Evidence map›Paper›PMID 28794181›Full record

ArticleJournal of clinical microbiology2017

Neutralization Assay for Zika and Dengue Viruses by Use of Real-Time-PCR-Based Endpoint Assessment.

Heather L Wilson, Thomas Tran, Julian Druce, Myrielle Dupont-Rouzeyrol, Michael Catton

Open access · bronzeAbstract read
In one paragraph

Article in Journal of clinical microbiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

15 citing papers in PubMed, 37 citations in OpenAlex.

  1. Application of Orthoflavivirus Pseudovirus Technology in Antiviral Research.International journal of molecular sciences · 2026
    Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Congenital Zika Virus Infection in a Birth Cohort in Vietnam, 2017-2018.The American journal of tropical medicine and hygiene · 2020
    Article
  7. Article
  8. Article
  9. Immunological Assays used to Support Efficacy of Zika Virus Vaccines.Tropical medicine and infectious disease · 2019
    Review
  10. Article
  11. Article
  12. Article
  13. Detection of Zika Virus Infection in Myanmar.The American journal of tropical medicine and hygiene · 2018
    Article
  14. Switch-on the LAMP to spot Zika.Annals of translational medicine · 2017
    Article
  15. 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

5 authors at 3 institutions in 2 countries.

Heather L WilsonVictorian Infectious Diseases Reference Laboratory, The Royal Melbourne Hospital at the Peter Doherty Institute, Melbourne, Victoria, Australia Heather.Wilson@act.gov.au.
Thomas TranVictorian Infectious Diseases Reference Laboratory, The Royal Melbourne Hospital at the Peter Doherty Institute, Melbourne, Victoria, Australia.
Julian DruceVictorian Infectious Diseases Reference Laboratory, The Royal Melbourne Hospital at the Peter Doherty Institute, Melbourne, Victoria, Australia.
Myrielle Dupont-RouzeyrolInstitut Pasteur in New Caledonia, Research and Expertise Unit on Dengue and Arboviruses, International Institut Pasteur Network, Noumea, New Caledonia.
Michael CattonVictorian Infectious Diseases Reference Laboratory, The Royal Melbourne Hospital at the Peter Doherty Institute, Melbourne, Victoria, Australia.
The Royal Melbourne Hospital · AUInstitut Pasteur de Nouvelle Calédonie · NCVictorian Infectious Diseases Reference Laboratory · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The global spread and infective complications of Zika virus (ZKV) and dengue virus (DENV) have made them flaviviruses of public health concern. Serological diagnosis can be challenging due to antibody cross-reactivity, particularly in secondary flavivirus infections or when there is a history of flavivirus vaccination. The virus neutralization assay is considered to be the most specific assay for measurement of anti-flavivirus antibodies. This study describes an assay where the neutralization endpoint is measured by real-time PCR, providing results within 72 h. It demonstrated 100% sensitivity (24/24 ZKV and 15/15 DENV) and 100% specificity (11/11 specimens) when testing well-characterized sera. In addition, the assay was able to determine the correct DENV serotype in 91.7% of cases. The high sensitivity and specificity of the real-time PCR neutralization assay makes it suitable to use as a confirmatory test for sera that are reactive in commercial IgM/IgG enzyme immunoassays. Results are objective and the PCR-based measurement of the neutralization endpoint lends itself to automation so that throughput may be increased in times of high demand.

Indexed as

AdultAntibodies, ViralDengueDengue VirusEnzyme-Linked Immunosorbent AssayHumansNeutralization TestsReal-Time Polymerase Chain ReactionZika VirusZika Virus InfectionAntibodies, ViraldengueflavivirusserologyZika

Identifiers

PMID28794181
PMCPMC5625395
OpenAlexW2744312063

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.