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SRX23940295: Nanopore WGS of Bacillus anthracis
1 OXFORD_NANOPORE (MinION) run: 367,783 spots, 1.1G bases, 942.4Mb downloads

Design: For nanopore sequencing, sequencing libraries were prepared with the Rapid Barcoding Kit (SQK-RBK004) with up to 8 different gDNA samples multiplexed in one library. Nanopore libraries were sequenced on a MinION Mk1B device with R9.4.1 flow cells (Oxford Nanopore Technologies)
Submitted by: CDC
Study: Clarithromycin resistance in Bacillus anthracis
show Abstracthide Abstract
The high consequence pathogen Bacillus anthracis causes human anthrax and often results in lethal infections without the rapid administration of effective antimicrobial treatment. Antimicrobial resistance profiling is therefore critical to inform post-exposure prophylaxis and treatment decisions, especially during emergencies such as outbreaks or where intentional release is suspected. Whole genome sequencing using a rapid long-read sequencer can uncover antimicrobial resistance patterns if genetic markers of resistance are known. To identify genomic markers associated with antimicrobial resistance, we isolated B. anthracis derived from the avirulent Sterne strain with elevated minimal inhibitory concentrations to clarithromycin. Mutants were characterized both phenotypically through broth microdilution susceptibility testing and observations during culturing, as well as genotypically with whole genome sequencing. The mutations associated with clarithromycin resistance described here will be used in conjunction with known genetic markers of resistance for other antimicrobials to strengthen prediction of antimicrobial resistance in B. anthracis.
Sample:
SAMN40399311 • SRS20743867 • All experiments • All runs
Library:
Name: Sterne-CLR2-46
Instrument: MinION
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: SINGLE
Runs: 1 run, 367,783 spots, 1.1G bases, 942.4Mb
Run# of Spots# of BasesSizePublished
SRR28332069367,7831.1G942.4Mb2024-03-27

ID:
32245492

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