Development and optimization of biologically contained Marburg virus for high-throughput antiviral screening

被引:2
作者
Vanmechelen, Bert [1 ]
Stroobants, Joren [2 ]
Chiu, Winston [2 ]
Naesens, Lieve [2 ]
Schepers, Joost [2 ]
Vermeire, Kurt [2 ]
Maes, Piet [1 ]
机构
[1] Katholieke Univ Leuven, Rega Inst, Dept Microbiol Immunol & Transplantat, Lab Clin & Epidemiol Virol, Herestr 49 box 1040, B-3000 Leuven, Belgium
[2] Katholieke Univ Leuven, Dept Microbiol Immunol & Transplantat, Lab Virol & Chemotherapy, Rega Inst, Herestr 49 box 1043, B-3000 Leuven, Belgium
关键词
REVERSE GENETICS SYSTEM; EBOLA-VIRUS; REPLICATION; GENERATION; CDNA;
D O I
10.1016/j.antiviral.2022.105426
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Comparable to the related Ebola virus, Marburg virus is an emerging zoonotic pathogen that causes hemorrhagic fever with a high mortality rate. Therefore, handling of Ebola virus and Marburg virus is limited to biosafety level 4 facilities, of which only a limited number exists worldwide. However, researchers have developed several virus alternatives that are safe to handle in lower biosafety settings. One particularly interesting approach is the engineering of biologically contained Ebola virus by removing an essential gene from the virus genome and providing this missing gene in trans in a specific cell line. Because the virus is confined to this specific cell line, this results in a system that is safe to handle. So far, Ebola virus is the only virus for which biological containment has been reported. Here, we describe the first successful rescue of biologically contained Marburg virus and demonstrate that biological containment is also feasible for other filoviruses. Specifically, we describe the development of containment cell lines for Marburg virus through lentiviral transduction and show the growth and safety characteristics of eGFP-expressing, biologically contained Marburg virus in these cell lines. Additionally, we exploited this newly established Marburg virus system to screen over 500 compounds from available libraries. Lastly, we also validated the applicability of our biologically contained Marburg virus system in a 384-well format, to further illustrate the usefulness of this novel system as an alternative for high-throughput MARV screening of compound libraries.
引用
收藏
页数:9
相关论文
共 38 条
  • [1] Development of a reverse genetics system to generate a recombinant Ebola virus Makona expressing a green fluorescent protein
    Albarino, Cesar G.
    Guerrero, Lisa Wiggleton
    Lo, Michael K.
    Nichol, Stuart T.
    Towner, Jonathan S.
    [J]. VIROLOGY, 2015, 484 : 259 - 264
  • [2] Development of a reverse genetics system to generate recombinant Marburg virus derived from a bat isolate
    Albarino, Cesar G.
    Uebelhoer, Luke S.
    Vincent, Joel P.
    Khristova, Marina L.
    Chakrabarti, Ayan K.
    McElroy, Anita
    Nichol, Stuart T.
    Towner, Jonathan S.
    [J]. VIROLOGY, 2013, 446 (1-2) : 230 - 237
  • [3] Regulation of VP30-Dependent Transcription by RNA Sequence and Structure in the Genomic Ebola Virus Promoter
    Bach, Simone
    Demper, Jana-Christin
    Gruenweller, Arnold
    Becker, Stephan
    Biedenkopf, Nadine
    Hartmann, Roland K.
    [J]. JOURNAL OF VIROLOGY, 2021, 95 (05)
  • [4] Transcriptional Regulation in Ebola Virus: Effects of Gene Border Structure and Regulatory Elements on Gene Expression and Polymerase Scanning Behavior
    Brauburger, Kristina
    Boehmann, Yannik
    Kraehling, Verena
    Muehlberger, Elke
    [J]. JOURNAL OF VIROLOGY, 2016, 90 (04) : 1898 - 1909
  • [5] Generation of bovine respiratory syncytial virus (BRSV) from cDNA: BRSV NS2 is not essential for virus replication in tissue culture, and the human RSV leader region acts as a functional BRSV genome promoter
    Buchholz, UJ
    Finke, S
    Conzelmann, KK
    [J]. JOURNAL OF VIROLOGY, 1999, 73 (01) : 251 - 259
  • [6] Chosewood L.C., 2009, Biosafety in microbiological and biomedical laboratories, Vfifth
  • [7] Interaction with Tsg101 Is Necessary for the Efficient Transport and Release of Nucleocapsids in Marburg Virus-Infected Cells
    Dolnik, Olga
    Kolesnikova, Larissa
    Welsch, Sonja
    Strecker, Thomas
    Schudt, Gordian
    Becker, Stephan
    [J]. PLOS PATHOGENS, 2014, 10 (10)
  • [8] Current status of small molecule drug development for Ebola virus and other filoviruses
    Edwards, Megan R.
    Basler, Christopher F.
    [J]. CURRENT OPINION IN VIROLOGY, 2019, 35 : 42 - 56
  • [9] Rescue of recombinant Marburg virus from cDNA is dependent on nucleocapsid protein VP30
    Enterlein, S
    Volchkov, V
    Weik, M
    Kolesnikova, L
    Volchkova, V
    Klenk, HD
    Mühlberger, E
    [J]. JOURNAL OF VIROLOGY, 2006, 80 (02) : 1038 - 1043
  • [10] European Medicines Agency,, 2020, NEW VACC PREV EB VIR