Evidence map›Paper›PMID 35889170›Full record

ArticleMicroorganisms2022

A Chikungunya Virus Multiepitope Recombinant Protein Expressed from the Binary System Insect Cell/Recombinant Baculovirus Is Useful for Laboratorial Diagnosis of Chikungunya.

Leonardo Assis da Silva, Monique da Rocha Queiroz Lima, Brenda Rabello de Camargo, Dyeferson Kened da Silva Coelho Guimarães, Anabele Azevedo Lima Barbastefano, Raquel Curtinhas de Lima, Paulo Vieira Damasco, Rivaldo Venâncio da Cunha, Luiz José de Souza, Elzinandes Leal de Azeredo and 5 more

Open access · goldAbstract read
In one paragraph

Article in Microorganisms, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Review
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

15 authors at 6 institutions in 1 country.

Leonardo Assis da SilvaLaboratory of Baculovirus, Cell Biology Department, University of Brasilia, Brasilia 70910-900, DF, Brazil.
Monique da Rocha Queiroz LimaViral Immunology Laboratory, Oswaldo Cruz Institute Rio de Janeiro, Oswaldo Cruz Foundation, Rio de Janeiro 21040-900, RJ, Brazil.
Brenda Rabello de CamargoLaboratory of Baculovirus, Cell Biology Department, University of Brasilia, Brasilia 70910-900, DF, Brazil.
Dyeferson Kened da Silva Coelho GuimarãesCentro Universitário de Brasília, UniCEUB, Brasilia 70790-075, DF, Brazil.
Anabele Azevedo Lima BarbastefanoCentro Universitário de Brasília, UniCEUB, Brasilia 70790-075, DF, Brazil.
Raquel Curtinhas de LimaViral Immunology Laboratory, Oswaldo Cruz Institute Rio de Janeiro, Oswaldo Cruz Foundation, Rio de Janeiro 21040-900, RJ, Brazil.
Paulo Vieira DamascoPathological Anatomy, Gaffrée Guinle University Hospital Rio de Janeiro, Federal University of the State of Rio de Janeiro, Rio de Janeiro 20270-004, RJ, Brazil.
Rivaldo Venâncio da CunhaMedical Clinic Department, Federal University of Mato Grosso do Sul (UFMS), Campo Grande 79050-010, MS, Brazil.
Luiz José de SouzaPlantadores de Cana Hospital, Campos dos Goytacazes, Rio de Janeiro 28025-496, RJ, Brazil.
Elzinandes Leal de AzeredoViral Immunology Laboratory, Oswaldo Cruz Institute Rio de Janeiro, Oswaldo Cruz Foundation, Rio de Janeiro 21040-900, RJ, Brazil.
Luzia Maria de-Oliveira-PintoViral Immunology Laboratory, Oswaldo Cruz Institute Rio de Janeiro, Oswaldo Cruz Foundation, Rio de Janeiro 21040-900, RJ, Brazil.
Tatsuya NagataLaboratory of Baculovirus, Cell Biology Department, University of Brasilia, Brasilia 70910-900, DF, Brazil.
Daniel M P Ardisson-AraújoLaboratory of Insect Viruses, Cell Biology Department, University of Brasilia, Brasilia 70910-900, DF, Brazil.
Flavia Barreto Dos SantosViral Immunology Laboratory, Oswaldo Cruz Institute Rio de Janeiro, Oswaldo Cruz Foundation, Rio de Janeiro 21040-900, RJ, Brazil.ORCID 0000-0002-1309-5366
Bergmann Morais RibeiroLaboratory of Baculovirus, Cell Biology Department, University of Brasilia, Brasilia 70910-900, DF, Brazil.ORCID 0000-0002-1061-196X
Fundação Oswaldo Cruz · BRUniversidade de Brasília · BRUniversity Center of Brasília · BRHospital Universitário Gaffrée e Guinle · BRPrefeitura Municipal de Campos dos Goytacazes · BRUniversidade Federal de Mato Grosso do Sul · BR

Funding

Coordenação de Aperfeicoamento de Pessoal de Nível Superior Financial code 001Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/202.003/2016Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/202.659/2019Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro E-26/211.569/2019Fundação da Apoio à Pesquisa do Distrito Federal 0193.001499/2017Fundação da Apoio à Pesquisa do Distrito Federal 193001532/2016National Council for Scientific and Technological Development 302462/2018-0National Council for Scientific and Technological Development 305468/2019-7
6 · The paper itself

Abstract

Chikungunya virus (CHIKV) is an arbovirus currently distributed worldwide, causing a disease that shares clinical signs and symptoms with other illnesses, such as dengue and Zika and leading to a challenging clinical differential diagnosis. In Brazil, CHIKV emerged in 2014 with the simultaneous introduction of both Asian and East/Central/South African (ECSA) genotypes. Laboratorial diagnosis of CHIKV is mainly performed by molecular and serological assays, with the latter more widely used. Although many commercial kits are available, their costs are still high for many underdeveloped and developing countries where the virus circulates. Here we described the development and evaluation of a multi-epitope recombinant protein-based IgG-ELISA (MULTREC IgG-ELISA) test for the specific detection of anti-CHIKV antibodies in clinical samples, as an alternative approach for laboratorial diagnosis. The MULTREC IgG-ELISA showed 86.36% of sensitivity and 100% of specificity, and no cross-reactivity with other exanthematic diseases was observed. The recombinant protein was expressed from the binary system insect cell/baculovirus using the crystal-forming baculoviral protein polyhedrin as a carrier of the target recombinant protein to facilitate recovery. The crystals were at least 10 times smaller in size and had an amorphous shape when compared to the polyhedrin wild-type crystal. The assay uses a multi-epitope antigen, representing two replicates of 18 amino acid sequences from the E2 region and a sequence of 17 amino acids from the nsP3 region of CHIKV. The recombinant protein was highly expressed, easy to purify and has demonstrated its usefulness in confirming chikungunya exposure, indeed showing a good potential tool for epidemiological surveillance.

Indexed as

baculovirus expressionchikungunyaE2IgG-ELISArecombinant protein

Identifiers

PMID35889170
PMCPMC9316945
OpenAlexW4285728597

What OpenQuestion holds

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LicenceCC BY
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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.