Cholesterol reducing agents inhibit assembly of type I parainfluenza viruses

被引:26
作者
Bajimaya, Shringkhala [1 ]
Hayashi, Tsuyoshi [1 ]
Frankl, Tunde [1 ]
Bryk, Peter [1 ]
Ward, Brian [1 ]
Takimoto, Toru [1 ]
机构
[1] Univ Rochester, Med Ctr, Dept Microbiol & Immunol, Box 672,601 Elmwood Ave, Rochester, NY 14642 USA
基金
美国国家卫生研究院;
关键词
Type I parainfluenza virus; Assembly; Cholesterol; Lipid rafts; Antiviral therapy; RESPIRATORY SYNCYTIAL VIRUS; LIPID-RAFTS; SENDAI-VIRUS; HN-PROTEINS; MEMBRANE; INFECTION; GEMFIBROZIL; COMPONENTS; PARTICLES; OUTBREAK;
D O I
10.1016/j.virol.2016.11.011
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Many enveloped RNA viruses utilize lipid rafts for the assembly of progeny virions, but the role of cholesterol, a major component of rafts, on paramyxovirus budding and virion formation is controversial. In this study, we analyzed the effects of FDA-approved cholesterol-reducing agents, gemfibrozil and lovastatin, on raft formation and assembly of human parainfluenza virus type 1 (hPIV1) and Sendai virus (SeV). Treatment of the human airway epithelial A549 cells with the agents, especially when combined, significantly decreased production of infectious hPIV1 and SeV. Mechanistic analysis indicated that depletion of cellular cholesterol reduced cell surface accumulation of envelope glycoproteins and association of viral matrix and nucleocapsids with raft membrane, which resulted in impaired virus budding and release from the cells. These results indicate that cellular cholesterol is required for assembly and formation of type 1 parainfluenza viruses and suggest that cholesterol could be an attractive target for antiviral agents against hPIV1.
引用
收藏
页码:127 / 135
页数:9
相关论文
共 48 条
[1]   Assembly of Sendai virus: M protein interacts with F and HN proteins and with the cytoplasmic tail and transmembrane domain of F protein [J].
Ali, A ;
Nayak, DP .
VIROLOGY, 2000, 276 (02) :289-303
[2]  
Ausubel F.M., 1995, SHORT PROTOCOLS MOL
[3]   Specific Residues in the 2009 H1N1 Swine-Origin Influenza Matrix Protein Influence Virion Morphology and Efficiency of Viral Spread In Vitro [J].
Bialas, Kristy M. ;
Desmet, Emily A. ;
Takimoto, Toru .
PLOS ONE, 2012, 7 (11)
[4]   Structure and function of sphingolipid- and cholesterol-rich membrane rafts [J].
Brown, DA ;
London, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (23) :17221-17224
[5]   Analysis of the interaction between respiratory syncytial virus and lipid-rafts in Hep2 cells during infection [J].
Brown, G ;
Jeffree, CE ;
McDonald, T ;
Rixon, HWM ;
Aitken, JD ;
Sugrue, RJ .
VIROLOGY, 2004, 327 (02) :175-185
[6]   Respiratory syncytial virus assembly occurs in GM1-rich regions of the host-cell membrane and alters the cellular distribution of tyrosine phosphorylated caveolin-1 [J].
Brown, G ;
Rixon, HWM ;
Sugrue, RJ .
JOURNAL OF GENERAL VIROLOGY, 2002, 83 :1841-1850
[7]   Caveolin-1 is incorporated into mature respiratory syncytial virus particles during virus assembly on the surface of virus-infected cells [J].
Brown, G ;
Aitken, J ;
Rixon, HWM ;
Sugrue, RJ .
JOURNAL OF GENERAL VIROLOGY, 2002, 83 :611-621
[8]   Increased survival after gemfibrozil treatment of severe mouse influenza [J].
Budd, Alison ;
Alleva, Lisa ;
Alsharifi, Mohammed ;
Koskinen, Aulikki ;
Smythe, Victoria ;
Mullbacher, Arno ;
Wood, Jeff ;
Clark, Ian .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2007, 51 (08) :2965-2968
[9]   Trafficking of Sendai Virus Nucleocapsids Is Mediated by Intracellular Vesicles [J].
Chambers, Raychel ;
Takimoto, Toru .
PLOS ONE, 2010, 5 (06)
[10]   Cholesterol-rich lipid rafts are required for release of infectious human respiratory syncytial virus particles [J].
Chang, Te-Hung ;
Segovia, Jesus ;
Sabbah, Ahmed ;
Mgbemena, Victoria ;
Bose, Santanu .
VIROLOGY, 2012, 422 (02) :205-213