The Genome of Burkholderia cenocepacia J2315, an Epidemic Pathogen of Cystic Fibrosis Patients

Геном Burkholderia cenocepacia J2315 — эпидемического патогена пациентов с муковисцидозом
Matthew T. G. Holden, Helena M. B. Seth-Smith, Lisa Crossman, Mohammed Sebaihia, Stephen D. Bentley, Ana Cerdeño-Tárraga, Nicholas R. Thomson, Nathalie Bason, Michael A. Quail, Sarah Sharp, Inna Cherevach, Carol Churcher, Ian Goodhead, Heidi Hauser, Nancy Holroyd, Karen Mungall, Paul J. Scott, Danielle Walker, Brian R. White, Helen L. Rose, Pernille Iversen, Dalila Mil‐Homens, Eduardo P. C. Rocha, Arsénio M. Fialho, Adam Baldwin, Christopher G. Dowson, Bart Barrell, John R. W. Govan, Peter Vandamme, C. Anthony Hart, Eshwar Mahenthiralingam, Julian Parkhill
2008-10-18

Burkholderia cenocepacia J2315ET12 epidemic lineageantibiotic resistancecystic fibrosis pathogengenome plasticity
Bacterial infections of the lungs of cystic fibrosis (CF) patients cause major complications in the treatment of this common genetic disease. Burkholderia cenocepacia infection is particularly problematic since this organism has high levels of antibiotic resistance, making it difficult to eradicate; the resulting chronic infections are associated with severe declines in lung function and increased mortality rates. B. cenocepacia strain J2315 was isolated from a CF patient and is a member of the epidemic ET12 lineage that originated in Canada or the United Kingdom and spread to Europe. The 8.06-Mb genome of this highly transmissible pathogen comprises three circular chromosomes and a plasmid and encodes a broad array of functions typical of this metabolically versatile genus, as well as numerous virulence and drug resistance functions. Although B. cenocepacia strains can be isolated from soil and can be pathogenic to both plants and man, J2315 is representative of a lineage of B. cenocepacia rarely isolated from the environment and which spreads between CF patients. Comparative analysis revealed that ca. 21% of the genome is unique in comparison to other strains of B. cenocepacia, highlighting the genomic plasticity of this species. Pseudogenes in virulence determinants suggest that the pathogenic response of J2315 may have been recently selected to promote persistence in the CF lung. The J2315 genome contains evidence that its unique and highly adapted genetic content has played a significant role in its success as an epidemic CF pathogen.
1
Approximately 21% of the J2315 genome is unique relative to other B. cenocepacia strains, demonstrating substantial genomic plasticity.
2
J2315 encodes extensive metabolic capabilities alongside numerous virulence and antibiotic-resistance functions, consistent with adaptation to persistent CF lung infection.
3
Pseudogenes in virulence determinants suggest recent selection toward persistence rather than acute pathogenicity in the CF lung.
4
The 8.06-Mb genome of epidemic B. cenocepacia strain J2315 consists of three circular chromosomes and one plasmid.
5
Unique, highly adapted genetic content likely contributed substantially to J2315’s transmissibility and success as an epidemic CF pathogen.

The 8.06-Mb genome of Burkholderia cenocepacia strain J2315, an epidemic ET12-lineage pathogen infecting cystic fibrosis patients

Genome organization, unique genetic content, genomic plasticity, virulence and antibiotic-resistance determinants, and genetic adaptations underlying persistence and epidemic transmission in the cystic fibrosis lung

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2008-10-18
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Authors
Matthew T. G. Holden
Helena M. B. Seth-Smith
Lisa Crossman
Mohammed Sebaihia
Stephen D. Bentley
Ana Cerdeño-Tárraga
Nicholas R. Thomson
Nathalie Bason
Michael A. Quail
Sarah Sharp
Inna Cherevach
Carol Churcher
Ian Goodhead
Heidi Hauser
Nancy Holroyd
Karen Mungall
Paul J. Scott
Danielle Walker
Brian R. White
Helen L. Rose
Pernille Iversen
Dalila Mil‐Homens
Eduardo P. C. Rocha
Arsénio M. Fialho
Adam Baldwin
Christopher G. Dowson
Bart Barrell
John R. W. Govan
Peter Vandamme
C. Anthony Hart
Eshwar Mahenthiralingam
Julian Parkhill
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