Evidence map›Paper›PMID 17160605›Full record

ArticleWiener klinische Wochenschrift2006

Binding of human complement regulators FHL-1 and factor H to CRASP-1 orthologs of Borrelia burgdorferi.

Peter Kraiczy, Evelyn Rossmann, Volker Brade, Markus M Simon, Christine Skerka, Peter F Zipfel, Reinhard Wallich

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Wiener klinische Wochenschrift, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 2 pooled it
2.1field-weighted citation impact, top 15% 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

24 citing papers in PubMed, 2 syntheses or guidelines pooled it, 35 citations in OpenAlex.

  1. Guideline
  2. Guideline
  3. Comparative evaluation of viability assays and functional analysis ofApplied and environmental microbiology · 2026
    Article
  4. Review
  5. Article
  6. Review
  7. Evolution of theMicrobiology spectrum · 2022
    Article
  8. Elucidating the Immune Evasion Mechanisms ofFrontiers in immunology · 2019
    Article
  9. Article
  10. Multifunctional and Redundant Roles ofFrontiers in immunology · 2016
    Review
  11. Article
  12. Article
  13. Review
  14. Plasminogen is a complement inhibitor.The Journal of biological chemistry · 2012
    Article
  15. Review
  16. Article
  17. Article
  18. Novel Diagnosis of Lyme Disease: Potential for CAM Intervention.Evidence-based complementary and alternative medicine : eCAM · 2009
    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

7 authors at 4 institutions in 1 country.

Peter KraiczyInstitute of Medical Microbiology and Infection Control, University Hospital of Frankfurt, Frankfurt, Germany. Kraiczy@em.uni-frankfurt.de
Evelyn Rossmann
Volker Brade
Markus M Simon
Christine Skerka
Peter F Zipfel
Reinhard Wallich
Heidelberg University · DELeibniz-Institut für Naturstoff-Forschung und Infektionsbiologie e. V. - Hans-Knöll-Institut (HKI) · DEUniversity Hospital Frankfurt · DEMax Planck Society · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The complement regulator-acquiring surface protein (CRASP)-1 is a member of the paralogous gene family gbb54 and the dominant FHL-1 and factor H binding protein of Borrelia burgdorferi sensu stricto (s.s.). It was shown recently that expression of BbCRASP-1 directly correlates with serum resistance of B. burgdorferi s.s. isolates. In the present study we have elucidated the putative potential of other members of the gbb54 paralogous family, including orthologs ZSA66, ZSA69, ZSA70, ZSA71, ZSA72 and ZSA73 of the European B. burgdorferi s.s. strain ZS7, to bind human FHL-1 and factor H. In spite of their overall similarity in protein sequence, between 47% and 67%, and the fact that the C-terminal region of ZSA69 shows 70% similarity with BbCRASP-1, none of the orthologous proteins was able to bind human FHL-1 and/or factor H. BbCRASP-1 is the only member of the paralogous gene family gbb54 that binds to human complement regulators, supporting the notion that BbCRASP-1 plays a critical role in evasion of complement by B. burgdorferi s.s. and thus may be helpful in the development of novel therapeutic strategies against Lyme borreliosis.

Indexed as

Immunity, InnateBacterial ProteinsBase SequenceBlood DonorsBorrelia burgdorferiComplement ActivationComplement C3b Inactivator ProteinsComplement Factor HDNA, BacterialHumansLyme DiseaseMembrane ProteinsReverse Transcriptase Polymerase Chain ReactionBacterial ProteinsCFHR1 protein, humanComplement C3b Inactivator ProteinsComplement Factor Hcomplement regulator-acquiring surface proteins, Borrelia burgdorferiDNA, BacterialMembrane Proteins

Identifiers

PMID17160605
OpenAlexW1995740522

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.