tetano
Editor, Senior Moderator
PLoS Pathog
. 2023 Jan 23;19(1):e1011128.
doi: 10.1371/journal.ppat.1011128. Online ahead of print.
Unconventional secretion of unglycosylated ORF8 is critical for the cytokine storm during SARS-CoV-2 infection
Xiaoyuan Lin[SUP] 1 2 [/SUP], Beibei Fu[SUP] 1 [/SUP], Yan Xiong[SUP] 1 [/SUP], Na Xing[SUP] 2 [/SUP], Weiwei Xue[SUP] 3 [/SUP], Dong Guo[SUP] 1 [/SUP], Mohamed Zaky[SUP] 4 [/SUP], Krishna Pavani[SUP] 5 [/SUP], Dusan Kunec[SUP] 2 [/SUP], Jakob Trimpert[SUP] 2 [/SUP], Haibo Wu[SUP] 1 [/SUP]
Affiliations
Abstract
Coronavirus disease 2019 is a respiratory infectious disease caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Evidence on the pathogenesis of SARS-CoV-2 is accumulating rapidly. In addition to structural proteins such as Spike and Envelope, the functional roles of non-structural and accessory proteins in regulating viral life cycle and host immune responses remain to be understood. Here, we show that open reading frame 8 (ORF8) acts as messenger for inter-cellular communication between alveolar epithelial cells and macrophages during SARS-CoV-2 infection. Mechanistically, ORF8 is a secretory protein that can be secreted by infected epithelial cells via both conventional and unconventional secretory pathways. Conventionally secreted ORF8 is glycosylated and loses the ability to recognize interleukin 17 receptor A of macrophages, possibly due to the steric hindrance imposed by N-glycosylation at Asn78. However, unconventionally secreted ORF8 does not undergo glycosylation without experiencing the ER-Golgi trafficking, thereby activating the downstream NF-κB signaling pathway and facilitating a burst of cytokine release. Furthermore, we show that ORF8 deletion in SARS-CoV-2 attenuates inflammation and yields less lung lesions in hamsters. Our data collectively highlights a role of ORF8 protein in the development of cytokine storms during SARS-CoV-2 infection.
. 2023 Jan 23;19(1):e1011128.
doi: 10.1371/journal.ppat.1011128. Online ahead of print.
Unconventional secretion of unglycosylated ORF8 is critical for the cytokine storm during SARS-CoV-2 infection
Xiaoyuan Lin[SUP] 1 2 [/SUP], Beibei Fu[SUP] 1 [/SUP], Yan Xiong[SUP] 1 [/SUP], Na Xing[SUP] 2 [/SUP], Weiwei Xue[SUP] 3 [/SUP], Dong Guo[SUP] 1 [/SUP], Mohamed Zaky[SUP] 4 [/SUP], Krishna Pavani[SUP] 5 [/SUP], Dusan Kunec[SUP] 2 [/SUP], Jakob Trimpert[SUP] 2 [/SUP], Haibo Wu[SUP] 1 [/SUP]
Affiliations
- PMID: 36689483
- DOI: 10.1371/journal.ppat.1011128
Abstract
Coronavirus disease 2019 is a respiratory infectious disease caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Evidence on the pathogenesis of SARS-CoV-2 is accumulating rapidly. In addition to structural proteins such as Spike and Envelope, the functional roles of non-structural and accessory proteins in regulating viral life cycle and host immune responses remain to be understood. Here, we show that open reading frame 8 (ORF8) acts as messenger for inter-cellular communication between alveolar epithelial cells and macrophages during SARS-CoV-2 infection. Mechanistically, ORF8 is a secretory protein that can be secreted by infected epithelial cells via both conventional and unconventional secretory pathways. Conventionally secreted ORF8 is glycosylated and loses the ability to recognize interleukin 17 receptor A of macrophages, possibly due to the steric hindrance imposed by N-glycosylation at Asn78. However, unconventionally secreted ORF8 does not undergo glycosylation without experiencing the ER-Golgi trafficking, thereby activating the downstream NF-κB signaling pathway and facilitating a burst of cytokine release. Furthermore, we show that ORF8 deletion in SARS-CoV-2 attenuates inflammation and yields less lung lesions in hamsters. Our data collectively highlights a role of ORF8 protein in the development of cytokine storms during SARS-CoV-2 infection.