Nonsense-mediated mRNA decay does not restrict influenza A virus propagation

被引:5
|
作者
Tran, Giao Vu Quynh [1 ]
Kleinehr, Jens [1 ]
Preugschas, Hannah Franziska [1 ]
Anhlan, Darisuren [1 ]
Mohamed, Fakry Fahmy [1 ]
Ehrhardt, Christina [1 ,2 ]
Ludwig, Stephan [1 ]
Hrincius, Eike Roman [1 ]
机构
[1] Univ Hosp Muenster UKM, Inst Virol Muenster IVM, Von Esmarch Str 56, D-48149 Munster, Germany
[2] Univ Hosp Jena, Inst Med Microbiol, Sect Expt Virol, Jena, Germany
关键词
diseases; infection; mRNA decay; viral replication; viruses;
D O I
10.1111/cmi.13323
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
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页数:11
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