Evidence map›Paper›PMID 16239539›Full record

ArticleInfection and immunity2005

Borrelia burgdorferi regulates expression of complement regulator-acquiring surface protein 1 during the mammal-tick infection cycle.

Kate von Lackum, Jennifer C Miller, Tomasz Bykowski, Sean P Riley, Michael E Woodman, Volker Brade, Peter Kraiczy, Brian Stevenson, Reinhard Wallich

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

34 citing papers in PubMed, 71 citations in OpenAlex.

  1. Article
  2. Article
  3. Lyme Disease Pathogenesis.Current issues in molecular biology · 2021
    Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Enolase FromFrontiers in immunology · 2019
    Article
  9. Review
  10. Article
  11. Spirochetal Lipoproteins and Immune Evasion.Frontiers in immunology · 2017
    Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  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

9 authors at 4 institutions in 2 countries.

Kate von LackumDepartment of Microbiology, Immunology, and Molecular Genetics, University of Kentucky College of Medicine, MS417 Chandler Medical Center, 800 Rose Street, Lexington, KY 40536-0298, USA.
Jennifer C Miller
Tomasz Bykowski
Sean P Riley
Michael E Woodman
Volker Brade
Peter Kraiczy
Brian Stevenson
Reinhard Wallich
University of Kentucky · USGoethe University Frankfurt · DEHeidelberg University · DEUniversity Hospital Frankfurt · DE

Funding

ANALYSIS OF BORRELIA BURGDORFERI ERP PROTEINSR01AI044254 · NIAID · UNIVERSITY OF KENTUCKY · PI STEVENSON, BRIAN · 2000 to 2010
$3.1M
Training Program in Microbial PathogenesisT32AI049795 · NIAID · UNIVERSITY OF KENTUCKY · PI STRALEY, SUSAN C · 2001 to 2005
$841k
NIAID NIH HHS 5T32AI49795NIAID NIH HHS R01 AI044254NIAID NIH HHS R01-AI44254NIAID NIH HHS T32 AI049795
6 · The paper itself

Abstract

During the natural mammal-tick infection cycle, the Lyme disease spirochete Borrelia burgdorferi comes into contact with components of the alternative complement pathway. B. burgdorferi, like many other human pathogens, has evolved the immune evasion strategy of binding two host-derived fluid-phase regulators of complement, factor H and factor H-like protein 1 (FHL-1). The borrelial complement regulator-acquiring surface protein 1 (CRASP-1) is a surface-exposed lipoprotein that binds both factor H and FHL-1. Analysis of CRASP-1 expression during the mammal-tick infectious cycle indicated that B. burgdorferi expresses this protein during mammalian infection, supporting the hypothesized role for CRASP-1 in immune evasion. However, CRASP-1 synthesis was repressed in bacteria during colonization of vector ticks. Analysis of cultured bacteria indicated that CRASP-1 is differentially expressed in response to changes in pH. Comparisons of CRASP-1 expression patterns with those of other infection-associated B. burgdorferi proteins, including the OspC, OspA, and Erp proteins, indicated that each protein is regulated through a unique mechanism.

Indexed as

Gene Expression Regulation, BacterialAnimalsBacterial ProteinsBlood ProteinsBorrelia burgdorferiComplement C3b Inactivator ProteinsComplement Factor HEvolution, MolecularFemaleHydrogen-Ion ConcentrationLarvaLyme DiseaseMaleMammalsMembrane ProteinsMiceBacterial ProteinsBlood ProteinsCFHR1 protein, humanComplement C3b Inactivator ProteinsComplement Factor Hcomplement regulator-acquiring surface proteins, Borrelia burgdorferiMembrane Proteins

Identifiers

PMID16239539
PMCPMC1273877
OpenAlexW2160286580

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.