Evidence map›Paper›PMID 38791660›Full record

ArticleAnimals : an open access journal from MDPI2024

Development of a Bead-Based Multiplex Fluorescent Immunoassay to Detect Antibodies against Maedi-Visna Virus in Sheep.

Anniken Jerre Borge, Barbara Colitti, Sergio Rosati, Anne B Nordstoga, Britt Gjerset, Kristin Udjus, Chiara Nogarol, Stalin Chellappa, Ingunn Anita Samdal, Kari Lybeck

Abstract read
In one paragraph

Article in Animals : an open access journal from MDPI, 2024. 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
–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

1 citing paper in PubMed.

  1. 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

10 authors.

Anniken Jerre BorgeNorwegian Veterinary Institute, P.O. Box 64, 1431 Ås, Norway.ORCID 0000-0002-3423-7271
Barbara ColittiDepartment of Veterinary Science, University of Turin, Largo P. Braccini 2, 10095 Grugliasco, TO, Italy.
Sergio RosatiDepartment of Veterinary Science, University of Turin, Largo P. Braccini 2, 10095 Grugliasco, TO, Italy.ORCID 0000-0002-8315-0316
Anne B NordstogaNorwegian Veterinary Institute, P.O. Box 64, 1431 Ås, Norway.
Britt GjersetNorwegian Veterinary Institute, P.O. Box 64, 1431 Ås, Norway.ORCID 0009-0005-6209-3024
Kristin UdjusNorwegian Veterinary Institute, P.O. Box 64, 1431 Ås, Norway.
Chiara NogarolIn3diagnostic s.r.l., Largo P. Braccini 2, 10095 Grugliasco, TO, Italy.
Stalin ChellappaNorwegian Veterinary Institute, P.O. Box 64, 1431 Ås, Norway.
Ingunn Anita SamdalNorwegian Veterinary Institute, P.O. Box 64, 1431 Ås, Norway.ORCID 0000-0001-5225-2494
Kari LybeckNorwegian Veterinary Institute, P.O. Box 64, 1431 Ås, Norway.

Funding

The Research Council of Norway NO 310753
6 · The paper itself

Abstract

The Maedi-visna virus (MVV) causes a persistent infection in small ruminants, and its high genetic heterogeneity affects the performance of diagnostic tests when used in different populations. Therefore, the aim of this study was to develop a bead-based multiplex immunoassay tailored to detect antibodies against a Norwegian MVV strain. We used tissue samples from 14 PCR-positive sheep from a recent MVV outbreak in Norway to sequence the viral strain and produced recombinant antigens based on sequences from one animal. The assay included commercial TM-A and recombinant Norwegian p25, p16-25 and SU5 antigens. Cut-off values for each antigen were determined using receiver operating characteristic curves on 40 ELISA-negative and 67 ELISA-positive samples from the outbreak. The intraplate and interplate repeatability were investigated by testing a quadruplicate of five samples over three days, while the analytical sensitivity (aSe) and specificity (aSp) were measured in comparison to a commercial ELISA. The repeatability showed a coefficient of variation below 15% for most positive samples. The aSe was equal or higher for the multiplex assay than the ELISA, and the aSp of each antigen was 91.7, 93.3, 95.0 and 93.3% for p25, p16-25, SU5 and TM-A, respectively. The assay shows promising results; however, further evaluations of diagnostic characteristics are necessary before implementation in the Norwegian surveillance programme.

Indexed as

diagnostic testluminex immunoassayMVVovinesmall ruminant lentivirusSRLV

Identifiers

PMID38791660
PMCPMC11117221

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Registered trials

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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.