U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Links from BioSample

ERX268120: Whole Genome Sequencing of Salmonella enterica subsp. enterica serovar Weltevreden
1 ILLUMINA (Illumina HiSeq 2000) run: 5M spots, 995.3M bases, 485.8Mb downloads

Design: Illumina sequencing of library 6742023, constructed from sample accession ERS208989 for study accession ERP002199. This is part of an Illumina multiplexed sequencing run (9472_3). This submission includes reads tagged with the sequence CAGATCTG.
Submitted by: The Wellcome Trust Sanger Institute (SC)
Study: Phylogenomic analysis of blood and stool isolates of Salmonella Weltevreden from Vietnam
show Abstracthide Abstract
Salmonella enterica serovar Weltevreden (S. Weltevreden) is an emerging cause of diarrheal and invasive disease in humans residing in tropical regions. Despite the regional and international emergence of this Salmonella serovar, relatively little is known about its genetic diversity, genomics or virulence potential in model systems. Here we used whole genome sequencing and bioinformatics analyses to define the phylogenetic structure of a diverse global selection of S. Weltevreden. Phylogenetic analysis of more than 100 isolates demonstrated that the population of S. Weltevreden can be segregated into two main phylogenetic clusters, one associated predominantly with continental Southeast Asia and the other more internationally dispersed. Subcluster analysis suggested the local evolution of S. Weltevreden within specific geographical regions. Four of the isolates were sequenced using long read sequencing to produce high quality reference genomes. Phenotypic analysis in Hep-2 cells and in a murine infection model indicated that S. Weltevreden were significantly attenuated in these models compared to the classical S. Typhimurium reference strain SL1344. Our work outlines novel insights into this important emerging pathogen and provides a baseline understanding for future research studies. This data is part of a pre-publication release. For information on the proper use of pre-publication data shared by the Wellcome Trust Sanger Institute (including details of any publication moratoria), please see http://www.sanger.ac.uk/about/who-we-are/policies/open-access-science
Library:
Name: 6742023
Instrument: Illumina HiSeq 2000
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Standard
Runs: 1 run, 5M spots, 995.3M bases, 485.8Mb
Run# of Spots# of BasesSizePublished
ERR2947874,976,700995.3M485.8Mb2013-06-10

ID:
414095

Supplemental Content

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...