Evidence map›Paper›PMID 34063385›Full record

ArticleViruses2021

Development and Validation of Confirmatory Foot-and-Mouth Disease Virus Antibody ELISAs to Identify Infected Animals in Vaccinated Populations.

Anuj Tewari, Helen Ambrose, Krupali Parekh, Toru Inoue, Javier Guitian, Antonello Di Nardo, David James Paton, Satya Parida

Open access · goldAbstract readValidation Study
In one paragraph

Article in Viruses, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. 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

8 authors at 3 institutions in 2 countries.

Anuj TewariThe Pirbright Institute, Ash Road, Pirbright, Surrey GU24 0NF, UK.ORCID 0000-0002-6602-6014
Helen AmbroseThe Pirbright Institute, Ash Road, Pirbright, Surrey GU24 0NF, UK.
Krupali ParekhThe Pirbright Institute, Ash Road, Pirbright, Surrey GU24 0NF, UK.
Toru InoueDepartment of Exotic Disease, National Institute of Animal Health, 6-20-1, Josuihoncho, Kodaira, Tokyo 187-0022, Japan.
Javier GuitianVeterinary Epidemiology, Economics and Public Health, The Royal Veterinary College, Hawkshead Lane, North Mymms, Hatfield, Hertfordshire AL9 7TA, UK.
Antonello Di NardoThe Pirbright Institute, Ash Road, Pirbright, Surrey GU24 0NF, UK.
David James PatonThe Pirbright Institute, Ash Road, Pirbright, Surrey GU24 0NF, UK.
Satya ParidaThe Pirbright Institute, Ash Road, Pirbright, Surrey GU24 0NF, UK.ORCID 0000-0001-8253-9461
The Pirbright Institute · GBNational Institute of Animal Health · JPRoyal Veterinary College · GB

Funding

Biotechnology and Biological Sciences Research Council BBS/E/I/00001703Biotechnology and Biological Sciences Research Council BBS/E/I/00007031Biotechnology and Biological Sciences Research Council BBS/E/I/00007036Biotechnology and Biological Sciences Research Council BBS/E/I/00007037
6 · The paper itself

Abstract

In foot-and-mouth disease (FMD)-endemic countries, vaccination is commonly used to control the disease, whilst in FMD-free countries, vaccination is considered as an option, in addition to culling the infected and in contact animals. FMD vaccines are mainly comprised of inactivated virions and stimulate protective antibodies to virus structural proteins. In contrast, infection with FMD virus leads to virus replication and additional antibody responses to viral nonstructural proteins (NSP). Therefore, antibodies against NSPs are used to differentiate infection in vaccinated animals (DIVA), in order to estimate the prevalence of infection or its absence. Another advantage of NSP antibody tests is that they detect FMD infection in the field, irrespective of the serotypes of virus in circulation. In cattle, the NSP tests that target the 3ABC polyprotein provides the highest sensitivity, detecting up to 90% of vaccinated animals that become carriers after exposure to infection, with a specificity of around 99%. Due to insufficient diagnostic sensitivity and specificity, detection of a low level of infection is difficult at the population level with a high degree of confidence. The low level of non-specific responses can be overcome by retesting samples scored positive using a second confirmatory test, which should have at least comparable sensitivity to the first test. In this study, six in-house tests were developed incorporating different NSP antigens, and validated using bovine sera from naïve animals, field cases and experimentally vaccinated and/or infected animals. In addition, two (short and long incubation) new commercial NSP tests based on 3ABC competitive blocking ELISAs (ID Screen

Indexed as

AnimalsAntibodies, ViralAntibody FormationCattleCattle DiseasesEnzyme-Linked Immunosorbent AssayFoot-and-Mouth DiseaseFoot-and-Mouth Disease VirusSensitivity and SpecificityVaccinationAntibodies, ViralDIVAfoot-and-mouth diseasemultiple testingNSP ELISAsero-surveillancevaccinate-to-live

Identifiers

PMID34063385
PMCPMC8156621
OpenAlexW3162313488

What OpenQuestion holds

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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.