KEVÉLY, Ádám, Veronika PRANČLOVÁ, Monika SLÁVIKOVÁ, Jan HAVIERNIK, Václav HÖNIG, Eva NOVÁKOVÁ, Martin PALUS, Daniel RŮŽEK, Boris KLEMPA and Juraj KOČI. Fitness of mCherry Reporter Tick-Borne Encephalitis Virus in Tick Experimental Models. Viruses. MDPI, 2022, vol. 14, No 12, p. 1-12. ISSN 1999-4915. Available from: https://dx.doi.org/10.3390/v14122673.
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Basic information
Original name Fitness of mCherry Reporter Tick-Borne Encephalitis Virus in Tick Experimental Models.
Authors KEVÉLY, Ádám, Veronika PRANČLOVÁ, Monika SLÁVIKOVÁ, Jan HAVIERNIK (203 Czech Republic, belonging to the institution), Václav HÖNIG (203 Czech Republic), Eva NOVÁKOVÁ, Martin PALUS (203 Czech Republic), Daniel RŮŽEK (203 Czech Republic, belonging to the institution), Boris KLEMPA and Juraj KOČI (guarantor).
Edition Viruses, MDPI, 2022, 1999-4915.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10607 Virology
Country of publisher Switzerland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 4.700
RIV identification code RIV/00216224:14310/22:00128502
Organization unit Faculty of Science
Doi http://dx.doi.org/10.3390/v14122673
UT WoS 000904310800001
Keywords in English tick-borne encephalitis virus; TBEV; mCherry reporter; viral reverse genetics; Ixodes ricinus; ticks; tick cell culture
Tags rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Marie Šípková, DiS., učo 437722. Changed: 8/2/2023 08:10.
Abstract
The tick-borne encephalitis virus (TBEV) causes a most important viral life-threatening illness transmitted by ticks. The interactions between the virus and ticks are largely unexplored, indicating a lack of experimental tools and systematic studies. One such tool is recombinant reporter TBEV, offering antibody-free visualization to facilitate studies of transmission and interactions between a tick vector and a virus. In this paper, we utilized a recently developed recombinant TBEV expressing the reporter gene mCherry to study its fitness in various tick-derived in vitro cell cultures and live unfed nymphal Ixodes ricinus ticks. The reporter virus was successfully replicated in tick cell lines and live ticks as confirmed by the plaque assay and the mCherry-specific polymerase chain reaction (PCR). Although a strong mCherry signal determined by fluorescence microscopy was detected in several tick cell lines, the fluorescence of the reporter was not observed in the live ticks, corroborated also by immunoblotting. Our data indicate that the mCherry reporter TBEV might be an excellent tool for studying TBEV-tick interactions using a tick in vitro model. However, physiological attributes of a live tick, likely contributing to the inactivity of the reporter, warrant further development of reporter-tagged viruses to study TBEV in ticks in vivo.
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