Chimaeric Rift Valley Fever Virus-Like Particle Vaccine Candidate Production in Nicotiana benthamiana

被引:13
作者
Mbewana, Sandiswa [1 ]
Meyers, Ann E. [1 ]
Rybicki, Edward P. [1 ,2 ]
机构
[1] Univ Cape Town, Dept Mol & Cell Biol, Biopharming Res Unit, Private Bag X3,22 Univ Ave, ZA-7700 Cape Town, South Africa
[2] Univ Cape Town, Fac Hlth Sci, Inst Infect Dis & Mol Med, Anzio Rd, ZA-7925 Cape Town, South Africa
基金
新加坡国家研究基金会;
关键词
agroinfiltration; chimaeric virus-like particles; Nicotiana benthamiana; Rift Valley fever; vaccine; ENVELOPE GLYCOPROTEINS; IMMUNE-RESPONSES; DISEASE VIRUS; EXPRESSION; PLANTS; PROTEINS; GENE; ORGANIZATION; REPLICATION; MATURATION;
D O I
10.1002/biot.201800238
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Rift Valley fever virus (RVFV) is an emerging mosquito-borne virus and hemorrhagic fever agent, which causes abortion storms in farmed small ruminants and potentially causes miscarriages in humans. Although live-attenuated vaccines are available for animals, they can only be used in endemic areas and there are currently no commercially available vaccines for humans. Here the authors describe the production of chimaeric RVFV virus-like particles transiently expressed in Nicotiana benthamiana by Agrobacterium tumefaciens-mediated gene transfer. The glycoprotein (Gn) gene is modified by removing its ectodomain (Gne) and fusing it to the transmembrane domain and cytosolic tail-encoding region of avian influenza H5N1 hemagglutinin. This is expressed transiently in N. benthamiana with purified protein yields calculated to be approximate to 57 mg kg(-1) fresh weight. Transmission electron microscopy shows putative chimaeric RVFV Gne-HA particles of 49-60 nm which are immunogenic, eliciting Gn-specific antibody responses in vaccinated mice without the use of adjuvant. To our knowledge, this is the first demonstration of the synthesis of Gne-HA chimaeric RVFV VLPs and the first demonstration of a detectable yield of RVFV Gn in plants.
引用
收藏
页数:9
相关论文
共 54 条
  • [1] Functional maturation of an antiviral cytotoxic T-cell response
    Bachmann, MF
    Speiser, DE
    Ohashi, PS
    [J]. JOURNAL OF VIROLOGY, 1997, 71 (08) : 5764 - 5768
  • [2] THE INFLUENCE OF ANTIGEN ORGANIZATION ON B-CELL RESPONSIVENESS
    BACHMANN, MF
    ROHRER, UH
    KUNDIG, TM
    BURKI, K
    HENGARTNER, H
    ZINKERNAGEL, RM
    [J]. SCIENCE, 1993, 262 (5138) : 1448 - 1451
  • [3] Baudin M, 2016, LANCET GLOB HEALTH, V4, pE864, DOI [10.1016/S2214-109X(16)30176-0, 10.1016/s2214-109x(16)30176-0]
  • [4] TOPOLOGICAL MAPPING OF ANTIGENIC SITES ON THE RIFT-VALLEY FEVER VIRUS ENVELOPE GLYCOPROTEINS USING MONOCLONAL-ANTIBODIES
    BESSELAAR, TG
    BLACKBURN, NK
    [J]. ARCHIVES OF VIROLOGY, 1991, 121 (1-4) : 111 - 124
  • [5] Reverse genetics technology for Rift Valley fever virus: Current and future applications for the development of therapeutics and vaccines
    Bouloy, Michele
    Flick, Ramon
    [J]. ANTIVIRAL RESEARCH, 2009, 84 (02) : 101 - 118
  • [6] Induction of autoantibodies to mouse CCR5 with recombinant papillomavirus particles
    Chackerian, B
    Lowy, DR
    Schiller, JT
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (05) : 2373 - 2378
  • [7] Collett M.S., 1987, The biology of negative strand viruses, P321
  • [8] Rift Valley fever virus subunit vaccines confer complete protection against a lethal virus challenge
    de Boer, S. M.
    Kortekaas, J.
    Antonis, A. F.
    Kant, J.
    van Oploo, J. L.
    Rottier, P. J. M.
    Moormann, R. J. M.
    Bosch, B. J.
    [J]. VACCINE, 2010, 28 (11) : 2330 - 2339
  • [9] Emerging viruses: The Bunyaviridae
    Elliott, RM
    [J]. MOLECULAR MEDICINE, 1997, 3 (09) : 572 - 577
  • [10] A Glycoprotein Subunit Vaccine Elicits a Strong Rift Valley Fever Virus Neutralizing Antibody Response in Sheep
    Faburay, Bonto
    Lebedev, Maxim
    McVey, D. Scott
    Wilson, William
    Morozov, Igor
    Young, Alan
    Richt, Juergen A.
    [J]. VECTOR-BORNE AND ZOONOTIC DISEASES, 2014, 14 (10) : 746 - 756