Evidence map›Paper›PMID 34099081›Full record

ArticleEpidemiology and infection2021

Improved diagnosis of SARS-CoV-2 by using nucleoprotein and spike protein fragment 2 in quantitative dual ELISA tests.

Carolina De Marco Verissimo, Carol O'Brien, Jesús López Corrales, Amber Dorey, Krystyna Cwiklinski, Richard Lalor, Jack M Doyle, Stephen Field, Claire Masterson, Eduardo Ribes Martinez and 8 more

Abstract read
In one paragraph

Article in Epidemiology and infection, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. COVID-19 and the Vasculature: Current Aspects and Long-Term Consequences.Frontiers in cell and developmental biology · 2022
    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

18 authors.

Carolina De Marco VerissimoMolecular Parasitology Lab (MPL), Centre for One Health and Ryan Institute, School of Natural Science, National University of Ireland Galway, Galway, Republic of Ireland.ORCID 0000-0003-1762-6387
Carol O'BrienDepartment of Biology, National University of Ireland Maynooth, Maynooth, Ireland.
Jesús López CorralesMolecular Parasitology Lab (MPL), Centre for One Health and Ryan Institute, School of Natural Science, National University of Ireland Galway, Galway, Republic of Ireland.
Amber DoreyMolecular Parasitology Lab (MPL), Centre for One Health and Ryan Institute, School of Natural Science, National University of Ireland Galway, Galway, Republic of Ireland.
Krystyna CwiklinskiMolecular Parasitology Lab (MPL), Centre for One Health and Ryan Institute, School of Natural Science, National University of Ireland Galway, Galway, Republic of Ireland.
Richard LalorMolecular Parasitology Lab (MPL), Centre for One Health and Ryan Institute, School of Natural Science, National University of Ireland Galway, Galway, Republic of Ireland.
Jack M DoyleDepartment of Biology, National University of Ireland Maynooth, Maynooth, Ireland.
Stephen FieldClinical Associate Professor (TCD), Medical and Scientific Director, Irish Blood Transfusion Service, Dublin, Ireland.
Claire MastersonSchool of Medicine, and Regenerative Medicine Institute (REMEDI) at CÚRAM Centre for Research in Medical Devices, Biomedical Sciences Building, National University of Ireland Galway, Galway, Ireland.
Eduardo Ribes MartinezSchool of Medicine, and Regenerative Medicine Institute (REMEDI) at CÚRAM Centre for Research in Medical Devices, Biomedical Sciences Building, National University of Ireland Galway, Galway, Ireland.
Gerry HughesSchool of Medicine, Trinity College Dublin, College Green, Dublin 2, Ireland.
Colm BerginSchool of Medicine, Trinity College Dublin, College Green, Dublin 2, Ireland.
Kieran WalsheDepartment of Biology, National University of Ireland Maynooth, Maynooth, Ireland.
Bairbre McNicholasDepartment of Anaesthesia and Intensive Care Medicine, University Hospital Galway, Saolta University Hospital Group, Galway, Ireland.
John G LaffeySchool of Medicine, and Regenerative Medicine Institute (REMEDI) at CÚRAM Centre for Research in Medical Devices, Biomedical Sciences Building, National University of Ireland Galway, Galway, Ireland.
John P DaltonMolecular Parasitology Lab (MPL), Centre for One Health and Ryan Institute, School of Natural Science, National University of Ireland Galway, Galway, Republic of Ireland.
Colm KerrSchool of Medicine, Trinity College Dublin, College Green, Dublin 2, Ireland.
Sean DoyleDepartment of Biology, National University of Ireland Maynooth, Maynooth, Ireland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The novel coronavirus, severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2), is the causative agent of the 2020 worldwide coronavirus pandemic. Antibody testing is useful for diagnosing historic infections of a disease in a population. These tests are also a helpful epidemiological tool for predicting how the virus spreads in a community, relating antibody levels to immunity and for assessing herd immunity. In the present study, SARS-CoV-2 viral proteins were recombinantly produced and used to analyse serum from individuals previously exposed, or not, to SARS-CoV-2. The nucleocapsid (Npro) and spike subunit 2 (S2Frag) proteins were identified as highly immunogenic, although responses to the former were generally greater. These two proteins were used to develop two quantitative enzyme-linked immunosorbent assays (ELISAs) that when used in combination resulted in a highly reliable diagnostic test. Npro and S2Frag-ELISAs could detect at least 10% more true positive coronavirus disease-2019 (COVID-19) cases than the commercially available ARCHITECT test (Abbott). Moreover, our quantitative ELISAs also show that specific antibodies to SARS-CoV-2 proteins tend to wane rapidly even in patients who had developed severe disease. As antibody tests complement COVID-19 diagnosis and determine population-level surveillance during this pandemic, the alternative diagnostic we present in this study could play a role in controlling the spread of the virus.

Indexed as

AdultAgedAntibodies, ViralCoronavirus Nucleocapsid ProteinsCOVID-19COVID-19 Serological TestingEnzyme-Linked Immunosorbent AssayFemaleHumansImmunoglobulin GKineticsMaleMiddle AgedPhosphoproteinsRecombinant ProteinsSARS-CoV-2Antibodies, ViralCoronavirus Nucleocapsid ProteinsImmunoglobulin Gnucleocapsid phosphoprotein, SARS-CoV-2PhosphoproteinsRecombinant ProteinsSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2COVID-19diagnosisnucleocapsid proteinSARS-CoV-2spike protein

Identifiers

PMID34099081
PMCPMC8207563

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.