U-73122, a phospholipase C inhibitor, impairs lymphocytic choriomeningitis virus virion infectivity

• Published in: Journal of general virology Vol. 105; no. 12
• Main Authors: Mizuma, Keita, Hashizume, Mei, Urata, Shuzo, Shindo, Keiko, Takashima, Ayako, Mizuta, Satoshi, Iwasaki, Masaharu
• Format: Journal Article
• Language: English
• Published: England 17.12.2024
• Subjects: Animals; Antiviral Agents - pharmacology; Cell Line; Chlorocebus aethiops; Estrenes - pharmacology; Humans; Lassa virus - drug effects; Lymphocytic choriomeningitis virus - drug effects; Lymphocytic choriomeningitis virus - genetics; Lymphocytic choriomeningitis virus - physiology; Pyrrolidinones - pharmacology; Type C Phospholipases - antagonists & inhibitors; Type C Phospholipases - genetics; Type C Phospholipases - metabolism; Vero Cells; Virion - drug effects; Virus Replication - drug effects; virion; Junín virus; LCMV; Lassa virus; antiviral
• DOI: 10.1099/jgv.0.002060

Lassa virus (LASV) is an Old World (OW) mammarenavirus that causes Lassa fever, a life-threatening acute febrile disease endemic in West Africa. Lymphocytic choriomeningitis virus (LCMV) is a worldwide-distributed, prototypic OW mammarenavirus of clinical significance that has been largely neglected as a human pathogen. No licensed OW mammarenavirus vaccines are available, and the current therapeutic option is limited to the off-label use of ribavirin, which offers only partial efficacy. This situation underscores the urgent need to develop novel antivirals against human pathogenic mammarenaviruses. Previously, we showed that afatinib, a pan-ErbB tyrosine kinase inhibitor, inhibited multiple steps of the life cycles of OW LASV and LCMV, as well as the New World Junín virus vaccine strain Candid#1. In the present study, we investigated the inhibitory effect of U-73122, a phospholipase C inhibitor that acts downstream of ErbB signalling, on LCMV multiplication. U-73122 inhibited WT recombinant (r) LCMV multiplication in cultured cells. Preincubation of cell-free LCMV virions with U-73122 resulted in impaired virion infectivity. U-73122 also inhibited the infection of rLCMVs expressing heterologous viral glycoproteins, including the vesicular stomatitis Indiana virus (VSIV) glycoprotein, whereas WT VSIV infection was not affected by U-73122 treatment. Our results show the novel bioactivity of U-73122 as an LCMV inhibitor and indicate the presence of a virion-associated molecule that is necessary for virion infectivity and can be exploited as a potential antiviral drug target against human pathogenic mammarenavirus infections.