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ERX028650: Whole Genome Sequencing of Streptococcus pneumoniae
1 ILLUMINA (Illumina HiSeq 2000) run: 5.9M spots, 882.1M bases, 477.1Mb downloads

Design: Illumina sequencing of library 3246256, constructed from sample accession ERS020566 for study accession ERP000483. This is part of an Illumina multiplexed sequencing run (6731_3). This submission includes reads tagged with the sequence TTGACTCT.
Submitted by: The Wellcome Trust Sanger Institute (SC)
Study: Streptococcus pneumoniae evolution and population structure during longitudinal sampling in a defined human population
show Abstracthide Abstract
"Dense genomic sampling identifies highways of pneumococcal recombination." Pubmed ID: 24509479. Evasion of clinical interventions by Streptococcus pneumoniae occurs through selection of non-susceptible genomic variants. We report whole-genome sequencing of 3,085 pneumococcal carriage isolates from a 2.4-km(2) refugee camp. This sequencing provides unprecedented resolution of the process of recombination and its impact on population evolution. Genomic recombination hotspots show remarkable consistency between lineages, indicating common selective pressures acting at certain loci, particularly those associated with antibiotic resistance. Temporal changes in antibiotic consumption are reflected in changes in recombination trends, demonstrating rapid spread of resistance when selective pressure is high. The highest frequencies of receipt and donation of recombined DNA fragments were observed in non-encapsulated lineages, implying that this largely overlooked pneumococcal group, which is beyond the reach of current vaccines, may have a major role in genetic exchange and the adaptation of the species as a whole. These findings advance understanding of pneumococcal population dynamics and provide information for the design of future intervention strategies. Includes studies ERP000435, ERP000483, ERP000485, ERP000487, ERP000598, ERP000599.
Sample: Streptococcus pneumoniae; Streptococcus pneumoniae
SAMEA1024794 • ERS020566 • All experiments • All runs
Library:
Name: 3246256
Instrument: Illumina HiSeq 2000
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Standard
Spot descriptor:
forward  reverse

Runs: 1 run, 5.9M spots, 882.1M bases, 477.1Mb
Run# of Spots# of BasesSizePublished
ERR0516025,880,789882.1M477.1Mb2012-04-14

ID:
169685

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