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Characterization of the virome of Paracoccus spp. (Alphaproteobacteria) by combined in silico and in vivo approaches

Bacteria of the genus Paracoccus inhabit various pristine and anthropologically-shaped environments. Many Paracoccus spp. have biotechnological value and several are opportunistic human pathogens. Despite extensive knowledge of their metabolic potential and genome architecture, little is known about...

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Autores principales: Decewicz, Przemyslaw, Dziewit, Lukasz, Golec, Piotr, Kozlowska, Patrycja, Bartosik, Dariusz, Radlinska, Monika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6536676/
https://www.ncbi.nlm.nih.gov/pubmed/31133656
http://dx.doi.org/10.1038/s41598-019-44460-4
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author Decewicz, Przemyslaw
Dziewit, Lukasz
Golec, Piotr
Kozlowska, Patrycja
Bartosik, Dariusz
Radlinska, Monika
author_facet Decewicz, Przemyslaw
Dziewit, Lukasz
Golec, Piotr
Kozlowska, Patrycja
Bartosik, Dariusz
Radlinska, Monika
author_sort Decewicz, Przemyslaw
collection PubMed
description Bacteria of the genus Paracoccus inhabit various pristine and anthropologically-shaped environments. Many Paracoccus spp. have biotechnological value and several are opportunistic human pathogens. Despite extensive knowledge of their metabolic potential and genome architecture, little is known about viruses of Paracoccus spp. So far, only three active phages infecting these bacteria have been identified. In this study, 16 Paracoccus strains were screened for the presence of active temperate phages, which resulted in the identification of five novel viruses. Mitomycin C-induced prophages were isolated, visualized and their genomes sequenced and thoroughly analyzed, including functional validation of their toxin-antitoxin systems. This led to the identification of the first active Myoviridae phage in Paracoccus spp. and four novel Siphoviridae phages. In addition, another 53 prophages were distinguished in silico within genomic sequences of Paracoccus spp. available in public databases. Thus, the Paracoccus virome was defined as being composed of 66 (pro)phages. Comparative analyses revealed the diversity and mosaicism of the (pro)phage genomes. Moreover, similarity networking analysis highlighted the uniqueness of Paracoccus (pro)phages among known bacterial viruses.
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spelling pubmed-65366762019-06-06 Characterization of the virome of Paracoccus spp. (Alphaproteobacteria) by combined in silico and in vivo approaches Decewicz, Przemyslaw Dziewit, Lukasz Golec, Piotr Kozlowska, Patrycja Bartosik, Dariusz Radlinska, Monika Sci Rep Article Bacteria of the genus Paracoccus inhabit various pristine and anthropologically-shaped environments. Many Paracoccus spp. have biotechnological value and several are opportunistic human pathogens. Despite extensive knowledge of their metabolic potential and genome architecture, little is known about viruses of Paracoccus spp. So far, only three active phages infecting these bacteria have been identified. In this study, 16 Paracoccus strains were screened for the presence of active temperate phages, which resulted in the identification of five novel viruses. Mitomycin C-induced prophages were isolated, visualized and their genomes sequenced and thoroughly analyzed, including functional validation of their toxin-antitoxin systems. This led to the identification of the first active Myoviridae phage in Paracoccus spp. and four novel Siphoviridae phages. In addition, another 53 prophages were distinguished in silico within genomic sequences of Paracoccus spp. available in public databases. Thus, the Paracoccus virome was defined as being composed of 66 (pro)phages. Comparative analyses revealed the diversity and mosaicism of the (pro)phage genomes. Moreover, similarity networking analysis highlighted the uniqueness of Paracoccus (pro)phages among known bacterial viruses. Nature Publishing Group UK 2019-05-27 /pmc/articles/PMC6536676/ /pubmed/31133656 http://dx.doi.org/10.1038/s41598-019-44460-4 Text en © The Author(s) 2019 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
Decewicz, Przemyslaw
Dziewit, Lukasz
Golec, Piotr
Kozlowska, Patrycja
Bartosik, Dariusz
Radlinska, Monika
Characterization of the virome of Paracoccus spp. (Alphaproteobacteria) by combined in silico and in vivo approaches
title Characterization of the virome of Paracoccus spp. (Alphaproteobacteria) by combined in silico and in vivo approaches
title_full Characterization of the virome of Paracoccus spp. (Alphaproteobacteria) by combined in silico and in vivo approaches
title_fullStr Characterization of the virome of Paracoccus spp. (Alphaproteobacteria) by combined in silico and in vivo approaches
title_full_unstemmed Characterization of the virome of Paracoccus spp. (Alphaproteobacteria) by combined in silico and in vivo approaches
title_short Characterization of the virome of Paracoccus spp. (Alphaproteobacteria) by combined in silico and in vivo approaches
title_sort characterization of the virome of paracoccus spp. (alphaproteobacteria) by combined in silico and in vivo approaches
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6536676/
https://www.ncbi.nlm.nih.gov/pubmed/31133656
http://dx.doi.org/10.1038/s41598-019-44460-4
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