Dennis Bamford

Prof. Dennis Bamford


Research Focus & Metrics

Academic Career Length

36Years (1991-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 March 2001 in Nature
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Journal Article
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SBSarah Butcher
Sarah Butcher
JGJonathan M. Grimes
Jonathan M. Grimes
EMEugeny V. Makeyev
Eugeny V. Makeyev
DBDennis Bamford
Dennis Bamford
DSDavid Ian Stuart
David Ian Stuart

1 December 2005 in Current Opinion in Structural Biology
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Journal Article
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DBDennis Bamford
Dennis Bamford
JGJonathan M Grimes
Jonathan M Grimes
DSDavid Ian Stuart
David Ian Stuart

7 July 2012 in Annual Review of Biochemistry
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Journal Article
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NANicola GA Abrescia
Nicola GA Abrescia
DBDennis Bamford
Dennis Bamford
JGJonathan M. Grimes
Jonathan M. Grimes
DSDavid Ian Stuart
David Ian Stuart
Is it possible to meaningfully comprehend the diversity of the viral world? We propose that it is. This is based on the observation that, although there is immense genomic variation, every infective virion is restricted by strict constraints in structure space (i.e., there are a limited number of ways to fold a protein chain, and only a small subset of these have the potential to construct a virion, the hallmark of a virus). We have previously suggested the use of structure for the higher-order classification of viruses, where genomic similarities are no longer observable. Here, we summarize the arguments behind this proposal, describe the current status of structural work, highlighting its power to infer common ancestry, and discuss the limitations and obstacles ahead of us. We also reflect on the future opportunities for a more concerted effort to provide high-throughput methods to facilitate the large-scale sampling of the virosphere.

14 May 2009 in Nature
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Journal Article
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HLHeng-Chi Lee
Heng-Chi Lee
SCShwu-Shin Chang
Shwu-Shin Chang
SCSwati Choudhary
Swati Choudhary
AAAntti P. Aalto
Antti P. Aalto
MMMekhala Maiti
Mekhala Maiti
YLYi Liu
Yi Liu

1 November 2004 in Nature
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Journal Article
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NANicola GA Abrescia
Nicola GA Abrescia
JCJoseph Cockburn
Joseph Cockburn
JGJonathan M. Grimes
Jonathan M. Grimes
GSGeoffrey C. Sutton
Geoffrey C. Sutton
JDJonathan M. Diprose
Jonathan M. Diprose
JBJaana K. H. Bamford
Jaana K. H. Bamford

1 December 2011 in Microbiology and Molecular Biology Reviews
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Journal Article
Closed access
MKMart Krupovic
Mart Krupovic
DPDavid Prangishvili
David Prangishvili
RHRoger W. Hendrix
Roger W. Hendrix
DBDennis Bamford
Dennis Bamford
SUMMARY: Prokaryotes, bacteria and archaea, are the most abundant cellular organisms among those sharing the planet Earth with human beings (among others). However, numerous ecological studies have revealed that it is actually prokaryotic viruses that predominate on our planet and outnumber their hosts by at least an order of magnitude. An understanding of how this viral domain is organized and what are the mechanisms governing its evolution is therefore of great interest and importance. The vast majority of characterized prokaryotic viruses belong to the order Caudovirales, double-stranded DNA (dsDNA) bacteriophages with tails. Consequently, these viruses have been studied (and reviewed) extensively from both genomic and functional perspectives. However, albeit numerous, tailed phages represent only a minor fraction of the prokaryotic virus diversity. Therefore, the knowledge which has been generated for this viral system does not offer a comprehensive view of the prokaryotic virosphere. In this review, we discuss all families of bacterial and archaeal viruses that contain more than one characterized member and for which evolutionary conclusions can be attempted by use of comparative genomic analysis. We focus on the molecular mechanisms of their genome evolution as well as on the relationships between different viral groups and plasmids. It becomes clear that evolutionary mechanisms shaping the genomes of prokaryotic viruses vary between different families and depend on the type of the nucleic acid, characteristics of the virion structure, as well as the mode of the life cycle. We also point out that horizontal gene transfer is not equally prevalent in different virus families and is not uniformly unrestricted for diverse viral functions.