Evidence map›Paper›PMID 17035489›Full record

ArticleJournal of clinical microbiology2006

Borrelia burgdorferi genetic markers and disseminated disease in patients with early Lyme disease.

Kathryn L Jones, Lisa J Glickstein, Nitin Damle, Vijay K Sikand, Gail McHugh, Allen C Steere

Open access · greenAbstract read
In one paragraph

Article in Journal of clinical microbiology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

59 citing papers in PubMed, 91 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Lyme Arthritis: A 50-Year Journey.The Journal of infectious diseases · 2024
    Article
  7. Article
  8. Suppression of host humoral immunity byInfection and immunity · 2024
    Article
  9. Article
  10. Article
  11. Whole genome sequencing ofbioRxiv : the preprint server for biology · 2023
    Article
  12. Detection of Borrelia burgdorferi Cell-free DNA in Human Plasma Samples for Improved Diagnosis of Early Lyme Borreliosis.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2021
    Article
  13. Review
  14. Laboratory Diagnosis of Lyme Borreliosis.Clinical microbiology reviews · 2021
    Review
  15. Lyme Disease Pathogenesis.Current issues in molecular biology · 2021
    Review
  16. Lyme Disease in Humans.Current issues in molecular biology · 2021
    Article
  17. Article
  18. Article
  19. The RpoS Gatekeeper inFrontiers in microbiology · 2019
    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

6 authors at 2 institutions in 1 country.

Kathryn L JonesDivision of Rheumatology, Allergy, and Immunology, Center for Immunology and Inflammatory Disease, Harvard Medical School, Massachusetts General Hospital, 55 Fruit St., CNY 149/8301, Boston, MA 02114, USA. KLJones@partners.org
Lisa J Glickstein
Nitin Damle
Vijay K Sikand
Gail McHugh
Allen C Steere
Harvard University · USMassachusetts General Hospital · US

Funding

LYME ARTHRITIS: A NEW EPIDEMIC DISEASER01AR020358 · NIAMS · YALE UNIVERSITY · PI STEERE, ALLEN C · 1986 to 2010
$4.0M
NIAMS NIH HHS AR-20358NIAMS NIH HHS R01 AR020358PHS HHS CCU110 291
6 · The paper itself

Abstract

Three genetic markers of Borrelia burgdorferi have been associated with disseminated disease: the OspC type, the 16S-23S rRNA intergenic spacer type (RST), and vlsE. Here, we modified previous methods so as to identify the three markers by PCR and restriction fragment length polymorphism in parallel, analyzed B. burgdorferi isolates from erythema migrans (EM) skin lesions in 91 patients, and correlated the results with evidence of dissemination. OspC type A was found approximately twice as frequently in patients with disseminated disease, whereas type K was identified approximately twice as often in those without evidence of dissemination, but these trends were not statistically significant. The remaining seven types identified were found nearly equally in patients with or without evidence of dissemination. RST 1 strains were significantly associated with dissemination (P=0.03), whereas RST 2 and RST 3 strains tended to have an inverse association with this outcome. The vlsE gene was identified in all 91 cases, using primer sets specific for an N-terminal sequence of B. burgdorferi strain B31 (vlsEB31) or strain 297 (vlsE297), but neither marker was associated with dissemination. Specific combinations of the three genetic markers usually occurred together. OspC type A was always found with RST 1 and vlsEB31, type K was always identified with RST 2 and more often with vlsE297, and types E and I were almost always found with RST 3 and equally often with vlsEB31 and vlsE297. We conclude that B. burgdorferi strains vary in their capacity to disseminate, but almost all strains isolated from EM lesions sometimes caused disseminated disease.

Indexed as

Polymerase Chain ReactionPolymorphism, Restriction Fragment LengthAntigens, BacterialBacterial Outer Membrane ProteinsBacterial ProteinsBiomarkersBorrelia burgdorferiDNA, BacterialDNA, Ribosomal SpacerGene FrequencyGenes, BacterialGenotypeHumansLipoproteinsLyme DiseaseSkinAntigens, BacterialBacterial Outer Membrane ProteinsBacterial ProteinsBiomarkersDNA, BacterialDNA, Ribosomal SpacerLipoproteinsOspC proteinVlsE protein, Borrelia burgdorferi

Identifiers

PMID17035489
PMCPMC1698394
OpenAlexW2156255552

What OpenQuestion holds

Textmetadata
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.