Microtubule-dependent transport of arenavirus matrix protein demonstrated using live-cell imaging microscopy. (11th November 2019)

• Record Type: Journal Article
• Authors: Takamatsu, Yuki; Kajikawa, Junichi; Muramoto, Yukiko; Nakano, Masahiro; Noda, Takeshi
• Is Part Of: Microscopy. Volume 68:Number 6(2019)
• Page Start: 450
• Page End: 456
• Publication Date: 2019-11-11
• Subjects: Arenavirus -- matrix protein -- transport -- microtubule -- live-cell imaging; Microscopy -- Periodicals; 502.825
• DOI: 10.1093/jmicro/dfz034
• Languages: English
• ISSNs: 2050-5698

Abstract

Abstract: Lassa virus (LASV), belonging to the family Arenaviridae, causes severe haemorrhagic manifestations and is associated with a high mortality rate in humans. Thus, it is classified as a biosafety level (BSL)-4 agent. Since countermeasures for LASV diseases are yet to be developed, it is important to elucidate the molecular mechanisms underlying the life cycle of the virus, including its viral and host cellular protein interactions. These underlying molecular mechanisms may serve as the key for developing novel therapeutic options. Lymphocytic choriomeningitis virus (LCMV), a close relative of LASV, is usually asymptomatic and is categorized as a BSL-2 agent. In the present study, we visualized the transport of viral matrix Z protein in LCMV-infected cells using live-cell imaging microscopy. We demonstrated that the transport of Z protein is mediated by polymerized microtubules. Interestingly, the transport of LASV Z protein showed characteristics similar to those of Z protein in LCMV-infected cells. The live-cell imaging system using LCMV provides an attractive surrogate measure for studying arenavirus matrix protein transport in BSL-2 laboratories. In addition, it could be also utilized to analyze the interactions between viral matrix proteins and the cellular cytoskeleton, as well as to evaluate the antiviral compounds that target the transport of viral matrix proteins.