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The Caulobacter crescentus phage phiCbK: genomics of a canonical phage

BACKGROUND: The bacterium Caulobacter crescentus is a popular model for the study of cell cycle regulation and senescence. The large prolate siphophage phiCbK has been an important tool in C. crescentus biology, and has been studied in its own right as a model for viral morphogenesis. Although a sys...

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Autores principales: Gill, Jason J, Berry, Joel D, Russell, William K, Lessor, Lauren, Escobar-Garcia, Diego A, Hernandez, Daniel, Kane, Ashley, Keene, Jennifer, Maddox, Matthew, Martin, Rebecca, Mohan, Sheba, Thorn, Ashlyn M, Russell, David H, Young, Ry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3556154/
https://www.ncbi.nlm.nih.gov/pubmed/23050599
http://dx.doi.org/10.1186/1471-2164-13-542
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author Gill, Jason J
Berry, Joel D
Russell, William K
Lessor, Lauren
Escobar-Garcia, Diego A
Hernandez, Daniel
Kane, Ashley
Keene, Jennifer
Maddox, Matthew
Martin, Rebecca
Mohan, Sheba
Thorn, Ashlyn M
Russell, David H
Young, Ry
author_facet Gill, Jason J
Berry, Joel D
Russell, William K
Lessor, Lauren
Escobar-Garcia, Diego A
Hernandez, Daniel
Kane, Ashley
Keene, Jennifer
Maddox, Matthew
Martin, Rebecca
Mohan, Sheba
Thorn, Ashlyn M
Russell, David H
Young, Ry
author_sort Gill, Jason J
collection PubMed
description BACKGROUND: The bacterium Caulobacter crescentus is a popular model for the study of cell cycle regulation and senescence. The large prolate siphophage phiCbK has been an important tool in C. crescentus biology, and has been studied in its own right as a model for viral morphogenesis. Although a system of some interest, to date little genomic information is available on phiCbK or its relatives. RESULTS: Five novel phiCbK-like C. crescentus bacteriophages, CcrMagneto, CcrSwift, CcrKarma, CcrRogue and CcrColossus, were isolated from the environment. The genomes of phage phiCbK and these five environmental phage isolates were obtained by 454 pyrosequencing. The phiCbK-like phage genomes range in size from 205 kb encoding 318 proteins (phiCbK) to 280 kb encoding 448 proteins (CcrColossus), and were found to contain nonpermuted terminal redundancies of 10 to 17 kb. A novel method of terminal ligation was developed to map genomic termini, which confirmed termini predicted by coverage analysis. This suggests that sequence coverage discontinuities may be useable as predictors of genomic termini in phage genomes. Genomic modules encoding virion morphogenesis, lysis and DNA replication proteins were identified. The phiCbK-like phages were also found to encode a number of intriguing proteins; all contain a clearly T7-like DNA polymerase, and five of the six encode a possible homolog of the C. crescentus cell cycle regulator GcrA, which may allow the phage to alter the host cell’s replicative state. The structural proteome of phage phiCbK was determined, identifying the portal, major and minor capsid proteins, the tail tape measure and possible tail fiber proteins. All six phage genomes are clearly related; phiCbK, CcrMagneto, CcrSwift, CcrKarma and CcrRogue form a group related at the DNA level, while CcrColossus is more diverged but retains significant similarity at the protein level. CONCLUSIONS: Due to their lack of any apparent relationship to other described phages, this group is proposed as the founding cohort of a new phage type, the phiCbK-like phages. This work will serve as a foundation for future studies on morphogenesis, infection and phage-host interactions in C. crescentus.
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spelling pubmed-35561542013-01-31 The Caulobacter crescentus phage phiCbK: genomics of a canonical phage Gill, Jason J Berry, Joel D Russell, William K Lessor, Lauren Escobar-Garcia, Diego A Hernandez, Daniel Kane, Ashley Keene, Jennifer Maddox, Matthew Martin, Rebecca Mohan, Sheba Thorn, Ashlyn M Russell, David H Young, Ry BMC Genomics Research Article BACKGROUND: The bacterium Caulobacter crescentus is a popular model for the study of cell cycle regulation and senescence. The large prolate siphophage phiCbK has been an important tool in C. crescentus biology, and has been studied in its own right as a model for viral morphogenesis. Although a system of some interest, to date little genomic information is available on phiCbK or its relatives. RESULTS: Five novel phiCbK-like C. crescentus bacteriophages, CcrMagneto, CcrSwift, CcrKarma, CcrRogue and CcrColossus, were isolated from the environment. The genomes of phage phiCbK and these five environmental phage isolates were obtained by 454 pyrosequencing. The phiCbK-like phage genomes range in size from 205 kb encoding 318 proteins (phiCbK) to 280 kb encoding 448 proteins (CcrColossus), and were found to contain nonpermuted terminal redundancies of 10 to 17 kb. A novel method of terminal ligation was developed to map genomic termini, which confirmed termini predicted by coverage analysis. This suggests that sequence coverage discontinuities may be useable as predictors of genomic termini in phage genomes. Genomic modules encoding virion morphogenesis, lysis and DNA replication proteins were identified. The phiCbK-like phages were also found to encode a number of intriguing proteins; all contain a clearly T7-like DNA polymerase, and five of the six encode a possible homolog of the C. crescentus cell cycle regulator GcrA, which may allow the phage to alter the host cell’s replicative state. The structural proteome of phage phiCbK was determined, identifying the portal, major and minor capsid proteins, the tail tape measure and possible tail fiber proteins. All six phage genomes are clearly related; phiCbK, CcrMagneto, CcrSwift, CcrKarma and CcrRogue form a group related at the DNA level, while CcrColossus is more diverged but retains significant similarity at the protein level. CONCLUSIONS: Due to their lack of any apparent relationship to other described phages, this group is proposed as the founding cohort of a new phage type, the phiCbK-like phages. This work will serve as a foundation for future studies on morphogenesis, infection and phage-host interactions in C. crescentus. BioMed Central 2012-10-10 /pmc/articles/PMC3556154/ /pubmed/23050599 http://dx.doi.org/10.1186/1471-2164-13-542 Text en Copyright ©2012 Gill et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Gill, Jason J
Berry, Joel D
Russell, William K
Lessor, Lauren
Escobar-Garcia, Diego A
Hernandez, Daniel
Kane, Ashley
Keene, Jennifer
Maddox, Matthew
Martin, Rebecca
Mohan, Sheba
Thorn, Ashlyn M
Russell, David H
Young, Ry
The Caulobacter crescentus phage phiCbK: genomics of a canonical phage
title The Caulobacter crescentus phage phiCbK: genomics of a canonical phage
title_full The Caulobacter crescentus phage phiCbK: genomics of a canonical phage
title_fullStr The Caulobacter crescentus phage phiCbK: genomics of a canonical phage
title_full_unstemmed The Caulobacter crescentus phage phiCbK: genomics of a canonical phage
title_short The Caulobacter crescentus phage phiCbK: genomics of a canonical phage
title_sort caulobacter crescentus phage phicbk: genomics of a canonical phage
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3556154/
https://www.ncbi.nlm.nih.gov/pubmed/23050599
http://dx.doi.org/10.1186/1471-2164-13-542
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