Literature DB >> 15476873

Molecular and transcriptional analysis of the temperate lactococcal bacteriophage Tuc2009.

Jos F M L Seegers1, Stephen Mc Grath, Mary O'Connell-Motherway, Elke K Arendt, Maarten van de Guchte, Martina Creaven, Gerald F Fitzgerald, Douwe van Sinderen.   

Abstract

The genome of bacteriophage Tuc2009 consists of 38347 base pairs on which 57 open reading frames (ORFs) were identified, divided in two oppositely transcribed regions. The leftward-transcribed region harbors three ORFs, two of which are involved in the establishment of lysogeny. The rightward-transcribed region contains 54 ORFs, which are assumed to be required for the lytic life cycle. An exception to the above organization is ORF 10, of unknown function, located within the rightward-transcribed region that has an orientation opposite to the ORFs surrounding it. Transcriptional analysis of the Tuc2009 genome following infection of a sensitive host revealed that most ORFs are transcribed in a sequential manner. ORFs that are presumed to form (part of) the genetic switch along with the superinfection exclusion-encoding gene are transcribed immediately after infection, followed by transcription of the presumed replication region. Subsequent to this, several small transcripts could be identified followed by a single 24-kb transcript. This latter transcript was shown to specify most of the identified structural proteins as well as two proteins required for host lysis. Interestingly, the 24-kb mRNA was shown to undergo splicing through the activity of a type I intron whose removal from the mRNA resulted in the formation of an ORF specifying a major structural protein. Primer extension analysis was employed to identify the 5' ends of mRNA transcripts and the genome and transcriptional data are discussed in relation to other lactococcal bacteriophages.

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Year:  2004        PMID: 15476873     DOI: 10.1016/j.virol.2004.07.003

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  24 in total

1.  Identification of the lower baseplate protein as the antireceptor of the temperate lactococcal bacteriophages TP901-1 and Tuc2009.

Authors:  Christina S Vegge; Finn K Vogensen; Stephen Mc Grath; Horst Neve; Douwe van Sinderen; Lone Brøndsted
Journal:  J Bacteriol       Date:  2006-01       Impact factor: 3.490

2.  Anatomy of a lactococcal phage tail.

Authors:  Stephen Mc Grath; Horst Neve; Jos F M L Seegers; Robyn Eijlander; Christina S Vegge; Lone Brøndsted; Knut J Heller; Gerald F Fitzgerald; Finn K Vogensen; Douwe van Sinderen
Journal:  J Bacteriol       Date:  2006-06       Impact factor: 3.490

3.  Genome sequence and global gene expression of Q54, a new phage species linking the 936 and c2 phage species of Lactococcus lactis.

Authors:  Louis-Charles Fortier; Ali Bransi; Sylvain Moineau
Journal:  J Bacteriol       Date:  2006-09       Impact factor: 3.490

4.  Identification and characterization of lactococcal-prophage-carried superinfection exclusion genes.

Authors:  Jennifer Mahony; Stephen McGrath; Gerald F Fitzgerald; Douwe van Sinderen
Journal:  Appl Environ Microbiol       Date:  2008-08-22       Impact factor: 4.792

5.  The lactococcal phages Tuc2009 and TP901-1 incorporate two alternate forms of their tail fiber into their virions for infection specialization.

Authors:  Stephen R Stockdale; Jennifer Mahony; Pascal Courtin; Marie-Pierre Chapot-Chartier; Jan-Peter van Pijkeren; Robert A Britton; Horst Neve; Knut J Heller; Bashir Aideh; Finn K Vogensen; Douwe van Sinderen
Journal:  J Biol Chem       Date:  2013-01-08       Impact factor: 5.157

6.  Identification of a new P335 subgroup through molecular analysis of lactococcal phages Q33 and BM13.

Authors:  Jennifer Mahony; Bruno Martel; Denise M Tremblay; Horst Neve; Knut J Heller; Sylvain Moineau; Douwe van Sinderen
Journal:  Appl Environ Microbiol       Date:  2013-05-10       Impact factor: 4.792

7.  Molecular characterization of three Lactobacillus delbrueckii subsp. bulgaricus phages.

Authors:  Eoghan Casey; Jennifer Mahony; Mary O'Connell-Motherway; Francesca Bottacini; Anneleen Cornelissen; Horst Neve; Knut J Heller; Jean-Paul Noben; Fabio Dal Bello; Douwe van Sinderen
Journal:  Appl Environ Microbiol       Date:  2014-07-07       Impact factor: 4.792

8.  Structural characterization and assembly of the distal tail structure of the temperate lactococcal bacteriophage TP901-1.

Authors:  Christina S Vegge; Lone Brøndsted; Horst Neve; Stephen Mc Grath; Douwe van Sinderen; Finn K Vogensen
Journal:  J Bacteriol       Date:  2005-06       Impact factor: 3.490

9.  The plasmid complement of Lactococcus lactis UC509.9 encodes multiple bacteriophage resistance systems.

Authors:  Stuart Ainsworth; Jennifer Mahony; Douwe van Sinderen
Journal:  Appl Environ Microbiol       Date:  2014-05-09       Impact factor: 4.792

10.  Morphology, genome sequence, and structural proteome of type phage P335 from Lactococcus lactis.

Authors:  Simon J Labrie; Jytte Josephsen; Horst Neve; Finn K Vogensen; Sylvain Moineau
Journal:  Appl Environ Microbiol       Date:  2008-06-06       Impact factor: 4.792

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