Interaction between the yellow fever virus nonstructural protein NS3 and the host protein Alix contributes to the release of infectious particles

被引:44
作者
Carpp, Lindsay N. [1 ]
Galler, Ricardo [2 ]
Bonaldo, Myrna C. [1 ]
机构
[1] Fiocruz MS, Inst Oswaldo Cruz, Lab Biol Mol Flavivirus, Fdn Oswaldo Cruz, BR-21045900 Manguinho, RJ, Brazil
[2] Biomanguinhos, BR-21045900 Manguinho, RJ, Brazil
关键词
Yellow fever virus; Flavivirus; Alix protein; Viral nonstructural proteins; ESCRT-III; CRYSTAL-STRUCTURE; HUMAN HOMOLOG; DOMAIN; COMPLEX; HELICASE; MUTAGENESIS; ASSOCIATION; AIP1/ALIX; MECHANISM;
D O I
10.1016/j.micinf.2010.10.010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
The ESCRT (endosomal sorting complex required for transport) machinery normally executes cargo sorting and internalization during multivesicular body biogenesis, but is also utilized by several enveloped viruses to facilitate their budding from cellular membranes. Although the mechanisms of flavivirus infectious particle assembly and release are poorly understood, the nonstructural protein NS3 has been reported to have an essential role via an undescribed mechanism. Here, we shed light on the role of NS3 by connecting it to the host factor Alix, a protein intimately connected with the ESCRT machinery. We demonstrate that NS3 and Alix interact and show that dominant negative versions of Alix inhibit YFV release. Furthermore, we show that NS3 supplied in trans rescues this effect. We propose that the interaction between NS3 and Alix contributes to YFV release. (C) 2010 Institut Pasteur. Published by Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:85 / 95
页数:11
相关论文
共 44 条
[1]
Mutagenesis of the NS2B-NS3-mediated cleavage site in the flavivirus capsid protein demonstrates a requirement for coordinated processing [J].
Amberg, SM ;
Rice, CM .
JOURNAL OF VIROLOGY, 1999, 73 (10) :8083-8094
[2]
The Vps4p AAA ATPase regulates membrane association of a Vps protein complex required for normal endosome function [J].
Babst, M ;
Wendland, B ;
Estepa, EJ ;
Emr, SD .
EMBO JOURNAL, 1998, 17 (11) :2982-2993
[3]
ESCRT-III: An endosome-associated heterooligomeric protein complex required for MVB sorting [J].
Babst, M ;
Katzmann, DJ ;
Estepa-Sabal, EJ ;
Meerloo, T ;
Emr, SD .
DEVELOPMENTAL CELL, 2002, 3 (02) :271-282
[4]
Surface expression of an immunodominant malaria protein B cell epitope by yellow fever virus [J].
Bonaldo, MC ;
Garratt, RC ;
Caufour, PS ;
Freire, MS ;
Rodrigeus, MM ;
Nussenzweig, RS ;
Galler, R .
JOURNAL OF MOLECULAR BIOLOGY, 2002, 315 (04) :873-885
[5]
PROCESSING OF THE YELLOW-FEVER VIRUS NONSTRUCTURAL POLYPROTEIN - A CATALYTICALLY ACTIVE NS3-PROTEINASE DOMAIN AND NS2B ARE REQUIRED FOR CLEAVAGES AT DIBASIC SITES [J].
CHAMBERS, TJ ;
GRAKOUI, A ;
RICE, CM .
JOURNAL OF VIROLOGY, 1991, 65 (11) :6042-6050
[6]
EVIDENCE THAT THE N-TERMINAL DOMAIN OF NONSTRUCTURAL PROTEIN NS3 FROM YELLOW-FEVER VIRUS IS A SERINE PROTEASE RESPONSIBLE FOR SITE-SPECIFIC CLEAVAGES IN THE VIRAL POLYPROTEIN [J].
CHAMBERS, TJ ;
WEIR, RC ;
GRAKOUI, A ;
MCCOURT, DW ;
BAZAN, JF ;
FLETTERICK, RJ ;
RICE, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (22) :8898-8902
[7]
Alix (ALG-2-interacting protein X), a protein involved in apoptosis, binds to endophilins and induces cytoplasmic vacuolization [J].
Chatellard-Causse, C ;
Blot, B ;
Cristina, N ;
Torch, S ;
Missotten, M ;
Sadoul, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (32) :29108-29115
[8]
Functions of early (AP-2) and late (AIP1/ALIX) Endocytic proteins in equine infectious anemia virus budding [J].
Chen, CP ;
Vincent, O ;
Jin, J ;
Weisz, OA ;
Montelaro, RC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (49) :40474-40480
[9]
Association of Japanese encephalitis virus NS3 protein with microtubules and tumour susceptibility gene 101 (TSG101) protein [J].
Chiou, CT ;
Hu, CCA ;
Chen, PH ;
Liao, CL ;
Lin, YL ;
Wang, JJ .
JOURNAL OF GENERAL VIROLOGY, 2003, 84 :2795-2805
[10]
Retrovirus budding [J].
Demirov, DG ;
Freed, EO .
VIRUS RESEARCH, 2004, 106 (02) :87-102