The calmodulin antagonist W-7 (N-(6-aminohexyl)-5-chloro-1-naphthalenesulfonamide hydrochloride) inhibits DENV infection in Huh-7 cells

被引:17
作者
Bautista-Carbajal, Patricia [1 ]
Soto-Acosta, Ruben [2 ]
Angel-Ambrocio, Antonio H. [1 ]
Cervantes-Salazar, Margot [1 ]
Loranca-Vega, Circe I. [1 ,2 ]
Herrera-Martinez, Mayra [1 ,2 ]
del Angel, Rosa M. [1 ]
机构
[1] IPN, CINVESTAV, Dept Infect & Patogenesis Mol, Mexico City 07360, DF, Mexico
[2] Univ Texas Med Branch, Dept Biochem & Mol Biol, Galveston, TX USA
关键词
Dengue virus (DENV) infection; Calmudulin (CaM); W7; Replicative complexes; NONSTRUCTURAL PROTEIN NS2A; WEST-NILE-VIRUS; DENGUE VIRUS; ENDOPLASMIC-RETICULUM; NS2B-NS3; PROTEASE; BINDING DOMAIN; REPLICATION; CONSTRUCTION; GLYCOPROTEIN; DYNAMICS;
D O I
10.1016/j.virol.2016.12.004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Dengue virus (DENV) replicative cycle occurs in the endoplasmic reticulum where calcium ions play an important role in cell signaling. Calmodulin (CaM) is the primary sensor of intracellular Ca2+ levels in eukaryotic cells. In this paper, the effect of the calmodulin antagonist W-7 in DENV infection in Huh-7 cells was evaluated. W7 inhibited viral yield, NS1 secretion and viral RNA and protein synthesis. Moreover, luciferase activity, encoded by a DENY replicon, was also reduced. A decrease in the replicative complexes formation was clearly observed in W7 treated cells. Docking simulations suggest 2 possible mechanisms of action for W7: the direct inhibition of NS2B-NS3 activity and/or inhibition of the interaction between NS2A with Ca2+-CaM complex. This last possibility was supported by the in vitro interaction observed between recombinant NS2A and CaM. These results indicate that Ca2+-CaM plays an important role in DENY replication.
引用
收藏
页码:188 / 198
页数:11
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