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ALKBH5 去甲基酶通过调节猪肺泡巨噬细胞中的表达来抑制 PEDV 感染。

mA Demethylase ALKBH5 Restrains PEDV Infection by Regulating Expression in Porcine Alveolar Macrophages.

机构信息

College of Animal Science and Technology, Yangzhou University, Yangzhou 225009, China.

Institute of Comparative Medicine, College of Veterinary Medicine, Yangzhou University, Yangzhou 225009, China.

出版信息

Int J Mol Sci. 2022 May 31;23(11):6191. doi: 10.3390/ijms23116191.

Abstract

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-methyladenosine (mA) 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 mA 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 , which is known to regulate virus infectivity. Further, MeRIP-qPCR and mRNA stability analyses suggest that ALKBH5 regulates the expression of via an mA-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 through an mA-YTHDF2-dependent mechanism.

摘要

猪流行性腹泻病毒(PEDV)是全球养猪业的一大负担。尽管其粪-口途径已被充分认识,但越来越多的证据表明,PEDV 也可以通过空气传播途径传播,这表明感染也可能发生在呼吸道。N6-甲基腺苷(m6A)已被证明可以调节病毒复制和宿主免疫,但它在胃肠道以外的 PEDV 感染中的调节作用和分子机制仍未被探索。在这项研究中,我们证明了 PEDV 可以感染猪肺组织和 3D4/21 肺泡巨噬细胞系,并且 PEDV 感染后关键的 m6A 去甲基酶 ALKBH5 被显著诱导。有趣的是,ALKBH5 表达的破坏显著增加了 PEDV 的感染能力。转录组谱分析确定了几十个 ALKBH5 的假定靶标,包括 ,它被认为可以调节病毒感染力。此外,MeRIP-qPCR 和 mRNA 稳定性分析表明,ALKBH5 通过 mA-YTHDF2 依赖性机制调节 的表达。总的来说,我们的研究表明 PEDV 可以感染猪肺组织和 3D4/21 细胞,并揭示了 ALKBH5 在抑制 PEDV 感染中的关键作用,至少部分是通过 mA-YTHDF2 依赖性机制影响 的表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b18d/9181496/b895af9fe1e5/ijms-23-06191-g001.jpg

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