Prostaglandin A1 inhibits avian influenza virus replication at a postentry level: Effect on virus protein synthesis and NF-κB activity

被引:6
作者
Carta, Stefania [1 ]
La Frazia, Simone [1 ]
Donatelli, Isabella [2 ]
Puzelli, Simona [2 ]
Rossi, Antonio [3 ]
Santoro, M. Gabriella [1 ,3 ]
机构
[1] Univ Roma Tor Vergata, Dept Biol, I-00133 Rome, Italy
[2] Ist Super Sanita, Dept Infect Dis, I-00161 Rome, Italy
[3] CNR, Inst Translat Pharmacol, Rome, Italy
来源
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS | 2014年 / 91卷 / 06期
关键词
Antiviral; Cyclopentenone prostanoids; Heat shock proteins; NF-kappaB; A H7N9 VIRUS; ANTIVIRAL ACTIVITY; CYCLOPENTENONE PROSTAGLANDINS; VIRAL-INFECTION; HUMAN-DISEASE; KINASE; H5N1; TRANSCRIPTION; RESISTANCE; THERAPY;
D O I
10.1016/j.plefa.2014.07.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Influenza A viruses (IAV) have the potential to cause devastating pandemics. In recent years, the emergence of new avian strains able to infect humans represents a serious threat to global human health. The increase in drug-resistant IAV strains underscores the need for novel approaches to anti-influenza chemotherapy. Herein we show that prostaglandin-A(1) (PGA(1)) possesses antiviral activity against avian IAV, including H5N9, H7N1 and H1N1 strains, acting at a level different from the currently available anti-influenza drugs. PGA(1) acts at postentry level, causing dysregulation of viral protein synthesis and preventing virus-induced disassembly of host microtubular network and activation of pro-inflammatory factor NF-kappa B. The antiviral activity is dependent on the presence of a cyclopentenone ring structure and is associated with activation of a cytoprotective heat shock response in infected cells. The results suggest that cyclopentenone prostanoids or prostanoids-derived molecules may represent a new tool to combat avian influenza virus infection. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:311 / 323
页数:13
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