A genetically engineered commercial chicken line is resistant to highly pathogenic avian leukosis virus subgroup j

  • Ahmed Kheimar
  • , Romina Klinger
  • , Luca D. Bertzbach
  • , Hicham Sid
  • , You Yu
  • , Andelé M. Conradie
  • , Benjamin Schade
  • , Brigitte Böhm
  • , Rudolf Preisinger
  • , Venugopal Nair
  • , Benedikt B. Kaufer
  • , Benjamin Schusser

Research output: Contribution to journalArticlepeer-review

23 Scopus citations

Abstract

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.

Original languageEnglish
Article number1066
JournalMicroorganisms
Volume9
Issue number5
DOIs
StatePublished - May 2021

Keywords

  • Avian leukosis virus subgroup J
  • Avian retrovirus
  • CRISPR/Cas9
  • ChNHE1
  • Gene editing
  • HPRS-103
  • Resistance
  • Viral escape

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