Přehled o publikaci
2025
Exploring Enterovirus 71 Genome Replication In Situ
NEPOVÍMOVÁ, Lucie; Milan EŠNER a Pavel PLEVKAZákladní údaje
Originální název
Exploring Enterovirus 71 Genome Replication In Situ
Autoři
NEPOVÍMOVÁ, Lucie; Milan EŠNER a Pavel PLEVKA
Vydání
Junior Group Workshop for the European Society for Virology: Imaging Viruses, Madrid, Spain, 2025
Další údaje
Jazyk
angličtina
Typ výsledku
Konferenční abstrakta
Stát vydavatele
Španělsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Označené pro přenos do RIV
Ne
Organizace
Středoevropský technologický institut – Masarykova univerzita – Repozitář
Klíčová slova anglicky
enterovirus; electron microscopy; cryo-electron tomography; replication dynamics; viral assembly; fluorescent visualisation
Návaznosti
EH22_008/0004607, projekt VaV.
Změněno: 15. 2. 2026 00:51, RNDr. Daniel Jakubík
Anotace
V originále
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.