Divisions of Human Biology and Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, United States; Department of Microbiology, University of Washington, Seattle, WA 98115, United States.
Divisions of Human Biology and Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, United States.
Virology. 2018 May;518:398-405. doi: 10.1016/j.virol.2018.03.023. Epub 2018 Apr 3.
Nitazoxanide (NTZ) is an FDA-approved anti-protozoal drug that inhibits several bacteria and viruses as well. However, its effect on poxviruses is unknown. Therefore, we investigated the impact of NTZ on vaccinia virus (VACV). We found that NTZ inhibits VACV production with an EC of ~2 μM, a potency comparable to that reported for several other viruses. The inhibitory block occurs early during the viral life cycle, prior to viral DNA replication. The mechanism of viral inhibition is likely not due to activation of intracellular innate immune pathways, such as protein kinase R (PKR) or interferon signaling, contrary to what has been suggested to mediate the effects of NTZ against some other viruses. Rather, our finding that addition of exogenous palmitate partially rescues VACV production from the inhibitory effect of NTZ suggests that NTZ impedes adaptations in cellular metabolism that are needed for efficient completion of the VACV replication cycle.
硝唑尼特(NTZ)是一种获得美国食品药品监督管理局批准的抗原生动物药物,它还能抑制多种细菌和病毒。然而,其对痘病毒的作用尚不清楚。因此,我们研究了硝唑尼特对牛痘病毒(VACV)的影响。我们发现,硝唑尼特抑制 VACV 的产生,其半数有效浓度(EC)约为 2 μM,这一效力与其他几种病毒相当。抑制作用发生在病毒生命周期的早期,在病毒 DNA 复制之前。病毒抑制的机制可能不是由于细胞内先天免疫途径的激活,如蛋白激酶 R(PKR)或干扰素信号通路,这与硝唑尼特对一些其他病毒的作用机制不同。相反,我们发现添加外源性棕榈酸部分挽救了硝唑尼特对 VACV 产生的抑制作用,这表明硝唑尼特阻碍了细胞代谢的适应性改变,而这些改变是 VACV 复制周期高效完成所必需的。