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Genomic dynamics of species and mobile genetic elements in a prolonged bla(IMP-4)-associated carbapenemase outbreak in an Australian hospital
BACKGROUND: Hospital outbreaks of carbapenemase-producing organisms, such as bla(IMP-4)-containing organisms, are an increasing threat to patient safety. OBJECTIVES: To investigate the genomic dynamics of a 10 year (2006–15) outbreak of bla(IMP-4)-containing organisms in a burns unit in a hospital i...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7069471/ https://www.ncbi.nlm.nih.gov/pubmed/31960024 http://dx.doi.org/10.1093/jac/dkz526 |
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author | Kizny Gordon, A Phan, H T T Lipworth, S I Cheong, E Gottlieb, T George, S Peto, T E A Mathers, A J Walker, A S Crook, D W Stoesser, N |
author_facet | Kizny Gordon, A Phan, H T T Lipworth, S I Cheong, E Gottlieb, T George, S Peto, T E A Mathers, A J Walker, A S Crook, D W Stoesser, N |
author_sort | Kizny Gordon, A |
collection | PubMed |
description | BACKGROUND: Hospital outbreaks of carbapenemase-producing organisms, such as bla(IMP-4)-containing organisms, are an increasing threat to patient safety. OBJECTIVES: To investigate the genomic dynamics of a 10 year (2006–15) outbreak of bla(IMP-4)-containing organisms in a burns unit in a hospital in Sydney, Australia. METHODS: All carbapenem-non-susceptible or MDR clinical isolates (2006–15) and a random selection of equivalent or ESBL-producing environmental isolates (2012–15) were sequenced [short-read (Illumina), long-read (Oxford Nanopore Technology)]. Sequence data were used to assess genetic relatedness of isolates (Mash; mapping and recombination-adjusted phylogenies), perform in silico typing (MLST, resistance genes and plasmid replicons) and reconstruct a subset of bla(IMP) plasmids for comparative plasmid genomics. RESULTS: A total of 46/58 clinical and 67/96 environmental isolates contained bla(IMP-4). All bla(IMP-4)-positive organisms contained five or more other resistance genes. Enterobacter cloacae was the predominant organism, with 12 other species mainly found in either the environment or patients, some persisting despite several cleaning methods. On phylogenetic analysis there were three genetic clusters of E. cloacae containing both clinical and environmental isolates, and an additional four clusters restricted to either reservoir. bla(IMP-4) was mostly found as part of a cassette array (bla(IMP-4)-qacG2-aacA4-catB3) in a class 1 integron within a previously described IncM2 plasmid (pEl1573), with almost complete conservation of this cassette across the species over the 10 years. Several other plasmids were also implicated, including an IncF plasmid backbone not previously widely described in association with bla(IMP-4.) CONCLUSIONS: Genetic backgrounds disseminating bla(IMP-4) can persist, diversify and evolve amongst both human and environmental reservoirs during a prolonged outbreak despite intensive prevention efforts. |
format | Online Article Text |
id | pubmed-7069471 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-70694712020-03-18 Genomic dynamics of species and mobile genetic elements in a prolonged bla(IMP-4)-associated carbapenemase outbreak in an Australian hospital Kizny Gordon, A Phan, H T T Lipworth, S I Cheong, E Gottlieb, T George, S Peto, T E A Mathers, A J Walker, A S Crook, D W Stoesser, N J Antimicrob Chemother Original Research BACKGROUND: Hospital outbreaks of carbapenemase-producing organisms, such as bla(IMP-4)-containing organisms, are an increasing threat to patient safety. OBJECTIVES: To investigate the genomic dynamics of a 10 year (2006–15) outbreak of bla(IMP-4)-containing organisms in a burns unit in a hospital in Sydney, Australia. METHODS: All carbapenem-non-susceptible or MDR clinical isolates (2006–15) and a random selection of equivalent or ESBL-producing environmental isolates (2012–15) were sequenced [short-read (Illumina), long-read (Oxford Nanopore Technology)]. Sequence data were used to assess genetic relatedness of isolates (Mash; mapping and recombination-adjusted phylogenies), perform in silico typing (MLST, resistance genes and plasmid replicons) and reconstruct a subset of bla(IMP) plasmids for comparative plasmid genomics. RESULTS: A total of 46/58 clinical and 67/96 environmental isolates contained bla(IMP-4). All bla(IMP-4)-positive organisms contained five or more other resistance genes. Enterobacter cloacae was the predominant organism, with 12 other species mainly found in either the environment or patients, some persisting despite several cleaning methods. On phylogenetic analysis there were three genetic clusters of E. cloacae containing both clinical and environmental isolates, and an additional four clusters restricted to either reservoir. bla(IMP-4) was mostly found as part of a cassette array (bla(IMP-4)-qacG2-aacA4-catB3) in a class 1 integron within a previously described IncM2 plasmid (pEl1573), with almost complete conservation of this cassette across the species over the 10 years. Several other plasmids were also implicated, including an IncF plasmid backbone not previously widely described in association with bla(IMP-4.) CONCLUSIONS: Genetic backgrounds disseminating bla(IMP-4) can persist, diversify and evolve amongst both human and environmental reservoirs during a prolonged outbreak despite intensive prevention efforts. Oxford University Press 2020-04 2020-01-20 /pmc/articles/PMC7069471/ /pubmed/31960024 http://dx.doi.org/10.1093/jac/dkz526 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Kizny Gordon, A Phan, H T T Lipworth, S I Cheong, E Gottlieb, T George, S Peto, T E A Mathers, A J Walker, A S Crook, D W Stoesser, N Genomic dynamics of species and mobile genetic elements in a prolonged bla(IMP-4)-associated carbapenemase outbreak in an Australian hospital |
title | Genomic dynamics of species and mobile genetic elements in a prolonged bla(IMP-4)-associated carbapenemase outbreak in an Australian hospital |
title_full | Genomic dynamics of species and mobile genetic elements in a prolonged bla(IMP-4)-associated carbapenemase outbreak in an Australian hospital |
title_fullStr | Genomic dynamics of species and mobile genetic elements in a prolonged bla(IMP-4)-associated carbapenemase outbreak in an Australian hospital |
title_full_unstemmed | Genomic dynamics of species and mobile genetic elements in a prolonged bla(IMP-4)-associated carbapenemase outbreak in an Australian hospital |
title_short | Genomic dynamics of species and mobile genetic elements in a prolonged bla(IMP-4)-associated carbapenemase outbreak in an Australian hospital |
title_sort | genomic dynamics of species and mobile genetic elements in a prolonged bla(imp-4)-associated carbapenemase outbreak in an australian hospital |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7069471/ https://www.ncbi.nlm.nih.gov/pubmed/31960024 http://dx.doi.org/10.1093/jac/dkz526 |
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