Type I and type III interferon receptor knockout chickens: Novel models for unraveling interferon dynamics in influenza infection
Mohanned Naif AlhussieniD, Hanna-Kaisa VikkulaiD, Romina Klinger, Christian ZenneriD, Simon FrühiD, Rashi NegiiD, Theresa von HeyliD, Sabrina SchleibingeriD, Milena Brunner, T.V.L. BerghofiD, Leora Avolio, Arne ReichiD, Benjamin SchadeiD, Bassel A Abukhadra, Silke RautenschleiniD, Rudolf PreisingeriD, Hicham SidiD, Benjamin SchusseriD
Abstract
The rapid cross-species transmission of highly pathogenic avian influenza presents a significant zoonotic threat. Elucidating the avian interferon (IFN) system, the primary antiviral defense in chickens, is critical for controlling the virus at its source and preventing its spillover into humans and other species. We engineered type I (IFN-/{beta}) and type III (IFN-{lambda}) IFN receptor knockout chickens to dissect the role of IFNs in viral infections. Results revealed that type I IFN predominantly modulates innate immune cell populations, T cell subsets, and their contribution to antibody production following immunization under physiological conditions. In ovo and in vivo challenge experiments utilizing diverse influenza A virus strains demonstrated strain-specific roles of both IFN-/{beta} and IFN-{lambda} in orchestrating viral pathogenesis, immunological responses, and tissue-tropism effects. Notably, type I IFN was particularly crucial in the initial defense mechanisms against H3N1 avian influenza A virus infection. These novel models offer unprecedented insights into avian IFN biology within the context of avian influenza, which is essential for developing more effective strategies to prevent and control this public health challenge.
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