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Journal article

Plasmid classification in an era of whole-genome sequencing: application in studies of antibiotic resistance epidemiology

Abstract:
Plasmids are extra-chromosomal genetic elements ubiquitous in bacteria, and commonly transmissible between host cells. Their genomes include variable repertoires of ‘accessory genes’, such as antibiotic resistance genes, as well as ‘backbone’ loci which are largely conserved within plasmid families, and often involved in key plasmid-specific functions (e.g. replication, stable inheritance, mobility). Classifying plasmids into different types according to their phylogenetic relatedness provides insight into the epidemiology of plasmid-mediated antibiotic resistance. Current typing schemes exploit backbone loci associated with replication (replicon typing), or plasmid mobility (MOB typing). Conventional PCR-based methods for plasmid typing remain widely used. With the emergence of whole-genome sequencing (WGS), large datasets can be analyzed using in silico plasmid typing methods. However, short reads from popular high-throughput sequencers can be challenging to assemble, so complete plasmid sequences may not be accurately reconstructed. Therefore, localizing resistance genes to specific plasmids may be difficult, limiting epidemiological insight. Long-read sequencing will become increasingly popular as costs decline, especially when resolving accurate plasmid structures is the primary goal. This review discusses the application of plasmid classification in WGS-based studies of antibiotic resistance epidemiology; novel in silico plasmid analysis tools are highlighted. Due to the diverse and plastic nature of plasmid genomes, current typing schemes do not classify all plasmids, and identifying conserved, phylogenetically concordant genes for subtyping and phylogenetics is challenging. Analyzing plasmids as nodes in a network that represents gene-sharing relationships between plasmids provides a complementary way to assess plasmid diversity, and allows inferences about horizontal gene transfer to be made.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.3389/fmicb.2017.00182

Authors


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Institution:
University of Oxford
Oxford college:
Wolfson College
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Role:
Author


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Grant:
HealthcareAssociatedInfections
AntimicrobialResistanceHPRU-2012-10041


Publisher:
Frontiers Media
Journal:
Frontiers in Microbiology More from this journal
Volume:
8
Article number:
182
Publication date:
2017-01-25
Acceptance date:
2017-01-25
DOI:
ISSN:
1664-302X


Keywords:
Pubs id:
pubs:675368
UUID:
uuid:2149e942-fd5f-4b53-9a97-6d6e1f301cc6
Local pid:
pubs:675368
Source identifiers:
675368
Deposit date:
2017-02-02

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