Clonal dissemination of Enterobacter cloacae harboring blaKPC-3 in the upper midwestern United States

Melissa L. Hargreaves, Kristin M. Shaw, Ginette Dobbins, Paula M Snippes Vagnone, Jane E. Harper, Dave Boxrud, Ruth Lynfield, Maliha Aziz, Lance B. Price, Kevin A T Silverstein, Jessica L. Danzeisen, Bonnie Youmans, Kyle Case, Srinand Sreevatsan, Timothy J. Johnson

Research output: Contribution to journalArticlepeer-review

42 Scopus citations

Abstract

Carbapenemase-producing, carbapenem-resistant Enterobacteriaceae, or CP-CRE, are an emerging threat to human and animal health, because they are resistant to many of the last-line antimicrobials available for disease treatment. Carbapenemase-producing Enterobacter cloacae harboring blaKPC-3 recently was reported in the upper midwestern United States and implicated in a hospital outbreak in Fargo, North Dakota (L. M. Kiedrowski, D. M. Guerrero, F. Perez, R. A. Viau, L. J. Rojas, M. F. Mojica, S. D. Rudin, A. M. Hujer, S. H. Marshall, and R. A. Bonomo, Emerg Infect Dis 20:1583-1585, 2014, http://dx.doi.org/10.3201/eid2009.1 40344). In early 2009, the Minnesota Department of Health began collecting and screening CP-CRE from patients throughout Minnesota. Here, we analyzed a retrospective group of CP-E. cloacae isolates (n=34) collected between 2009 and 2013. Wholegenome sequencing and analysis revealed that 32 of the strains were clonal, belonging to the ST171 clonal complex and differing collectively by 211 single-nucleotide polymorphisms, and it revealed a dynamic clone under positive selection. The phylogeography of these strains suggests that this clone existed in eastern North Dakota and western Minnesota prior to 2009 and subsequently was identified in the Minneapolis and St. Paul metropolitan area. All strains harbored identical IncFIA-like plasmids conferring a CP-CRE phenotype and an additional IncX3 plasmid. In a single patient with multiple isolates submitted over several months, we found evidence that these plasmids had transferred from the E. cloacae clone to an Escherichia coli ST131 bacterium, rendering it as a CP-CRE. The spread of this clone throughout the upper midwestern United States is unprecedented for E. cloacae and highlights the importance of continued surveillance to identify such threats to human health.

Original languageEnglish (US)
Pages (from-to)7723-7734
Number of pages12
JournalAntimicrobial agents and chemotherapy
Volume59
Issue number12
DOIs
StatePublished - Dec 1 2015

Bibliographical note

Funding Information:
This work was supported in part by University of Minnesota College of Veterinary Medicine funding. Computing resources were provided by the University of Minnesota Supercomputing Institute. MDH CRE surveillance was funded by CDC EIP Cooperative Agreement 1U50CK000204-01. This research was also supported in part by an appointment to the Emerging Infectious Diseases (EID) Fellowship Program administered by the Association of Public Health Laboratories (APHL) and funded by the Centers for Disease Control and Prevention (CDC). We thank Cristian Flores Figueroa and Jeannette Munoz Aguayo for their assistance with the S1 PFGE.

Publisher Copyright:
Copyright © 2015, American Society for Microbiology. All Rights Reserved.

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