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甲氨蝶呤抗寨卡病毒的作用机制。

Mechanism of Action of Methotrexate Against Zika Virus.

机构信息

Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California, San Diego, La Jolla, CA 92093, USA.

Sanford Consortium for Regenerative Medicine, La Jolla, CA 92093, USA.

出版信息

Viruses. 2019 Apr 10;11(4):338. doi: 10.3390/v11040338.

Abstract

Zika virus (ZIKV), which is associated with microcephaly in infants and Guillain-Barré syndrome, reemerged as a serious public health threat in Latin America in recent years. Previous high-throughput screening (HTS) campaigns have revealed several potential hit molecules against ZIKV, including methotrexate (MTX), which is clinically used as an anti-cancer chemotherapy and anti-rheumatoid agent. We studied the mechanism of action of MTX against ZIKV in relation to its inhibition of dihydrofolate reductase (DHFR) in vitro using Vero and human neural stem cells (hNSCs). As expected, an antiviral effect for MTX against ZIKV was observed, showing up to 10-fold decrease in virus titer during MTX treatment. We also observed that addition of leucovorin (a downstream metabolite of DHFR pathway) rescued the ZIKV replication impaired by MTX treatment in ZIKV-infected cells, explaining the antiviral effect of MTX through inhibition of DHFR. We also found that addition of adenosine to ZIKV-infected cells was able to rescue ZIKV replication inhibited by MTX, suggesting that restriction of de novo synthesis adenosine triphosphate (ATP) pools suppresses viral replication. These results confirm that the DHFR pathway can be targeted to inhibit replication of ZIKV, similar to other published results showing this effect in related flaviviruses.

摘要

寨卡病毒(ZIKV)与婴儿小头畸形和吉兰-巴雷综合征有关,近年来在拉丁美洲再次成为严重的公共卫生威胁。以前的高通量筛选(HTS)活动揭示了几种针对 ZIKV 的潜在候选药物,包括甲氨蝶呤(MTX),它在临床上用作抗癌化疗药物和抗风湿药物。我们研究了 MTX 对 ZIKV 的作用机制,以及它在体外对二氢叶酸还原酶(DHFR)的抑制作用,使用了 Vero 和人神经干细胞(hNSCs)。正如预期的那样,MTX 对 ZIKV 表现出抗病毒作用,在 MTX 治疗期间病毒滴度降低了 10 倍。我们还观察到,DHFR 途径的下游代谢产物亚叶酸的添加挽救了 MTX 处理后 ZIKV 复制受损的情况,这解释了 MTX 通过抑制 DHFR 发挥抗病毒作用。我们还发现,向感染 ZIKV 的细胞中添加腺苷能够挽救被 MTX 抑制的 ZIKV 复制,这表明限制从头合成三磷酸腺苷(ATP)池可抑制病毒复制。这些结果证实,DHFR 途径可以作为抑制 ZIKV 复制的靶点,这与其他已发表的结果相似,这些结果表明在相关黄病毒中也有这种作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d86f/6521145/85475d77fe85/viruses-11-00338-g001.jpg

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