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Bacteriophages are the major drivers of Shigella flexneri serotype 1c genome plasticity: a complete genome analysis

BACKGROUND: Shigella flexneri is the primary cause of bacillary dysentery in the developing countries. S. flexneri serotype 1c is a novel serotype, which is found to be endemic in many developing countries, but little is known about its genomic architecture and virulence signatures. We have sequence...

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Autores principales: Parajuli, Pawan, Adamski, Marcin, Verma, Naresh K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596473/
https://www.ncbi.nlm.nih.gov/pubmed/28899344
http://dx.doi.org/10.1186/s12864-017-4109-4
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author Parajuli, Pawan
Adamski, Marcin
Verma, Naresh K.
author_facet Parajuli, Pawan
Adamski, Marcin
Verma, Naresh K.
author_sort Parajuli, Pawan
collection PubMed
description BACKGROUND: Shigella flexneri is the primary cause of bacillary dysentery in the developing countries. S. flexneri serotype 1c is a novel serotype, which is found to be endemic in many developing countries, but little is known about its genomic architecture and virulence signatures. We have sequenced for the first time, the complete genome of S. flexneri serotype 1c strain Y394, to provide insights into its diversity and evolution. RESULTS: We generated a high-quality reference genome of S. flexneri serotype 1c using the hybrid methods of long-read single-molecule real-time (SMRT) sequencing technology and short-read MiSeq (Illumina) sequencing technology. The Y394 chromosome is 4.58 Mb in size and shares the basic genomic features with other S. flexneri complete genomes. However, it possesses unique and highly modified O-antigen structure comprising of three distinct O-antigen modifying gene clusters that potentially came from three different bacteriophages. It also possesses a large number of hypothetical unique genes compared to other S. flexneri genomes. CONCLUSIONS: Despite a high level of structural and functional similarities of Y394 genome with other S. flexneri genomes, there are marked differences in the pathogenic islands. The diversity in the pathogenic islands suggests that these bacterial pathogens are well adapted to respond to the selection pressures during their evolution, which might contribute to the differences in their virulence potential. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-017-4109-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-55964732017-09-15 Bacteriophages are the major drivers of Shigella flexneri serotype 1c genome plasticity: a complete genome analysis Parajuli, Pawan Adamski, Marcin Verma, Naresh K. BMC Genomics Research Article BACKGROUND: Shigella flexneri is the primary cause of bacillary dysentery in the developing countries. S. flexneri serotype 1c is a novel serotype, which is found to be endemic in many developing countries, but little is known about its genomic architecture and virulence signatures. We have sequenced for the first time, the complete genome of S. flexneri serotype 1c strain Y394, to provide insights into its diversity and evolution. RESULTS: We generated a high-quality reference genome of S. flexneri serotype 1c using the hybrid methods of long-read single-molecule real-time (SMRT) sequencing technology and short-read MiSeq (Illumina) sequencing technology. The Y394 chromosome is 4.58 Mb in size and shares the basic genomic features with other S. flexneri complete genomes. However, it possesses unique and highly modified O-antigen structure comprising of three distinct O-antigen modifying gene clusters that potentially came from three different bacteriophages. It also possesses a large number of hypothetical unique genes compared to other S. flexneri genomes. CONCLUSIONS: Despite a high level of structural and functional similarities of Y394 genome with other S. flexneri genomes, there are marked differences in the pathogenic islands. The diversity in the pathogenic islands suggests that these bacterial pathogens are well adapted to respond to the selection pressures during their evolution, which might contribute to the differences in their virulence potential. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-017-4109-4) contains supplementary material, which is available to authorized users. BioMed Central 2017-09-12 /pmc/articles/PMC5596473/ /pubmed/28899344 http://dx.doi.org/10.1186/s12864-017-4109-4 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Parajuli, Pawan
Adamski, Marcin
Verma, Naresh K.
Bacteriophages are the major drivers of Shigella flexneri serotype 1c genome plasticity: a complete genome analysis
title Bacteriophages are the major drivers of Shigella flexneri serotype 1c genome plasticity: a complete genome analysis
title_full Bacteriophages are the major drivers of Shigella flexneri serotype 1c genome plasticity: a complete genome analysis
title_fullStr Bacteriophages are the major drivers of Shigella flexneri serotype 1c genome plasticity: a complete genome analysis
title_full_unstemmed Bacteriophages are the major drivers of Shigella flexneri serotype 1c genome plasticity: a complete genome analysis
title_short Bacteriophages are the major drivers of Shigella flexneri serotype 1c genome plasticity: a complete genome analysis
title_sort bacteriophages are the major drivers of shigella flexneri serotype 1c genome plasticity: a complete genome analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5596473/
https://www.ncbi.nlm.nih.gov/pubmed/28899344
http://dx.doi.org/10.1186/s12864-017-4109-4
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