Co-Occurrence of Plasmid-Mediated AmpC β-Lactamase Activity Among and .

Open Microbiol J

Laboratoire de Microorganismes et Biomolécules Actives Faculté des Sciences de Tunis, Université de Tunis El-Manar, 2098 El-Manar II, Tunisie.

Published: September 2017

Introduction: Extended-spectrum β-lactamases (ESBLs), including the AmpC type, are important mechanisms of resistance among and isolates.

Objective: The aim of the study was to investigate the occurrence of AmpC-type β-lactamase producers isolated from two hospitals in Tripoli, Libya.

Methods: All clinical isolates (76 and 75 ) collected over two years (2013-2014) were evaluated for susceptibility to a panel of antimicrobials and were analyzed phenotypically for the ESBL and AmpC phenotype using E-test and ESBL and AmpC screen disc test. Both ESBL and AmpC-positive isolates were then screened for the presence of genes encoding plasmid-mediated AmpC β-lactamases by polymerase chain reaction (PCR).

Results: Of the and tested, 75% and 16% were resistant to gentamicin, 74% and 1.3% to imipenem, 71% and 12% to cefoxitin, 80% and 12% to cefepime, 69% and 22.6% to ciprofloxacin, respectively. None of the isolates were multidrug resistant compared with (65.8%). ESBL producers were significantly higher (85.5%) compared with (17.3%) isolates (P <0.0001, OR=4.93). Plasmid-mediated AmpC genes were detected in 7.9% of , and 4% isolates. There was low agreement between phenotypic and genotypic methods, phenotypic testing underestimated detection of AmpC enzyme and did not correlate well with molecular results. The gene encoding CMY enzyme was the most prevalent (66.6%) of AmpC positive isolates followed by MOX, DHA and EBC. Only one AmpC gene was detected in 5/9 isolates, i.e, (n=3), (n=1), (n=1). However, co-occurrence of AmpC genes were evident in 3/9 isolates with the following distribution: and (n=1), and and (n=2). Neither nor was detected in all tested isolates. All AmpC positive strains were resistant to cefoxitin and isolated from patients admitted to intensive care units.

Conclusion: Further studies are needed for detection of other AmpC variant enzyme production among such isolates. Continued surveillance and judicious antibiotic usage together with the implementation of efficient infection control measures are absolutely required.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678236PMC
http://dx.doi.org/10.2174/1874285801711010195DOI Listing

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