Evidence map›Paper›PMID 17509142›Full record

ArticleBMC genomics2007

Phase variation and microevolution at homopolymeric tracts in Bordetella pertussis.

Emily B Gogol, Craig A Cummings, Ryan C Burns, David A Relman

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 33 citations in OpenAlex.

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  7. Fha DeficientIranian journal of public health · 2021
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  16. Review
  17. Simple sequence repeats in Haemophilus influenzae.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2009
    Article
  18. Article
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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

4 authors at 3 institutions in 1 country.

Emily B GogolDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, California 94305, USA. emily.gogol@ucsf.edu <emily.gogol@ucsf.edu>
Craig A Cummings
Ryan C Burns
David A Relman
Stanford University · USUniversity of San Francisco · USVA Palo Alto Health Care System · 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 AI054970NIAID NIH HHS AI057188NIAID NIH HHS R03 AI054970NIAID NIH HHS R21 AI057188NIAID NIH HHS R33 AI057188
6 · The paper itself

Abstract

backgroundBordetella pertussis, the causative agent of whooping cough, is a highly clonal pathogen of the respiratory tract. Its lack of genetic diversity, relative to many bacterial pathogens, could limit its ability to adapt to a hostile and changing host environment. This limitation might be overcome by phase variation, as observed for other mucosal pathogens. One of the most common mechanisms of phase variation is reversible expansion or contraction of homopolymeric tracts (HPTs).

resultsThe genomes of B. pertussis and the two closely related species, B. bronchiseptica and B. parapertussis, were screened for homopolymeric tracts longer than expected on the basis of chance, given their nucleotide compositions. Sixty-nine such HPTs were found in total among the three genomes, 74% of which were polymorphic among the three species. Nine HPTs were genotyped in a collection of 90 geographically and temporally diverse B. pertussis strains using the polymerase chain reaction/ligase detection reaction (PCR/LDR) assay. Six HPTs were polymorphic in this collection of B. pertussis strains. Of note, one of these polymorphic HPTs was found in the fimX promoter, where a single base insertion variant was present in seven strains, all of which were isolated prior to introduction of the pertussis vaccine. Transcript abundance of fimX was found to be 3.8-fold lower in strains carrying the longer allele. HPTs in three other genes, tcfA, bapC, and BP3651, varied widely in composition across the strain collection and displayed allelic polymorphism within single cultures.

conclusionAllelic polymorphism at homopolymeric tracts is common within the B. pertussis genome. Phase variability may be an important mechanism in B. pertussis for evasion of the immune system and adaptation to different niches in the human host. High sensitivity and specificity make the PCR/LDR assay a powerful tool for investigating allelic variation at HPTs. Using this method, allelic diversity and phase variation were demonstrated at several B. pertussis loci.

Indexed as

Evolution, MolecularPolymorphism, GeneticRepetitive Sequences, Nucleic AcidAllelesBacterial ProteinsBordetella bronchisepticaBordetella parapertussisBordetella pertussisDNA, BacterialFimbriae ProteinsGenome, BacterialHumansPolymerase Chain ReactionPromoter Regions, GeneticBacterial ProteinsDNA, BacterialFimbriae Proteins

Identifiers

PMID17509142
PMCPMC1891110
OpenAlexW2082877580

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.