Evidence map›Paper›PMID 32851044›Full record

ArticleFrontiers in veterinary science2020

Diagnostic and Epitope Mapping Potential of Single-Chain Antibody Fragments Against Foot-and-Mouth Disease Virus Serotypes A, SAT1, and SAT3.

Melanie Chitray, Pamela Anne Opperman, Lia Rotherham, Jeanni Fehrsen, Wouter van Wyngaardt, Janine Frischmuth, Elizabeth Rieder, Francois Frederick Maree

Open access · goldAbstract read
In one paragraph

Article in Frontiers in veterinary science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.5field-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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
  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

8 authors at 4 institutions in 2 countries.

Melanie ChitrayAgricultural Research Council, Onderstepoort Veterinary Research, Vaccines and Diagnostic Development, Onderstepoort, Pretoria, South Africa.
Pamela Anne OppermanAgricultural Research Council, Onderstepoort Veterinary Research, Vaccines and Diagnostic Development, Onderstepoort, Pretoria, South Africa.
Lia RotherhamAgricultural Research Council, Onderstepoort Veterinary Research, Vaccines and Diagnostic Development, Onderstepoort, Pretoria, South Africa.
Jeanni FehrsenAgricultural Research Council, Onderstepoort Veterinary Research, Vaccines and Diagnostic Development, Onderstepoort, Pretoria, South Africa.
Wouter van WyngaardtAgricultural Research Council, Onderstepoort Veterinary Research, Vaccines and Diagnostic Development, Onderstepoort, Pretoria, South Africa.
Janine FrischmuthBiotechnology Division, National Bioproducts Institute, Pinetown, South Africa.
Elizabeth RiederPlum Island Animal Disease Centre, U.S. Department of Agriculture, Agricultural Research Service, Greenport, NY, United States.
Francois Frederick MareeAgricultural Research Council, Onderstepoort Veterinary Research, Vaccines and Diagnostic Development, Onderstepoort, Pretoria, South Africa.
University of Pretoria · ZAOnderstepoort Veterinary Institute · ZANational Bioproducts Institute (South Africa) · ZAPlum Island Animal Disease Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Foot-and-mouth disease (FMD) affects cloven-hoofed domestic and wildlife animals and an outbreak can cause severe losses in milk production, reduction in meat production and death amongst young animals. Several parts of Asia, most of Africa, and the Middle East remain endemic, thus emphasis on improved FMD vaccines, diagnostic assays, and control measures are key research areas. FMD virus (FMDV) populations are quasispecies, which pose serious implications in vaccine design and efficacy where an effective vaccine should include multiple independent neutralizing epitopes to elicit an adequate immune response. Further investigation of the residues that comprise the antigenic determinants of the virus will allow the identification of mutations in outbreak strains that potentially lessen the efficacy of a vaccine. Additionally, of utmost importance in endemic regions, is the accurate diagnosis of FMDV infection for the control and eradication of the disease. To this end, a phage display library was explored to identify FMDV epitopes for recombinant vaccines and for the generation of reagents for improved diagnostic FMD enzyme-linked immunosorbent assays (ELISAs). A naïve semi-synthetic chicken single chain variable fragment (scFv) phage display library i.e., the

Indexed as

ELISAepitopefoot-and-mouth diseasephage displaySAT1SAT3serotype Asingle-chain variable fragment

Identifiers

PMID32851044
PMCPMC7432252
OpenAlexW3048152682

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.