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中国大鲵(Oligoadenylate synthetase)的鉴定、表达模式及抗病毒活性。

Characterization, expression pattern and antiviral activities of oligoadenylate synthetase in Chinese Giant Salamander, Andrias davidianus.

机构信息

National Demonstration Center for Experimental Fisheries Science Education, Shanghai Ocean University, Shanghai, 201306, China; Yangtze River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Wuhan, 430223, China.

Yangtze River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Wuhan, 430223, China.

出版信息

Dev Comp Immunol. 2022 Apr;129:104347. doi: 10.1016/j.dci.2022.104347. Epub 2022 Jan 8.

Abstract

The enzyme 2'-5'-oligoadenylate synthetase (OAS) is an antiviral protein induced by interferons (IFNs), which plays an important role in IFN-mediated antiviral signaling pathway. In this study, the OAS of Chinese Giant Salamander, Andrias davidianus (AdOAS) was identified for the first time, and the expression profiles in vivo and the antiviral activities in vitro were investigated. The open reading frame (ORF) of AdOAS gene is 1185 bp in length, encoding a putative protein of 394 amino acids, in which a Nucleotidyltransferase (NTase) domain (40-143 aa) and a conserved OAS1 C superfamily domain (165-341 aa) are included. qRT-PCR analysis revealed a broad expression of AdOAS in vivo, with the highest expression level in intestine and heart. After infection with Chinese giant salamander iridovirus (GSIV), the mRNA level of AdOAS in liver increased significantly at 24 h and 48 h post infection and reached the peak at 72 h compared with the control group. The AdOAS mRNA level in kidney increased slightly at 6 h and 12 h post infection, declined to the initial level at 24 h and peaked at 48 h post infection, while in spleen it was slightly up-regulated at 6 h, inhibited at 12 h, 24 h and 48 h, and then significantly increased to the peak at 72 h post infection. In vitro, AdOAS mRNA level in Chinese giant salamander muscle (GSM) cells was not noticeably up-regulated until 24 h and then peaked at 48 h post GSIV infection. In antiviral activity test, the mRNA transcription and protein level of virus major capsid protein (MCP) in AdOAS over-expressed cells was significantly reduced compared with that in control cells by qRT-PCR and western blot analysis. In addition, ddPCR results showed that lower MCP gene copy was found in AdOAS over-expressed cells compared with the control group. These results collectively suggest that AdOAS plays a crucial role against GSIV infection in Chinese giant salamander, and provide a solid base for the further studies on the mechanism of immune defense and the control of the disease in this animal.

摘要

2'-5'-寡聚腺苷酸合成酶(OAS)是一种干扰素(IFN)诱导的抗病毒蛋白,在 IFN 介导的抗病毒信号通路中发挥重要作用。本研究首次鉴定了中国大鲵的 OAS(AdOAS),并研究了其体内表达谱和体外抗病毒活性。AdOAS 基因的开放阅读框(ORF)长 1185bp,编码一个由 394 个氨基酸组成的假定蛋白,其中包含一个核苷酸转移酶(NTase)结构域(40-143aa)和一个保守的 OAS1 C 超家族结构域(165-341aa)。qRT-PCR 分析显示,AdOAS 在体内广泛表达,在肠和心脏中表达水平最高。感染中国大鲵虹彩病毒(GSIV)后,与对照组相比,肝组织中 AdOAS 的 mRNA 水平在感染后 24 和 48h 显著升高,并在 72h 达到峰值。肾组织中 AdOAS 的 mRNA 水平在感染后 6 和 12h 略有升高,在 24h 降至初始水平,并在 48h 达到峰值,而脾组织中 AdOAS 的 mRNA 水平在 6h 略有上调,在 12、24 和 48h 被抑制,然后在 72h 感染后显著增加到峰值。在体外,AdOAS 在中华大鲵肌肉(GSM)细胞中的 mRNA 水平在感染 GSIV 24h 后才明显上调,然后在 48h 达到峰值。在抗病毒活性试验中,通过 qRT-PCR 和 Western blot 分析,与对照组相比,AdOAS 过表达细胞中的病毒主要衣壳蛋白(MCP)的 mRNA 转录和蛋白水平均显著降低。此外,ddPCR 结果显示,AdOAS 过表达细胞中的 MCP 基因拷贝数低于对照组。这些结果共同表明,AdOAS 在中华大鲵抵抗 GSIV 感染中发挥关键作用,为进一步研究该动物的免疫防御机制和疾病控制提供了坚实的基础。

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