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The M25 gene products are critical for the cytopathic effect of mouse cytomegalovirus
Cell rounding is a hallmark of the cytopathic effect induced by cytomegaloviruses. By screening a panel of deletion mutants of mouse cytomegalovirus (MCMV) a mutant was identified that did not elicit cell rounding and lacked the ability to form typical plaques. Altered cell morphology was assigned t...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686157/ https://www.ncbi.nlm.nih.gov/pubmed/29138436 http://dx.doi.org/10.1038/s41598-017-15783-x |
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author | Kutle, Ivana Sengstake, Sarah Templin, Corinna Glaß, Mandy Kubsch, Tobias Keyser, Kirsten A. Binz, Anne Bauerfeind, Rudolf Sodeik, Beate Čičin-Šain, Luka Dezeljin, Martina Messerle, Martin |
author_facet | Kutle, Ivana Sengstake, Sarah Templin, Corinna Glaß, Mandy Kubsch, Tobias Keyser, Kirsten A. Binz, Anne Bauerfeind, Rudolf Sodeik, Beate Čičin-Šain, Luka Dezeljin, Martina Messerle, Martin |
author_sort | Kutle, Ivana |
collection | PubMed |
description | Cell rounding is a hallmark of the cytopathic effect induced by cytomegaloviruses. By screening a panel of deletion mutants of mouse cytomegalovirus (MCMV) a mutant was identified that did not elicit cell rounding and lacked the ability to form typical plaques. Altered cell morphology was assigned to the viral M25 gene. We detected an early 2.8 kb M25 mRNA directing the synthesis of a 105 kDa M25 protein, and confirmed that a late 3.1 kb mRNA encodes a 130 kDa M25 tegument protein. Virions lacking the M25 tegument protein were of smaller size because the tegument layer between capsid and viral envelope was reduced. The ΔM25 mutant did not provoke the rearrangement of the actin cytoskeleton observed after wild-type MCMV infection, and isolated expression of the M25 proteins led to cell size reduction, confirming that they contribute to the morphological changes. Yields of progeny virus and cell-to-cell spread of the ΔM25 mutant in vitro were diminished and replication in vivo was impaired. The identification of an MCMV gene involved in cell rounding provides the basis for investigating the role of this cytopathic effect in CMV pathogenesis. |
format | Online Article Text |
id | pubmed-5686157 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56861572017-11-21 The M25 gene products are critical for the cytopathic effect of mouse cytomegalovirus Kutle, Ivana Sengstake, Sarah Templin, Corinna Glaß, Mandy Kubsch, Tobias Keyser, Kirsten A. Binz, Anne Bauerfeind, Rudolf Sodeik, Beate Čičin-Šain, Luka Dezeljin, Martina Messerle, Martin Sci Rep Article Cell rounding is a hallmark of the cytopathic effect induced by cytomegaloviruses. By screening a panel of deletion mutants of mouse cytomegalovirus (MCMV) a mutant was identified that did not elicit cell rounding and lacked the ability to form typical plaques. Altered cell morphology was assigned to the viral M25 gene. We detected an early 2.8 kb M25 mRNA directing the synthesis of a 105 kDa M25 protein, and confirmed that a late 3.1 kb mRNA encodes a 130 kDa M25 tegument protein. Virions lacking the M25 tegument protein were of smaller size because the tegument layer between capsid and viral envelope was reduced. The ΔM25 mutant did not provoke the rearrangement of the actin cytoskeleton observed after wild-type MCMV infection, and isolated expression of the M25 proteins led to cell size reduction, confirming that they contribute to the morphological changes. Yields of progeny virus and cell-to-cell spread of the ΔM25 mutant in vitro were diminished and replication in vivo was impaired. The identification of an MCMV gene involved in cell rounding provides the basis for investigating the role of this cytopathic effect in CMV pathogenesis. Nature Publishing Group UK 2017-11-14 /pmc/articles/PMC5686157/ /pubmed/29138436 http://dx.doi.org/10.1038/s41598-017-15783-x Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kutle, Ivana Sengstake, Sarah Templin, Corinna Glaß, Mandy Kubsch, Tobias Keyser, Kirsten A. Binz, Anne Bauerfeind, Rudolf Sodeik, Beate Čičin-Šain, Luka Dezeljin, Martina Messerle, Martin The M25 gene products are critical for the cytopathic effect of mouse cytomegalovirus |
title | The M25 gene products are critical for the cytopathic effect of mouse cytomegalovirus |
title_full | The M25 gene products are critical for the cytopathic effect of mouse cytomegalovirus |
title_fullStr | The M25 gene products are critical for the cytopathic effect of mouse cytomegalovirus |
title_full_unstemmed | The M25 gene products are critical for the cytopathic effect of mouse cytomegalovirus |
title_short | The M25 gene products are critical for the cytopathic effect of mouse cytomegalovirus |
title_sort | m25 gene products are critical for the cytopathic effect of mouse cytomegalovirus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686157/ https://www.ncbi.nlm.nih.gov/pubmed/29138436 http://dx.doi.org/10.1038/s41598-017-15783-x |
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