Role of the ERK1/2 Signaling Pathway in the Replication of Junín and Tacaribe Viruses

QUINTANA, VERÓNICA; CASTILLA, VIVIANA; QUINTANA, VERÓNICA; CASTILLA, VIVIANA; BRUNETTI, JESÚS; SCOLARO, LUIS; BRUNETTI, JESÚS; FOSCALDI, SABRINA; SCOLARO, LUIS; LÓPEZ, NORA; FOSCALDI, SABRINA; LÓPEZ, NORA

Viruses

MDPI AG

Lugar: Basel; Año: 2018 vol. 10

1999-4915

Abstract: We have previously shown that the infection of cell cultures with the arenaviruses Junín (JUNV), Tacaribe (TCRV), and Pichindé promotes the phosphorylation of mitogen-activated protein kinases (MAPKs) extracellular signal-regulated kinases 1 and 2 (ERK1/2) and that this activation is required for the achievement of a productive infection. Here we examined the contribution of ERK1/2 in early steps of JUNV and TCRV multiplication. JUNV adsorption, internalization, and uncoating were not affected by treatment of cultured cells with U0126, an inhibitor of the ERK1/2 signaling pathway. In contrast, U0126 caused a marked reduction in viral protein expression and RNA synthesis, while JUNV RNA synthesis was significantly augmented in the presence of an activator of the ERK1/2 pathway. Moreover, U0126 impaired the expression of a reporter gene in a TCRV-based replicon system, confirming the ability of the compound to hinder arenavirus macromolecular synthesis. By using a cell-based assay, we determined that the inhibitor did not affect the translation of a synthetic TCRV-like mRNA. No changes in the phosphorylation pattern of the translation factor eIF2α were found in U0126-treated cells. Our results indicate that U0126 impairs viral RNA synthesis, thereby leading to a subsequent reduction in viral protein expression. Thus, we conclude that ERK1/2 signaling activation is required for an efficient arenavirus RNA synthesis.