Evidence map›Paper›PMID 25454607›Full record

ArticleTicks and tick-borne diseases2015

Amblyomma americanum tick calreticulin binds C1q but does not inhibit activation of the classical complement cascade.

Tae Kwon Kim, Adriana Mércia Guaratini Ibelli, Albert Mulenga

Open access · greenAbstract read
In one paragraph

Article in Ticks and tick-borne diseases, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.6field-weighted citation impact, top 12% 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

21 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. RecombinantPathogens (Basel, Switzerland) · 2024
    Article
  5. The many faces of parasite calreticulin.Frontiers in immunology · 2023
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Identification ofPathogens (Basel, Switzerland) · 2020
    Article
  11. Review
  12. TNF-α/calreticulin dual signaling induced NLRP3 inflammasome activation associated with HuR nucleocytoplasmic shuttling in rheumatoid arthritis.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2019
    Article
  13. Review
  14. Article
  15. Review
  16. Immunomodulatory Effects ofFrontiers in cellular and infection microbiology · 2017
    Article
  17. DecipheringFrontiers in cellular and infection microbiology · 2017
    Review
  18. 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

3 authors at 1 institution in 1 country.

Tae Kwon KimTexas A & M University AgriLife Research, Department of Entomology, 2475 TAMU, College Station, TX 77843, United States.
Adriana Mércia Guaratini Ibelli
Albert Mulenga
Texas A&M University · US

Funding

Molecular Mechanisms Regulating Early Stage Tick FeedingR21AI081093 · NIAID · TEXAS A&M UNIVERSITY · PI MULENGA, ALBERT · 2011 to 2012
$404k
NIAID NIH HHS AI081093NIAID NIH HHS R21 AI081093
6 · The paper itself

Abstract

In this study we characterized Amblyomma americanum (Aam) tick calreticulin (CRT) homolog in tick feeding physiology. In nature, different tick species can be found feeding on the same animal host. This suggests that different tick species found feeding on the same host can modulate the same host anti-tick defense pathways to successfully feed. From this perspective it's plausible that different tick species can utilize universally conserved proteins such as CRT to regulate and facilitate feeding. CRT is a multi-functional protein found in most taxa that is injected into the vertebrate host during tick feeding. Apart from it's current use as a biomarker for human tick bites, role(s) of this protein in tick feeding physiology have not been elucidated. Here we show that annotated functional CRT amino acid motifs are well conserved in tick CRT. However our data show that despite high amino acid identity levels to functionally characterized CRT homologs in other organisms, AamCRT is apparently functionally different. Pichia pastoris expressed recombinant (r) AamCRT bound C1q, the first component of the classical complement system, but it did not inhibit activation of this pathway. This contrast with reports of other parasite CRT that inhibited activation of the classical complement pathway through sequestration of C1q. Furthermore rAamCRT did not bind factor Xa in contrast to reports of parasite CRT binding factor Xa, an important protease in the blood clotting system. Consistent with this observation, rAamCRT did not affect plasma clotting or platelet aggregation. We discuss our findings in the context of tick feeding physiology.

Indexed as

Amino Acid MotifsAmino Acid SequenceAnimalsCalreticulinComplement C1qComplement Pathway, ClassicalFeeding BehaviorHumansIxodidaeMolecular Sequence AnnotationMolecular Sequence DataPichiaRecombinant ProteinsSequence AlignmentCalreticulinComplement C1qRecombinant Proteins

Identifiers

PMID25454607
PMCPMC4304940
OpenAlexW1986701745

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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.