Pregled bibliografske jedinice broj: 1218984
Design of recombinant viral vaccines based on mumps virus
Design of recombinant viral vaccines based on mumps virus // 15th Vaccine Congress
online, 2021. (predavanje, međunarodna recenzija, ostalo, znanstveni)
CROSBI ID: 1218984 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Design of recombinant viral vaccines
based on mumps virus
Autori
Pali, Dorotea ; Košutić Gulija, Tanja ; Slović, Anamarija ; Ivančić Jelečki, Jelena ; Forčić, Dubravko
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, ostalo, znanstveni
Skup
15th Vaccine Congress
Mjesto i datum
Online, 04.10.2021. - 06.10.2021
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
dizajn rekombinantnih cjepiva, mumps virus
(design of recombinant vaccines, mumps virus)
Sažetak
Recombinant viral vectors are particularly interesting for the development of vaccines against emerging viral diseases. So far, only few studies have shown the potential of mumps virus (Mumps orthorubulavirus, family Paramyxoviridae) to be used as a recombinant vector. The objective of this research is to develop recombinant vaccines for hepatitis C virus (HCV) and human respiratory syncytial virus (RSV) based on mumps recombinant virus (vMRV2). Virus vMRV2 was generated using a reverse genetics technology (rescue) and has a genome sequence based on the consensus of vaccine strain L-Zagreb. The rescue method we use comprises a co- transfection of BSRT7 cells with three expression plasmids that encode nucleocapsid protein and components of viral RNA-dependant RNA polymerase, and a plasmid with full-length virus genome (pMRV2). Additional transcription units were added to pMRV2 in order to produce recombinant live attenuated vaccines for HCV or RSV. Sequences encoding ectodomains of RSV F protein and HCV E1 and E2 proteins were cloned into the pMRV2 with or without the addition of transmembrane and cytoplasmic domain (TMD/CD) of mumps F protein. We expect that RSV and HCV genes will be expressed in infected cells ; proteins with the addition of TMD/CD of mumps F protein will be incorporated in viral particles as well. We have produced recombinant viruses vMRV2, vF RSV-MRV2 (vector vaccine for RSV) and vE1E2TMD HCV-MRV2 (vector vaccine 1 for HCV) ; rescue for vCE1E2 HCV-MRV2 (vector vaccine 2 for HCV) is currently in progress. Viral genetic stability was analysed by next generation sequencing after passaging of vF RSV-MRV2 in Vero cells, a putative production cell line. The biological significance of subconsensus population variability, as well as nucleotide changes observed on the level of viral population consensus, is being analyzed, as minor variant of virus quasispecies can affect the attenuation status of live viral vaccines.
Izvorni jezik
Engleski
POVEZANOST RADA
Profili:
Dorotea Pali
(autor)
Jelena Ivančić-Jelečki
(autor)
Anamarija Slović
(autor)
Dubravko Forčić
(autor)
Tanja Košutić Gulija
(autor)