首页> 外文期刊>Antiviral Research >Peptidomimetic furin inhibitor MI-701 in combination with oseltamivir and ribavirin efficiently blocks propagation of highly pathogenic avian influenza viruses and delays high level oseltamivir resistance in MDCK cells
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Peptidomimetic furin inhibitor MI-701 in combination with oseltamivir and ribavirin efficiently blocks propagation of highly pathogenic avian influenza viruses and delays high level oseltamivir resistance in MDCK cells

机译:拟肽弗林蛋白酶抑制剂MI-701与奥司他韦和利巴韦林合用可有效阻断高致病性禽流感病毒的繁殖并延迟MDCK细胞对奥司他韦的高水平耐药性

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摘要

Antiviral medication is used for the treatment of severe influenza infections, of which the neuraminidase inhibitors (NAIs) are the most effective drugs, approved so far. Here, we investigated the antiviral efficacy of the peptidomimetic furin inhibitor MI-701 in combination with oseltamivir carboxylate and ribavirin against the infection of highly pathogenic avian influenza viruses (HPAIV) that are activated by the host protease furin. Cell cultures infected with the strains A/Thailand/1(KAN-1)/2004 (H5N1) and A/FPV/Rostock/1934 (H7N1) were treated with each agent alone, or in double and triple combinations. MI-701 alone achieved a concentration-dependent reduction of virus propagation. Double treatment of MI-701 with oseltamivir carboxylate and triple combination with ribavirin showed synergistic inhibition and a pronounced delay of virus propagation. MI-701 resistant mutants were not observed. Emergence of NA mutation H275Y conferring high oseltamivir resistance was significantly delayed in the presence of MI-701. Our data indicate that combination with a potent furin inhibitor significantly enhances the therapeutic efficacy of conventional antivirals drugs against HPAIV infection. (C) 2015 Elsevier B.V. All rights reserved.
机译:抗病毒药物用于治疗严重的流感感染,到目前为止,神经氨酸酶抑制剂(NAIs)是最有效的药物。在这里,我们研究了拟肽弗林蛋白酶抑制剂MI-701与oseltamivir羧酸盐和利巴韦林联合使用对由宿主蛋白酶弗林蛋白酶激活的高致病性禽流感病毒(HPAIV)感染的抗病毒效果。用每种试剂单独或以双重和三重组合处理感染菌株A / Thailand / 1(KAN-1)/ 2004(H5N1)和A / FPV / Rostock / 1934(H7N1)的细胞培养物。仅MI-701即可实现浓度依赖性的病毒繁殖减少。 MI-701用奥司他韦羧酸酯的双重处理和利巴韦林的三次组合显示出协同抑制作用和明显的病毒传播延迟。未观察到MI-701抗性突变体。 MI-701的存在大大延迟了赋予高奥司他韦耐药性的NA突变H275Y的出现。我们的数据表明,与有效的弗林蛋白酶抑制剂组合可显着增强常规抗病毒药物对HPAIV感染的治疗功效。 (C)2015 Elsevier B.V.保留所有权利。

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