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Article ; Online: Cluster K mycobacteriophages

Welkin H Pope / Christina M Ferreira / Deborah Jacobs-Sera / Robert C Benjamin / Ariangela J Davis / Randall J DeJong / Sarah C R Elgin / Forrest R Guilfoile / Mark H Forsyth / Alexander D Harris / Samuel E Harvey / Lee E Hughes / Peter M Hynes / Arrykka S Jackson / Marilyn D Jalal / Elizabeth A MacMurray / Coreen M Manley / Molly J McDonough / Jordan L Mosier /
Larissa J Osterbann / Hannah S Rabinowitz / Corwin N Rhyan / Daniel A Russell / Margaret S Saha / Christopher D Shaffer / Stephanie E Simon / Erika F Sims / Isabel G Tovar / Emilie G Weisser / John T Wertz / Kathleen A Weston-Hafer / Kurt E Williamson / Bo Zhang / Steven G Cresawn / Paras Jain / Mariana Piuri / William R Jacobs / Roger W Hendrix / Graham F Hatfull

PLoS ONE, Vol 6, Iss 10, p e

insights into the evolutionary origins of mycobacteriophage TM4.

2011  Volume 26750

Abstract: Five newly isolated mycobacteriophages--Angelica, CrimD, Adephagia, Anaya, and Pixie--have similar genomic architectures to mycobacteriophage TM4, a previously characterized phage that is widely used in mycobacterial genetics. The nucleotide sequence ... ...

Abstract Five newly isolated mycobacteriophages--Angelica, CrimD, Adephagia, Anaya, and Pixie--have similar genomic architectures to mycobacteriophage TM4, a previously characterized phage that is widely used in mycobacterial genetics. The nucleotide sequence similarities warrant grouping these into Cluster K, with subdivision into three subclusters: K1, K2, and K3. Although the overall genome architectures of these phages are similar, TM4 appears to have lost at least two segments of its genome, a central region containing the integration apparatus, and a segment at the right end. This suggests that TM4 is a recent derivative of a temperate parent, resolving a long-standing conundrum about its biology, in that it was reportedly recovered from a lysogenic strain of Mycobacterium avium, but it is not capable of forming lysogens in any mycobacterial host. Like TM4, all of the Cluster K phages infect both fast- and slow-growing mycobacteria, and all of them--with the exception of TM4--form stable lysogens in both Mycobacterium smegmatis and Mycobacterium tuberculosis; immunity assays show that all five of these phages share the same immune specificity. TM4 infects these lysogens suggesting that it was either derived from a heteroimmune temperate parent or that it has acquired a virulent phenotype. We have also characterized a widely-used conditionally replicating derivative of TM4 and identified mutations conferring the temperature-sensitive phenotype. All of the Cluster K phages contain a series of well conserved 13 bp repeats associated with the translation initiation sites of a subset of the genes; approximately one half of these contain an additional sequence feature composed of imperfectly conserved 17 bp inverted repeats separated by a variable spacer. The K1 phages integrate into the host tmRNA and the Cluster K phages represent potential new tools for the genetics of M. tuberculosis and related species.
Keywords Medicine ; R ; Science ; Q
Subject code 572
Language English
Publishing date 2011-01-01T00:00:00Z
Publisher Public Library of Science (PLoS)
Document type Article ; Online
Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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