The kinase inhibitor SFV785 dislocates dengue virus envelope protein from the replication complex and blocks virus assembly.

Imagen de Mariano Garcia-Blanco
TítuloThe kinase inhibitor SFV785 dislocates dengue virus envelope protein from the replication complex and blocks virus assembly.
Publication TypeJournal Article
Year of Publication2011
AutoresAnwar, A, Hosoya, T, Leong, KM, Onogi, H, Okuno, Y, Hiramatsu, T, Koyama, H, Suzuki, M, Hagiwara, M, García-Blanco, MA
JournalPLoS One
Volume6
Issue8
Paginatione23246
Date Published2011
ISSN1932-6203
Palabras claveAnimals, Antiviral Agents, Azocines, Body Weight, Cell Line, Cell Line, Tumor, Cercopithecus aethiops, Dengue Virus, Endoplasmic Reticulum, Hepacivirus, Humans, Mice, Mice, Inbred ICR, Microscopy, Electron, Microscopy, Fluorescence, Molecular Structure, Nucleocapsid, Protein Kinase Inhibitors, Thiourea, Vero Cells, Viral Envelope Proteins, Virion, Virus Assembly, Virus Replication
Abstract

Dengue virus (DENV) is the etiologic agent for dengue fever, for which there is no approved vaccine or specific anti-viral drug. As a remedy for this, we explored the use of compounds that interfere with the action of required host factors and describe here the characterization of a kinase inhibitor (SFV785), which has selective effects on NTRK1 and MAPKAPK5 kinase activity, and anti-viral activity on Hepatitis C, DENV and yellow fever viruses. SFV785 inhibited DENV propagation without inhibiting DENV RNA synthesis or translation. The compound did not cause any changes in the cellular distribution of non-structural 3, a protein critical for DENV RNA synthesis, but altered the distribution of the structural envelope protein from a reticulate network to enlarged discrete vesicles, which altered the co-localization with the DENV replication complex. Ultrastructural electron microscopy analyses of DENV-infected SFV785-treated cells showed the presence of viral particles that were distinctly different from viable enveloped virions within enlarged ER cisternae. These viral particles were devoid of the dense nucleocapsid. The secretion of the viral particles was not inhibited by SFV785, however a reduction in the amount of secreted infectious virions, DENV RNA and capsid were observed. Collectively, these observations suggest that SFV785 inhibited the recruitment and assembly of the nucleocapsid in specific ER compartments during the DENV assembly process and hence the production of infectious DENV. SFV785 and derivative compounds could be useful biochemical probes to explore the DENV lifecycle and could also represent a new class of anti-virals.

DOI10.1371/journal.pone.0023246
Alternate JournalPLoS ONE
PubMed ID21858043