Characterization of Carbapenem-Resistant Enterobacteriaceae Clinical Isolates in Al Thawra University Hospital, Sana'a, Yemen.

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ID: 42583
2019
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Abstract
The aim of this study was to investigate the resistance mechanisms of carbapenem-resistant Enterobacteriaceae clinical strains recovered from Al Thawra University Hospital, Sana'a, Yemen. A total of 27 isolates showing decreased susceptibility to carbapenems were obtained from different clinical specimens in Al Thawra Hospital, Sana'a, Yemen. Strains were identified by Matrix Assisted Laser Desorption Ionization Time-Of-Flight spectroscopy. Susceptibility to antibiotics was determined by the disk diffusion method on Mueller Hinton agar. Carbapenemases-encoding genes, extended-spectrum β-lactamases (ESBLs), and plasmid-mediated quinolone resistance (PMQR) genes were screened by PCR. Bacterial isolates were typed by multilocus sequence typing (MLST). Carbapenemase genes detection and sequencing showed that 18 (66.7%) isolates were (NDM-1,  = 13; NDM-1 + OXA-48,  = 3; OXA-48,  = 1; OXA-232,  = 1), 6 (22.2%) were (NDM-5,  = 3; OXA-181,  = 2; OXA-48,  = 1), and 3 (11.1%) were (NDM-1,  = 1; OXA-181,  = 2). In addition the ESBL gene was detected in 14 and 2 isolates, and the was found in 1 isolate. Fifteen isolates were PMQR positive including ( = 1), ( = 5), ( = 2), and ( = 7). The MLST typing showed a diversity of sequence type (ST) clones including ST410 (3), ST448 (2), and ST648; ST78 and ST270; and ST395 (2), ST309, ST23, ST35, ST1728, ST15, ST231, and ST1428. This study reports the first description of OXA-48-like-producing Enterobacteriaceae and NDM-5 enzymes in in Yemen.
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alsharapy2019characterizationmicrobial Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Alsharapy, Sameer Ahmed;Gharout-Sait, Alima;Muggeo, Anaelle;Guillard, Thomas;Cholley, Pascal;Brasme, Lucien;Bertrand, Xavier;Moghram, Ghuzlan Saeed;Touati, Abdelaziz;De Champs, Christophe;
Journal microbial drug resistance (larchmont, ny)
Year 2019
DOI
10.1089/mdr.2018.0443
URL
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