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Modeling The Lifecycle Of Ebola Virus Under Biosafety Level 2 Conditions With Virus-like Particles Containing Tetracistronic Minigenomes
Published on: September 27, 2014
Identification of gemcitabine as an anti-Lassa virus inhibitor using a robust biosafety Level-2 system modeling the
Xiaoyou Hu1, Qian Guang1, Wenting Mao2
1Infectious Disease Research Center, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China; Shanghai Institute of Immunity and Infection, Chinese Academy of Sciences, Shanghai, 200031, China; University of Chinese Academy of Sciences, Beijing, 100049, China.
Abstract:
The Lassa virus (LASV), a member of the Old World arenaviruses and classified as a risk-group 4 pathogen, causes severe hemorrhagic fever in humans with significant mortality. Here, we developed a robust LASV reverse genetics system designated LASVsg that models the complete LASV life cycle under biosafety level-2 (BSL-2) conditions. Using this system, we screened a library of nucleoside/nucleotide analogs for anti-LASV activity. Gemcitabine, a clinically approved nucleoside analog, was identified to exhibit pronounced antiviral efficacy against LASVsg, which was further confirmed using authentic LASV in a BSL-4 laboratory. Mechanistic analyses revealed that gemcitabine suppresses LASV infection by reducing viral protein levels without directly inhibiting viral RNA replication or transcription. In summary, we developed a robust BSL-2 reverse genetics system for LASV research, enabling the identification of gemcitabine as a potential antiviral candidate.
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