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Tracking of antibiotic resistance transfer and rapid plasmid evolution in a hospital setting by Nanopore sequencing

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dc.contributor.author Peter, Silke
dc.contributor.author Bosio, Mattia
dc.contributor.author Gross, Caspar
dc.contributor.author Bezdan, Daniela
dc.contributor.author Gutiérrez, Javier
dc.contributor.author Oberhettinger, Philipp
dc.contributor.author Liese, Jan
dc.contributor.author Vogel, Wichard
dc.contributor.author Dörfel, Daniela
dc.contributor.author Berger, Lennard
dc.contributor.author Marschal, Matthias
dc.contributor.author Willmann, Matthias
dc.contributor.author Gut, Ivo Glynne
dc.contributor.author Gut, Marta
dc.contributor.author Autenrieth, Ingo B.
dc.contributor.author Ossowski, Stephan
dc.date.accessioned 2020-10-29T06:55:17Z
dc.date.available 2020-10-29T06:55:17Z
dc.date.issued 2020
dc.identifier.citation Peter S, Bosio M, Gross C, Bezdan D, Gutierrez J, Oberhettinger P, Liese J, Vogel W, Dörfel D, Berger L, Marschal M, Willmann M, Gut I, Gut M, Autenrieth I, Ossowski S. Tracking of antibiotic resistance transfer and rapid plasmid evolution in a hospital setting by Nanopore sequencing. mSphere. 2020; 5(4):e00525-20. DOI: 10.1128/mSphere.00525-20
dc.identifier.issn 2379-5042
dc.identifier.uri http://hdl.handle.net/10230/45612
dc.description.abstract Infections with multidrug-resistant bacteria often leave limited or no treatment options. The transfer of antimicrobial resistance genes (ARG) carrying plasmids between bacterial species by horizontal gene transfer represents an important mode of expansion of ARGs. Here, we demonstrate the application of Nanopore sequencing in a hospital setting for monitoring transfer and rapid evolution of antibiotic resistance plasmids within and across multiple species. In 2009, we experienced an outbreak with extensively multidrug-resistant Pseudomonas aeruginosa harboring the carbapenemase-encoding bla IMP-8 gene. In 2012, the first Citrobacter freundii and Citrobacter cronae strains harboring the same gene were detected. Using Nanopore and Illumina sequencing, we conducted comparative analysis of all bla IMP-8 bacteria isolated in our hospital over a 6-year period (n = 54). We developed the computational platform plasmIDent for Nanopore-based characterization of clinical isolates and monitoring of ARG transfer, comprising de novo assembly of genomes and plasmids, plasmid circularization, ARG annotation, comparative genome analysis of multiple isolates, and visualization of results. Using plasmIDent, we identified a 40-kb plasmid carrying bla IMP-8 in P. aeruginosa and C. freundii, verifying the plasmid transfer. Within C. freundii, the plasmid underwent further evolution and plasmid fusion, resulting in a 164-kb megaplasmid, which was transferred to C. cronae Multiple rearrangements of the multidrug resistance gene cassette were detected in P. aeruginosa, including deletions and translocations of complete ARGs. In summary, plasmid transfer, plasmid fusion, and rearrangement of the ARG cassette mediated the rapid evolution of opportunistic pathogens in our hospital. We demonstrated the feasibility of near-real-time monitoring of plasmid evolution and ARG transfer in clinical settings, enabling successful countermeasures to contain plasmid-mediated outbreaks.IMPORTANCE Infections with multidrug-resistant bacteria represent a major threat to global health. While the spread of multidrug-resistant bacterial clones is frequently studied in the hospital setting, surveillance of the transfer of mobile genetic elements between different bacterial species was difficult until recent advances in sequencing technologies. Nanopore sequencing technology was applied to track antimicrobial gene transfer in a long-term outbreak of multidrug-resistant Pseudomonas aeruginosa, Citrobacter freundii, and Citrobacter cronae in a German hospital over 6 years. We developed a novel computational pipeline, pathoLogic, which enables de novo assembly of genomes and plasmids, antimicrobial resistance gene annotation and visualization, and comparative analysis. Applying this approach, we detected plasmid transfer between different bacterial species as well as plasmid fusion and frequent rearrangements of the antimicrobial resistance gene cassette. This study demonstrated the feasibility of near-real-time tracking of plasmid-based antimicrobial resistance gene transfer in hospitals, enabling countermeasures to contain plasmid-mediated outbreaks.
dc.format.mimetype application/pdf
dc.language.iso eng
dc.publisher American Society for Microbiology
dc.relation.ispartof mSphere. 2020; 5(4):e00525-20
dc.rights © 2020 Peter et al. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/).
dc.rights.uri https://creativecommons.org/licenses/by/4.0/
dc.title Tracking of antibiotic resistance transfer and rapid plasmid evolution in a hospital setting by Nanopore sequencing
dc.type info:eu-repo/semantics/article
dc.identifier.doi http://dx.doi.org/10.1128/mSphere.00525-20
dc.subject.keyword IMP-8
dc.subject.keyword Nanopore
dc.subject.keyword Nanopore sequencing
dc.subject.keyword Pseudomonas aeruginosa
dc.subject.keyword Antimicrobial resistance
dc.subject.keyword Genome assembly
dc.subject.keyword Horizontal gene transfer
dc.subject.keyword Long read
dc.subject.keyword PathoLogic
dc.subject.keyword PlasmIDent
dc.subject.keyword Plasmid-mediated resistance
dc.subject.keyword Plasmids
dc.subject.keyword Surveillance studies
dc.rights.accessRights info:eu-repo/semantics/openAccess
dc.type.version info:eu-repo/semantics/publishedVersion

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