Evidence map›Paper›PMID 32405826›Full record

ArticleArchives of virology2020

Generation of recombinant VP3 protein of infectious bursal disease virus in three different expression systems, antigenic analysis of the obtained polypeptides and development of an ELISA test.

Dmitriy A Shirokov, Valentin A Manuvera, Olga A Miroshina, Alexandr S Dubovoi, Galina N Samuseva, Margarita E Dmitrieva, Vassili N Lazarev

Abstract read
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In one paragraph

Article in Archives of virology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 23% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. 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 3 institutions in 1 country.

Dmitriy A ShirokovFederal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency, Moscow, Russian Federation. dmitry.a.shirokov@gmail.com.ORCID http://orcid.org/0000-0001-6080-3348
Valentin A ManuveraFederal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency, Moscow, Russian Federation.
Olga A MiroshinaFederal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency, Moscow, Russian Federation.
Alexandr S DubovoiAll-Russian Research Veterinary Institute of Poultry Science, Branch of All-Russian Research and Technological Poultry Institute of the Russian Academy of Sciences, Sergiyev Posad, Russian Federation, St. Petersburg, Russian Federation.
Galina N SamusevaAll-Russian Research Veterinary Institute of Poultry Science, Branch of All-Russian Research and Technological Poultry Institute of the Russian Academy of Sciences, Sergiyev Posad, Russian Federation, St. Petersburg, Russian Federation.
Margarita E DmitrievaAll-Russian Research Veterinary Institute of Poultry Science, Branch of All-Russian Research and Technological Poultry Institute of the Russian Academy of Sciences, Sergiyev Posad, Russian Federation, St. Petersburg, Russian Federation.
Vassili N LazarevFederal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency, Moscow, Russian Federation.
Russian Academy of Sciences · RUMoscow Institute of Physics and Technology · RUMoscow State Academy of Veterinary Medicine and Biotechnology named after Skryabin · RU

Funding

Russian Science Foundation 16-16-04051
6 · The paper itself

Abstract

Infectious bursal disease virus (IBDV), which infects young chickens, is one of the most important pathogens that harm the poultry industry. Evaluation of the immune status of birds before and after vaccination is of great importance for controlling the disease caused by this virus. Therefore, the development of low-cost and easy-to-manufacture test systems for IBDV antibody detection remains an urgent issue. In this study, three expression systems (bacteria, yeast, and human cells) were used to produce recombinant VP3 protein of IBDV. VP3 is a group-specific antigen and hence may be a good candidate for use in diagnostic tests. Comparison of the antigenic properties of the obtained polypeptides showed that the titres of antibodies raised in chickens against bacteria- or human-cell-derived recombinant VP3 were high, whereas the antibody level against yeast-derived recombinant VP3 was low. The results of an enzyme-linked immunosorbent assay (ELISA) of sera from IBDV-infected chickens demonstrated that the recombinant VP3 produced in E. coli would be the best choice for use in test systems.

Indexed as

AnimalsAntibodies, ViralBirnaviridae InfectionsChickensEnzyme-Linked Immunosorbent AssayEpitope MappingEscherichia coliInfectious bursal disease virusPeptidesPoultry DiseasesRecombinant ProteinsViral Structural ProteinsAntibodies, ViralPeptidesRecombinant ProteinsViral Structural ProteinsVP3 protein, infectious bursal disease virus

Identifiers

PMID32405826
OpenAlexW3025316276

What OpenQuestion holds

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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.