Proteolysis of the Ebola virus glycoproteins enhances virus binding and infectivity

被引:136
作者
Kaletsky, Rachel L. [1 ]
Simmons, Graham [1 ]
Bates, Paul [1 ]
机构
[1] Univ Penn, Sch Med, Dept Microbiol, Philadelphia, PA 19104 USA
关键词
D O I
10.1128/JVI.01170-07
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Cellular cathepsins are required for Ebola virus infection and are believed to proteolytically process the Ebola virus glycoprotein (GP) during entry. However, the significance of cathepsin cleavage during infection remains unclear. Here we demonstrate a role for cathepsin L (CatL) cleavage of Ebola virus GP in the generation of a stable 18-kDa GP1 viral intermediate that exhibits increased binding to and infectivity for susceptible cell targets. Cell binding to a lymphocyte line was increased when CatL-proteolysed pseudovirions were used, but lymphocytes remained resistant to Ebola virus GP-mediated infection. Genetic removal of the highly glycosylated mucin domain in Ebola virus GP resulted in cell binding similar to that observed with CatL-treated full-length GP, and no overall enhancement of binding or infectivity was observed when mucin-deleted virions were treated with CatL. These results suggest that cathepsin cleavage of Ebola virus GP facilitates an interaction with a cellular receptor(s) and that removal of the mucin domain may facilitate receptor binding. The influence of CatL in Ebola virus GP receptor binding should be useful in future studies characterizing the mechanism of Ebola virus entry.
引用
收藏
页码:13378 / 13384
页数:7
相关论文
共 25 条
[1]   Avian sarcoma and leukosis virus-receptor interactions: From classical genetics to novel insights into virus-cell membrane fusion [J].
Barnard, RJO ;
Elleder, D ;
Young, JAT .
VIROLOGY, 2006, 344 (01) :25-29
[2]   Distinct mechanisms of entry by envelope glycoproteins of Marburg and Ebola (Zaire) viruses [J].
Chan, SY ;
Speck, RF ;
Ma, MC ;
Goldsmith, MA .
JOURNAL OF VIROLOGY, 2000, 74 (10) :4933-4937
[3]   Endosomal proteolysis of the Ebola virus glycoprotein is necessary for infection [J].
Chandran, K ;
Sullivan, NJ ;
Felbor, U ;
Whelan, SP ;
Cunningham, JM .
SCIENCE, 2005, 308 (5728) :1643-1645
[4]   VPR IS REQUIRED FOR EFFICIENT REPLICATION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 IN MONONUCLEAR PHAGOCYTES [J].
CONNOR, RI ;
CHEN, BK ;
CHOE, S ;
LANDAU, NR .
VIROLOGY, 1995, 206 (02) :935-944
[5]   Differentiation of filoviruses by electron microscopy [J].
Geisbert, TW ;
Jahrling, PB .
VIRUS RESEARCH, 1995, 39 (2-3) :129-150
[6]   SARS coronavirus, but not human coronavirus NL63, utilizes cathepsin L to infect ACE2-expressing cells [J].
Huang, IC ;
Bosch, BJ ;
Li, F ;
Li, WH ;
Lee, KH ;
Ghiran, S ;
Vasilieva, N ;
Dermody, TS ;
Harrison, SC ;
Dormitzer, PR ;
Farzan, M ;
Rottier, PJM ;
Choe, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (06) :3198-3203
[7]   Conserved receptor-binding domains of Lake Victoria marburgvirus and Zaire ebolavirus bind a common receptor [J].
Kuhn, Jens H. ;
Radoshitzky, Sheli R. ;
Guth, Alexander C. ;
Warfield, Kelly L. ;
Li, Wenhui ;
Vincent, Martin J. ;
Towner, Jonathan S. ;
Nichol, Stuart T. ;
Bavari, Sina ;
Choe, Hyeryun ;
Aman, M. Javad ;
Farzan, Michael .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (23) :15951-15958
[8]   Core structure of the envelope glycoprotein GP2 from Ebola virus at 1.9-Å resolution [J].
Malashkevich, VN ;
Schneider, BJ ;
McNally, ML ;
Milhollen, MA ;
Pang, JX ;
Kim, PS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (06) :2662-2667
[9]   Comprehensive analysis of Ebola virus GP1 in viral entry [J].
Manicassamy, B ;
Wang, JZ ;
Jiang, HQ ;
Rong, LJ .
JOURNAL OF VIROLOGY, 2005, 79 (08) :4793-4805
[10]   Virus entry: Open sesame [J].
Marsh, M ;
Helenius, A .
CELL, 2006, 124 (04) :729-740