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SRX25692636: WGS of P. brasiliense
1 ILLUMINA (Illumina NovaSeq 6000) run: 13.5M spots, 4.1G bases, 1.3Gb downloads

Design: For the purpose of genome sequencing, DNA was extracted from pure bacterial cultures obtained by growing the strains on TSA medium. Per isolate approximately one inoculation loop (10__l) of bacterial slime was collected from multiple colonies. The DNA extraction was performed by using the Wizard Magnetic DNA Purification System for Food (Promega, Leiden, the Netherlands) according to the manufacturers protocol. The NEBNext Ultra II DNA Library Prep kit for Illumina (cat# NEB #E7645S/L) was used to prepare sequencing libraries. Fragmentation of the DNA using the Biorupor Pico (Diagenode), ligation of sequencing adapters, and PCR amplification of the resulting product was performed according to the procedure described in the NEBNext Ultra DNA Library Prep kit for Illumina Instruction Manual. The quality and yield after sample preparation was measured with the Fragment Analyzer (Table 2 and Appendices). The size of the resulting product was consistent with the expected size of approximately 500-700 bp. Clustering and 150bp paired-end DNA sequencing using the NovaSeq6000 was performed according to manufacturer's protocols. A concentration of 1.1 nM of DNA was used.
Submitted by: Wageningen University & Research
Study: Pangenomics to understand the prophage dynamics in the radiating lineages of P. brasiliense
show Abstracthide Abstract
Bacterial pathogens of the genus Pectobacterium are responsible for soft rot and blackleg disease ina wide range of crops and have a global impact on food production. Pangenome studies of this genushave shown that genetic diversity is particularly high in pathogenic species. The emergence of newstrains and their competitive succession is frequently observed in Pectobacterium species, in particularP. brasiliense. With a focus on one such recently emerged P. brasiliense lineage in the Netherlands thatcause blackleg in potatoes, we studied genome evolution in this genus using the pangenome approach.We identified 30,156 homology groups in the pangenome build with the 454 Pectobacterium speciesgenomes. The expansion of this pangenome was mainly contributed by the accessory genome andprophages contributed 16% of the pangenome. Blackleg causing P. brasiliense isolates had increasedgenome size with high levels of prophage integration compared to the non-causing isolates. To studythe diversity and dynamics of these prophages across pangenome, we developed an approach to traceprophages across genomes using pangenome homology group signatures. Our approach identified lineage-specific as well as generalist bacteriophages infecting Pectobacterium species. Our results capture ongoingdynamics of mobile genetic elements even in the clonal lineage as per the core genome phylogeny andprovide mechanistic insights into diverse strain emergence in P. brasiliense.
Sample: NAK673
SAMN42841166 • SRS22334695 • All experiments • All runs
Library:
Name: NAK673
Instrument: Illumina NovaSeq 6000
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Runs: 1 run, 13.5M spots, 4.1G bases, 1.3Gb
Run# of Spots# of BasesSizePublished
SRR3023074813,507,6144.1G1.3Gb2024-08-14

ID:
34721283

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