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Predominance of Non-carbapenemase Producing Carbapenem-Resistant Enterobacterales in South Texas.

Authors :
Black CA
So W
Dallas SS
Gawrys G
Benavides R
Aguilar S
Chen CJ
Shurko JF
Lee GC
Source :
Frontiers in microbiology [Front Microbiol] 2021 Feb 10; Vol. 11, pp. 623574. Date of Electronic Publication: 2021 Feb 10 (Print Publication: 2020).
Publication Year :
2021

Abstract

Background: Carbapenem-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.<br />Materials and Methods: We 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.<br />Results: The majority (59%) of the CRE isolates were NCPE while 41% of isolates harbored carbapenemases, predmonantly bla <subscript>KPC</subscript> -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%.<br />Conclusions: This 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.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2021 Black, So, Dallas, Gawrys, Benavides, Aguilar, Chen, Shurko and Lee.)

Details

Language :
English
ISSN :
1664-302X
Volume :
11
Database :
MEDLINE
Journal :
Frontiers in microbiology
Publication Type :
Academic Journal
Accession number :
33643226
Full Text :
https://doi.org/10.3389/fmicb.2020.623574