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


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 23 08 2019
accepted: 31 01 2020
entrez: 16 4 2020
pubmed: 16 4 2020
medline: 2 7 2020
Statut: epublish

Résumé

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.

Identifiants

pubmed: 32294099
doi: 10.1371/journal.pone.0229196
pii: PONE-D-19-23810
pmc: PMC7159214
doi:

Substances chimiques

Antibodies, Monoclonal 0
Capsid Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0229196

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Références

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Auteurs

Shogo Miyoshi (S)

Division of Cell-Free Sciences, Proteo-Science Center, Ehime University, Matsuyama, Ehime, Japan.

Soh Tokunaga (S)

Division of Cell-Free Sciences, Proteo-Science Center, Ehime University, Matsuyama, Ehime, Japan.

Tatsuhiko Ozawa (T)

Department of Immunology, Graduate School of Medical and Pharmacological Science, University of Toyama, Toyama, Toyama, Japan.

Hiroyuki Takeda (H)

Division of Proteo-Drug-Discovery Sciences, Proteo-Science Center, Ehime University, Matsuyama, Ehime, Japan.

Mitsuo Aono (M)

Fruit Tree Research Center, Ehime Research Institute of Agriculture, Forestry and Fisheries, Matsuyama, Ehime, Japan.

Takanori Miyoshi (T)

Fruit Tree Research Center, Ehime Research Institute of Agriculture, Forestry and Fisheries, Matsuyama, Ehime, Japan.

Hiroyuki Kishi (H)

Department of Immunology, Graduate School of Medical and Pharmacological Science, University of Toyama, Toyama, Toyama, Japan.

Atsushi Muraguchi (A)

Department of Immunology, Graduate School of Medical and Pharmacological Science, University of Toyama, Toyama, Toyama, Japan.

Shin-Ichi Shimizu (SI)

Fruit Tree Research Center, Ehime Research Institute of Agriculture, Forestry and Fisheries, Matsuyama, Ehime, Japan.

Akira Nozawa (A)

Division of Cell-Free Sciences, Proteo-Science Center, Ehime University, Matsuyama, Ehime, Japan.

Tatsuya Sawasaki (T)

Division of Cell-Free Sciences, Proteo-Science Center, Ehime University, Matsuyama, Ehime, Japan.

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Classifications MeSH