Abstract

Here, we determined the genes encoding antibiotic resistance enzymes and virulence factors and evaluated the genetic relationship between Enterobacter spp. isolated from different clinical samples. A total of 57 clinical isolates of Enterobacter spp. were tested for the production of extended-spectrum β-lactamases (ESBLs), carbapenemase, and AmpC using phenotypic and genotypic methods. The most common ESBLs and AmpC β-lactamases were bla TEM (63.3%) and bla EBC (57.7%), respectively. The most prevalent virulence gene was rpos (87.7%). The random amplified polymorphic DNA (RAPD) patterns of strains were genetically unrelated. RAPD polymerase chain reaction analysis revealed high genetic diversity among isolates.

Highlights

  • We determined the genes encoding antibiotic resistance enzymes and virulence factors and evaluated the genetic relationship between Enterobacter spp. isolated from different clinical samples

  • A total of 57 isolates of Enterobacter spp. were obtained from different patients admitted to three teaching hospitals of the Tehran University of Medical Sciences between September 2013 and April 2014

  • The phenotypic and genotypic characteristics of ESBL and AmpC-producing isolates of E. cloacae and E. aerogenes are shown in Table 2 and Table 3, respectively

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Summary

Short Communication

Clonal relation and antimicrobial resistance pattern of extended-spectrum β-lactamase- and AmpC β-lactamaseproducing Enterobacter spp. isolated from different clinical samples in Tehran, Iran. Roya Ghanavati[1], Mohammad Emaneini[1], Davood Kalantar-Neyestanaki[2], Azin Sattari Maraji[1], Mosayyeb Dalvand[1], Reza Beigverdi[1] and Fereshteh Jabalameli[1].

Bacterial isolates
Susceptibility testing
Findings
RAPD type blaEBC
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