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NanoBiT System and Hydrofurimazine for Optimized Detection of Viral Infection in Mice—A Novel in Vivo Imaging Platform
Reporter genes are used to visualize intracellular biological phenomena, including viral infection. Here we demonstrate bioluminescent imaging of viral infection using the NanoBiT system in combination with intraperitoneal injection of a furimazine analogue, hydrofurimazine. This recently developed...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7461499/ https://www.ncbi.nlm.nih.gov/pubmed/32824188 http://dx.doi.org/10.3390/ijms21165863 |
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author | Gaspar, Natasa Zambito, Giorgia Dautzenberg, Iris J. C. Cramer, Steve J. Hoeben, Rob C. Lowik, Clemens Walker, Joel R. Kirkland, Thomas A. Smith, Thomas P. van Weerden, Wytske M. de Vrij, Jeroen Mezzanotte, Laura |
author_facet | Gaspar, Natasa Zambito, Giorgia Dautzenberg, Iris J. C. Cramer, Steve J. Hoeben, Rob C. Lowik, Clemens Walker, Joel R. Kirkland, Thomas A. Smith, Thomas P. van Weerden, Wytske M. de Vrij, Jeroen Mezzanotte, Laura |
author_sort | Gaspar, Natasa |
collection | PubMed |
description | Reporter genes are used to visualize intracellular biological phenomena, including viral infection. Here we demonstrate bioluminescent imaging of viral infection using the NanoBiT system in combination with intraperitoneal injection of a furimazine analogue, hydrofurimazine. This recently developed substrate has enhanced aqueous solubility allowing delivery of higher doses for in vivo imaging. The small high-affinity peptide tag (HiBiT), which is only 11 amino-acids in length, was engineered into a clinically used oncolytic adenovirus, and the complementary large protein (LgBiT) was constitutively expressed in tumor cells. Infection of the LgBiT expressing cells with the HiBiT oncolytic virus will reconstitute NanoLuc in the cytosol of the cell, providing strong bioluminescence upon treatment with substrate. This new bioluminescent system served as an early stage quantitative viral transduction reporter in vitro and also in vivo in mice, for longitudinal monitoring of oncolytic viral persistence in infected tumor cells. This platform provides novel opportunities for studying the biology of viruses in animal models. |
format | Online Article Text |
id | pubmed-7461499 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74614992020-09-14 NanoBiT System and Hydrofurimazine for Optimized Detection of Viral Infection in Mice—A Novel in Vivo Imaging Platform Gaspar, Natasa Zambito, Giorgia Dautzenberg, Iris J. C. Cramer, Steve J. Hoeben, Rob C. Lowik, Clemens Walker, Joel R. Kirkland, Thomas A. Smith, Thomas P. van Weerden, Wytske M. de Vrij, Jeroen Mezzanotte, Laura Int J Mol Sci Article Reporter genes are used to visualize intracellular biological phenomena, including viral infection. Here we demonstrate bioluminescent imaging of viral infection using the NanoBiT system in combination with intraperitoneal injection of a furimazine analogue, hydrofurimazine. This recently developed substrate has enhanced aqueous solubility allowing delivery of higher doses for in vivo imaging. The small high-affinity peptide tag (HiBiT), which is only 11 amino-acids in length, was engineered into a clinically used oncolytic adenovirus, and the complementary large protein (LgBiT) was constitutively expressed in tumor cells. Infection of the LgBiT expressing cells with the HiBiT oncolytic virus will reconstitute NanoLuc in the cytosol of the cell, providing strong bioluminescence upon treatment with substrate. This new bioluminescent system served as an early stage quantitative viral transduction reporter in vitro and also in vivo in mice, for longitudinal monitoring of oncolytic viral persistence in infected tumor cells. This platform provides novel opportunities for studying the biology of viruses in animal models. MDPI 2020-08-15 /pmc/articles/PMC7461499/ /pubmed/32824188 http://dx.doi.org/10.3390/ijms21165863 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gaspar, Natasa Zambito, Giorgia Dautzenberg, Iris J. C. Cramer, Steve J. Hoeben, Rob C. Lowik, Clemens Walker, Joel R. Kirkland, Thomas A. Smith, Thomas P. van Weerden, Wytske M. de Vrij, Jeroen Mezzanotte, Laura NanoBiT System and Hydrofurimazine for Optimized Detection of Viral Infection in Mice—A Novel in Vivo Imaging Platform |
title | NanoBiT System and Hydrofurimazine for Optimized Detection of Viral Infection in Mice—A Novel in Vivo Imaging Platform |
title_full | NanoBiT System and Hydrofurimazine for Optimized Detection of Viral Infection in Mice—A Novel in Vivo Imaging Platform |
title_fullStr | NanoBiT System and Hydrofurimazine for Optimized Detection of Viral Infection in Mice—A Novel in Vivo Imaging Platform |
title_full_unstemmed | NanoBiT System and Hydrofurimazine for Optimized Detection of Viral Infection in Mice—A Novel in Vivo Imaging Platform |
title_short | NanoBiT System and Hydrofurimazine for Optimized Detection of Viral Infection in Mice—A Novel in Vivo Imaging Platform |
title_sort | nanobit system and hydrofurimazine for optimized detection of viral infection in mice—a novel in vivo imaging platform |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7461499/ https://www.ncbi.nlm.nih.gov/pubmed/32824188 http://dx.doi.org/10.3390/ijms21165863 |
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