Ogawa Motohiko, Shirasago Yoshitaka, Ando Shuji, Shimojima Masayuki, Saijo Masayuki, Fukasawa Masayoshi
Department of Virology I, National Institute of Infectious Diseases, 1-23-1, Toyama, Shinjuku-ku, Tokyo, 162-8640, Japan.
Department of Biochemistry and Cell Biology, National Institute of Infectious Diseases, 1-23-1, Toyama, Shinjuku-ku, Tokyo, 162-8640, Japan.
J Infect Chemother. 2018 Aug;24(8):597-601. doi: 10.1016/j.jiac.2018.03.005. Epub 2018 Apr 5.
Severe fever with thrombocytopenia syndrome (SFTS) virus (SFTSV) causes tick-borne hemorrhagic fever in East Asia. The disease is characterized by high morbidity and mortality. Here, we evaluated the effects of caffeic acid (CA), a coffee-related organic acid with antiviral effects, against SFTSV infection. CA dose-dependently inhibited SFTSV infection in permissive human hepatoma Huh7.5.1-8 cells when SFTSV was added into the culture medium with CA. However, quinic acid (QA), another coffee-related organic acid, did not inhibit SFTSV infection. The 50% inhibitory concentration (IC) of CA against SFTSV was 0.048 mM, whereas its 50% cytotoxic concentration was 7.6 mM. The selectivity index (SI) was 158. Pre-incubation of SFTSV with CA for 4 h resulted in a greater inhibition of SFTSV infection (IC = 0.019 mM; SI = 400). The pre-incubation substantially decreased viral attachment to the cells. CA treatment of the SFTSV-infected cells also inhibited the infection, albeit less effectively. CA activity after cell infection with SFTSV was more pronounced at a low multiplicity of infection (MOI) of 0.01 per cell (IC = 0.18 mM) than at a high MOI of 1 per cell (IC > 1 mM). Thus, CA inhibited virus spread by acting directly on the virus rather than on the infected cells. In conclusion, CA acted on SFTSV and inhibited viral infection and spread, mainly by inhibiting the binding of SFTSV to the cells. We therefore demonstrated CA to be a potential anti-SFTSV drug for preventing and treating SFTS.
严重发热伴血小板减少综合征(SFTS)病毒(SFTSV)在东亚地区引发蜱传出血热。该疾病具有高发病率和高死亡率的特点。在此,我们评估了咖啡相关的具有抗病毒作用的有机酸咖啡酸(CA)对SFTSV感染的影响。当将SFTSV添加到含有CA的培养基中时,CA在人肝癌Huh7.5.1 - 8允许性细胞中剂量依赖性地抑制SFTSV感染。然而,另一种咖啡相关的有机酸奎尼酸(QA)并未抑制SFTSV感染。CA对SFTSV的50%抑制浓度(IC)为0.048 mM,而其50%细胞毒性浓度为7.6 mM。选择性指数(SI)为158。将SFTSV与CA预孵育4小时导致对SFTSV感染的抑制作用增强(IC = 0.019 mM;SI = 400)。预孵育显著降低了病毒对细胞的附着。对感染SFTSV的细胞进行CA处理也能抑制感染,尽管效果较差。在每个细胞感染复数(MOI)为0.01的低感染复数下(IC = 0.18 mM),SFTSV感染细胞后CA的活性比在每个细胞感染复数为1的高感染复数下(IC > 1 mM)更明显。因此,CA通过直接作用于病毒而非感染细胞来抑制病毒传播。总之,CA作用于SFTSV并抑制病毒感染和传播,主要是通过抑制SFTSV与细胞的结合。因此,我们证明CA是一种预防和治疗SFTS的潜在抗SFTSV药物。