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Nonsense-mediated mRNA decay does not restrict influenza A virus propagation.
Tran, Giao Vu Quynh; Kleinehr, Jens; Preugschas, Hannah Franziska; Anhlan, Darisuren; Mohamed, Fakry Fahmy; Ehrhardt, Christina; Ludwig, Stephan; Hrincius, Eike Roman.
Afiliação
  • Tran GVQ; Institute of Virology Muenster (IVM), University Hospital Muenster (UKM), Muenster, Germany.
  • Kleinehr J; Institute of Virology Muenster (IVM), University Hospital Muenster (UKM), Muenster, Germany.
  • Preugschas HF; Institute of Virology Muenster (IVM), University Hospital Muenster (UKM), Muenster, Germany.
  • Anhlan D; Institute of Virology Muenster (IVM), University Hospital Muenster (UKM), Muenster, Germany.
  • Mohamed FF; Institute of Virology Muenster (IVM), University Hospital Muenster (UKM), Muenster, Germany.
  • Ehrhardt C; Institute of Virology Muenster (IVM), University Hospital Muenster (UKM), Muenster, Germany.
  • Ludwig S; Section of Experimental Virology, Institute of Medical Microbiology, University Hospital Jena, Jena, Germany.
  • Hrincius ER; Institute of Virology Muenster (IVM), University Hospital Muenster (UKM), Muenster, Germany.
Cell Microbiol ; 23(6): e13323, 2021 06.
Article em En | MEDLINE | ID: mdl-33655690
ABSTRACT
Nonsense-mediated mRNA decay (NMD) was identified as a process to degrade flawed cellular messenger RNA (mRNA). Within the last decades it was also shown that NMD carries virus-restricting capacities and thus could be considered a part of the cellular antiviral system. As this was shown to affect primarily positive-sense single stranded RNA ((+)ssRNA) viruses there is only scarce knowledge if this also applies to negative-sense single stranded RNA ((-)ssRNA) viruses. Influenza A viruses (IAVs) harbour a segmented (-)ssRNA genome. During their replication IAVs produce numerous RNA transcripts and simultaneously impair cellular transcription and translation. The viral mRNAs hold several molecular patterns which can elicit NMD and in turn would lead to their degradation. This, in consequence, may mitigate viral propagation. Thus, we examined if a knockdown or a pharmacological inhibition of NMD key components may influence IAV replication. Additionally, we performed similar experiments with respiratory syncytial virus (RSV), another (-)ssRNA virus, but with a non-segmented genome. Although it seemed that a knockdown of up-frameshift protein 1 (UPF1), the central NMD factor, slightly increased viral mRNA and protein levels, no significant alteration of viral replication could be observed, implying that the NMD machinery may not have restricting capacities against (-)ssRNA viruses.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vírus da Influenza A / RNA Mensageiro / RNA Viral / Interações Hospedeiro-Patógeno / Degradação do RNAm Mediada por Códon sem Sentido Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vírus da Influenza A / RNA Mensageiro / RNA Viral / Interações Hospedeiro-Patógeno / Degradação do RNAm Mediada por Códon sem Sentido Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article