tetano
Editor, Senior Moderator
Emerg Microbes Infect
. 2023 Oct 12:2270073.
doi: 10.1080/22221751.2023.2270073. Online ahead of print. ABTB1 facilitates the replication of influenza A virus by counteracting TRIM4-mediated degradation of viral NP protein
Wenjun Shi[SUP] 1 [/SUP], Zhibo Shan[SUP] 1 [/SUP], Li Jiang[SUP] 1 [/SUP], Guangwen Wang[SUP] 1 [/SUP], Xuyuan Wang[SUP] 1 [/SUP], Yu Chang[SUP] 1 [/SUP], Yuzhen Hu[SUP] 1 [/SUP], Bo Wang[SUP] 1 [/SUP], Qibing Li[SUP] 1 [/SUP], Yihan Wang[SUP] 1 [/SUP], Guohua Deng[SUP] 1 [/SUP], Jianzhong Shi[SUP] 1 [/SUP], Yongping Jiang[SUP] 1 [/SUP], Xianying Zeng[SUP] 1 [/SUP], Guobin Tian[SUP] 1 [/SUP], Hualan Chen[SUP] 1 [/SUP], Chengjun Li[SUP] 1 [/SUP]
Affiliations
Influenza A viruses (IAVs) continue to cause tremendous economic losses to the global animal industry and respiratory diseases and deaths among humans. The nuclear import of the vRNP complex, composed of polymerase basic protein 1 (PB1), polymerase basic protein 2 (PB2), polymerase acidic protein (PA), nucleoprotein (NP), and viral RNA, is essential for the efficient replication of IAV. Host factors involved in this process can be targeted for the development of countermeasures against IAV infection. Here, we found that Ankyrin Repeat and BTB Domain Containing 1 (ABTB1) promotes the replication of IAV, and positively regulates the nuclear import of the vRNP complex. ABTB1 did not interact directly with NP, indicating that ABTB1 plays an indirect role in facilitating the nuclear import of the vRNP complex. Immunoprecipitation and mass spectrometry revealed that Tripartite Motif Containing 4 (TRIM4) interacts with ABTB1. We found that TRIM4 relies on its E3 ubiquitin ligase activity to inhibit the replication of IAV by targeting and degrading NP within the incoming vRNP complex as well as the newly synthesized NP. ABTB1 interacted with TRIM4, leading to TRIM4 degradation through the proteasome system. Notably, ABTB1-mediated degradation of TRIM4 blocked the effect of TRIM4 on NP stability, and largely counteracted the inhibitory effect of TRIM4 on IAV replication. Our findings define a novel role for ABTB1 in aiding the nuclear import of the vRNP complex of IAV by counteracting the destabilizing effect of TRIM4 on the viral NP protein.
Keywords: Influenza A virus; NP; ABTB1; TRIM4; Nuclear import of vRNP.
. 2023 Oct 12:2270073.
doi: 10.1080/22221751.2023.2270073. Online ahead of print. ABTB1 facilitates the replication of influenza A virus by counteracting TRIM4-mediated degradation of viral NP protein
Wenjun Shi[SUP] 1 [/SUP], Zhibo Shan[SUP] 1 [/SUP], Li Jiang[SUP] 1 [/SUP], Guangwen Wang[SUP] 1 [/SUP], Xuyuan Wang[SUP] 1 [/SUP], Yu Chang[SUP] 1 [/SUP], Yuzhen Hu[SUP] 1 [/SUP], Bo Wang[SUP] 1 [/SUP], Qibing Li[SUP] 1 [/SUP], Yihan Wang[SUP] 1 [/SUP], Guohua Deng[SUP] 1 [/SUP], Jianzhong Shi[SUP] 1 [/SUP], Yongping Jiang[SUP] 1 [/SUP], Xianying Zeng[SUP] 1 [/SUP], Guobin Tian[SUP] 1 [/SUP], Hualan Chen[SUP] 1 [/SUP], Chengjun Li[SUP] 1 [/SUP]
Affiliations
- PMID: 37823597
- DOI: 10.1080/22221751.2023.2270073
Influenza A viruses (IAVs) continue to cause tremendous economic losses to the global animal industry and respiratory diseases and deaths among humans. The nuclear import of the vRNP complex, composed of polymerase basic protein 1 (PB1), polymerase basic protein 2 (PB2), polymerase acidic protein (PA), nucleoprotein (NP), and viral RNA, is essential for the efficient replication of IAV. Host factors involved in this process can be targeted for the development of countermeasures against IAV infection. Here, we found that Ankyrin Repeat and BTB Domain Containing 1 (ABTB1) promotes the replication of IAV, and positively regulates the nuclear import of the vRNP complex. ABTB1 did not interact directly with NP, indicating that ABTB1 plays an indirect role in facilitating the nuclear import of the vRNP complex. Immunoprecipitation and mass spectrometry revealed that Tripartite Motif Containing 4 (TRIM4) interacts with ABTB1. We found that TRIM4 relies on its E3 ubiquitin ligase activity to inhibit the replication of IAV by targeting and degrading NP within the incoming vRNP complex as well as the newly synthesized NP. ABTB1 interacted with TRIM4, leading to TRIM4 degradation through the proteasome system. Notably, ABTB1-mediated degradation of TRIM4 blocked the effect of TRIM4 on NP stability, and largely counteracted the inhibitory effect of TRIM4 on IAV replication. Our findings define a novel role for ABTB1 in aiding the nuclear import of the vRNP complex of IAV by counteracting the destabilizing effect of TRIM4 on the viral NP protein.
Keywords: Influenza A virus; NP; ABTB1; TRIM4; Nuclear import of vRNP.