Abstract
The human pathogenic orthoflavivirus St. Louis encephalitis virus (SLEV) reemerged in the western United States in 2015 after more than a decade of apparent absence and has since expanded throughout California with sustained, interannual transmission. This shift from the historically sporadic pattern of SLEV activity prior to 2003 raises the question of whether contemporary SLEV strains differ in fitness in Culex vectors compared with earlier strains. To determine whether reemerging SLEV possess augmented infectivity and transmissibility that may have facilitated reestablishment, we compared the vector competence of five genotype III SLEV strains detected in California between 2016 and 2023 with a historic genotype V strain from 2003. Laboratory colonies of the two primary California vectors, Culex (Cx.) tarsalis and Cx. quinquefasciatus, were orally exposed to bloodmeals containing 3, 5, or 6.7 log(10) plaque forming units (PFU)/mL of SLEV, and infection, dissemination, and transmission were assessed 13,14, or 15 days later by quantifying SLEV RNA in individual mosquitoes. Both species exhibited strong dose-dependent responses, with minimal infection at 3 log(10) PFU/mL and uniformly high infection, dissemination, and saliva positivity at 6.7 log(10) PFU/mL. At 5 log(10) PFU/mL, genotype III strains infected Cx. quinquefasciatus more efficiently than the historical 2003 strain, which failed to infect this species. In Cx. tarsalis, fitness differences among SLEV strains were more modest and strain-specific. These findings demonstrate that multiple genotype III SLEV strains exhibit equal or greater vector infectivity in Cx. quinquefasciatus than the 2003 genotype V strain, suggesting that enhanced fitness in this vector may contribute to the persistence and geographic spread of SLEV in California since its reemergence and underscoring the need for continued vector surveillance and targeted control efforts to reduce SLEV transmission to humans.