Evidence map›Paper›PMID 17919281›Full record

ArticleMolecular microbiology2007

Genetic basis for retention of a critical virulence plasmid of Borrelia burgdorferi.

Mollie W Jewett, Rebecca Byram, Aaron Bestor, Kit Tilly, Kevin Lawrence, Mary N Burtnick, Frank Gherardini, Patricia A Rosa

Open access · bronzeAbstract read
In one paragraph

Article in Molecular microbiology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

56 citing papers in PubMed, 71 citations in OpenAlex.

  1. Article
  2. Article
  3. Virulence Regulation inMicroorganisms · 2025
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  7. Broadly conserved FlgV controls flagellar assembly andbioRxiv : the preprint server for biology · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Probing the Role ofInfection and immunity · 2021
    Article
  12. Article
  13. Article
  14. Lyme Disease Pathogenesis.Current issues in molecular biology · 2021
    Review
  15. Genetic Manipulation ofCurrent issues in molecular biology · 2021
    Review
  16. Infection and immunity · 2019
    Article
  17. Article
  18. Article
  19. Article
  20. Article
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

8 authors at 2 institutions in 1 country.

Mollie W JewettLaboratory of Zoonotic Pathogens, Rocky Mountain Laboratories, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, MT 59840, USA.
Rebecca Byram
Aaron Bestor
Kit Tilly
Kevin Lawrence
Mary N Burtnick
Frank Gherardini
Patricia A Rosa
National Institutes of Health · USUniversity of Wyoming · US

Funding

Molecular Genetic Basis of the Infectious Cycle of Borrelia burgdorferiZIAAI000917 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI ROSA, PATRICIA A · 2009 to 2023
$13.7M
The Roles of Key Transcription Factors on the Pathogenesis of B. Burgdorferi, the Causative Agent of Lyme DiseaseZIAAI000905 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI GHERARDINI, FRANK · 2009 to 2023
$12.4M
Molecular Genetics Of Infectious Borrelia BurgdorferiZ01AI000917 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI ROSA, PATRICIA A · 2002 to 2008
$2.2M
The Oxidative Stress Response In B. burgdorferiZ01AI000905 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI GHERARDINI, FRANK · 2002 to 2008
$744k
Intramural NIH HHS
6 · The paper itself

Abstract

The genome of Borrelia burgdorferi is composed of one linear chromosome and approximately 20 linear and circular plasmids. Although some plasmids are required by B. burgdorferi in vivo, most plasmids are dispensable for growth in vitro. However, circular plasmid (cp) 26 is present in all natural isolates and has never been lost during in vitro growth. This plasmid carries ospC, which is critical for mammalian infection. We previously showed that cp26 encodes essential functions, including the telomere resolvase, ResT, and hence cannot be displaced. Here we identify two additional essential genes on cp26, bbb26 and bbb27, through a systematic attempt to inactivate each open reading frame (ORF). Furthermore, an incompatible plasmid carrying resT, bbb26 and bbb27 could displace cp26. Computational and experimental analyses suggested that both BBB26 and BBB27 are membrane-associated, periplasmic proteins. These data indicate that bbb26 and bbb27 encode essential but possibly redundant functions and that one or the other of these cp26 genes, in addition to resT, is required for bacterial viability. We conclude that the genetic linkage of critical physiological and virulence functions on cp26 is pertinent to its stable maintenance throughout the evolution of B. burgdorferi.

Indexed as

Genes, EssentialBacterial ProteinsBorrelia burgdorferiDNA, BacterialDNA, CircularElectroporationGene SilencingGenetic VectorsPlasmidsRecombination, GeneticTransformation, BacterialVirulenceBacterial ProteinsDNA, BacterialDNA, Circular

Identifiers

PMID17919281
PMCPMC2229028
OpenAlexW2131492700

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.