Evidence map›Paper›PMID 19114549›Full record

ArticleInfection and immunity2009

Immune evasion of leptospira species by acquisition of human complement regulator C4BP.

Angela S Barbosa, Patricia A E Abreu, Sílvio A Vasconcellos, Zenaide M Morais, Amane P Gonçales, Aldacilene S Silva, Mohamed R Daha, Lourdes Isaac

Abstract read
In one paragraph

Article in Infection and immunity, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
–field-weighted citation impact
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

38 citing papers in PubMed.

  1. Trial
  2. Article
  3. Complement Resistance Assays.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  4. Neuroimmune cross-talk inFrontiers in immunology · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. The structure ofFrontiers in immunology · 2023
    Article
  9. Review
  10. Review
  11. Article
  12. A Review on Host-Frontiers in cellular and infection microbiology · 2021
    Review
  13. Interactions Between PathogenicFrontiers in cellular and infection microbiology · 2021
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Role of Murine Complement Component C5 in AcuteFrontiers in cellular and infection microbiology · 2018
    Article
  20. Frontiers in cellular and infection microbiology · 2018
    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.

Angela S BarbosaLaboratório de Bacteriologia, Instituto Butantan, São Paulo, Brazil. angelabarbosa@butantan.gov.br
Patricia A E Abreu
Sílvio A Vasconcellos
Zenaide M Morais
Amane P Gonçales
Aldacilene S Silva
Mohamed R Daha
Lourdes Isaac

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Leptospirosis is a spirochetal zoonotic disease of global distribution with a high incidence in tropical regions. In the last 15 years it has been recognized as an important emerging infectious disease due to the occurrence of large outbreaks in warm-climate countries and, occasionally, in temperate regions. Pathogenic leptospires efficiently colonize target organs after penetrating the host. Their invasiveness is attributed to the ability to multiply in blood, adhere to host cells, and penetrate into tissues. Therefore, they must be able to evade the innate host defense. The main purpose of the present study was to evaluate how several Leptospira strains evade the protective function of the complement system. The serum resistance of six Leptospira strains was analyzed. We demonstrate that the pathogenic strain isolated from infected hamsters avoids serum bactericidal activity more efficiently than the culture-attenuated or the nonpathogenic Leptospira strains. Moreover, both the alternative and the classical pathways of complement seem to be responsible for the killing of leptospires. Serum-resistant and serum-intermediate strains are able to bind C4BP, whereas the serum-sensitive strain Patoc I is not. Surface-bound C4BP promotes factor I-mediated cleavage of C4b. Accordingly, we found that pathogenic strains displayed reduced deposition of the late complement components C5 to C9 upon exposure to serum. We conclude that binding of C4BP contributes to leptospiral serum resistance against host complement.

Indexed as

AnimalsComplement C4b-Binding ProteinCricetinaeHistocompatibility AntigensHumansImmunoenzyme TechniquesLeptospiraLeptospirosisC4BPA protein, humanComplement C4b-Binding ProteinHistocompatibility Antigens

Identifiers

PMID19114549
PMCPMC2643629

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.