tetano
Editor, Senior Moderator
Viruses
. 2022 Jan 20;14(2):199.
doi: 10.3390/v14020199.
Heterogeneous Ribonucleoprotein A1 (hnRNPA1) Interacts with the Nucleoprotein of the Influenza a Virus and Impedes Virus Replication
Ramandeep Kaur[SUP] 1 [/SUP], Jyoti Batra[SUP] 1 [/SUP], Olga Stuchlik[SUP] 2 [/SUP], Matthew S Reed[SUP] 2 [/SUP], Jan Pohl[SUP] 2 [/SUP], Suryaprakash Sambhara[SUP] 2 [/SUP], Sunil Kumar Lal[SUP] 1 3 [/SUP]
Affiliations
Abstract
Influenza A virus (IAV), like other viruses, depends on the host cellular machinery for replication and production of progeny. The relationship between a virus and a host is complex, shaped by many spatial and temporal interactions between viral and host proteome, ultimately dictating disease outcome. Therefore, it is imperative to identify host-virus interactions as crucial determinants of disease pathogenies. Heterogeneous ribonucleoprotein A1 (hnRNPA1) is an RNA binding protein involved in the life cycle of many DNA and RNA viruses; however, its role in IAV remains undiscovered. Here we report that human hnRNPA1 physically interacts with the nucleoprotein (NP) of IAV in mammalian cells at different time points of the viral replication cycle. Temporal distribution studies identify hnRNPA1 and NP co-localize in the same cellular milieu in both nucleus and mitochondria in NP-transfected and IAV-infected mammalian cells. Interestingly, hnRNPA1 influenced NP gene expression and affected viral replication. Most importantly, hnRNPA1 knockdown caused a significant increase in NP expression and enhanced viral replication (93.82%) in IAV infected A549 cells. Conversely, hnRNPA1 overexpression reduced NP expression at the mRNA and protein levels and impeded virus replication by (60.70%), suggesting antagonistic function. Taken together, results from this study demonstrate that cellular hnRNPA1 plays a protective role in the host hitherto unknown and may hold potential as an antiviral target to develop host-based therapeutics against IAV.
Keywords: IAV replication; hnRNPA1; host-virus relationships; nucleoprotein; protein-protein interactions.
. 2022 Jan 20;14(2):199.
doi: 10.3390/v14020199.
Heterogeneous Ribonucleoprotein A1 (hnRNPA1) Interacts with the Nucleoprotein of the Influenza a Virus and Impedes Virus Replication
Ramandeep Kaur[SUP] 1 [/SUP], Jyoti Batra[SUP] 1 [/SUP], Olga Stuchlik[SUP] 2 [/SUP], Matthew S Reed[SUP] 2 [/SUP], Jan Pohl[SUP] 2 [/SUP], Suryaprakash Sambhara[SUP] 2 [/SUP], Sunil Kumar Lal[SUP] 1 3 [/SUP]
Affiliations
- PMID: 35215793
- PMCID: PMC8880450
- DOI: 10.3390/v14020199
Abstract
Influenza A virus (IAV), like other viruses, depends on the host cellular machinery for replication and production of progeny. The relationship between a virus and a host is complex, shaped by many spatial and temporal interactions between viral and host proteome, ultimately dictating disease outcome. Therefore, it is imperative to identify host-virus interactions as crucial determinants of disease pathogenies. Heterogeneous ribonucleoprotein A1 (hnRNPA1) is an RNA binding protein involved in the life cycle of many DNA and RNA viruses; however, its role in IAV remains undiscovered. Here we report that human hnRNPA1 physically interacts with the nucleoprotein (NP) of IAV in mammalian cells at different time points of the viral replication cycle. Temporal distribution studies identify hnRNPA1 and NP co-localize in the same cellular milieu in both nucleus and mitochondria in NP-transfected and IAV-infected mammalian cells. Interestingly, hnRNPA1 influenced NP gene expression and affected viral replication. Most importantly, hnRNPA1 knockdown caused a significant increase in NP expression and enhanced viral replication (93.82%) in IAV infected A549 cells. Conversely, hnRNPA1 overexpression reduced NP expression at the mRNA and protein levels and impeded virus replication by (60.70%), suggesting antagonistic function. Taken together, results from this study demonstrate that cellular hnRNPA1 plays a protective role in the host hitherto unknown and may hold potential as an antiviral target to develop host-based therapeutics against IAV.
Keywords: IAV replication; hnRNPA1; host-virus relationships; nucleoprotein; protein-protein interactions.