College of Veterinary Medicine, Henan Agricultural University, Zhengzhou, China; Key Laboratory of Animal Biochemistry and Nutrition, Ministry of Agriculture and Rural Affairs, Zhengzhou, China; Key Laboratory of Animal Growth and Development of Henan Province, Henan Agricultural University, Zhengzhou, China.
National Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, China; Hubei Hongshan Laboratory, Wuhan, China.
J Biol Chem. 2024 Jul;300(7):107453. doi: 10.1016/j.jbc.2024.107453. Epub 2024 Jun 7.
Identification of a conserved G-quadruplex in E165R of ASFVAfrican swine fever virus (ASFV) is a double-stranded DNA arbovirus with high transmissibility and mortality rates. It has caused immense economic losses to the global pig industry. Currently, no effective vaccines or medications are to combat ASFV infection. G-quadruplex (G4) structures have attracted increasing interest because of their regulatory role in vital biological processes. In this study, we identified a conserved G-rich sequence within the E165R gene of ASFV. Subsequently, using various methods, we verified that this sequence could fold into a parallel G4. In addition, the G4-stabilizers pyridostatin and 5,10,15,20-tetrakis-(N-methyl-4-pyridyl) porphin (TMPyP4) can bind and stabilize this G4 structure, thereby inhibiting E165R gene expression, and the inhibitory effect is associated with G4 formation. Moreover, the G4 ligand pyridostatin substantially impeded ASFV proliferation in Vero cells by reducing gene copy number and viral protein expression. These compelling findings suggest that G4 structures may represent a promising and novel antiviral target against ASFV.
非洲猪瘟病毒(ASFV)E165R 中的保守 G-四链体的鉴定:ASFV 是一种双链 DNA 虫媒病毒,具有高传染性和高死亡率。它给全球养猪业造成了巨大的经济损失。目前,尚无有效的疫苗或药物可用于对抗 ASFV 感染。G-四链体(G4)结构因其在重要生物过程中的调节作用而引起了越来越多的关注。在本研究中,我们在 ASFV 的 E165R 基因内鉴定出了一个保守的富含 G 的序列。随后,我们使用各种方法验证了该序列可以折叠成平行的 G4。此外,G4 稳定剂吡啶并[4,3-d]嘧啶(pyridostatin)和 5,10,15,20-四(N-甲基-4-吡啶基)卟啉(TMPyP4)可以结合并稳定该 G4 结构,从而抑制 E165R 基因表达,且抑制作用与 G4 形成相关。此外,G4 配体吡啶并[4,3-d]嘧啶通过降低基因拷贝数和病毒蛋白表达,显著抑制了 ASFV 在 Vero 细胞中的增殖。这些令人信服的发现表明,G4 结构可能成为对抗 ASFV 的一种有前途的新型抗病毒靶点。