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Journal of Bacteriology, March 2008, p. 2150-2160, Vol. 190, No. 6
0021-9193/08/$08.00+0     doi:10.1128/JB.01598-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Genome of the Actinomycete Plant Pathogen Clavibacter michiganensis subsp. sepedonicus Suggests Recent Niche Adaptation{triangledown} ,{dagger}

Stephen D. Bentley,1 Craig Corton,1 Susan E. Brown,2 Andrew Barron,1 Louise Clark,1 Jon Doggett,1 Barbara Harris,1 Doug Ormond,1 Michael A. Quail,1 Georgiana May,3 David Francis,4 Dennis Knudson,2 Julian Parkhill,1 and Carol A. Ishimaru2,5*

Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton CB10 1SA, United Kingdom,1 Department of Biological Sciences and Pest Management, Colorado State University, Fort Collins, Colorado 80523,2 Department of Ecology, Evolution and Behavior, University of Minnesota, St. Paul, Minnesota 55108,3 Department of Horticulture and Crop Science Ohio Agricultural Research and Development Center, The Ohio State University, Wooster, Ohio 44691,4 Department of Plant Pathology, University of Minnesota, St. Paul, Minnesota 551085

Received 2 October 2007/ Accepted 1 January 2008

Clavibacter michiganensis subsp. sepedonicus is a plant-pathogenic bacterium and the causative agent of bacterial ring rot, a devastating agricultural disease under strict quarantine control and zero tolerance in the seed potato industry. This organism appears to be largely restricted to an endophytic lifestyle, proliferating within plant tissues and unable to persist in the absence of plant material. Analysis of the genome sequence of C. michiganensis subsp. sepedonicus and comparison with the genome sequences of related plant pathogens revealed a dramatic recent evolutionary history. The genome contains 106 insertion sequence elements, which appear to have been active in extensive rearrangement of the chromosome compared to that of Clavibacter michiganensis subsp. michiganensis. There are 110 pseudogenes with overrepresentation in functions associated with carbohydrate metabolism, transcriptional regulation, and pathogenicity. Genome comparisons also indicated that there is substantial gene content diversity within the species, probably due to differential gene acquisition and loss. These genomic features and evolutionary dating suggest that there was recent adaptation for life in a restricted niche where nutrient diversity and perhaps competition are low, correlated with a reduced ability to exploit previously occupied complex niches outside the plant. Toleration of factors such as multiplication and integration of insertion sequence elements, genome rearrangements, and functional disruption of many genes and operons seems to indicate that there has been general relaxation of selective pressure on a large proportion of the genome.


* Corresponding author. Mailing address: 495 Borlaug Hall, 1991 Upper Buford Circle, University of Minnesota, St. Paul, MN 55108. Phone: (612) 625-9736. Fax: (612) 625-9728. E-mail: cishimar{at}umn.edu

{triangledown} Published ahead of print on 11 January 2008.

{dagger} Supplemental material for this article may be found at http://jb.asm.org/.


Journal of Bacteriology, March 2008, p. 2150-2160, Vol. 190, No. 6
0021-9193/08/$08.00+0     doi:10.1128/JB.01598-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.




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