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Synthetic rewiring and boosting type I interferon responses for visualization and counteracting viral infections
Mammalian first line of defense against viruses is accomplished by the interferon (IFN) system. Viruses have evolved numerous mechanisms to reduce the IFN action allowing them to invade the host and/or to establish latency. We generated an IFN responsive intracellular hub by integrating the syntheti...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7672444/ https://www.ncbi.nlm.nih.gov/pubmed/33137201 http://dx.doi.org/10.1093/nar/gkaa961 |
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author | Gödecke, Natascha Riedel, Jan Herrmann, Sabrina Behme, Sara Rand, Ulfert Kubsch, Tobias Cicin-Sain, Luka Hauser, Hansjörg Köster, Mario Wirth, Dagmar |
author_facet | Gödecke, Natascha Riedel, Jan Herrmann, Sabrina Behme, Sara Rand, Ulfert Kubsch, Tobias Cicin-Sain, Luka Hauser, Hansjörg Köster, Mario Wirth, Dagmar |
author_sort | Gödecke, Natascha |
collection | PubMed |
description | Mammalian first line of defense against viruses is accomplished by the interferon (IFN) system. Viruses have evolved numerous mechanisms to reduce the IFN action allowing them to invade the host and/or to establish latency. We generated an IFN responsive intracellular hub by integrating the synthetic transactivator tTA into the chromosomal Mx2 locus for IFN-based activation of tTA dependent expression modules. The additional implementation of a synthetic amplifier module with positive feedback even allowed for monitoring and reacting to infections of viruses that can antagonize the IFN system. Low and transient IFN amounts are sufficient to trigger these amplifier cells. This gives rise to higher and sustained—but optionally de-activatable—expression even when the initial stimulus has faded out. Amplification of the IFN response induced by IFN suppressing viruses is sufficient to protect cells from infection. Together, this interfaced sensor/actuator system provides a toolbox for robust sensing and counteracting viral infections. |
format | Online Article Text |
id | pubmed-7672444 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-76724442020-11-24 Synthetic rewiring and boosting type I interferon responses for visualization and counteracting viral infections Gödecke, Natascha Riedel, Jan Herrmann, Sabrina Behme, Sara Rand, Ulfert Kubsch, Tobias Cicin-Sain, Luka Hauser, Hansjörg Köster, Mario Wirth, Dagmar Nucleic Acids Res Synthetic Biology and Bioengineering Mammalian first line of defense against viruses is accomplished by the interferon (IFN) system. Viruses have evolved numerous mechanisms to reduce the IFN action allowing them to invade the host and/or to establish latency. We generated an IFN responsive intracellular hub by integrating the synthetic transactivator tTA into the chromosomal Mx2 locus for IFN-based activation of tTA dependent expression modules. The additional implementation of a synthetic amplifier module with positive feedback even allowed for monitoring and reacting to infections of viruses that can antagonize the IFN system. Low and transient IFN amounts are sufficient to trigger these amplifier cells. This gives rise to higher and sustained—but optionally de-activatable—expression even when the initial stimulus has faded out. Amplification of the IFN response induced by IFN suppressing viruses is sufficient to protect cells from infection. Together, this interfaced sensor/actuator system provides a toolbox for robust sensing and counteracting viral infections. Oxford University Press 2020-11-02 /pmc/articles/PMC7672444/ /pubmed/33137201 http://dx.doi.org/10.1093/nar/gkaa961 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Synthetic Biology and Bioengineering Gödecke, Natascha Riedel, Jan Herrmann, Sabrina Behme, Sara Rand, Ulfert Kubsch, Tobias Cicin-Sain, Luka Hauser, Hansjörg Köster, Mario Wirth, Dagmar Synthetic rewiring and boosting type I interferon responses for visualization and counteracting viral infections |
title | Synthetic rewiring and boosting type I interferon responses for visualization and counteracting viral infections |
title_full | Synthetic rewiring and boosting type I interferon responses for visualization and counteracting viral infections |
title_fullStr | Synthetic rewiring and boosting type I interferon responses for visualization and counteracting viral infections |
title_full_unstemmed | Synthetic rewiring and boosting type I interferon responses for visualization and counteracting viral infections |
title_short | Synthetic rewiring and boosting type I interferon responses for visualization and counteracting viral infections |
title_sort | synthetic rewiring and boosting type i interferon responses for visualization and counteracting viral infections |
topic | Synthetic Biology and Bioengineering |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7672444/ https://www.ncbi.nlm.nih.gov/pubmed/33137201 http://dx.doi.org/10.1093/nar/gkaa961 |
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