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Screening and characterization of prophages in Desulfovibrio genomes

Bacteria of the genus Desulfovibrio belong to the group of Sulphate Reducing Bacteria (SRB). SRB generate significant liabilities in the petroleum industry, mainly due to their ability to microbiologically induce corrosion, biofilm formation and H(2)S production. Bacteriophages are an alternative co...

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Autores principales: Crispim, Josicelli Souza, Dias, Roberto Sousa, Vidigal, Pedro Marcus Pereira, de Sousa, Maíra Paula, da Silva, Cynthia Canêdo, Santana, Mateus Ferreira, de Paula, Sérgio Oliveira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6006170/
https://www.ncbi.nlm.nih.gov/pubmed/29915307
http://dx.doi.org/10.1038/s41598-018-27423-z
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author Crispim, Josicelli Souza
Dias, Roberto Sousa
Vidigal, Pedro Marcus Pereira
de Sousa, Maíra Paula
da Silva, Cynthia Canêdo
Santana, Mateus Ferreira
de Paula, Sérgio Oliveira
author_facet Crispim, Josicelli Souza
Dias, Roberto Sousa
Vidigal, Pedro Marcus Pereira
de Sousa, Maíra Paula
da Silva, Cynthia Canêdo
Santana, Mateus Ferreira
de Paula, Sérgio Oliveira
author_sort Crispim, Josicelli Souza
collection PubMed
description Bacteria of the genus Desulfovibrio belong to the group of Sulphate Reducing Bacteria (SRB). SRB generate significant liabilities in the petroleum industry, mainly due to their ability to microbiologically induce corrosion, biofilm formation and H(2)S production. Bacteriophages are an alternative control method for SRB, whose information for this group of bacteria however, is scarce. The present study developed a workflow for the identification of complete prophages in Desulfovibrio. Poly-lysogenesis was shown to be common in Desulfovibrio. In the 47 genomes analyzed 53 complete prophages were identified. These were classified within the order Caudovirales, with 69.82% belonging to the Myoviridade family. More than half the prophages identified have genes coding for lysozyme or holin. Four of the analyzed bacterial genomes present prophages with identity above 50% in the same strain, whose comparative analysis demonstrated the existence of colinearity between the sequences. Of the 17 closed bacterial genomes analyzed, 6 have the CRISPR-Cas system classified as inactive. The identification of bacterial poly-lysogeny, the proximity between the complete prophages and the possible inactivity of the CRISPR-Cas in closed bacterial genomes analyzed allowed the choice of poly-lysogenic strains with prophages belonging to the Myoviridae family for the isolation of prophages and testing of related strains for subsequent studies.
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spelling pubmed-60061702018-06-26 Screening and characterization of prophages in Desulfovibrio genomes Crispim, Josicelli Souza Dias, Roberto Sousa Vidigal, Pedro Marcus Pereira de Sousa, Maíra Paula da Silva, Cynthia Canêdo Santana, Mateus Ferreira de Paula, Sérgio Oliveira Sci Rep Article Bacteria of the genus Desulfovibrio belong to the group of Sulphate Reducing Bacteria (SRB). SRB generate significant liabilities in the petroleum industry, mainly due to their ability to microbiologically induce corrosion, biofilm formation and H(2)S production. Bacteriophages are an alternative control method for SRB, whose information for this group of bacteria however, is scarce. The present study developed a workflow for the identification of complete prophages in Desulfovibrio. Poly-lysogenesis was shown to be common in Desulfovibrio. In the 47 genomes analyzed 53 complete prophages were identified. These were classified within the order Caudovirales, with 69.82% belonging to the Myoviridade family. More than half the prophages identified have genes coding for lysozyme or holin. Four of the analyzed bacterial genomes present prophages with identity above 50% in the same strain, whose comparative analysis demonstrated the existence of colinearity between the sequences. Of the 17 closed bacterial genomes analyzed, 6 have the CRISPR-Cas system classified as inactive. The identification of bacterial poly-lysogeny, the proximity between the complete prophages and the possible inactivity of the CRISPR-Cas in closed bacterial genomes analyzed allowed the choice of poly-lysogenic strains with prophages belonging to the Myoviridae family for the isolation of prophages and testing of related strains for subsequent studies. Nature Publishing Group UK 2018-06-18 /pmc/articles/PMC6006170/ /pubmed/29915307 http://dx.doi.org/10.1038/s41598-018-27423-z Text en © The Author(s) 2018 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
Crispim, Josicelli Souza
Dias, Roberto Sousa
Vidigal, Pedro Marcus Pereira
de Sousa, Maíra Paula
da Silva, Cynthia Canêdo
Santana, Mateus Ferreira
de Paula, Sérgio Oliveira
Screening and characterization of prophages in Desulfovibrio genomes
title Screening and characterization of prophages in Desulfovibrio genomes
title_full Screening and characterization of prophages in Desulfovibrio genomes
title_fullStr Screening and characterization of prophages in Desulfovibrio genomes
title_full_unstemmed Screening and characterization of prophages in Desulfovibrio genomes
title_short Screening and characterization of prophages in Desulfovibrio genomes
title_sort screening and characterization of prophages in desulfovibrio genomes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6006170/
https://www.ncbi.nlm.nih.gov/pubmed/29915307
http://dx.doi.org/10.1038/s41598-018-27423-z
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