Evidence map›Paper›PMID 27136199›Full record

ArticlePloS one2016

Composition and Potency Characterization of Mycobacterium avium subsp. paratuberculosis Purified Protein Derivatives.

Randal T Capsel, Charles O Thoen, Timothy A Reinhardt, John D Lippolis, Renee Olsen, Judith R Stabel, John P Bannantine

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Lateral-flow assays for bovine paratuberculosis diagnosis.Frontiers in veterinary science · 2023
    Review
  3. Article
  4. Article
  5. Article
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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 3 institutions in 1 country.

Randal T CapselNational Veterinary Services Laboratories, U.S. Department of Agriculture-AHPIS, Ames, Iowa, United States of America.
Charles O ThoenDepartment of Veterinary Microbiology and Preventive Medicine, Iowa State University, College of Veterinary Medicine, Ames, Iowa, United States of America.
Timothy A ReinhardtNational Animal Disease Center, U.S. Department of Agriculture-ARS, Ames, Iowa, United States of America.
John D LippolisNational Animal Disease Center, U.S. Department of Agriculture-ARS, Ames, Iowa, United States of America.
Renee OlsenCenter for Veterinary Biologics, U.S. Department of Agriculture-APHIS, Ames, Iowa, United States of America.
Judith R StabelNational Animal Disease Center, U.S. Department of Agriculture-ARS, Ames, Iowa, United States of America.
John P BannantineNational Animal Disease Center, U.S. Department of Agriculture-ARS, Ames, Iowa, United States of America.
National Animal Disease Center · USAnimal and Plant Health Inspection Service · USIowa State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mycobacterium avium subsp. paratuberculosis (MAP) purified protein derivatives (PPDs) are immunologic reagents prepared from cultured filtrates of the type strain. Traditional production consists of floating culture incubation at 37°C, organism inactivation by autoclaving, coarse filtration, and protein precipitation. Three traditional production PPDs were used in this study including lot 9801, which served as a reference and has been used in the field for decades. Alternative production PPDs (0902A and 0902B), in which the autoclaving step was removed, were also analyzed in this study. SDS-PAGE analysis revealed protein smearing in traditional PPDs, but distinct bands were observed in the alternative PPD preparations. Antibody bound distinct protein bands in the alternative PPDs by immunoblot analysis, whereas an immunoreactive smear was observed with the traditional PPDs. Mass spectrometry identified 194 proteins among three PPD lots representing the two different production methods, ten of which were present in all PPDs examined. Selected proteins identified by mass spectrometry were recombinantly expressed and purified from E. coli and evaluated by the guinea pig potency test. Seven recombinant proteins showed greater erythema as compared to the reference PPD lot 9801 in paired guinea pigs and were able to stimulate interferon-gamma production in blood from Johne's positive animals. These results suggest that autoclaving culture suspensions is not a necessary step in PPD production and specific proteins could supplant the PPD antigen for intradermal skin testing procedures and for use as in-vitro assay reagents.

Indexed as

AnimalsCattleElectrophoresis, Polyacrylamide GelEscherichia coliGuinea PigsImmunity, HumoralImmunoblottingInterferon-gammaMass SpectrometryMycobacterium avium subsp. paratuberculosisRecombinant ProteinsInterferon-gammaRecombinant Proteins

Identifiers

PMID27136199
PMCPMC4852940
OpenAlexW2342554633

What OpenQuestion holds

Textmetadata
LicenceCC0
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.