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A Genetically Engineered Commercial Chicken Line Is Resistant to Highly Pathogenic Avian Leukosis Virus Subgroup J

Viral diseases remain a major concern for animal health and global food production in modern agriculture. In chickens, avian leukosis virus subgroup J (ALV-J) represents an important pathogen that causes severe economic loss. Until now, no vaccine or antiviral drugs are available against ALV-J and s...

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Autores principales: Kheimar, Ahmed, Klinger, Romina, Bertzbach, Luca D., Sid, Hicham, Yu, You, Conradie, Andelé M., Schade, Benjamin, Böhm, Brigitte, Preisinger, Rudolf, Nair, Venugopal, Kaufer, Benedikt B., Schusser, Benjamin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8157034/
https://www.ncbi.nlm.nih.gov/pubmed/34069313
http://dx.doi.org/10.3390/microorganisms9051066
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author Kheimar, Ahmed
Klinger, Romina
Bertzbach, Luca D.
Sid, Hicham
Yu, You
Conradie, Andelé M.
Schade, Benjamin
Böhm, Brigitte
Preisinger, Rudolf
Nair, Venugopal
Kaufer, Benedikt B.
Schusser, Benjamin
author_facet Kheimar, Ahmed
Klinger, Romina
Bertzbach, Luca D.
Sid, Hicham
Yu, You
Conradie, Andelé M.
Schade, Benjamin
Böhm, Brigitte
Preisinger, Rudolf
Nair, Venugopal
Kaufer, Benedikt B.
Schusser, Benjamin
author_sort Kheimar, Ahmed
collection PubMed
description Viral diseases remain a major concern for animal health and global food production in modern agriculture. In chickens, avian leukosis virus subgroup J (ALV-J) represents an important pathogen that causes severe economic loss. Until now, no vaccine or antiviral drugs are available against ALV-J and strategies to combat this pathogen in commercial flocks are desperately needed. CRISPR/Cas9 targeted genome editing recently facilitated the generation of genetically modified chickens with a mutation of the chicken ALV-J receptor Na(+)/H(+) exchanger type 1 (chNHE1). In this study, we provide evidence that this mutation protects a commercial chicken line (NHE1ΔW38) against the virulent ALV-J prototype strain HPRS-103. We demonstrate that replication of HPRS-103 is severely impaired in NHE1ΔW38 birds and that ALV-J-specific antigen is not detected in cloacal swabs at later time points. Consistently, infected NHE1ΔW38 chickens gained more weight compared to their non-transgenic counterparts (NHE1W38). Histopathology revealed that NHE1W38 chickens developed ALV-J typical pathology in various organs, while no pathological lesions were detected in NHE1ΔW38 chickens. Taken together, our data revealed that this mutation can render a commercial chicken line resistant to highly pathogenic ALV-J infection, which could aid in fighting this pathogen and improve animal health in the field.
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spelling pubmed-81570342021-05-28 A Genetically Engineered Commercial Chicken Line Is Resistant to Highly Pathogenic Avian Leukosis Virus Subgroup J Kheimar, Ahmed Klinger, Romina Bertzbach, Luca D. Sid, Hicham Yu, You Conradie, Andelé M. Schade, Benjamin Böhm, Brigitte Preisinger, Rudolf Nair, Venugopal Kaufer, Benedikt B. Schusser, Benjamin Microorganisms Communication Viral diseases remain a major concern for animal health and global food production in modern agriculture. In chickens, avian leukosis virus subgroup J (ALV-J) represents an important pathogen that causes severe economic loss. Until now, no vaccine or antiviral drugs are available against ALV-J and strategies to combat this pathogen in commercial flocks are desperately needed. CRISPR/Cas9 targeted genome editing recently facilitated the generation of genetically modified chickens with a mutation of the chicken ALV-J receptor Na(+)/H(+) exchanger type 1 (chNHE1). In this study, we provide evidence that this mutation protects a commercial chicken line (NHE1ΔW38) against the virulent ALV-J prototype strain HPRS-103. We demonstrate that replication of HPRS-103 is severely impaired in NHE1ΔW38 birds and that ALV-J-specific antigen is not detected in cloacal swabs at later time points. Consistently, infected NHE1ΔW38 chickens gained more weight compared to their non-transgenic counterparts (NHE1W38). Histopathology revealed that NHE1W38 chickens developed ALV-J typical pathology in various organs, while no pathological lesions were detected in NHE1ΔW38 chickens. Taken together, our data revealed that this mutation can render a commercial chicken line resistant to highly pathogenic ALV-J infection, which could aid in fighting this pathogen and improve animal health in the field. MDPI 2021-05-14 /pmc/articles/PMC8157034/ /pubmed/34069313 http://dx.doi.org/10.3390/microorganisms9051066 Text en © 2021 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 Communication
Kheimar, Ahmed
Klinger, Romina
Bertzbach, Luca D.
Sid, Hicham
Yu, You
Conradie, Andelé M.
Schade, Benjamin
Böhm, Brigitte
Preisinger, Rudolf
Nair, Venugopal
Kaufer, Benedikt B.
Schusser, Benjamin
A Genetically Engineered Commercial Chicken Line Is Resistant to Highly Pathogenic Avian Leukosis Virus Subgroup J
title A Genetically Engineered Commercial Chicken Line Is Resistant to Highly Pathogenic Avian Leukosis Virus Subgroup J
title_full A Genetically Engineered Commercial Chicken Line Is Resistant to Highly Pathogenic Avian Leukosis Virus Subgroup J
title_fullStr A Genetically Engineered Commercial Chicken Line Is Resistant to Highly Pathogenic Avian Leukosis Virus Subgroup J
title_full_unstemmed A Genetically Engineered Commercial Chicken Line Is Resistant to Highly Pathogenic Avian Leukosis Virus Subgroup J
title_short A Genetically Engineered Commercial Chicken Line Is Resistant to Highly Pathogenic Avian Leukosis Virus Subgroup J
title_sort genetically engineered commercial chicken line is resistant to highly pathogenic avian leukosis virus subgroup j
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8157034/
https://www.ncbi.nlm.nih.gov/pubmed/34069313
http://dx.doi.org/10.3390/microorganisms9051066
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