Department of Veterinary Microbiology, Graduate School of Agricultural and Life Sciences, University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo, Japan.
Dev Comp Immunol. 2010 May;34(5):598-602. doi: 10.1016/j.dci.2010.01.004. Epub 2010 Jan 15.
Bats are now known as the source of several diseases in humans, but few studies regarding immune responses and factors associated with bats have so far been reported. In this study, we focused on STAT1, one of the critical components in interferon (IFN)-signaling and antiviral activity, which is often targeted by viral proteins to reduce antiviral activity and increase viral replication. We found that Rousettus aegyptiacus STAT1 (bat STAT1) is phosphorylatable and translocates to the nucleus when stimulated with human IFN-alpha (hIFN-alpha). Furthermore, phosphorylation of bat STAT1 and inhibition of nuclear translocation was observed in IFN-stimulated cells infected with the HEP-Flury strain of rabies virus, in the same manner as in other mammals. Additionally, quantitative real-time RT-PCR revealed that bat STAT1 mRNA was highly expressed in the liver, while low in muscle and spleen.
蝙蝠现在被认为是人类几种疾病的源头,但迄今为止,关于蝙蝠的免疫反应和相关因素的研究很少。在这项研究中,我们专注于 STAT1,它是干扰素(IFN)信号和抗病毒活性的关键组成部分之一,通常是病毒蛋白的靶标,以降低抗病毒活性并增加病毒复制。我们发现 Rousettus aegyptiacus STAT1(蝙蝠 STAT1)在受到人干扰素-α(hIFN-α)刺激时可磷酸化并转位到细胞核。此外,在感染HEP-Flury 株狂犬病病毒的 IFN 刺激细胞中观察到蝙蝠 STAT1 的磷酸化和核转位抑制,与其他哺乳动物相同。此外,定量实时 RT-PCR 显示,蝙蝠 STAT1 mRNA 在肝脏中高度表达,而在肌肉和脾脏中表达较低。