2023
DOI: 10.1016/j.vetmic.2023.109851
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Newcastle disease virus nucleocapsid protein mediates the degradation of 14–3–3ε to antagonize the interferon response and promote viral replication

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Cited by 2 publications
(1 citation statement)
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“…14–3–3ε, known for its interactions with retinoic acid-inducible gene I (RIG-I) and mitochondrial antiviral signalling protein (MAVS), serves as a crucial component within IFN-related host cascades [ 34 ]. Xu et al [ 35 ] investigated the role of 14–3–3ε in NDV infection and observed that viral replication was promoted via the enhanced degradation of 14–3–3ε. Meanwhile, activation of the IFN pathway necessitated the presence of 14-3-3ε, which facilitated the interaction between MDA5 and MAVS during NDV infection.…”
Section: Main Textmentioning
confidence: 99%
“…14–3–3ε, known for its interactions with retinoic acid-inducible gene I (RIG-I) and mitochondrial antiviral signalling protein (MAVS), serves as a crucial component within IFN-related host cascades [ 34 ]. Xu et al [ 35 ] investigated the role of 14–3–3ε in NDV infection and observed that viral replication was promoted via the enhanced degradation of 14–3–3ε. Meanwhile, activation of the IFN pathway necessitated the presence of 14-3-3ε, which facilitated the interaction between MDA5 and MAVS during NDV infection.…”
Section: Main Textmentioning
confidence: 99%