病毒学
病毒
生物
蛋白酶
神经氨酸酶
病毒复制
NS2-3蛋白酶
效价
甲型流感病毒
正粘病毒科
微生物学
酶
生物化学
作者
Zhirnov Op,А. В. Овчаренко,A. G. Bukrinskaya
标识
DOI:10.1099/0022-1317-65-1-191
摘要
SUMMARY Administration of the protease inhibitors, ε-aminocaproic acid or aprotinins, to mice infected with mouse-adapted influenza virus strain A/PR/8/34 (H0N1) and A/Aichi/2/68 (H3N2) reduced virus replication in the lungs. Up to 100-fold reduction of virus titre and virus-induced neuraminidase activity were revealed in mouse lungs under protease inhibitor treatment. As a result, drug-treated mice rapidly cleared the virus from their lungs. The predominant synthesis was of non-infectious virions with uncleaved haemagglutinin in the lungs of drug-treated mice, in contrast to the production of highly infectious virions with proteolytically cleaved haemagglutinin in untreated mice. These observations suggest that protease inhibitors suppress influenza virus replication in mouse lungs due to prevention of haemagglutinin cleavage and virus proteolytic activation.
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