Cargando…

Co-occurrence of NDM-5, OXA-181, and CMY-2 in a Clinical E. coli Isolate From a Patient in the United States

BACKGROUND: Carbapenem-resistant Enterobacteriacae (CRE) are an important public health problem. A mechanism of expansion of the CRE epidemic is transcontinental spread of multidrug-resistant organisms. Here, we present a patient with an intra-abdominal abscess due to Escherichia coli with an unusua...

Descripción completa

Detalles Bibliográficos
Autores principales: Miller, William, Rios, Rafael, Diaz, Lorena, Panesso, Diana, Chang, Michael, Sun, Zhizeng, Palzkill, Timothy, Arias, Cesar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5631959/
http://dx.doi.org/10.1093/ofid/ofx163.177
_version_ 1783269600227491840
author Miller, William
Rios, Rafael
Diaz, Lorena
Panesso, Diana
Chang, Michael
Sun, Zhizeng
Palzkill, Timothy
Arias, Cesar
author_facet Miller, William
Rios, Rafael
Diaz, Lorena
Panesso, Diana
Chang, Michael
Sun, Zhizeng
Palzkill, Timothy
Arias, Cesar
author_sort Miller, William
collection PubMed
description BACKGROUND: Carbapenem-resistant Enterobacteriacae (CRE) are an important public health problem. A mechanism of expansion of the CRE epidemic is transcontinental spread of multidrug-resistant organisms. Here, we present a patient with an intra-abdominal abscess due to Escherichia coli with an unusual multidrug resistance phenotype who was admitted to a tertiary hospital in Houston, TX after treatment in a country from the Middle East. METHODS: Identification and antimicrobial susceptibility testing were performed by standard methods. Whole-genome sequencing (WGS) was performed on an Illumina platform, with resistance genes identified by ResFinder 2.1 and plasmids recognized using PlasmidFinder 1.3. Results. It is confirmed via PCR, S1 pulsed field gel electrophoresis, and Southern blotting. Carbapenemase activity of bacterial lysates was assayed using 50 µM imipenem in the presence of both EDTA and zinc. RESULTS: The E. coli isolate was resistant to all β-lactams, including ceftazidime/avibactam. The organism belonged to ST410 and harbored bla(NDM-5), bla(OXA-181), bla(CMY-2), and bla(TEM-1B). The bla(OXA-181) gene was located on an IncX3 plasmid of ca. 50 Kb in association with the ISEcp1 mobile element and the qnrS21 gene encoding quinolone resistance. The bla(NDM-5) gene was located on an FIA/FIB plasmid of ~100 Kb, in association with ΔISAba125, and upstream of a putative bleomycin resistance gene, a conserved arrangement among NDM expressing Gram-negative organisms. Cell lysate assays showed decreasing carbapenemase activity with increasing concentrations of EDTA and an increase in activity with the addition of zinc, suggesting the NDM-5 metallo-β-lactamase is largely responsible for the observed carbapenemase activity. Comparison with plasmid sequences available suggested convergence of resistance determinants captured from a wide geographic area. CONCLUSION: Plasmid-mediated spread of β-lactamases among Enterobacteriaceae is a rapidly evolving threat, with the introduction of NDM-5 and OXA-181 in the United States being a particularly disturbing development. Introduction of multidrug-resistant organisms from areas of high prevalence of resistance may change the landscape of antimicrobial resistance in the United States. DISCLOSURES: All authors: No reported disclosures.
format Online
Article
Text
id pubmed-5631959
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-56319592017-11-07 Co-occurrence of NDM-5, OXA-181, and CMY-2 in a Clinical E. coli Isolate From a Patient in the United States Miller, William Rios, Rafael Diaz, Lorena Panesso, Diana Chang, Michael Sun, Zhizeng Palzkill, Timothy Arias, Cesar Open Forum Infect Dis Abstracts BACKGROUND: Carbapenem-resistant Enterobacteriacae (CRE) are an important public health problem. A mechanism of expansion of the CRE epidemic is transcontinental spread of multidrug-resistant organisms. Here, we present a patient with an intra-abdominal abscess due to Escherichia coli with an unusual multidrug resistance phenotype who was admitted to a tertiary hospital in Houston, TX after treatment in a country from the Middle East. METHODS: Identification and antimicrobial susceptibility testing were performed by standard methods. Whole-genome sequencing (WGS) was performed on an Illumina platform, with resistance genes identified by ResFinder 2.1 and plasmids recognized using PlasmidFinder 1.3. Results. It is confirmed via PCR, S1 pulsed field gel electrophoresis, and Southern blotting. Carbapenemase activity of bacterial lysates was assayed using 50 µM imipenem in the presence of both EDTA and zinc. RESULTS: The E. coli isolate was resistant to all β-lactams, including ceftazidime/avibactam. The organism belonged to ST410 and harbored bla(NDM-5), bla(OXA-181), bla(CMY-2), and bla(TEM-1B). The bla(OXA-181) gene was located on an IncX3 plasmid of ca. 50 Kb in association with the ISEcp1 mobile element and the qnrS21 gene encoding quinolone resistance. The bla(NDM-5) gene was located on an FIA/FIB plasmid of ~100 Kb, in association with ΔISAba125, and upstream of a putative bleomycin resistance gene, a conserved arrangement among NDM expressing Gram-negative organisms. Cell lysate assays showed decreasing carbapenemase activity with increasing concentrations of EDTA and an increase in activity with the addition of zinc, suggesting the NDM-5 metallo-β-lactamase is largely responsible for the observed carbapenemase activity. Comparison with plasmid sequences available suggested convergence of resistance determinants captured from a wide geographic area. CONCLUSION: Plasmid-mediated spread of β-lactamases among Enterobacteriaceae is a rapidly evolving threat, with the introduction of NDM-5 and OXA-181 in the United States being a particularly disturbing development. Introduction of multidrug-resistant organisms from areas of high prevalence of resistance may change the landscape of antimicrobial resistance in the United States. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2017-10-04 /pmc/articles/PMC5631959/ http://dx.doi.org/10.1093/ofid/ofx163.177 Text en © The Author 2017. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Miller, William
Rios, Rafael
Diaz, Lorena
Panesso, Diana
Chang, Michael
Sun, Zhizeng
Palzkill, Timothy
Arias, Cesar
Co-occurrence of NDM-5, OXA-181, and CMY-2 in a Clinical E. coli Isolate From a Patient in the United States
title Co-occurrence of NDM-5, OXA-181, and CMY-2 in a Clinical E. coli Isolate From a Patient in the United States
title_full Co-occurrence of NDM-5, OXA-181, and CMY-2 in a Clinical E. coli Isolate From a Patient in the United States
title_fullStr Co-occurrence of NDM-5, OXA-181, and CMY-2 in a Clinical E. coli Isolate From a Patient in the United States
title_full_unstemmed Co-occurrence of NDM-5, OXA-181, and CMY-2 in a Clinical E. coli Isolate From a Patient in the United States
title_short Co-occurrence of NDM-5, OXA-181, and CMY-2 in a Clinical E. coli Isolate From a Patient in the United States
title_sort co-occurrence of ndm-5, oxa-181, and cmy-2 in a clinical e. coli isolate from a patient in the united states
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5631959/
http://dx.doi.org/10.1093/ofid/ofx163.177
work_keys_str_mv AT millerwilliam cooccurrenceofndm5oxa181andcmy2inaclinicalecoliisolatefromapatientintheunitedstates
AT riosrafael cooccurrenceofndm5oxa181andcmy2inaclinicalecoliisolatefromapatientintheunitedstates
AT diazlorena cooccurrenceofndm5oxa181andcmy2inaclinicalecoliisolatefromapatientintheunitedstates
AT panessodiana cooccurrenceofndm5oxa181andcmy2inaclinicalecoliisolatefromapatientintheunitedstates
AT changmichael cooccurrenceofndm5oxa181andcmy2inaclinicalecoliisolatefromapatientintheunitedstates
AT sunzhizeng cooccurrenceofndm5oxa181andcmy2inaclinicalecoliisolatefromapatientintheunitedstates
AT palzkilltimothy cooccurrenceofndm5oxa181andcmy2inaclinicalecoliisolatefromapatientintheunitedstates
AT ariascesar cooccurrenceofndm5oxa181andcmy2inaclinicalecoliisolatefromapatientintheunitedstates