Evidence map›Paper›PMID 32294099›Full record

ArticlePloS one2020

Production of a rabbit monoclonal antibody for highly sensitive detection of citrus mosaic virus and related viruses.

Shogo Miyoshi, Soh Tokunaga, Tatsuhiko Ozawa, Hiroyuki Takeda, Mitsuo Aono, Takanori Miyoshi, Hiroyuki Kishi, Atsushi Muraguchi, Shin-Ichi Shimizu, Akira Nozawa and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.5field-weighted citation impact, top 26% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

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

11 authors at 3 institutions in 1 country.

Shogo MiyoshiDivision of Cell-Free Sciences, Proteo-Science Center, Ehime University, Matsuyama, Ehime, Japan.
Soh TokunagaDivision of Cell-Free Sciences, Proteo-Science Center, Ehime University, Matsuyama, Ehime, Japan.
Tatsuhiko OzawaDepartment of Immunology, Graduate School of Medical and Pharmacological Science, University of Toyama, Toyama, Toyama, Japan.ORCID 0000-0002-3112-452X
Hiroyuki TakedaDivision of Proteo-Drug-Discovery Sciences, Proteo-Science Center, Ehime University, Matsuyama, Ehime, Japan.
Mitsuo AonoFruit Tree Research Center, Ehime Research Institute of Agriculture, Forestry and Fisheries, Matsuyama, Ehime, Japan.
Takanori MiyoshiFruit Tree Research Center, Ehime Research Institute of Agriculture, Forestry and Fisheries, Matsuyama, Ehime, Japan.
Hiroyuki KishiDepartment of Immunology, Graduate School of Medical and Pharmacological Science, University of Toyama, Toyama, Toyama, Japan.
Atsushi MuraguchiDepartment of Immunology, Graduate School of Medical and Pharmacological Science, University of Toyama, Toyama, Toyama, Japan.
Shin-Ichi ShimizuFruit Tree Research Center, Ehime Research Institute of Agriculture, Forestry and Fisheries, Matsuyama, Ehime, Japan.
Akira NozawaDivision of Cell-Free Sciences, Proteo-Science Center, Ehime University, Matsuyama, Ehime, Japan.ORCID 0000-0003-4886-0213
Tatsuya SawasakiDivision of Cell-Free Sciences, Proteo-Science Center, Ehime University, Matsuyama, Ehime, Japan.
CellFree Sciences (Japan) · JPUniversity of Toyama · JPEhime University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Citrus mosaic virus (CiMV) is one of the causal viruses of citrus mosaic disease in satsuma mandarins (Citrus unshiu). Prompt detection of trees infected with citrus mosaic disease is important for preventing the spread of this disease. Although rabbit monoclonal antibodies (mAbs) exhibit high specificity and affinity, their applicability is limited by technical difficulties associated with the hybridoma-based technology used for raising these mAbs. Here, we demonstrate a feasible CiMV detection system using a specific rabbit mAb against CiMV coat protein. A conserved peptide fragment of the small subunit of CiMV coat protein was designed and used to immunize rabbits. Antigen-specific antibody-producing cells were identified by the immunospot array assay on a chip method. After cloning of variable regions in heavy or light chain by RT-PCR from these cells, a gene set of 33 mAbs was constructed and these mAbs were produced using Expi293F cells. Screening with the AlphaScreen system revealed eight mAbs exhibiting strong interaction with the antigen peptide. From subsequent sequence analysis, they were grouped into three mAbs denoted as No. 4, 9, and 20. Surface plasmon resonance analysis demonstrated that the affinity of these mAbs for the antigen peptide ranged from 8.7 × 10-10 to 5.5 × 10-11 M. In addition to CiMV, mAb No. 9 and 20 could detect CiMV-related viruses in leaf extracts by ELISA. Further, mAb No. 20 showed a high sensitivity to CiMV and CiMV-related viruses, simply by dot blot analysis. The anti-CiMV rabbit mAbs obtained in this study are envisioned to be extremely useful for practical applications of CiMV detection, such as in a virus detection kit.

Indexed as

Amino Acid SequenceAnimalsAntibodies, MonoclonalAntibody SpecificityCapsid ProteinsCitrusKineticsMosaic VirusesPlant LeavesRabbitsAntibodies, MonoclonalCapsid Proteins

Identifiers

PMID32294099
PMCPMC7159214
OpenAlexW3015732787

What OpenQuestion holds

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LicenceCC BY
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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.