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Development of Monoclonal Antibody Specific to Foot-and-Mouth Disease Virus Type A for Serodiagnosis

Foot-and-mouth disease (FMD) is a highly contagious and economically devastating disease affecting cloven-hoofed livestock worldwide. FMD virus (FMDV) type A is one of the most common causes of FMD outbreaks among the seven FMDV serotypes, and its serological diagnosis is therefore important to conf...

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Autores principales: Nguyen, Quyen Thi, Yang, Jihyun, Byun, Jae-Won, Pyo, Hyun Mi, Park, Mi-Young, Ku, Bok Kyung, Nah, Jinju, Ryoo, Soyoon, Wee, Sung-Hwan, Choi, Kang-Seuk, Poo, Haryoung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963590/
https://www.ncbi.nlm.nih.gov/pubmed/31861046
http://dx.doi.org/10.3390/pathogens8040301
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author Nguyen, Quyen Thi
Yang, Jihyun
Byun, Jae-Won
Pyo, Hyun Mi
Park, Mi-Young
Ku, Bok Kyung
Nah, Jinju
Ryoo, Soyoon
Wee, Sung-Hwan
Choi, Kang-Seuk
Poo, Haryoung
author_facet Nguyen, Quyen Thi
Yang, Jihyun
Byun, Jae-Won
Pyo, Hyun Mi
Park, Mi-Young
Ku, Bok Kyung
Nah, Jinju
Ryoo, Soyoon
Wee, Sung-Hwan
Choi, Kang-Seuk
Poo, Haryoung
author_sort Nguyen, Quyen Thi
collection PubMed
description Foot-and-mouth disease (FMD) is a highly contagious and economically devastating disease affecting cloven-hoofed livestock worldwide. FMD virus (FMDV) type A is one of the most common causes of FMD outbreaks among the seven FMDV serotypes, and its serological diagnosis is therefore important to confirm FMDV type A infection and to determine FMD vaccine efficacy. Here, we generated monoclonal antibodies (mAbs) specific to FMDV type A via hybridoma systems using an inactivated FMDV type A (A22/Iraq/1964) and found 4 monoclones (#29, #106, #108, and #109) with high binding reactivity to FMDV type A among 594 primary clones. In particular, the #106 mAb had a higher binding reactivity to the inactivated FMDV type A than the other mAbs and a commercial mAb. Moreover, the #106 mAb showed no cross-reactivity to inactivated FMDV type South African territories 1, 2, and 3, and low reactivity to inactivated FMDV type O (O(1) Manisa). Importantly, the solid-phase competitive ELISA (SPCE) using horseradish peroxidase (HRP)-conjugated #106 mAb detected FMDV type A-specific Abs in sera from FMD type A-vaccinated cattle more effectively than a commercial SPCE. These results suggest that the newly developed FMDV type A-specific mAb might be useful for diagnostic approaches for detecting Abs against FMDV type A.
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spelling pubmed-69635902020-01-30 Development of Monoclonal Antibody Specific to Foot-and-Mouth Disease Virus Type A for Serodiagnosis Nguyen, Quyen Thi Yang, Jihyun Byun, Jae-Won Pyo, Hyun Mi Park, Mi-Young Ku, Bok Kyung Nah, Jinju Ryoo, Soyoon Wee, Sung-Hwan Choi, Kang-Seuk Poo, Haryoung Pathogens Article Foot-and-mouth disease (FMD) is a highly contagious and economically devastating disease affecting cloven-hoofed livestock worldwide. FMD virus (FMDV) type A is one of the most common causes of FMD outbreaks among the seven FMDV serotypes, and its serological diagnosis is therefore important to confirm FMDV type A infection and to determine FMD vaccine efficacy. Here, we generated monoclonal antibodies (mAbs) specific to FMDV type A via hybridoma systems using an inactivated FMDV type A (A22/Iraq/1964) and found 4 monoclones (#29, #106, #108, and #109) with high binding reactivity to FMDV type A among 594 primary clones. In particular, the #106 mAb had a higher binding reactivity to the inactivated FMDV type A than the other mAbs and a commercial mAb. Moreover, the #106 mAb showed no cross-reactivity to inactivated FMDV type South African territories 1, 2, and 3, and low reactivity to inactivated FMDV type O (O(1) Manisa). Importantly, the solid-phase competitive ELISA (SPCE) using horseradish peroxidase (HRP)-conjugated #106 mAb detected FMDV type A-specific Abs in sera from FMD type A-vaccinated cattle more effectively than a commercial SPCE. These results suggest that the newly developed FMDV type A-specific mAb might be useful for diagnostic approaches for detecting Abs against FMDV type A. MDPI 2019-12-17 /pmc/articles/PMC6963590/ /pubmed/31861046 http://dx.doi.org/10.3390/pathogens8040301 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Nguyen, Quyen Thi
Yang, Jihyun
Byun, Jae-Won
Pyo, Hyun Mi
Park, Mi-Young
Ku, Bok Kyung
Nah, Jinju
Ryoo, Soyoon
Wee, Sung-Hwan
Choi, Kang-Seuk
Poo, Haryoung
Development of Monoclonal Antibody Specific to Foot-and-Mouth Disease Virus Type A for Serodiagnosis
title Development of Monoclonal Antibody Specific to Foot-and-Mouth Disease Virus Type A for Serodiagnosis
title_full Development of Monoclonal Antibody Specific to Foot-and-Mouth Disease Virus Type A for Serodiagnosis
title_fullStr Development of Monoclonal Antibody Specific to Foot-and-Mouth Disease Virus Type A for Serodiagnosis
title_full_unstemmed Development of Monoclonal Antibody Specific to Foot-and-Mouth Disease Virus Type A for Serodiagnosis
title_short Development of Monoclonal Antibody Specific to Foot-and-Mouth Disease Virus Type A for Serodiagnosis
title_sort development of monoclonal antibody specific to foot-and-mouth disease virus type a for serodiagnosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963590/
https://www.ncbi.nlm.nih.gov/pubmed/31861046
http://dx.doi.org/10.3390/pathogens8040301
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