Isolation of single-domain antibody fragments that preferentially detect intact (146s) particles of foot-and-mouth disease virus for use in vaccine quality control

Intact (146S) foot-and-mouth disease virus (FMDVs) can dissociate into specific (12S) viral capsid degradation products. FMD vaccines normally consist of inactivated virions. Vaccine quality is dependent on 146S virus particles rather than 12S particles. We earlier isolated two llama single-domain antibody fragments (VHHs) that specifically recognize 146S particles of FMDV strain O1 Manisa and shown their potential use in quality control of FMD vaccines during manufacturing. These 146S-specific VHHs were specific for particular O serotype strains and did not bind strains from other FMDV serotypes. Here, we describe the isolation of 146S-specific VHHs against FMDV SAT2 and Asia 1 strains by phage display selection from llama immune libraries. VHHs that bind both 12S and 146S particles were readily isolated but VHHs that bind specifically to 146S particles could only be isolated by phage display selection using prior depletion for 12S particles. We obtained one 146S-specific VHH—M332F—that binds to strain Asia 1 Shamir and several VHHs that preferentially bind 146S particles of SAT2 strain SAU/2/00, from which we selected VHH M379F for further characterization. Both M332F and M379F did not bind FMDV strains from other serotypes. In a sandwich enzyme-linked immunosorbent assay (ELISA) employing unlabeled and biotinylated versions of the same VHH M332F showed high specificity for 146S particles but M379F showed lower 146S-specificity with some cross-reaction with 12S particles. These ELISAs could detect 146S particle concentrations as low as 2.3–4.6 µg/l. They can be used for FMD vaccine quality control and research and development, for example, to identify virion stabilizing excipients.

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Main Authors: Harmsen, Michael, Seago, Julian, Perez, Eva, Charleston, Bryan, Eblé, Phaedra L., Dekker, Aldo
Format: Article/Letter to editor biblioteca
Language:English
Subjects:Enzyme-linked immunosorbent assay, Foot-and-mouth disease, Foot-and-mouth disease virion, Single-domain antibody, Vaccine quality control, Virion stability,
Online Access:https://research.wur.nl/en/publications/isolation-of-single-domain-antibody-fragments-that-preferentially
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spelling dig-wur-nl-wurpubs-5259302025-01-17 Harmsen, Michael Seago, Julian Perez, Eva Charleston, Bryan Eblé, Phaedra L. Dekker, Aldo Article/Letter to editor Frontiers in Immunology 8 (2017) ISSN: 1664-3224 Isolation of single-domain antibody fragments that preferentially detect intact (146s) particles of foot-and-mouth disease virus for use in vaccine quality control 2017 Intact (146S) foot-and-mouth disease virus (FMDVs) can dissociate into specific (12S) viral capsid degradation products. FMD vaccines normally consist of inactivated virions. Vaccine quality is dependent on 146S virus particles rather than 12S particles. We earlier isolated two llama single-domain antibody fragments (VHHs) that specifically recognize 146S particles of FMDV strain O1 Manisa and shown their potential use in quality control of FMD vaccines during manufacturing. These 146S-specific VHHs were specific for particular O serotype strains and did not bind strains from other FMDV serotypes. Here, we describe the isolation of 146S-specific VHHs against FMDV SAT2 and Asia 1 strains by phage display selection from llama immune libraries. VHHs that bind both 12S and 146S particles were readily isolated but VHHs that bind specifically to 146S particles could only be isolated by phage display selection using prior depletion for 12S particles. We obtained one 146S-specific VHH—M332F—that binds to strain Asia 1 Shamir and several VHHs that preferentially bind 146S particles of SAT2 strain SAU/2/00, from which we selected VHH M379F for further characterization. Both M332F and M379F did not bind FMDV strains from other serotypes. In a sandwich enzyme-linked immunosorbent assay (ELISA) employing unlabeled and biotinylated versions of the same VHH M332F showed high specificity for 146S particles but M379F showed lower 146S-specificity with some cross-reaction with 12S particles. These ELISAs could detect 146S particle concentrations as low as 2.3–4.6 µg/l. They can be used for FMD vaccine quality control and research and development, for example, to identify virion stabilizing excipients. en application/pdf https://research.wur.nl/en/publications/isolation-of-single-domain-antibody-fragments-that-preferentially 10.3389/fimmu.2017.00960 https://edepot.wur.nl/422403 Enzyme-linked immunosorbent assay Foot-and-mouth disease Foot-and-mouth disease virion Single-domain antibody Vaccine quality control Virion stability https://creativecommons.org/licenses/by/4.0/ Wageningen University & Research
institution WUR NL
collection DSpace
country Países bajos
countrycode NL
component Bibliográfico
access En linea
databasecode dig-wur-nl
tag biblioteca
region Europa del Oeste
libraryname WUR Library Netherlands
language English
topic Enzyme-linked immunosorbent assay
Foot-and-mouth disease
Foot-and-mouth disease virion
Single-domain antibody
Vaccine quality control
Virion stability
Enzyme-linked immunosorbent assay
Foot-and-mouth disease
Foot-and-mouth disease virion
Single-domain antibody
Vaccine quality control
Virion stability
spellingShingle Enzyme-linked immunosorbent assay
Foot-and-mouth disease
Foot-and-mouth disease virion
Single-domain antibody
Vaccine quality control
Virion stability
Enzyme-linked immunosorbent assay
Foot-and-mouth disease
Foot-and-mouth disease virion
Single-domain antibody
Vaccine quality control
Virion stability
Harmsen, Michael
Seago, Julian
Perez, Eva
Charleston, Bryan
Eblé, Phaedra L.
Dekker, Aldo
Isolation of single-domain antibody fragments that preferentially detect intact (146s) particles of foot-and-mouth disease virus for use in vaccine quality control
description Intact (146S) foot-and-mouth disease virus (FMDVs) can dissociate into specific (12S) viral capsid degradation products. FMD vaccines normally consist of inactivated virions. Vaccine quality is dependent on 146S virus particles rather than 12S particles. We earlier isolated two llama single-domain antibody fragments (VHHs) that specifically recognize 146S particles of FMDV strain O1 Manisa and shown their potential use in quality control of FMD vaccines during manufacturing. These 146S-specific VHHs were specific for particular O serotype strains and did not bind strains from other FMDV serotypes. Here, we describe the isolation of 146S-specific VHHs against FMDV SAT2 and Asia 1 strains by phage display selection from llama immune libraries. VHHs that bind both 12S and 146S particles were readily isolated but VHHs that bind specifically to 146S particles could only be isolated by phage display selection using prior depletion for 12S particles. We obtained one 146S-specific VHH—M332F—that binds to strain Asia 1 Shamir and several VHHs that preferentially bind 146S particles of SAT2 strain SAU/2/00, from which we selected VHH M379F for further characterization. Both M332F and M379F did not bind FMDV strains from other serotypes. In a sandwich enzyme-linked immunosorbent assay (ELISA) employing unlabeled and biotinylated versions of the same VHH M332F showed high specificity for 146S particles but M379F showed lower 146S-specificity with some cross-reaction with 12S particles. These ELISAs could detect 146S particle concentrations as low as 2.3–4.6 µg/l. They can be used for FMD vaccine quality control and research and development, for example, to identify virion stabilizing excipients.
format Article/Letter to editor
topic_facet Enzyme-linked immunosorbent assay
Foot-and-mouth disease
Foot-and-mouth disease virion
Single-domain antibody
Vaccine quality control
Virion stability
author Harmsen, Michael
Seago, Julian
Perez, Eva
Charleston, Bryan
Eblé, Phaedra L.
Dekker, Aldo
author_facet Harmsen, Michael
Seago, Julian
Perez, Eva
Charleston, Bryan
Eblé, Phaedra L.
Dekker, Aldo
author_sort Harmsen, Michael
title Isolation of single-domain antibody fragments that preferentially detect intact (146s) particles of foot-and-mouth disease virus for use in vaccine quality control
title_short Isolation of single-domain antibody fragments that preferentially detect intact (146s) particles of foot-and-mouth disease virus for use in vaccine quality control
title_full Isolation of single-domain antibody fragments that preferentially detect intact (146s) particles of foot-and-mouth disease virus for use in vaccine quality control
title_fullStr Isolation of single-domain antibody fragments that preferentially detect intact (146s) particles of foot-and-mouth disease virus for use in vaccine quality control
title_full_unstemmed Isolation of single-domain antibody fragments that preferentially detect intact (146s) particles of foot-and-mouth disease virus for use in vaccine quality control
title_sort isolation of single-domain antibody fragments that preferentially detect intact (146s) particles of foot-and-mouth disease virus for use in vaccine quality control
url https://research.wur.nl/en/publications/isolation-of-single-domain-antibody-fragments-that-preferentially
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