Evidence map›Paper›PMID 16369028›Full record

ArticleInfection and immunity2006

Differentially expressed and secreted major immunoreactive protein orthologs of Ehrlichia canis and E. chaffeensis elicit early antibody responses to epitopes on glycosylated tandem repeats.

C Kuyler Doyle, Kimberly A Nethery, Vsevolod L Popov, Jere W McBride

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

62 citing papers in PubMed, 104 citations in OpenAlex.

  1. Veterinary sciences · 2024
    Review
  2. Immuno- and expression analysis ofFrontiers in veterinary science · 2024
    Article
  3. Article
  4. Infection and immunity · 2023
    Article
  5. Costa Rican Genotype ofVeterinary sciences · 2023
    Article
  6. Antibody reactive immunomes ofFrontiers in cellular and infection microbiology · 2023
    Article
  7. Type 1 secretion system and effectors in Rickettsiales.Frontiers in cellular and infection microbiology · 2023
    Review
  8. Article
  9. mBio · 2022
    Article
  10. Exposure of Domestic Cats to DistinctVeterinary sciences · 2021
    Article
  11. Article
  12. Effect of GP19 Peptide Hyperimmune Antiserum on Activated Macrophage duringAnimals : an open access journal from MDPI · 2021
    Article
  13. Article
  14. Article
  15. Geographic Distribution ofVeterinary sciences · 2020
    Article
  16. Article
  17. NPJ vaccines · 2020
    Article
  18. Article
  19. Emergence of a NovelMicroorganisms · 2019
    Article
  20. Review

2 more citing papers are in PubMed but not listed here.

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

4 authors at 1 institution in 2 countries.

C Kuyler DoyleDepartment of Pathology, University of Texas Medical Branch, Galveston, TX 77555, USA.
Kimberly A Nethery
Vsevolod L Popov
Jere W McBride
The University of Texas Medical Branch at Galveston · US

Funding

Protective Glycopeptide Immunodeterminants of Ehrlichia chaffeensisR01AI071145 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI MCBRIDE, JERE W · 2006 to 2010
$1.9M
NIAID NIH HHS R01 AI071145
6 · The paper itself

Abstract

Ehrlichia canis major immunoreactive proteins of 36 and 19 kDa elicit the earliest detectable antibody responses during the acute phase of canine monocytic ehrlichiosis. Genes encoding the major immunoreactive 36-kDa protein of E. canis and the corresponding ortholog of E. chaffeensis (47 kDa) were identified and the proteins characterized. The molecular masses of the strongly immunoreactive recombinant proteins were larger than predicted (26.7 and 32.9 kDa, respectively) but were consistent with those of the corresponding native proteins (36 and 47 kDa). Similar to other reported ehrlichial immunoreactive glycoproteins, carbohydrate was detected on the recombinant expressed proteins, indicating that they were glycoproteins. Both glycoproteins (gp36 and gp47) have carboxy-terminal serine/threonine-rich tandem repeat regions containing repeats that vary in number (4 to 16 repeats) and amino acid sequence among different isolates of each species. E. canis gp36 was recognized by early acute-phase antibodies (day 14), and species-specific antibody epitopes were mapped to C-terminal nonhomologous repeat units of gp36 and gp47. Periodate treatment of recombinant gp36 reduced the antibody reactivity, and nonglycosylated synthetic peptide repeat units from E. canis gp36 and E. chaffeensis gp47 were substantially less immunoreactive than corresponding recombinant peptides, demonstrating that glycans are important epitope determinants that are structurally conserved on the recombinant proteins expressed in Escherichia coli. E. canis gp36 and E. chaffeensis gp47 were differentially expressed only on the surface of dense-cored ehrlichiae and detected in the Ehrlichia-free supernatants, indicating that these proteins are released extracellularly during infection.

Indexed as

Amino Acid SequenceAnimalsAntigens, BacterialBacterial ProteinsDogsEhrlichia canisEhrlichia chaffeensisEhrlichiosisGlycoproteinsGlycosylationImmunodominant EpitopesImmunohistochemistryMiceMice, Inbred BALB CMolecular Sequence DataTandem Repeat SequencesAntigens, BacterialBacterial ProteinsGlycoproteinsImmunodominant Epitopes

Identifiers

PMID16369028
PMCPMC1346619
OpenAlexW2118903939

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.