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Investigation of the “Antigen Hook Effect” in Lateral Flow Sandwich Immunoassay: The Case of Lumpy Skin Disease Virus Detection
Lumpy skin disease (LSD) is an infectious disease affecting bovine with severe symptomatology. The implementation of effective control strategies to prevent infection outbreak requires rapid diagnostic tools. Two monoclonal antibodies (mAbs), targeting different epitopes of the LSDV structural prote...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9496205/ https://www.ncbi.nlm.nih.gov/pubmed/36140124 http://dx.doi.org/10.3390/bios12090739 |
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author | Cavalera, Simone Pezzoni, Giulia Grazioli, Santina Brocchi, Emiliana Baselli, Stefano Lelli, Davide Colitti, Barbara Serra, Thea Nardo, Fabio Di Chiarello, Matteo Testa, Valentina Rosati, Sergio Baggiani, Claudio Anfossi, Laura |
author_facet | Cavalera, Simone Pezzoni, Giulia Grazioli, Santina Brocchi, Emiliana Baselli, Stefano Lelli, Davide Colitti, Barbara Serra, Thea Nardo, Fabio Di Chiarello, Matteo Testa, Valentina Rosati, Sergio Baggiani, Claudio Anfossi, Laura |
author_sort | Cavalera, Simone |
collection | PubMed |
description | Lumpy skin disease (LSD) is an infectious disease affecting bovine with severe symptomatology. The implementation of effective control strategies to prevent infection outbreak requires rapid diagnostic tools. Two monoclonal antibodies (mAbs), targeting different epitopes of the LSDV structural protein p32, and gold nanoparticles (AuNPs) were used to set up a colorimetric sandwich-type lateral flow immunoassay (LFIA). Combinations including one or two mAbs, used either as the capture or detection reagent, were explored to investigate the hook effect due to antigen saturation by the detector antibody. The mAb-AuNP preparations were optimized by a full-factorial design of experiment to achieve maximum sensitivity. Opposite optimal conditions were selected when one Mab was used for capture and detection instead of two mAbs; thus, two rational routes for developing a highly sensitive LFIA according to Mab availability were outlined. The optimal LFIA for LSDV showed a low limit of detection (10(3.4) TCID(50)/mL), high inter- and intra-assay repeatability (CV% < 5.3%), and specificity (no cross-reaction towards 12 other viruses was observed), thus proving to be a good candidate as a useful tool for the point-of-need diagnosis of LSD. |
format | Online Article Text |
id | pubmed-9496205 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-94962052022-09-23 Investigation of the “Antigen Hook Effect” in Lateral Flow Sandwich Immunoassay: The Case of Lumpy Skin Disease Virus Detection Cavalera, Simone Pezzoni, Giulia Grazioli, Santina Brocchi, Emiliana Baselli, Stefano Lelli, Davide Colitti, Barbara Serra, Thea Nardo, Fabio Di Chiarello, Matteo Testa, Valentina Rosati, Sergio Baggiani, Claudio Anfossi, Laura Biosensors (Basel) Article Lumpy skin disease (LSD) is an infectious disease affecting bovine with severe symptomatology. The implementation of effective control strategies to prevent infection outbreak requires rapid diagnostic tools. Two monoclonal antibodies (mAbs), targeting different epitopes of the LSDV structural protein p32, and gold nanoparticles (AuNPs) were used to set up a colorimetric sandwich-type lateral flow immunoassay (LFIA). Combinations including one or two mAbs, used either as the capture or detection reagent, were explored to investigate the hook effect due to antigen saturation by the detector antibody. The mAb-AuNP preparations were optimized by a full-factorial design of experiment to achieve maximum sensitivity. Opposite optimal conditions were selected when one Mab was used for capture and detection instead of two mAbs; thus, two rational routes for developing a highly sensitive LFIA according to Mab availability were outlined. The optimal LFIA for LSDV showed a low limit of detection (10(3.4) TCID(50)/mL), high inter- and intra-assay repeatability (CV% < 5.3%), and specificity (no cross-reaction towards 12 other viruses was observed), thus proving to be a good candidate as a useful tool for the point-of-need diagnosis of LSD. MDPI 2022-09-08 /pmc/articles/PMC9496205/ /pubmed/36140124 http://dx.doi.org/10.3390/bios12090739 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Cavalera, Simone Pezzoni, Giulia Grazioli, Santina Brocchi, Emiliana Baselli, Stefano Lelli, Davide Colitti, Barbara Serra, Thea Nardo, Fabio Di Chiarello, Matteo Testa, Valentina Rosati, Sergio Baggiani, Claudio Anfossi, Laura Investigation of the “Antigen Hook Effect” in Lateral Flow Sandwich Immunoassay: The Case of Lumpy Skin Disease Virus Detection |
title | Investigation of the “Antigen Hook Effect” in Lateral Flow Sandwich Immunoassay: The Case of Lumpy Skin Disease Virus Detection |
title_full | Investigation of the “Antigen Hook Effect” in Lateral Flow Sandwich Immunoassay: The Case of Lumpy Skin Disease Virus Detection |
title_fullStr | Investigation of the “Antigen Hook Effect” in Lateral Flow Sandwich Immunoassay: The Case of Lumpy Skin Disease Virus Detection |
title_full_unstemmed | Investigation of the “Antigen Hook Effect” in Lateral Flow Sandwich Immunoassay: The Case of Lumpy Skin Disease Virus Detection |
title_short | Investigation of the “Antigen Hook Effect” in Lateral Flow Sandwich Immunoassay: The Case of Lumpy Skin Disease Virus Detection |
title_sort | investigation of the “antigen hook effect” in lateral flow sandwich immunoassay: the case of lumpy skin disease virus detection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9496205/ https://www.ncbi.nlm.nih.gov/pubmed/36140124 http://dx.doi.org/10.3390/bios12090739 |
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