Evidence map›Paper›PMID 16389302›Full record

ArticlePLoS pathogens2005

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

Dimitri A Diavatopoulos, Craig A Cummings, Leo M Schouls, Mary M Brinig, David A Relman, Frits R Mooi

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 162 papers.

0numbers the graph read from it
0cells of the map it votes in
162citing papers in PubMed
8.8field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

162 citing papers in PubMed, 288 citations in OpenAlex.

  1. Article
  2. History of whooping cough in Colombia: Endemic infant deaths, outbreaks and epidemicsBiomedica : revista del Instituto Nacional de Salud · 2026
    Article
  3. Review
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  11. Article
  12. Article
  13. Genetic diversity ofFrontiers in microbiology · 2025
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Non-classicalThe Journal of international medical research · 2024
    Article
  20. Genomic epidemiology and multilevel genome typing ofEmerging microbes & infections · 2023
    Article

102 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Dimitri A DiavatopoulosLaboratory for Vaccine-Preventable Diseases, National Institute of Public Health and the Environment, Bilthoven, The Netherlands.
Craig A Cummings
Leo M Schouls
Mary M Brinig
David A Relman
Frits R Mooi
National Institute for Public Health and the Environment · NLVA Palo Alto Health Care System · USStanford University · US

Funding

Analytical Tools for Comparative Microbial GenomicsR33AI057188 · NIAID · STANFORD UNIVERSITY · PI RELMAN, DAVID ARNOLD · 2005 to 2006
$823k
Analytical Tools for Comparative Microbial GenomicsR21AI057188 · NIAID · STANFORD UNIVERSITY · PI RELMAN, DAVID ARNOLD · 2003 to 2004
$287k
Bordetella Response to Host Cues and Cell SignalsR03AI054970 · NIAID · STANFORD UNIVERSITY · PI RELMAN, DAVID ARNOLD · 2003 to 2004
$130k
NIAID NIH HHS R03 AI054970NIAID NIH HHS R21 AI057188NIAID NIH HHS R33 AI057188
6 · The paper itself

Abstract

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(hu), 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.

Identifiers

PMID16389302
PMCPMC1323478
OpenAlexW2066284041

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.