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Dual-RNAseq Analysis Unravels Virus-Host Interactions of MetSV and Methanosarcina mazei

Methanosarcina spherical virus (MetSV), infecting Methanosarcina species, encodes 22 genes, but their role in the infection process in combination with host genes has remained unknown. To study the infection process in detail, infected and uninfected M. mazei cultures were compared using dual-RNAseq...

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Autores principales: Gehlert, Finn O., Sauerwein, Till, Weidenbach, Katrin, Repnik, Urska, Hallack, Daniela, Förstner, Konrad U., Schmitz, Ruth A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9694453/
https://www.ncbi.nlm.nih.gov/pubmed/36423194
http://dx.doi.org/10.3390/v14112585
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author Gehlert, Finn O.
Sauerwein, Till
Weidenbach, Katrin
Repnik, Urska
Hallack, Daniela
Förstner, Konrad U.
Schmitz, Ruth A.
author_facet Gehlert, Finn O.
Sauerwein, Till
Weidenbach, Katrin
Repnik, Urska
Hallack, Daniela
Förstner, Konrad U.
Schmitz, Ruth A.
author_sort Gehlert, Finn O.
collection PubMed
description Methanosarcina spherical virus (MetSV), infecting Methanosarcina species, encodes 22 genes, but their role in the infection process in combination with host genes has remained unknown. To study the infection process in detail, infected and uninfected M. mazei cultures were compared using dual-RNAseq, qRT-PCRs, and transmission electron microscopy (TEM). The transcriptome analysis strongly indicates a combined role of virus and host genes in replication, virus assembly, and lysis. Thereby, 285 host and virus genes were significantly regulated. Within these 285 regulated genes, a network of the viral polymerase, MetSVORF6, MetSVORF5, MetSVORF2, and the host genes encoding NrdD, NrdG, a CDC48 family protein, and a SSB protein with a role in viral replication was postulated. Ultrastructural analysis at 180 min p.i. revealed many infected cells with virus particles randomly scattered throughout the cytoplasm or attached at the cell surface, and membrane fragments indicating cell lysis. Dual-RNAseq and qRT-PCR analyses suggested a multifactorial lysis reaction in potential connection to the regulation of a cysteine proteinase, a pirin-like protein and a HicB-solo protein. Our study’s results led to the first preliminary infection model of MetSV infecting M. mazei, summarizing the key infection steps as follows: replication, assembly, and host cell lysis.
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spelling pubmed-96944532022-11-26 Dual-RNAseq Analysis Unravels Virus-Host Interactions of MetSV and Methanosarcina mazei Gehlert, Finn O. Sauerwein, Till Weidenbach, Katrin Repnik, Urska Hallack, Daniela Förstner, Konrad U. Schmitz, Ruth A. Viruses Article Methanosarcina spherical virus (MetSV), infecting Methanosarcina species, encodes 22 genes, but their role in the infection process in combination with host genes has remained unknown. To study the infection process in detail, infected and uninfected M. mazei cultures were compared using dual-RNAseq, qRT-PCRs, and transmission electron microscopy (TEM). The transcriptome analysis strongly indicates a combined role of virus and host genes in replication, virus assembly, and lysis. Thereby, 285 host and virus genes were significantly regulated. Within these 285 regulated genes, a network of the viral polymerase, MetSVORF6, MetSVORF5, MetSVORF2, and the host genes encoding NrdD, NrdG, a CDC48 family protein, and a SSB protein with a role in viral replication was postulated. Ultrastructural analysis at 180 min p.i. revealed many infected cells with virus particles randomly scattered throughout the cytoplasm or attached at the cell surface, and membrane fragments indicating cell lysis. Dual-RNAseq and qRT-PCR analyses suggested a multifactorial lysis reaction in potential connection to the regulation of a cysteine proteinase, a pirin-like protein and a HicB-solo protein. Our study’s results led to the first preliminary infection model of MetSV infecting M. mazei, summarizing the key infection steps as follows: replication, assembly, and host cell lysis. MDPI 2022-11-21 /pmc/articles/PMC9694453/ /pubmed/36423194 http://dx.doi.org/10.3390/v14112585 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gehlert, Finn O.
Sauerwein, Till
Weidenbach, Katrin
Repnik, Urska
Hallack, Daniela
Förstner, Konrad U.
Schmitz, Ruth A.
Dual-RNAseq Analysis Unravels Virus-Host Interactions of MetSV and Methanosarcina mazei
title Dual-RNAseq Analysis Unravels Virus-Host Interactions of MetSV and Methanosarcina mazei
title_full Dual-RNAseq Analysis Unravels Virus-Host Interactions of MetSV and Methanosarcina mazei
title_fullStr Dual-RNAseq Analysis Unravels Virus-Host Interactions of MetSV and Methanosarcina mazei
title_full_unstemmed Dual-RNAseq Analysis Unravels Virus-Host Interactions of MetSV and Methanosarcina mazei
title_short Dual-RNAseq Analysis Unravels Virus-Host Interactions of MetSV and Methanosarcina mazei
title_sort dual-rnaseq analysis unravels virus-host interactions of metsv and methanosarcina mazei
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9694453/
https://www.ncbi.nlm.nih.gov/pubmed/36423194
http://dx.doi.org/10.3390/v14112585
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