Complete Assembly of Escherichia coli Sequence Type 131 Genomes Using Long Reads Demonstrates Antibiotic Resistance Gene Variation within Diverse Plasmid and Chromosomal Contexts
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- Arun Gonzales Decano
- School of Biotechnology, Dublin City University, Dublin, Ireland
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- Catherine Ludden
- Wellcome Trust Sanger Institute, Hinxton, United Kingdom
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- Theresa Feltwell
- Wellcome Trust Sanger Institute, Hinxton, United Kingdom
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- Kim Judge
- Wellcome Trust Sanger Institute, Hinxton, United Kingdom
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- Julian Parkhill
- Wellcome Trust Sanger Institute, Hinxton, United Kingdom
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- Tim Downing
- School of Biotechnology, Dublin City University, Dublin, Ireland
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- Brandi M. Limbago
- editor
説明
<jats:p> Drug-resistant bacteria are a major cause of illness worldwide, and a specific subtype called <jats:named-content content-type="genus-species">Escherichia coli</jats:named-content> ST131 causes a significant number of these infections. ST131 bacteria become resistant to treatments by modifying their DNA and by transferring genes among one another via large packages of genes called plasmids, like a game of pass-the-parcel. Tackling infections more effectively requires a better understanding of what plasmids are being exchanged and their exact contents. To achieve this, we applied new high-resolution DNA sequencing technology to six ST131 samples from infected patients and compared the output to that of an existing approach. A combination of methods shows that drug resistance genes on plasmids are highly mobile because they can jump into ST131’s chromosomes. We found that the plasmids are very elastic and undergo extensive rearrangements even in closely related samples. This application of DNA sequencing technologies illustrates at a new level the highly dynamic nature of ST131 genomes. </jats:p>
収録刊行物
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- mSphere
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mSphere 4 (3), 2019-06-26
American Society for Microbiology