Inhibition of betanodavirus infection by inhibitors of endosomal acidification

被引:28
作者
Adachi, K.
Ichinose, T.
Takizawa, N.
Watanabe, K.
Kitazato, K.
Kobayashi, N.
机构
[1] Nagasaki Univ, Grad Sch Biomed Sci, Lab Mol Biol Infect Agents, Nagasaki 8528521, Japan
[2] AVSS Corp, Ctr Res Ctr, Nagasaki, Japan
[3] Nagasaki Univ, Ctr Int Collaborat Res, Nagasaki, Japan
关键词
D O I
10.1007/s00705-007-1061-7
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Betanodaviruses, members of the family Nodaviridae, have small positive-stranded bipartite RNA genomes and are the causal agent of viral nervous necrosis (VNN) in many species of marine farmed fish. In the aquaculture industry, outbreaks of betanodavirus infection and spread in larval and juvenile fish result in devastating damage and heavy economic loss. Although an urgent need exists to develop drugs that inhibit betanodavirus infection, there have been no reports about anti-betanodavirus drugs. Recently, it was reported that betanodaviruses were detected in the endosomes of infected cells, suggesting that betanodaviruses enter fish cells by endocytosis. This finding prompted us to examine whether blocking this endosomal pathway could provide a target for antiviral drug development. In this study, we examined the inhibitory effect of several lysosomotropic agents against betanodavirus infection in fish E-11 cells. The presence of 1mM NH4Cl or 1 mu M chloroquine in the medium inhibited the entry of betanodaviruses into cells and inhibited viral infection. The lysosomotropic agents bafilomycin A1 and monensin also inhibited virus-induced cytopathology and virus production. Our data demonstrate that inhibitors of endosomal acidification are candidates as antiviral agents against betanodavirus.
引用
收藏
页码:2217 / 2224
页数:8
相关论文
共 36 条
  • [1] Endocytosis and a low-pH step are required for productive entry of equine infectious anemia virus
    Brindley, MA
    Maury, W
    [J]. JOURNAL OF VIROLOGY, 2005, 79 (23) : 14482 - 14488
  • [2] The avian coronavirus infectious bronchitis virus undergoes direct low-pH-dependent fusion activation during entry into host cells
    Chu, VC
    McElroy, LJ
    Chu, V
    Bauman, BE
    Whittaker, GR
    [J]. JOURNAL OF VIROLOGY, 2006, 80 (07) : 3180 - 3188
  • [3] Internalization and trafficking mechanisms of coxsackievirus B3 in HeLa cells
    Chung, SK
    Kim, JY
    Kim, IB
    Park, SI
    Paek, KH
    Nam, JH
    [J]. VIROLOGY, 2005, 333 (01) : 31 - 40
  • [4] De Clercq Erik, 2006, Expert Rev Anti Infect Ther, V4, P291, DOI 10.1586/14787210.4.2.291
  • [5] The clathrin endocytic pathway in viral infection
    De Tulleo, L
    Kirchhausen, T
    [J]. EMBO JOURNAL, 1998, 17 (16) : 4585 - 4593
  • [6] INHIBITION OF VESICULAR STOMATITIS-VIRUS GLYCOPROTEIN EXPRESSION BY CHLOROQUINE
    DILLE, BJ
    JOHNSON, TC
    [J]. JOURNAL OF GENERAL VIROLOGY, 1982, 62 (SEP) : 91 - 103
  • [7] Sequestration and protection of double-stranded RNA by the betanodavirus B2 protein
    Fenner, Beau J.
    Goh, Winnie
    Kwang, Jimmy
    [J]. JOURNAL OF VIROLOGY, 2006, 80 (14) : 6822 - 6833
  • [8] Betanodavirus B2 is an RNA interference antagonist that facilitates intracellular viral RNA accumulation
    Fenner, BJ
    Thiagarajan, R
    Chua, HK
    Kwang, J
    [J]. JOURNAL OF VIROLOGY, 2006, 80 (01) : 85 - 94
  • [9] Weak bases affect late stages of Mayaro virus replication cycle in vertebrate cells
    Ferreira, DF
    Santo, MPE
    Rebello, MA
    Rebello, MCS
    [J]. JOURNAL OF MEDICAL MICROBIOLOGY, 2000, 49 (04) : 313 - 318
  • [10] Membrane association of greasy grouper nervous necrosis virus protein A and characterization of its mitochondrial localization targeting signal
    Guo, YX
    Chan, SW
    Kwang, J
    [J]. JOURNAL OF VIROLOGY, 2004, 78 (12) : 6498 - 6508