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Diversity of pili-specific bacteriophages: genome sequence of IncM plasmid-dependent RNA phage M

BACKGROUND: Bacteriophages of the Leviviridae family are small RNA viruses with linear, positive-sense, single-stranded RNA genomes that encode only four proteins. All phages of this family require bacterial pili to attach to and infect cells. Leviviridae phages utilizing F-pili for this purpose hav...

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Autores principales: Rumnieks, Janis, Tars, Kaspars
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3561173/
https://www.ncbi.nlm.nih.gov/pubmed/23176223
http://dx.doi.org/10.1186/1471-2180-12-277
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author Rumnieks, Janis
Tars, Kaspars
author_facet Rumnieks, Janis
Tars, Kaspars
author_sort Rumnieks, Janis
collection PubMed
description BACKGROUND: Bacteriophages of the Leviviridae family are small RNA viruses with linear, positive-sense, single-stranded RNA genomes that encode only four proteins. All phages of this family require bacterial pili to attach to and infect cells. Leviviridae phages utilizing F-pili for this purpose have been extensively studied. RNA phages specific for conjugative plasmid-encoded pili other than that of plasmid F have been isolated, but are much less understood and their relation to the F-pili-specific phages in many cases is not known. RESULTS: Phage M has the smallest known Leviviridae genome to date and has the typical genome organization with maturation, coat and replicase genes in the 5′ to 3′ direction. The lysis gene is located in a different position than in other known Leviviridae phages and completely overlaps with the replicase gene in a different reading frame. It encodes a 37 residue long polypeptide that contains a transmembrane helix like the other known lysis proteins of leviviruses. Sequence identities of M proteins to those of other phages do not exceed 25% for maturation protein, 51% for coat protein and 41% for replicase. Similarities in protein sequences and RNA secondary structures at the 3′ untranslated region place phage M together with phages specific for IncP, IncC and IncH, but not IncF plasmid-encoded pili. Phylogenetic analysis using the complete genome sequences and replicase proteins suggests that phage M represents a lineage that branched off early in the course of RNA phage specialization on different conjugative plasmids. CONCLUSIONS: The genome sequence of phage M shows that it is clearly related to other conjugative pili-specific leviviruses but has an atypical location of the lysis gene. It provides a better view on the remarkable diversification of the plasmid-specific RNA phages.
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spelling pubmed-35611732013-02-05 Diversity of pili-specific bacteriophages: genome sequence of IncM plasmid-dependent RNA phage M Rumnieks, Janis Tars, Kaspars BMC Microbiol Research Article BACKGROUND: Bacteriophages of the Leviviridae family are small RNA viruses with linear, positive-sense, single-stranded RNA genomes that encode only four proteins. All phages of this family require bacterial pili to attach to and infect cells. Leviviridae phages utilizing F-pili for this purpose have been extensively studied. RNA phages specific for conjugative plasmid-encoded pili other than that of plasmid F have been isolated, but are much less understood and their relation to the F-pili-specific phages in many cases is not known. RESULTS: Phage M has the smallest known Leviviridae genome to date and has the typical genome organization with maturation, coat and replicase genes in the 5′ to 3′ direction. The lysis gene is located in a different position than in other known Leviviridae phages and completely overlaps with the replicase gene in a different reading frame. It encodes a 37 residue long polypeptide that contains a transmembrane helix like the other known lysis proteins of leviviruses. Sequence identities of M proteins to those of other phages do not exceed 25% for maturation protein, 51% for coat protein and 41% for replicase. Similarities in protein sequences and RNA secondary structures at the 3′ untranslated region place phage M together with phages specific for IncP, IncC and IncH, but not IncF plasmid-encoded pili. Phylogenetic analysis using the complete genome sequences and replicase proteins suggests that phage M represents a lineage that branched off early in the course of RNA phage specialization on different conjugative plasmids. CONCLUSIONS: The genome sequence of phage M shows that it is clearly related to other conjugative pili-specific leviviruses but has an atypical location of the lysis gene. It provides a better view on the remarkable diversification of the plasmid-specific RNA phages. BioMed Central 2012-11-24 /pmc/articles/PMC3561173/ /pubmed/23176223 http://dx.doi.org/10.1186/1471-2180-12-277 Text en Copyright ©2012 Rumnieks and Tars; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Rumnieks, Janis
Tars, Kaspars
Diversity of pili-specific bacteriophages: genome sequence of IncM plasmid-dependent RNA phage M
title Diversity of pili-specific bacteriophages: genome sequence of IncM plasmid-dependent RNA phage M
title_full Diversity of pili-specific bacteriophages: genome sequence of IncM plasmid-dependent RNA phage M
title_fullStr Diversity of pili-specific bacteriophages: genome sequence of IncM plasmid-dependent RNA phage M
title_full_unstemmed Diversity of pili-specific bacteriophages: genome sequence of IncM plasmid-dependent RNA phage M
title_short Diversity of pili-specific bacteriophages: genome sequence of IncM plasmid-dependent RNA phage M
title_sort diversity of pili-specific bacteriophages: genome sequence of incm plasmid-dependent rna phage m
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3561173/
https://www.ncbi.nlm.nih.gov/pubmed/23176223
http://dx.doi.org/10.1186/1471-2180-12-277
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