Open AccessInfluenza A virus NS1 protein‐induced JNK activation and apoptosis are not functionally linked
Author(s) -
Nacken Wolfgang,
Wixler Viktor,
Ehrhardt Christina,
Ludwig Stephan
Publication year - 2017
Publication title -
cellular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.542
H-Index - 138
eISSN - 1462-5822
pISSN - 1462-5814
DOI - 10.1111/cmi.12721
Subject(s) - biology , apoptosis , microbiology and biotechnology , kinase , signal transduction , protein kinase r , phosphorylation , mutant , protein kinase a , gene , mitogen activated protein kinase kinase , genetics
Expression of the influenza A virus (IAV) nonstructural protein (NS1) results in the activation of c‐Jun N‐terminal kinase (JNK). Both NS1 and JNK are involved in apoptosis induction. To investigate their interrelationship, we stably expressed a tamoxifen inducible NS1 oestrogen receptor fusion‐protein (NS1ERT) in mammalian cells. Upon tamoxifen stimulation, NS1ERT‐expressing cells partially rescued the attenuated replication of NS1‐deficient IAVs and also inhibited interferon up‐regulation, confirming the functional competence of NS1ERT. Tamoxifen‐induced NS1ERT created a cytopathic phenotype and led to the activation of JNK and apoptosis. Induction of NS1F103SERT mutant failed to activate JNK, but induced apoptosis, whereas the induction of NS1M106IERT led to JNK phosphorylation, but not apoptosis, indicating that JNK activation and apoptosis induction are not functionally linked. Further mutational analysis highlighted that apoptosis induction is a function of the C‐terminal effector domain of NS1. Finally, IAVs encoding mutant NS1 revealed a modulating effect of NS1 on apoptosis induction in a genuine infection. With respect to apoptogenicity, an NS1 mutant virus that results in a super activation of JNK behaves similarly to the JNK nonactivating virus expressing NS1F103S, thus confirming that NS1‐mediated JNK activation and apoptosis induction are also functionally independent from each other in vivo.