Immune Dynamics in Viral Infections, National Research Center for the Control and Prevention of Infectious Diseases, Nagasaki University, Nagasaki, Japan.
Laboratory of Molecular Immunobiology, Division of Biological Science, Graduate School of Science and Technology, Nagasaki, Japan.
PLoS Negl Trop Dis. 2024 Sep 30;18(9):e0012553. doi: 10.1371/journal.pntd.0012553. eCollection 2024 Sep.
Crimean-Congo Hemorrhagic Fever virus (CCHFV) is a tick-borne pathogen that causes severe acute fever disease in humans and requires a biosafety level 4 laboratory for handling. Hazara virus (HAZV), belonging to the same virus genus as CCHFV, does not exhibit pathogenesis in humans. To investigate host RNA-binding proteins (RBPs) that regulate CCHFV replication, we generated a series of mutant RAW264.7 cells by CRISPR/Cas9 system and these cells were infected with HAZV. The viral titers in the supernatant of these cells was investigated, and HuR (ELAVL1) was identified. HuR KO RAW264.7 cells reduced HAZV replication. HuR is an RBP that enhances mRNA stability by binding to adenyl-uridine (AU)-rich regions in their 3' non-coding region (NCR). HuR regulates innate immune response by binding to host mRNAs of signaling molecules. The expression of cytokine genes such as Ifnb, Il6, and Tnf was reduced in HuR KO cells after HAZV infection. Although HuR supports the innate immune response during HAZV infection, we found that innate immune activation by HAZV infection did not affect its replication. We then investigated whether HuR regulates HAZV genome RNA stability. HAZV RNA genome was precipitated with an anti-HuR antibody, and HAZV genome RNA stability was lowered in HuR KO cells. We found that HuR associated with HAZV RNA and stabilized it to enhance HAZV replication. Furthermore, HuR-deficiency reduced CCHFV minigenome replication. CCHFV is a negative-strand RNA virus and positive-strand RNA is produced during replication. HuR was associated with positive-strand RNA rather than negative-strand RNA, and AU-rich region in 3'-NCR of S segment was responsible for immunoprecipitation with anti-HuR antibody and minigenome replication. Additionally, HuR inhibitor treatment reduced CCHFV minigenome replication. Our results indicate that HuR aids replication of the CCHFV minigenome by associating with the AU-rich region in the 3'-NCR.
克里米亚-刚果出血热病毒(CCHFV)是一种蜱传病原体,可导致人类严重急性发热疾病,需要生物安全 4 级实验室进行处理。同为同一病毒属的哈扎拉病毒(HAZV)在人类中不表现出致病性。为了研究调控 CCHFV 复制的宿主 RNA 结合蛋白(RBPs),我们通过 CRISPR/Cas9 系统生成了一系列突变 RAW264.7 细胞,并用 HAZV 感染这些细胞。研究了这些细胞上清液中的病毒滴度,并鉴定出 HuR(ELAVL1)。HuR KO RAW264.7 细胞减少了 HAZV 复制。HuR 是一种通过与 3'非编码区(NCR)中富含腺嘌呤-尿嘧啶(AU)的区域结合来增强 mRNA 稳定性的 RBP。HuR 通过与信号分子的宿主 mRNA 结合来调节先天免疫反应。HAZV 感染后,HuR KO 细胞中细胞因子基因如 Ifnb、Il6 和 Tnf 的表达减少。尽管 HuR 在 HAZV 感染期间支持先天免疫反应,但我们发现 HAZV 感染引起的先天免疫激活并不影响其复制。我们随后研究了 HuR 是否调节 HAZV 基因组 RNA 稳定性。用抗 HuR 抗体沉淀 HAZV RNA 基因组,发现 HuR KO 细胞中 HAZV 基因组 RNA 稳定性降低。我们发现 HuR 与 HAZV RNA 结合并稳定它以增强 HAZV 复制。此外,HuR 缺陷降低了 CCHFV 小基因组长复制。CCHFV 是一种负链 RNA 病毒,复制过程中产生正链 RNA。HuR 与正链 RNA 而非负链 RNA 结合,S 片段 3'-NCR 中的 AU 富含区负责与抗 HuR 抗体的免疫沉淀和小基因组长复制。此外,HuR 抑制剂处理降低了 CCHFV 小基因组长复制。我们的结果表明,HuR 通过与 3'-NCR 中的 AU 富含区结合来辅助 CCHFV 小基因组长复制。