tetano
Editor, Senior Moderator
J Virol
. 2022 Jan 12;jvi0199021.
doi: 10.1128/jvi.01990-21. Online ahead of print.
Influenza A virus uses PSMA2 for downregulation of NRF2-mediated oxidative stress response
Mahamud-Ur Rashid[SUP] 1 2 [/SUP], Ang Gao[SUP] 2 [/SUP], Kevin M Coombs[SUP] 1 2 3 [/SUP]
Affiliations
Abstract
Influenza A virus (IAV), an obligatory intracellular parasite, uses host cellular molecules to complete its replication cycle and suppress immune responses. Proteasome subunit alpha type-2 (PSMA2) is a cellular protein highly expressed in IAV-infected human lung epithelial A549 cells. PSMA2 is part of the 20S proteasome complex that degrades or recycles defective proteins and involves proteolytic modification of many cellular regulatory proteins. However, the role of PSMA2 in IAV replication is not well understood. In this study, PSMA2 knockdown (KD) in A549 cells caused a significant reduction in extracellular progeny IAV, but intracellular viral protein translation and viral RNA transcription were not affected. This indicates PSMA2 is a critical host factor for IAV maturation. To better understand the interplay between PSMA2 KD and IAV infection at the proteomic level, we used the SOMAScan 1.3K version that measures 1307 proteins to analyze alterations induced by these treatments. We found seven cellular signaling pathways, including Phospholipase C signaling, Pak signaling, and NRF2- mediated oxidative stress response signaling that were inhibited by IAV infection but significantly activated by PSMA2 KD. Further analysis of NRF2-mediated oxidative stress response signaling indicated IAV inhibits accumulation of reactive oxygen species (ROS), but ROS levels significantly increased during IAV infection in PSMA2 KD cells. However, IAV infection caused significantly higher NFR2 nuclear translocation that was inhibited in PSMA2 KD cells. This indicates that PSMA2 is required for NRF2-mediated ROS neutralization and that IAV uses PSMA2 to escape viral clearance via NRF2-mediated cellular oxidative response. Importance Influenza A virus (IAV) remains one of the most significant infectious agents, responsible for 3 - 5 million illnesses each year and more than 50 million deaths during the 20[SUP]th[/SUP] century. The cellular processes that promote and inhibit IAV infection and pathogenesis remain only partially understood. PSMA2 is a critical component of the 20S proteasome and ubiquitin-proteasome system, which is important in the replication of numerous viruses. This study examined host protein responses to IAV infection alone, PSMA2 knockdown alone, and IAV infection in the presence of PSMA2 knockdown and determined that interfering with PSMA2 function affected IAV maturation. These results help us better understand the importance of PSMA2 in IAV replication and may pave the way for designing additional IAV antivirals targeting PSMA2 or the host proteasome for the treatment of seasonal flu.
. 2022 Jan 12;jvi0199021.
doi: 10.1128/jvi.01990-21. Online ahead of print.
Influenza A virus uses PSMA2 for downregulation of NRF2-mediated oxidative stress response
Mahamud-Ur Rashid[SUP] 1 2 [/SUP], Ang Gao[SUP] 2 [/SUP], Kevin M Coombs[SUP] 1 2 3 [/SUP]
Affiliations
- PMID: 35019712
- DOI: 10.1128/jvi.01990-21
Abstract
Influenza A virus (IAV), an obligatory intracellular parasite, uses host cellular molecules to complete its replication cycle and suppress immune responses. Proteasome subunit alpha type-2 (PSMA2) is a cellular protein highly expressed in IAV-infected human lung epithelial A549 cells. PSMA2 is part of the 20S proteasome complex that degrades or recycles defective proteins and involves proteolytic modification of many cellular regulatory proteins. However, the role of PSMA2 in IAV replication is not well understood. In this study, PSMA2 knockdown (KD) in A549 cells caused a significant reduction in extracellular progeny IAV, but intracellular viral protein translation and viral RNA transcription were not affected. This indicates PSMA2 is a critical host factor for IAV maturation. To better understand the interplay between PSMA2 KD and IAV infection at the proteomic level, we used the SOMAScan 1.3K version that measures 1307 proteins to analyze alterations induced by these treatments. We found seven cellular signaling pathways, including Phospholipase C signaling, Pak signaling, and NRF2- mediated oxidative stress response signaling that were inhibited by IAV infection but significantly activated by PSMA2 KD. Further analysis of NRF2-mediated oxidative stress response signaling indicated IAV inhibits accumulation of reactive oxygen species (ROS), but ROS levels significantly increased during IAV infection in PSMA2 KD cells. However, IAV infection caused significantly higher NFR2 nuclear translocation that was inhibited in PSMA2 KD cells. This indicates that PSMA2 is required for NRF2-mediated ROS neutralization and that IAV uses PSMA2 to escape viral clearance via NRF2-mediated cellular oxidative response. Importance Influenza A virus (IAV) remains one of the most significant infectious agents, responsible for 3 - 5 million illnesses each year and more than 50 million deaths during the 20[SUP]th[/SUP] century. The cellular processes that promote and inhibit IAV infection and pathogenesis remain only partially understood. PSMA2 is a critical component of the 20S proteasome and ubiquitin-proteasome system, which is important in the replication of numerous viruses. This study examined host protein responses to IAV infection alone, PSMA2 knockdown alone, and IAV infection in the presence of PSMA2 knockdown and determined that interfering with PSMA2 function affected IAV maturation. These results help us better understand the importance of PSMA2 in IAV replication and may pave the way for designing additional IAV antivirals targeting PSMA2 or the host proteasome for the treatment of seasonal flu.