Genome-wide RNAi Screen Identifies SEC61A and VCP as Conserved Regulators of Sindbis Virus Entry

被引:58
作者
Panda, Debasis [1 ]
Rose, Patrick P. [1 ]
Hanna, Sheri L. [1 ]
Gold, Beth [1 ]
Hopkins, Kaycie C. [1 ]
Lyde, Randolph B. [3 ,4 ]
Marks, Michael S. [3 ,4 ]
Cherry, Sara [1 ,2 ]
机构
[1] Univ Penn, Dept Microbiol, Philadelphia, PA 19104 USA
[2] Univ Penn, Penn Genome Frontiers Inst, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[4] Univ Penn, Dept Physiol, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
UNFOLDED PROTEIN RESPONSE; CELLULAR RECEPTOR; TRANSPORTER DMT1; IRON; DROSOPHILA; ALPHAVIRUSES; INHIBITOR; MEMBRANE; MODEL; REPLICATION;
D O I
10.1016/j.celrep.2013.11.028
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Alphaviruses are a large class of insect-borne human pathogens and little is known about the host-factor requirements for infection. To identify such factors, we performed a genome-wide RNAi screen using model Drosophila cells and validated 94 genes that impacted infection of Sindbis virus (SINV), the prototypical alphavirus. We identified a conserved role for SEC61A and valosin-containing protein (VCP) in facilitating SINV entry in insects and mammals. SEC61A and VCP selectively regulate trafficking of the entry receptor NRAMP2, and loss or pharmacological inhibition of these proteins leads to altered NRAMP2 trafficking to lysosomal compartments and proteolytic digestion within lysosomes. NRAMP2 is the major iron transporter in cells, and loss of NRAMP2 attenuates intracellular iron transport. Thus, this study reveals genes and pathways involved in both infection and iron homeostasis that may serve as targets for antiviral therapeutics or for iron-imbalance disorders.
引用
收藏
页码:1737 / 1748
页数:12
相关论文
共 57 条
[1]   Iron homeostasis [J].
Andrews, Nancy C. ;
Schmidt, Paul J. .
ANNUAL REVIEW OF PHYSIOLOGY, 2007, 69 :69-85
[2]  
Atkins Gregory J., 2008, Expert Reviews in Molecular Medicine, V10, P1, DOI 10.1017/S1462399408000859
[3]   Intestinal DMT1 Cotransporter Is Down-regulated by Hepcidin via Proteasome Internalization and Degradation [J].
Brasse-Lagnel, Carole ;
Karim, Zoubida ;
Letteron, Philippe ;
Bekri, Soumeya ;
Bado, Andre ;
Beaumont, Carole .
GASTROENTEROLOGY, 2011, 140 (04) :1261-+
[4]   Protein Quality Control in the Cytosol and the Endoplasmic Reticulum: Brothers in Arms [J].
Buchberger, Alexander ;
Bukau, Bernd ;
Sommer, Thomas .
MOLECULAR CELL, 2010, 40 (02) :238-252
[5]   Heterogeneous nuclear ribonuclear protein K interacts with Sindbis virus nonstructural proteins and viral subgenomic mRNA [J].
Burnham, Andrew J. ;
Gong, Lei ;
Hardy, Richard W. .
VIROLOGY, 2007, 367 (01) :212-221
[6]   A fluorescence assay for assessing chelation of intracellular iron in a membrane model system and in mammalian cells [J].
Cabantchik, ZI ;
Glickstein, H ;
Milgram, P ;
Breuer, W .
ANALYTICAL BIOCHEMISTRY, 1996, 233 (02) :221-227
[7]   Genome-wide RNAi screen reveals a specific sensitivity of IRES-containing RNA viruses to host translation inhibition [J].
Cherry, S ;
Doukas, T ;
Armknecht, S ;
Whelan, S ;
Wang, H ;
Sarnow, P ;
Perrimon, N .
GENES & DEVELOPMENT, 2005, 19 (04) :445-452
[8]   Entry is a rate-limiting step for viral infection in a Drosophila melanogaster model of pathogenesis [J].
Cherry, S ;
Perrimon, N .
NATURE IMMUNOLOGY, 2004, 5 (01) :81-87
[9]   Genomic RNAi screening in Drosophila S2 cells:: what have we learned about host-pathogen interactions? [J].
Cherry, Sara .
CURRENT OPINION IN MICROBIOLOGY, 2008, 11 (03) :262-270
[10]   Reversible inhibitor of p97, DBeQ, impairs both ubiquitin-dependent and autophagic protein clearance pathways [J].
Chou, Tsui-Fen ;
Brown, Steve J. ;
Minond, Dmitriy ;
Nordin, Brian E. ;
Li, Kelin ;
Jones, Amanda C. ;
Chase, Peter ;
Porubsky, Patrick R. ;
Stoltz, Brian M. ;
Schoenen, Frank J. ;
Patricelli, Matthew P. ;
Hodder, Peter ;
Rosen, Hugh ;
Deshaies, Raymond J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (12) :4834-4839