Exploiting <i>V</i>-Gene Bias for Rapid, High-Throughput Monoclonal Antibody Isolation from Horses
Horses and humans share a close relationship that includes both species’ viromes. Many emerging infectious diseases can be transmitted between horses and humans and can exhibit mortality rates as high as 90% in both populations. Antibody biologics represents an emerging field of rapidly discoverable...
Main Authors: | , |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2022-09-01
|
Series: | Viruses |
Subjects: | |
Online Access: | https://www.mdpi.com/1999-4915/14/10/2172 |
_version_ | 1827647748302700544 |
---|---|
author | Constantinos Kurt Wibmer Poppy Mashilo |
author_facet | Constantinos Kurt Wibmer Poppy Mashilo |
author_sort | Constantinos Kurt Wibmer |
collection | DOAJ |
description | Horses and humans share a close relationship that includes both species’ viromes. Many emerging infectious diseases can be transmitted between horses and humans and can exhibit mortality rates as high as 90% in both populations. Antibody biologics represents an emerging field of rapidly discoverable and potent antiviral therapeutics. These biologics can be used to provide passive immunity, as well as blueprints for the rational design of novel active vaccine antigens. Here, we exploit the limited diversity of immunoglobulin variable genes used by horses to develop a rapid, high-throughput monoclonal antibody discovery pipeline. The antibodies isolated from two horses in this study were developed with near exclusivity from a few highly related germline genes within a single IgHV and IgλV gene family and could be recovered for cloning with just three primer pairs. This variable gene pairing was compatible with both horse and human immunoglobulin G isotypes, confirming the suitability of an equine antibody discovery pipeline for developing novel therapeutics to meet the One Health approach to infectious diseases. |
first_indexed | 2024-03-09T19:23:56Z |
format | Article |
id | doaj.art-643c84ad584f4a3598fec288f8a1c30d |
institution | Directory Open Access Journal |
issn | 1999-4915 |
language | English |
last_indexed | 2024-03-09T19:23:56Z |
publishDate | 2022-09-01 |
publisher | MDPI AG |
record_format | Article |
series | Viruses |
spelling | doaj.art-643c84ad584f4a3598fec288f8a1c30d2023-11-24T03:08:43ZengMDPI AGViruses1999-49152022-09-011410217210.3390/v14102172Exploiting <i>V</i>-Gene Bias for Rapid, High-Throughput Monoclonal Antibody Isolation from HorsesConstantinos Kurt Wibmer0Poppy Mashilo1National Institute for Communicable Diseases, Johannesburg 2131, South AfricaNational Institute for Communicable Diseases, Johannesburg 2131, South AfricaHorses and humans share a close relationship that includes both species’ viromes. Many emerging infectious diseases can be transmitted between horses and humans and can exhibit mortality rates as high as 90% in both populations. Antibody biologics represents an emerging field of rapidly discoverable and potent antiviral therapeutics. These biologics can be used to provide passive immunity, as well as blueprints for the rational design of novel active vaccine antigens. Here, we exploit the limited diversity of immunoglobulin variable genes used by horses to develop a rapid, high-throughput monoclonal antibody discovery pipeline. The antibodies isolated from two horses in this study were developed with near exclusivity from a few highly related germline genes within a single IgHV and IgλV gene family and could be recovered for cloning with just three primer pairs. This variable gene pairing was compatible with both horse and human immunoglobulin G isotypes, confirming the suitability of an equine antibody discovery pipeline for developing novel therapeutics to meet the One Health approach to infectious diseases.https://www.mdpi.com/1999-4915/14/10/2172antibody discoveryimmunotherapeutics and biologicsimmunoglobulin repertoireantigen-specific B-cell sortingequine humoral immune system |
spellingShingle | Constantinos Kurt Wibmer Poppy Mashilo Exploiting <i>V</i>-Gene Bias for Rapid, High-Throughput Monoclonal Antibody Isolation from Horses Viruses antibody discovery immunotherapeutics and biologics immunoglobulin repertoire antigen-specific B-cell sorting equine humoral immune system |
title | Exploiting <i>V</i>-Gene Bias for Rapid, High-Throughput Monoclonal Antibody Isolation from Horses |
title_full | Exploiting <i>V</i>-Gene Bias for Rapid, High-Throughput Monoclonal Antibody Isolation from Horses |
title_fullStr | Exploiting <i>V</i>-Gene Bias for Rapid, High-Throughput Monoclonal Antibody Isolation from Horses |
title_full_unstemmed | Exploiting <i>V</i>-Gene Bias for Rapid, High-Throughput Monoclonal Antibody Isolation from Horses |
title_short | Exploiting <i>V</i>-Gene Bias for Rapid, High-Throughput Monoclonal Antibody Isolation from Horses |
title_sort | exploiting i v i gene bias for rapid high throughput monoclonal antibody isolation from horses |
topic | antibody discovery immunotherapeutics and biologics immunoglobulin repertoire antigen-specific B-cell sorting equine humoral immune system |
url | https://www.mdpi.com/1999-4915/14/10/2172 |
work_keys_str_mv | AT constantinoskurtwibmer exploitingivigenebiasforrapidhighthroughputmonoclonalantibodyisolationfromhorses AT poppymashilo exploitingivigenebiasforrapidhighthroughputmonoclonalantibodyisolationfromhorses |