4.7 Article

An adenosine nucleoside analogue NITD008 inhibits EV71 proliferation

期刊

ANTIVIRAL RESEARCH
卷 112, 期 -, 页码 47-58

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.antiviral.2014.10.009

关键词

Enterovirus 71; NITD008; Nucleoside analogue; Polymerase

资金

  1. National Natural Science Foundation of China [81322023, 31370733, 31170678, 31100208, 31000332, 21202087]
  2. National Basic Research Program of China (973 program) [2013CB911100, 2014CB542800]
  3. Fundamental Research Funds for the Central Universities [65124002]
  4. Specialized Research Fund for the Doctoral Program of Higher Education Ministry of Education of China [20120031120049]
  5. Tianjin Science and Technology Program [13JCYBJC24300, 13JCQNJC13100]
  6. 111 Project of the Ministry of Education of China [B06005]
  7. Tsinghua University Initiative Scientific Research Program [2009THZ01]

向作者/读者索取更多资源

Enterovirus 71 (EV71), one of the major causative agents of Hand Foot Mouth Disease (HFMD), causes severe pandemics and hundreds of deaths in the Asia-Pacific region annually and is an enormous public health threat. However, effective therapeutic antiviral drugs against EV71 are rare. Nucleoside analogues have been successfully used in the clinic for the treatment of various viral infections. We evaluated a total of 27 nucleoside analogues and discovered that an adenosine nucleoside analogue NITD008, which has been reported to be an antiviral reagent that specifically inhibits flaviviruses, effectively suppressed the propagation of different strains of EV71 in RD, 293T and Vero cells with a relatively high selectivity index. Triphosphorylated NITD008 (ppp-NITD008) functions as a chain terminator to directly inhibit the RNA-dependent RNA polymerase activity of EV71, and it does not affect the EV71 VPg uridylylation process. A significant synergistic anti-EV71 effect of NITD008 with rupintrivir (AG7088) (a protease inhibitor) was documented, supporting the potential combination therapy of NITD008 with other inhibitors for the treatment of EV71 infections. (C) 2014 Elsevier B.V. All rights reserved.

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