome contains a copy of regA which has similarity to the repressors of lambdoid bacteriophages, suggesting that the maintenance of DinoHI and the intB element may be co-ordinately controlled. Bentham Science Publishers Ltd 2008-01-14 /pmc/articles/PMC2593044/ /pubmed/19088904 http://dx.doi.org/10.2174/1874285800802010001 Text en 2008 Bentham Science Publishers Ltd. http://creativecommons.org/licenses/by/2.5/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.5/), which permits unrestrictive use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Cheetham, Brian F Parker, Dane Bloomfield, Garry A Shaw, Bruce E Sutherland, Megan Hyman, Jessica A Druitt, Jenifer Kennan, Ruth M Rood, Julian I Katz, Margaret E Isolation of the Bacteriophage DinoHI from Dichelobacter nodosus and its Interactions with other Integrated Genetic Elements |
title | Isolation of the Bacteriophage DinoHI from Dichelobacter nodosus and its Interactions with other Integrated Genetic Elements |
title_full | Isolation of the Bacteriophage DinoHI from Dichelobacter nodosus and its Interactions with other Integrated Genetic Elements |
title_fullStr | Isolation of the Bacteriophage DinoHI from Dichelobacter nodosus and its Interactions with other Integrated Genetic Elements |
title_full_unstemmed | Isolation of the Bacteriophage DinoHI from Dichelobacter nodosus and its Interactions with other Integrated Genetic Elements |
title_short | Isolation of the Bacteriophage DinoHI from Dichelobacter nodosus and its Interactions with other Integrated Genetic Elements |
title_sort | isolation of the bacteriophage dinohi from dichelobacter nodosus and its interactions with other integrated genetic elements |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2593044/ https://www.ncbi.nlm.nih.gov/pubmed/19088904 http://dx.doi.org/10.2174/1874285800802010001 |
work_keys_str_mv | AT cheethambrianf isolationofthebacteriophagedinohifromdichelobacternodosusanditsinteractionswithotherintegratedgeneticelements AT parkerdane isolationofthebacteriophagedinohifromdichelobacternodosusanditsinteractionswithotherintegratedgeneticelements AT bloomfieldgarrya isolationofthebacteriophagedinohifromdichelobacternodosusanditsinteractionswithotherintegratedgeneticelements AT shawbrucee isolationofthebacteriophagedinohifromdichelobacternodosusanditsinteractionswithotherintegratedgeneticelements AT sutherlandmegan isolationofthebacteriophagedinohifromdichelobacternodosusanditsinteractionswithotherintegratedgeneticelements AT hymanjessicaa isolationofthebacteriophagedinohifromdichelobacternodosusanditsinteractionswithotherintegratedgeneticelements AT druittjenifer isolationofthebacteriophagedinohifromdichelobacternodosusanditsinteractionswithotherintegratedgeneticelements AT kennanruthm isolationofthebacteriophagedinohifromdichelobacternodosusanditsinteractionswithotherintegratedgeneticelements AT roodjuliani isolationofthebacteriophagedinohifromdichelobacternodosusanditsinteractionswithotherintegratedgeneticelements AT katzmargarete isolationofthebacteriophagedinohifromdichelobacternodosusanditsinteractionswithotherintegratedgeneticelements |