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Comparative analysis of the genome sequences of Bordetella pertussis,Bordetella parapertussis and Bordetella bronchiseptica
Authors:Parkhill Julian  Sebaihia Mohammed  Preston Andrew  Murphy Lee D  Thomson Nicholas  Harris David E  Holden Matthew T G  Churcher Carol M  Bentley Stephen D  Mungall Karen L  Cerdeño-Tárraga Ana M  Temple Louise  James Keith  Harris Barbara  Quail Michael A  Achtman Mark  Atkin Rebecca  Baker Steven  Basham David  Bason Nathalie  Cherevach Inna  Chillingworth Tracey  Collins Matthew  Cronin Anne  Davis Paul  Doggett Jonathan  Feltwell Theresa  Goble Arlette  Hamlin Nancy  Hauser Heidi  Holroyd Simon  Jagels Kay  Leather Sampsa  Moule Sharon  Norberczak Halina  O'Neil Susan  Ormond Doug  Price Claire  Rabbinowitsch Ester
Institution:The Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK. parkhill@sanger.ac.uk
Abstract:Bordetella pertussis, Bordetella parapertussis and Bordetella bronchiseptica are closely related Gram-negative beta-proteobacteria that colonize the respiratory tracts of mammals. B. pertussis is a strict human pathogen of recent evolutionary origin and is the primary etiologic agent of whooping cough. B. parapertussis can also cause whooping cough, and B. bronchiseptica causes chronic respiratory infections in a wide range of animals. We sequenced the genomes of B. bronchiseptica RB50 (5,338,400 bp; 5,007 predicted genes), B. parapertussis 12822 (4,773,551 bp; 4,404 genes) and B. pertussis Tohama I (4,086,186 bp; 3,816 genes). Our analysis indicates that B. parapertussis and B. pertussis are independent derivatives of B. bronchiseptica-like ancestors. During the evolution of these two host-restricted species there was large-scale gene loss and inactivation; host adaptation seems to be a consequence of loss, not gain, of function, and differences in virulence may be related to loss of regulatory or control functions.
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