Generation of biologically contained Ebola viruses

被引:93
作者
Halfmann, Peter [1 ]
Kim, Jin Hyun
Ebihara, Hideki [3 ,4 ]
Noda, Takeshi [3 ]
Neumann, Gabriele [1 ]
Feldmann, Heinz [4 ]
Kawaoka, Yoshihiro [2 ,3 ]
机构
[1] Univ Wisconsin, Sch Vet Med, Dept Pathobiol Sci, Madison, WI 53706 USA
[2] Univ Tokyo, Dept Microbiol & Immunol, Div Virol, Tokyo 1130033, Japan
[3] Univ Tokyo, Int Res Ctr Infect Dis, Inst Med Sci, Tokyo 1130033, Japan
[4] Univ Manitoba, Dept Med Microbiol, Publ Hlth Agcy Canada, Special Pathogens Program, Winnipeg, MB R3E3R2, Canada
关键词
antiviral screening; areverse genetics; avaccine development;
D O I
10.1073/pnas.0708057105
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Ebola virus (EBOV), a public health concern in Africa and a potential biological weapon, is classified as a biosafety level-4 agent because of its high mortality rate and the lack of approved vaccines and antivirals. Basic research into the mechanisms of EBOV pathogenicity and the development of effective countermeasures are restricted by the current biosafety classification of EBOVs. We therefore developed biologically contained EBOV that express a reporter gene instead of the VP30 gene, which encodes an essential transcription factor. A Vero cell line that stably expresses VP30 provides this essential protein in trans and biologically confines the virus to its complete replication cycle in this cell line. This complementation approach is highly efficient because biologically contained EBOVs lacking the VP30 gene grow to titers similar to those obtained with wild-type virus. Moreover, EBOVs lacking the VP30 gene are indistinguishable in their morphology from wild-type virus and are genetically stable, as determined by sequence analysis after seven serial passages in VP30-expressing Vero cells. We propose that this system provides a safe means to handle EBOV outside a biosafety level-4 facility and will stimulate critical studies on the EBOV life cycle as well as large-scale screening efforts for compounds with activity against this lethal virus.
引用
收藏
页码:1129 / 1133
页数:5
相关论文
共 28 条
[1]   A reconstituted replication and transcription system for Ebola virus Reston and comparison with Ebola virus Zaire [J].
Boehmann, Y ;
Enterlein, S ;
Randolf, A ;
Mühlberger, E .
VIROLOGY, 2005, 332 (01) :406-417
[2]   Folate receptor-α is a cofactor for cellular entry by Marburg and Ebola viruses [J].
Chan, SY ;
Empig, CJ ;
Welte, FJ ;
Speck, RF ;
Schmaljohn, A ;
Kreisberg, JF ;
Goldsmith, MA .
CELL, 2001, 106 (01) :117-126
[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]   Molecular determinants of Ebola virus virulence in mice [J].
Ebihara, Hideki ;
Takada, Ayato ;
Kobasa, Darwyn ;
Jones, Steven ;
Neumann, Gabriele ;
Theriault, Steven ;
Bray, Mike ;
Feldmann, Heinz ;
Kawaoka, Yoshihiro .
PLOS PATHOGENS, 2006, 2 (07) :705-711
[5]  
Feldmann H, 2004, VIRUS TAXONOMY, P645
[6]   RNA polymerase I-driven minigenome system for Ebola viruses [J].
Groseth, A ;
Feldmann, H ;
Theriault, S ;
Mehmetoglu, G ;
Flick, R .
JOURNAL OF VIROLOGY, 2005, 79 (07) :4425-4433
[7]   A PPxY motif within the VP40 protein of Ebola virus interacts physically and functionally with a ubiquitin ligase: Implications for filovirus budding [J].
Harty, RN ;
Brown, ME ;
Wang, GL ;
Huibregtse, J ;
Hayes, FP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (25) :13871-13876
[8]   The assembly of Ebola virus nucleocapsid requires virion-associated proteins 35 and 24 and posttranslational modification of nucleoprotein [J].
Huang, Y ;
Xu, L ;
Sun, YN ;
Nabel, GJ .
MOLECULAR CELL, 2002, 10 (02) :307-316
[9]   Ebola virus VP40-induced particle formation and association with the lipid bilayer [J].
Jasenosky, LD ;
Neumann, G ;
Lukashevich, I ;
Kawaoka, Y .
JOURNAL OF VIROLOGY, 2001, 75 (11) :5205-5214
[10]   Effect of Ebola virus proteins GP, NP and VP35 on VP40VLP morphology [J].
Johnson, Reed F. ;
Bell, Peter ;
Harty, Ronald N. .
VIROLOGY JOURNAL, 2006, 3 (1)