Přehled o publikaci
2025
Exploring Enterovirus 71 Genome Replication In Situ
NEPOVÍMOVÁ, Lucie; Milan EŠNER and Pavel PLEVKABasic information
Original name
Exploring Enterovirus 71 Genome Replication In Situ
Authors
NEPOVÍMOVÁ, Lucie; Milan EŠNER and Pavel PLEVKA
Edition
Junior Group Workshop for the European Society for Virology: Imaging Viruses, Madrid, Spain, 2025
Other information
Language
English
Type of outcome
Konferenční abstrakta
Country of publisher
Spain
Confidentiality degree
is not subject to a state or trade secret
References:
Marked to be transferred to RIV
No
Organization
Středoevropský technologický institut – Repository – Repository
Keywords in English
enterovirus; electron microscopy; cryo-electron tomography; replication dynamics; viral assembly; fluorescent visualisation
Links
EH22_008/0004607, research and development project.
Changed: 15/2/2026 00:51, RNDr. Daniel Jakubík
Abstract
In the original language
Background and Aims. Enterovirus 71 (EV71), a Picornaviridae family member, is a major cause of hand-foot-and-mouth disease, predominantly affecting young children. Severe cases can result in neurological complications with mortality rates reaching 19%. Escalating outbreaks in the Asia-Pacific region highlight the urgent need for novel therapeutic approaches. Current vaccines target specific serotypes but lack evidence of cross-protection, and antiviral therapies remain unavailable due to limited knowledge of EV71's replication cycle. This study aims to investigate unexplored aspects of EV71 RNA replication, including its coupling with genome packaging and viral assembly. Methods. We developed a fluorescent reporter system to specifically label EV71 replication sites while preserving the natural viral genome and replication process. The reporter serves as a key tool for advanced imaging techniques, including correlative light and electron microscopy and cryo-electron tomography, to visualise replication dynamics and viral assembly at molecular level. Results. Preliminary results demonstrate successful cloning of the fluorescent reporter system. Functional validation is underway using fluorescence microscopy, providing insights into the reporter’s potential to track replication in both live and fixed cells.