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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
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