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Autophagy
. 2022 Oct 27.
doi: 10.1080/15548627.2022.2139922. Online ahead of print.
A/(H1N1) pdm09 NS1 promotes viral replication by enhancing autophagy through hijacking the IAV negative regulatory factor LRPPRC
Xing Guo 1 2 3 , Zhenyu Zhang 1 , Chaohui Lin 1 , Huiling Ren 1 , Yijing Li 2 , Yuan Zhang 1 , Yuxing Qu 1 , Hongxin Li 1 , Saiwen Ma 1 , Huijuan Xia 1 , Rongkuan Sun 1 , Haoyu Zu 1 , Yuezhi Lin 1 , Xiaojun Wang 1
Affiliations
- PMID: 36300799
- DOI: 10.1080/15548627.2022.2139922
Abstract
The quadrilateral reassortant IAV A/(H1N1) pdm09 is the pathogen responsible for the first influenza pandemic of the 21st century. The virus spread rapidly among hosts causing high mortality within human population. Efficient accumulation of virions is known to be important for the rapid transmission of virus. However, the mechanism by which A/(H1N1) pdm09 promotes its rapid replication has not been fully studied. Here, we found the NS1 of A/(H1N1) pdm09 mediated complete macroautophagy/autophagy, and then facilitated self-replication, which may be associated with the more rapid spread of this virus compared with H1N1WSN and H3N8JL89. We found that the promotion of self-replication could be mainly attributed to NS1pdm09 strongly antagonizing the inhibitory effect of LRPPRC on autophagy. The interaction between NS1pdm09 and LRPPRC competitively blocked the interaction of LRPPRC with BECN1/Beclin1, resulting in increased recruitment of BECN1 for PIK3C3 (phosphatidylinositol 3-kinase catalytic subunit type 3) and induction of the initiation of autophagy. In conclusion, we uncover the unique molecular mechanism by which A/(H1N1) pdm09 utilizes autophagy to promote self-replication, and we provide theoretical basics for the analysis of the etiological characteristics of the A/(H1N1) pdm09 pandemic and the development of anti-influenza drugs and vaccines.
Keywords: BECN1; IAVs; LRPPRC; NS1; autophagy.