Visualizing lymphocytic choriomeningitis virus infection in cells and living mice
Yuxi Wen, Huan Xu, Weiwei Wan, Weijuan Shang, Runming Jin, Fen Zhou, Heng Mei, Jingshi Wang, Gengfu Xiao, Hongbo Chen, Xiaoyan Wu, Leike Zhang
Abstract
Yuxi Wen, Huan Xu, Weiwei Wan, Weijuan Shang, Runming Jin, Fen Zhou, Heng Mei, Jingshi Wang, Gengfu Xiao, Hongbo Chen, Xiaoyan Wu, Leike Zhang
Abstract
Mammarenavirus are a large family of enveloped negative-strand RNA viruses that include several agents responsible for severe hemorrhagic fevers. Until now, no FDA-licensed drug has been admitted for treating an arenavirus infection, and only few effective anti-arenavirus drugs have been tested in vivo . In this work, we designed a recombinant reporter arenavirus lymphocytic choriomeningitis virus that stably expressed nanoluciferase (LCMV-Nluc). The LCMV-Nluc was proved to share similar biological properties with wild-type LCMV and the Nluc intensity reliably reflected viral replication both in vitro and in vivo . Replication of the Nluc-encoding virus in living mice can be visualized by real-time bioluminescent imaging, and bioluminescence can be detected in a variety of organs of infected mice. This work provides a novel approach that enables real-time study of the arenavirus infection and is a convenient and valuable tool for screening of compounds that are active against arenaviruses in vitro and in living mice.
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Mammarenavirus are a large family of enveloped negative-strand RNA viruses that include several agents responsible for severe hemorrhagic fevers. Until now, no FDA-licensed drug has been admitted for treating an arenavirus infection, and only few effective anti-arenavirus drugs have been tested in vivo . In this work, we designed a recombinant reporter arenavirus lymphocytic choriomeningitis virus that stably expressed nanoluciferase (LCMV-Nluc). The LCMV-Nluc was proved to share similar biological properties with wild-type LCMV and the Nluc intensity reliably reflected viral replication both in vitro and in vivo . Replication of the Nluc-encoding virus in living mice can be visualized by real-time bioluminescent imaging, and bioluminescence can be detected in a variety of organs of infected mice. This work provides a novel approach that enables real-time study of the arenavirus infection and is a convenient and valuable tool for screening of compounds that are active against arenaviruses in vitro and in living mice.
Key concepts: Arenavirus, Lymphocytic choriomeningitis, Virology, Biology, Virus, Viral replication, In vivo, Antiviral drug