m6A Demethylase ALKBH5 Restrains PEDV Infection by Regulating GAS6 Expression in Porcine Alveolar Macrophages

被引:7
|
作者
Jin, Jian [1 ,2 ]
Xu, Chao [1 ]
Wu, Sen [1 ]
Wu, Zhengchang [1 ]
Wu, Shenglong [1 ]
Sun, Mingan [2 ]
Bao, Wenbin [1 ]
机构
[1] Yangzhou Univ, Coll Anim Sci & Technol, Yangzhou 225009, Jiangsu, Peoples R China
[2] Yangzhou Univ, Coll Vet Med, Inst Comparat Med, Yangzhou 225009, Jiangsu, Peoples R China
关键词
ALKBH5; PEDV; alveolar macrophages; N-6-methyladenosine; GAS6; pig; DIARRHEA VIRUS-INFECTION; GENE-EXPRESSION; RNA MODIFICATIONS; MESSENGER-RNA; METHYLATION; RECEPTORS;
D O I
10.3390/ijms23116191
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Porcine epidemic diarrhea virus (PEDV) is a burdensome coronavirus for the global pig industry. Although its fecal-oral route has been well-recognized, increasing evidence suggests that PEDV can also spread through airborne routes, indicating that the infection may also occur in the respiratory tract. N-6-methyladenosine (m(6)A) has been known to regulate viral replication and host immunity, yet its regulatory role and molecular mechanism regarding PEDV infection outside the gastrointestinal tract remain unexplored. In this study, we demonstrate that PEDV can infect porcine lung tissue and the 3D4/21 alveolar macrophage cell line, and the key m(6)A demethylase ALKBH5 is remarkably induced after PEDV infection. Interestingly, the disruption of ALKBH5 expression remarkably increases the infection's capacity for PEDV. Transcriptome profiling identified dozens of putative targets of ALKBH5, including GAS6, which is known to regulate virus infectivity. Further, MeRIP-qPCR and mRNA stability analyses suggest that ALKBH5 regulates the expression of GAS6 via an m(6)A-YTHDF2-dependent mechanism. Overall, our study demonstrates that PEDV can infect porcine lung tissue and 3D4/21 cells and reveals the crucial role of ALKBH5 in restraining PEDV infections, at least partly, by influencing GAS6 through an m(6)A-YTHDF2-dependent mechanism.
引用
收藏
页数:15
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