Evidence map›Paper›PMID 20032216›Full record

ArticleClinical and vaccine immunology : CVI2010

The borrelial fibronectin-binding protein RevA is an early antigen of human Lyme disease.

Catherine A Brissette, Evelyn Rossmann, Amy Bowman, Anne E Cooley, Sean P Riley, Klaus-Peter Hunfeld, Michael Bechtel, Peter Kraiczy, Brian Stevenson

Open access · diamondAbstract read
In one paragraph

Article in Clinical and vaccine immunology : CVI, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 24% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Borrelia surface proteins: new horizons in Lyme disease diagnosis.Applied microbiology and biotechnology · 2025
    Review
  3. Article
  4. Electrochemical Detection ofACS measurement science au · 2023
    Article
  5. Review
  6. Laboratory Diagnosis of Lyme Borreliosis.Clinical microbiology reviews · 2021
    Review
  7. Review
  8. Review
  9. Microorganisms' Footprint in Neurodegenerative Diseases.Frontiers in cellular neuroscience · 2018
    Review
  10. Article
  11. Article
  12. Article
  13. That's my story, and I'm sticking to it--an update on B. burgdorferi adhesins.Frontiers in cellular and infection microbiology · 2014
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. 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

9 authors at 2 institutions in 2 countries.

Catherine A BrissetteDepartment of Microbiology, Immunology and Molecular Genetics, University of Kentucky College of Medicine, Chandler Medical Center MN469, 800 Rose Street, Lexington, KY 40536-0298, USA. catherine.brissette@uky.edu
Evelyn Rossmann
Amy Bowman
Anne E Cooley
Sean P Riley
Klaus-Peter Hunfeld
Michael Bechtel
Peter Kraiczy
Brian Stevenson
University of Kentucky · USUniversity Hospital Frankfurt · DE

Funding

Role of a Borrelia burgdorferi fibronection-binding protein in Lyme DiseaseF32AI081480 · NIAID · UNIVERSITY OF KENTUCKY · PI BRISSETTE, CATHERINE AYN · 2009 to 2010
$65k
NIAID NIH HHS F32 AI081480NIAID NIH HHS F32-AI081480
6 · The paper itself

Abstract

Previous studies using small numbers of serum samples from human patients and experimentally infected animals identified the frequent presence of antibodies recognizing RevA, a borrelial fibronectin-binding outer surface protein. We now demonstrate that most examined Lyme disease spirochetes from North America and Europe contain genes encoding RevA proteins, some with extensive regions of conservation and others with moderate diversity. Line blot analyses using recombinant RevA from two diverse Lyme disease spirochetes of RevA and serum samples from culture-confirmed human Lyme disease patients from the United States (n = 46, mainly with early Lyme disease) and Germany (>500, with early and late manifestations of Lyme disease) were performed. The results indicated that a sizable proportion of patients produced antibodies that recognized recombinant RevA. Overall, RevA-based serological studies were less sensitive and less specific than other assay types, such as the VlsE-based C6 peptide assay. However, sera from patients in the initial stages of Lyme disease contained antibodies against RevA, demonstrating that this protein is expressed early in human infection. Thus, RevA may be a useful target for preventative or curative therapies.

Indexed as

Adhesins, BacterialAnimalsAntibodies, BacterialAntigens, BacterialBacterial Outer Membrane ProteinsBacteriological TechniquesBorreliaConserved SequenceEuropeHumansImmunoblottingLyme DiseaseNorth AmericaPolymorphism, GeneticRecombinant ProteinsSensitivity and SpecificityAdhesins, BacterialAntibodies, BacterialAntigens, BacterialBacterial Outer Membrane Proteinsfibronectin-binding proteins, bacterialRecombinant Proteins

Identifiers

PMID20032216
PMCPMC2815533
OpenAlexW2133165002

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.