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Transcriptome Kinetics of Saccharomyces cerevisiae in Response to Viral Killer Toxin K1
The K1 A/B toxin secreted by virus-infected Saccharomyces cerevisiae strains kills sensitive cells via disturbance of cytoplasmic membrane functions. Despite decades of research, the mechanisms underlying K1 toxicity and immunity have not been elucidated yet. In a novel approach, this study aimed to...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531845/ https://www.ncbi.nlm.nih.gov/pubmed/31156606 http://dx.doi.org/10.3389/fmicb.2019.01102 |
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author | Gier, Stefanie Simon, Martin Nordström, Karl Khalifa, Salem Schulz, Marcel H. Schmitt, Manfred J. Breinig, Frank |
author_facet | Gier, Stefanie Simon, Martin Nordström, Karl Khalifa, Salem Schulz, Marcel H. Schmitt, Manfred J. Breinig, Frank |
author_sort | Gier, Stefanie |
collection | PubMed |
description | The K1 A/B toxin secreted by virus-infected Saccharomyces cerevisiae strains kills sensitive cells via disturbance of cytoplasmic membrane functions. Despite decades of research, the mechanisms underlying K1 toxicity and immunity have not been elucidated yet. In a novel approach, this study aimed to characterize transcriptome changes in K1-treated sensitive yeast cells in a time-dependent manner. Global transcriptional profiling revealed substantial cellular adaptations in target cells resulting in 1,189 differentially expressed genes in total. Killer toxin K1 induced oxidative, cell wall and hyperosmotic stress responses as well as rapid down-regulation of transcription and translation. Essential pathways regulating energy metabolism were also significantly affected by the toxin. Remarkably, a futile cycle of the osmolytes trehalose and glycogen was identified probably representing a critical feature of K1 intoxication. In silico analysis suggested several transcription factors involved in toxin-triggered signal transduction. The identified transcriptome changes provide valuable hints to illuminate the still unknown molecular events leading to K1 toxicity and immunity implicating an evolutionarily conserved response at least initially counteracting ionophoric toxin action. |
format | Online Article Text |
id | pubmed-6531845 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65318452019-05-31 Transcriptome Kinetics of Saccharomyces cerevisiae in Response to Viral Killer Toxin K1 Gier, Stefanie Simon, Martin Nordström, Karl Khalifa, Salem Schulz, Marcel H. Schmitt, Manfred J. Breinig, Frank Front Microbiol Microbiology The K1 A/B toxin secreted by virus-infected Saccharomyces cerevisiae strains kills sensitive cells via disturbance of cytoplasmic membrane functions. Despite decades of research, the mechanisms underlying K1 toxicity and immunity have not been elucidated yet. In a novel approach, this study aimed to characterize transcriptome changes in K1-treated sensitive yeast cells in a time-dependent manner. Global transcriptional profiling revealed substantial cellular adaptations in target cells resulting in 1,189 differentially expressed genes in total. Killer toxin K1 induced oxidative, cell wall and hyperosmotic stress responses as well as rapid down-regulation of transcription and translation. Essential pathways regulating energy metabolism were also significantly affected by the toxin. Remarkably, a futile cycle of the osmolytes trehalose and glycogen was identified probably representing a critical feature of K1 intoxication. In silico analysis suggested several transcription factors involved in toxin-triggered signal transduction. The identified transcriptome changes provide valuable hints to illuminate the still unknown molecular events leading to K1 toxicity and immunity implicating an evolutionarily conserved response at least initially counteracting ionophoric toxin action. Frontiers Media S.A. 2019-05-16 /pmc/articles/PMC6531845/ /pubmed/31156606 http://dx.doi.org/10.3389/fmicb.2019.01102 Text en Copyright © 2019 Gier, Simon, Nordström, Khalifa, Schulz, Schmitt and Breinig. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Gier, Stefanie Simon, Martin Nordström, Karl Khalifa, Salem Schulz, Marcel H. Schmitt, Manfred J. Breinig, Frank Transcriptome Kinetics of Saccharomyces cerevisiae in Response to Viral Killer Toxin K1 |
title | Transcriptome Kinetics of Saccharomyces cerevisiae in Response to Viral Killer Toxin K1 |
title_full | Transcriptome Kinetics of Saccharomyces cerevisiae in Response to Viral Killer Toxin K1 |
title_fullStr | Transcriptome Kinetics of Saccharomyces cerevisiae in Response to Viral Killer Toxin K1 |
title_full_unstemmed | Transcriptome Kinetics of Saccharomyces cerevisiae in Response to Viral Killer Toxin K1 |
title_short | Transcriptome Kinetics of Saccharomyces cerevisiae in Response to Viral Killer Toxin K1 |
title_sort | transcriptome kinetics of saccharomyces cerevisiae in response to viral killer toxin k1 |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531845/ https://www.ncbi.nlm.nih.gov/pubmed/31156606 http://dx.doi.org/10.3389/fmicb.2019.01102 |
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