Bordetella pertussis, the causative agent of whooping cough, evolved from a distinct, human-associated lineage of B-bronchiseptica

被引:218
作者
Diavatopoulos, Dimitri A.
Cummings, Craig A.
Schouls, Leo M.
Brinig, Mary M.
Relman, David A.
Mooi, Frits R. [5 ]
机构
[1] Univ Utrecht, Eijkman Winkler Inst, Ctr Med, Utrecht, Netherlands
[2] Stanford Univ, Dept Microbiol & Immunol, Sch Med, Stanford, CA 94305 USA
[3] VA Palo Alto Hlth Care Syst, Palo Alto, CA USA
[4] Stanford Univ, Sch Med, Dept Med, Stanford, CA 94305 USA
[5] Natl Inst Publ Hlth & Environm, Lab Vaccine Preventable Dis, NL-3720 BA Bilthoven, Netherlands
关键词
D O I
10.1371/journal.ooat.0010045
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Bordetella pertussis, B. bronchiseptica, B. parapertussis(hu) and B. parapertussis(ov) are closely related respiratory pathogens that infect mammalian species. B. pertussis and B. parapertussis(hu) are exclusively human pathogens and cause whooping cough, or pertussis, a disease that has resurged despite vaccination. Although it most often infects animals, infrequently B. bronchiseptica is isolated from humans, and these infections are thought to be zoonotic. B. pertussis and B. parapertussis(hu) are assumed to have evolved from a B. bronchiseptica-like ancestor independently. To determine the phylogenetic relationships among these species, housekeeping and virulence genes were sequenced, comparative genomic hybridizations were performed using DNA microarrays, and the distribution of insertion sequence elements was determined, using a collection of 132 strains. This multifaceted approach distinguished four complexes, representing B. pertussis, B. parapertussis(hur) and two distinct B. bronchiseptica subpopulations, designated complexes I and IV. Of the two B. bronchiseptica complexes, complex IV was more closely related to B. pertussis. Of interest, while only 32% of the complex I strains were isolated from humans, 80% of the complex IV strains were human isolates. Comparative genomic hybridization analysis identified the absence of the pertussis toxin locus and dermonecrotic toxin gene, as well as a polymorphic lipopolysaccharide biosynthesis locus, as associated with adaptation of complex IV strains to the human host. Lipopolysaccharide structural diversity among these strains was confirmed by gel electrophoresis. Thus, complex IV strains may comprise a human-associated lineage of B. bronchiseptica from which B. pertussis evolved. These findings will facilitate the study of pathogen host-adaptation. Our results shed light on the origins of the disease pertussis and suggest that the association of B. pertussis with humans may be more ancient than previously assumed.
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页码:373 / 383
页数:11
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