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Integrating multiple genomic technologies to investigate an outbreak of carbapenemase-producing Enterobacter hormaechei

Leah W. Roberts, View ORCID ProfilePatrick N. A. Harris, Brian M. Forde, Nouri L. Ben Zakour, Mitchell Stanton-Cook, Elizabeth Catchpoole, Minh-Duy Phan, Hanna E. Sidjabat, Haakon Bergh, Claire Heney, Jayde A. Gawthorne, Jeffrey Lipman, Anthony Allworth, Kok-Gan Chan, Teik Min Chong, Wai-Fong Yin, Mark A. Schembri, David L. Paterson, View ORCID ProfileScott A. Beatson
doi: https://doi.org/10.1101/172536
Leah W. Roberts
1School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD, Australia
2Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, QLD, Australia
3Australian Centre for Ecogenomics, The University of Queensland, Brisbane, QLD, Australia
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Patrick N. A. Harris
4The University of Queensland, UQ Centre for Clinical Research, Brisbane, QLD, Australia
5Pathology Queensland, Central Microbiology, Brisbane, QLD, Australia
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  • For correspondence: p.harris@uq.edu.au
Brian M. Forde
1School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD, Australia
2Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, QLD, Australia
3Australian Centre for Ecogenomics, The University of Queensland, Brisbane, QLD, Australia
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Nouri L. Ben Zakour
1School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD, Australia
2Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, QLD, Australia
3Australian Centre for Ecogenomics, The University of Queensland, Brisbane, QLD, Australia
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Mitchell Stanton-Cook
1School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD, Australia
2Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, QLD, Australia
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Elizabeth Catchpoole
5Pathology Queensland, Central Microbiology, Brisbane, QLD, Australia
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Minh-Duy Phan
1School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD, Australia
2Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, QLD, Australia
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Hanna E. Sidjabat
4The University of Queensland, UQ Centre for Clinical Research, Brisbane, QLD, Australia
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Haakon Bergh
5Pathology Queensland, Central Microbiology, Brisbane, QLD, Australia
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Claire Heney
5Pathology Queensland, Central Microbiology, Brisbane, QLD, Australia
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Jayde A. Gawthorne
1School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD, Australia
2Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, QLD, Australia
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Jeffrey Lipman
4The University of Queensland, UQ Centre for Clinical Research, Brisbane, QLD, Australia
6Burns Trauma and Critical Care Research Centre, The University of Queensland, Brisbane, QLD, Australia
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Anthony Allworth
7Infectious Disease Unit, Royal Brisbane & Women’s Hospital, Brisbane, QLD, Australia
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Kok-Gan Chan
8Division of Genetics and Molecular Biology, Institute of Biological Sciences, Faculty of Science, University of Malaya, Kuala Lumpur, Malaysia
9International Genome Centre, Jiangsu University, Zhenjiang, China
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Teik Min Chong
8Division of Genetics and Molecular Biology, Institute of Biological Sciences, Faculty of Science, University of Malaya, Kuala Lumpur, Malaysia
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Wai-Fong Yin
8Division of Genetics and Molecular Biology, Institute of Biological Sciences, Faculty of Science, University of Malaya, Kuala Lumpur, Malaysia
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Mark A. Schembri
1School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD, Australia
2Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, QLD, Australia
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David L. Paterson
2Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, QLD, Australia
4The University of Queensland, UQ Centre for Clinical Research, Brisbane, QLD, Australia
10Wesley Medical Research, The Wesley Hospital, Auchenflower, QLD, Australia
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Scott A. Beatson
1School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD, Australia
2Australian Infectious Diseases Research Centre, The University of Queensland, Brisbane, QLD, Australia
3Australian Centre for Ecogenomics, The University of Queensland, Brisbane, QLD, Australia
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  • For correspondence: s.beatson@uq.edu.au
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Abstract

Carbapenem-resistant Enterobacteriaceae (CRE) represent one of the most urgent threats to human health posed by antibiotic resistant bacteria. Enterobacter hormaechei and other members of the Enterobacter cloacae complex are the most commonly encountered Enterobacter spp. within clinical settings, responsible for numerous outbreaks and ultimately poorer patient outcomes. Here we applied three complementary whole genome sequencing (WGS) technologies to characterise a hospital cluster of blaIMP-4 carbapenemase-producing E. hormaechei.

In response to a suspected CRE outbreak in 2015 within an Intensive Care Unit (ICU)/Burns Unit in a Brisbane tertiary referral hospital we used Illumina sequencing to determine that all outbreak isolates were sequence type (ST)90 and near-identical at the core genome level. Comparison to publicly available data unequivocally linked all 10 isolates to a 2013 isolate from the same ward, confirming the hospital environment as the most likely original source of infection in the 2015 cases. No clonal relationship was found to IMP-4-producing isolates identified from other local hospitals. However, using Pacific Biosciences long-read sequencing we were able to resolve the complete context of the blaIMP-4 gene, which was found to be on a large IncHI2 plasmid carried by all IMP-4-producing isolates. Continued surveillance of the hospital environment was carried out using Oxford Nanopore long-read sequencing, which was able to rapidly resolve the true relationship of subsequent isolates to the initial outbreak. Shotgun metagenomic sequencing of environmental samples also found evidence of ST90 E. hormaechei and the IncHI2 plasmid within the hospital plumbing.

Overall, our strategic application of three WGS technologies provided an in-depth analysis of the outbreak, including the transmission dynamics of a carbapenemase-producing E. hormaechei cluster, identification of possible hospital reservoirs and the full context of blaIMP-4 on a multidrug resistant IncHI2 plasmid that appears to be widely distributed in Australia.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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Posted April 17, 2019.
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Integrating multiple genomic technologies to investigate an outbreak of carbapenemase-producing Enterobacter hormaechei
Leah W. Roberts, Patrick N. A. Harris, Brian M. Forde, Nouri L. Ben Zakour, Mitchell Stanton-Cook, Elizabeth Catchpoole, Minh-Duy Phan, Hanna E. Sidjabat, Haakon Bergh, Claire Heney, Jayde A. Gawthorne, Jeffrey Lipman, Anthony Allworth, Kok-Gan Chan, Teik Min Chong, Wai-Fong Yin, Mark A. Schembri, David L. Paterson, Scott A. Beatson
bioRxiv 172536; doi: https://doi.org/10.1101/172536
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Integrating multiple genomic technologies to investigate an outbreak of carbapenemase-producing Enterobacter hormaechei
Leah W. Roberts, Patrick N. A. Harris, Brian M. Forde, Nouri L. Ben Zakour, Mitchell Stanton-Cook, Elizabeth Catchpoole, Minh-Duy Phan, Hanna E. Sidjabat, Haakon Bergh, Claire Heney, Jayde A. Gawthorne, Jeffrey Lipman, Anthony Allworth, Kok-Gan Chan, Teik Min Chong, Wai-Fong Yin, Mark A. Schembri, David L. Paterson, Scott A. Beatson
bioRxiv 172536; doi: https://doi.org/10.1101/172536

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