Abstract

BackgroundCarbapenem-resistant Enterobacterales (CRE) pose a significant global public health threat. Resistance among CRE is particularly complex, owing to numerous possible resistance mechanisms and broad definitions. We aimed to characterize the clinical and molecular profiles of CRE in the South Texas region.Materials and methodsWe compared the clinical, genotypic, and phenotypic profiles of carbapenemase producing Enterobacterales (CPE) with those of non-carbapenemase producers (NCPE) isolated from South Texas, United States between 2011 and 2019. Molecular characteristics and resistance mechanisms were analyzed using whole-genome sequences.ResultsThe majority (59%) of the CRE isolates were NCPE while 41% of isolates harbored carbapenemases, predmonantly blaKPC-type. The most common CPE was Klebsiella pneumoniae while majority of Enterobacter cloacae and Escherichia coli were NCPE Among K. pneumoniae, the clonal group 307 has emerged as a predmoninant group and was associated with as many CRE infections as the previous common clonal group 258. Patients with NCPE compared to CPE infections were associated with higher antimicrobial exposure prior to culture collection (days of therapy, 795 vs. 242; p < 0.001) and emergency department visits within past 90 days (22% vs. 4%; p = 0.011). The all cause 30-day mortality was 21%.ConclusionsThis study highlights the diversity of resistance mechanisms underlying CRE in South Texas, with 59% not harboring a carbapenemase. Individuals with NCPE infections were more likely to have had prior antimicrobial therapy and emergency department visits compared to those with CPE. Identification and distinction of these mechanisms by rapid identification of species and carbapenemase would allow for optimal treatment and infection control efforts.

Highlights

  • Carbapenem-resistant Enterobacterales(CRE), formerly known as Enterobacteriaceae, are a group of organisms that are among the most difficult to treat

  • We identified 99 CRE isolates collected from 85 patients

  • In 58 (59%), in vitro resistance to at least one carbapenem was confirmed in the absence of any carbapenemase gene, referred as non-carbapenemase producers (NCPE)

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Summary

Introduction

Carbapenem-resistant Enterobacterales(CRE), formerly known as Enterobacteriaceae, are a group of organisms that are among the most difficult to treat. It was given a level one priority by the World Health Organization in 2017 (WHO, 2020), and remains one of the top five most urgent public health threat in 2019 by U.S Centers of Disease Control and Prevention (Centers for Disease Control and Prevention (U.S.), 2019). CREs can include those due to porin-deficient Enterobacterales, Enterobacterales with intrinsic imipenem resistance, and Enterobacterales with carbapenemase enzymes that remain “susceptible” to carbapenems. Common carbapenemases in Enterobacterales include the Klebsiella pneumoniae carbapenemases (KPC), oxacillinase (OXA)-48-like β-lactamases, and metallo-β-lactamases, such as New-Delhimetallo-β-lactamases (NDM), the active-in-imipenem family of carbapenemases, and Verona integron-encoded metallo-βlactamases (VIM). We aimed to characterize the clinical and molecular profiles of CRE in the South Texas region

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