Skip to content Skip to navigation
University of Warwick
  • Study
  • |
  • Research
  • |
  • Business
  • |
  • Alumni
  • |
  • News
  • |
  • About

University of Warwick
Publications service & WRAP

Highlight your research

  • WRAP
    • Home
    • Search WRAP
    • Browse by Warwick Author
    • Browse WRAP by Year
    • Browse WRAP by Subject
    • Browse WRAP by Department
    • Browse WRAP by Funder
    • Browse Theses by Department
  • Publications Service
    • Home
    • Search Publications Service
    • Browse by Warwick Author
    • Browse Publications service by Year
    • Browse Publications service by Subject
    • Browse Publications service by Department
    • Browse Publications service by Funder
  • Statistics
  • Help & Advice
University of Warwick

The Library

  • Login

Evidence for the intense exchange of MazG in marine cyanophages by horizontal gene transfer

Tools
- Tools
+ Tools

Bryan, Michael J., Burroughs, Nigel John, Spence, Edward M., Clokie, Martha R. J., Mann, Nicholas H. and Bryan, Samantha J.. (2008) Evidence for the intense exchange of MazG in marine cyanophages by horizontal gene transfer. PL o S One, Vol.3 (No.4). ISSN 1932-6203

[img]
Preview
PDF
WRAP_Burroughs_Intense_exchange_MazG.pdf - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader

Download (848Kb)
Official URL: http://dx.doi.org/10.1371/journal.pone.0002048

Abstract

Background: S-PM2 is a phage capable of infecting strains of unicellular cyanobacteria belonging to the genus Synechococcus. S-PM2, like other myoviruses infecting marine cyanobacteria, encodes a number of bacterial-like genes. Amongst these genes is one encoding a MazG homologue that is hypothesized to be involved in the adaption of the infected host for production of progeny phage. Methodology/Principal Findings: This study focuses on establishing the occurrence of mazG homologues in other cyanophages isolated from different oceanic locations. Degenerate PCR primers were designed using the mazG gene of S-PM2. The mazG gene was found to be widely distributed and highly conserved among Synechococcus myoviruses and podoviruses from diverse oceanic provinces. Conclusions/Significance: This study provides evidence of a globally connected cyanophage gene pool, the cyanophage mazG gene having a small effective population size indicative of rapid lateral gene transfer despite being present in a substantial fraction of cyanophage. The Prochlorococcus and Synechococcus phage mazG genes do not cluster with the host mazG gene, suggesting that their primary hosts are not the source of the mazG gene.

Item Type: Journal Article
Subjects: Q Science > QR Microbiology > QR355 Virology
Divisions: Faculty of Science > Life Sciences (2010- ) > Biological Sciences ( -2010)
Faculty of Science > Mathematics
Faculty of Science > Centre for Systems Biology
Library of Congress Subject Headings (LCSH): Cyanobacteria -- Viruses -- Genetics
Journal or Publication Title: PL o S One
Publisher: Public Library of Science
ISSN: 1932-6203
Date: 23 April 2008
Volume: Vol.3
Number: No.4
Number of Pages: 12
Identification Number: 10.1371/journal.pone.0002048
Status: Peer Reviewed
Publication Status: Published
Access rights to Published version: Open Access
Funder: University of Warwick
References: 1. Mann NH (2003) Phages of the marine cyanobacterial picophytoplankton. Fems Microbiology Reviews 27: 17–34. 2. Mann NH, Clokie MRJ, Millard A, Cook A, Wilson WH, et al. (2005) The genome of S-PM2, a ‘‘photosynthetic’’ T4-type bacteriophage that infects marine Synechococcus strains. Journal of Bacteriology 187: 3188–3200. 3. Bailey S, Clokie MRJ, Millard A, Mann NH (2004) Cyanophage infection and photoinhibition in marine cyanobacteria. Research inMicrobiology 155: 720–725. 4. Galperin MY, Moroz OV, Wilson KS, Murzin AG (2006) House cleaning, a part of good housekeeping. Mol Microbiol 59: 5–19. 5. Gross M, Marianovsky I, Glaser G (2006) MazG - a regulator of programmed cell death in Escherichia coli. Molecular Microbiology 59: 590–601. 6. Magnusson LU, Farewell A, Nystrom T (2005) ppGpp: a global regulator in Escherichia coli. Trends in Microbiology 13: 236–242. 7. Wang JD, Sanders GM, Grossman AD (2007) Nutritional control of elongation of DNA replication by (p)ppGpp. Cell 128: 865–875. 8. Mann N, Carr NG, Midgley JE (1975) RNA synthesis and the accumulation of guanine nucleotides during growth shift down in the blue-green alga Anacystis nidulans. Biochim Biophys Acta 402: 41–50. 9. Friga GM, Borbely G, Farkas GL (1981) Accumulation of guanosine tetraphosphate (ppGpp) under nitrogen starvation in Anacystis nidulans, a cyanobacterium. Arch Microbiol 129: 341–343. 10. Borbely G, Kaki C, Gulyas A, Farkas GL (1980) Bacteriophage infection interferes with guanosine 39-diphosphate-59-diphosphate accumulation induced by energy and nitrogen starvation in the cyanobacterium Anacystis nidulans. Journal of Bacteriology 144: 859–864. 11. Clokie MRJ, Mann NH (2006) Marine cyanophages and light. Environmental Microbiology 8: 2074–2082. 12. Fuller NJ, Wilson WH, Joint IR, Mann NH (1998) Occurrence of a sequence in marine cyanophages similar to that of T4 g20 and its application to PCR-based detection and quantification techniques. Applied and Environmental Microbiology 64: 2051–2060. 13. Breitbart M, Miyake JH, Rohwer F (2006) Global distribution of nearly identical phage-encoded DNA sequences (vol 236, pg 249, 2004). Fems Microbiology Letters 254: 332–332. 14. Short CM, Suttle CA (2005) Nearly identical bacteriophage structural gene sequences are widely distributed in both marine and freshwater environments. Applied and Environmental Microbiology 71: 480–486. 15. Sprague SG, Staehelin LA, DiBartolomeis MJ, Fuller RC (1981) Isolation and development of chlorosomes in the green bacterium Chloroflexus aurantiacus. Journal of Bacteriology 147: 1021–1031. 16. Morris RM, Rappe MS, Urbach E, Connon SA, Giovannoni SJ (2004) Prevalence of the Chloroflexi-related SAR202 bacterioplankton cluster throughout the mesopelagic zone and deep ocean. Appl Environ Microbiol 70: 2836–2842. 17. Hendrix RW, Smith MCM, Burns RN, Ford ME, Hatfull GF (1999) Evolutionary relationships among diverse bacteriophages and prophages: All the world’s a phage. Proceedings of the National Academy of Sciences of the United States of America 96: 2192–2197. 18. DeLong EF, Preston CM, Mincer T, Rich V, Hallam SJ, et al. (2006) Community genomics among stratified microbial assemblages in the ocean’s interior. Science 311: 496–503. 19. Gelman A, Rubin DB (1992) Inference from iterative simulation using multiple sequences. Statistical Science 7: 457–511.
URI: http://wrap.warwick.ac.uk/id/eprint/16663

Data sourced from Thomson Reuters' Web of Knowledge

Request changes to a record

Actions (login required)

View Item View Item

Document Downloads

More statistics for this item...
twitter

Email us: publications@warwick.ac.uk
Contact Details
About Us