| Literature DB >> 33256205 |
Franck Gallardo1, Doris Schmitt2, Renée Brandely2, Catherine Brua2, Nathalie Silvestre2, Annie Findeli2, Johann Foloppe2, Sokunthea Top1, Sandrine Kappler-Gratias1, Charlotte Quentin-Froignant1, Renaud Morin3, Jean-Michel Lagarde3, Kerstin Bystricky4,5, Stéphane Bertagnoli6, Philippe Erbs2.
Abstract
As a live biologic agent, oncolytic vaccinia virus has the ability to target and selectively amplify at tumor sites. We have previously reported that deletion of thymidine kinase and ribonucleotide reductase genes in vaccinia virus can increase the safety and efficacy of the virus. Here, to allow direct visualization of the viral genome in living cells, we incorporated the ANCH target sequence and the OR3-Santaka gene in the double-deleted vaccinia virus. Infection of human tumor cells with ANCHOR3-tagged vaccinia virus enables visualization and quantification of viral genome dynamics in living cells. The results show that the ANCHOR technology permits the measurement of the oncolytic potential of the double deleted vaccinia virus. Quantitative analysis of infection kinetics and of viral DNA replication allow rapid and efficient identification of inhibitors and activators of oncolytic activity. Our results highlight the potential application of the ANCHOR technology to track vaccinia virus and virtually any kind of poxvirus in living cells.Entities:
Keywords: fluorescence labeling; live cell imaging; oncolytic vaccinia virus; poxvirus modulators
Year: 2020 PMID: 33256205 PMCID: PMC7760631 DOI: 10.3390/biomedicines8120543
Source DB: PubMed Journal: Biomedicines ISSN: 2227-9059