Molecular Identification of MefE and AmpC Resistance Genes in ATCC Bacteria

Enterococci are gram-positive bacteria and the source of recurrent nosocomial infections with high levels of antibiotic resistance (1), of which we can name resistance to cephalosporins, aminoglycosides, monobactams, penicillinase resistance penicillins, and most importantly, vancomycin (2). Between 85% to 90% of the enterococci infections are caused by Enterococcus faecium (2), and macrolide-lincosamide-streptogramin is an antibiotic, which can be useful for treating enterococcal infections (1). M phenotype refers to a resistance mechanism to macrolides (such as erythromycin) and includes activedrug efflux pumps that are encoded by mef genes (3,4). For the first time, bacterial antibiotic efflux was reported in 1970 (3). The presence of mef genes have been reported in previous studies (6). In the current study, we reported mefE gene in E. faecium ATCC (American Type Culture Collection) 51559. Acinetobacter baumannii is a gramnegative bacterium that has turned into a great concern in the health care centers especially in intensive care units (4). The name Acinetobacter is originated from akinetos, a Greek word meaning non-motile (4). A. baumannii is a member of “ESKAPE” (Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, A. baumannii, Pseudomonas aeruginosa and Enterobacter spp.) group which consist of multi-drug resistant organisms (4). It is one of the important causes of nosocomial infections (5). Among these multi-drug resistance traits, chromosomal AmpC, a non-inducible cephalosporinase, was already reported in A. baumannii genome (4). In this study, we reported AmpC resistance gene in A. baumannii ATCC 19606. The mentioned ATCC bacteria, which were isolated from clinical samples for the first time (6,7), were bought commercially. The Clinical and Laboratory Standards Institute (CLSI) guidelines were followed for the determination of resistance phenotypes (8). Suspensions of both A. baumannii ATCC 19606 and E. faecium ATCC 51559 were prepared with an opacity equivalent to 0.5 McFarland solution, and subsequently cultured on separate Mueller-Hinton agar plates. An ampicillin (10 μg) disc was used to check the phenotypic resistance in A. baumannii ATCC 19606 and an erythromycin (15 μg) disc for E. faecium ATCC 51559. The plates were then incubated for 24 hours at 35 ̊C. Staphylococcus aureus ATCC 25923 was used for the quality control of both discs. Both A. baumannii ATCC 19606 and E. faecium ATCC 51559 exhibited resistance to the above-mentioned antibiotic discs as shown in Figure 1. In the next step, DNA was extracted using boiling method (9); a loopful of each bacterium was suspended in 1 mL of distilled water and boiled for 15 minutes. Then each microtube was centrifuged at 15 000 g for 10 minutes. The DNA containing supernatants were used for PCR. The primers F: 5’-CAATATGGGCAGGGCAAG-3’ and R: 5’-AAGCTGTTCCAATGCTACGG-3’ were utilized for MefE gene detection (10), and the primers F: 5’TAAACACCACATATGTTCCG-3’ and R: 5’ACTTACTTCAACTCGCGACG-3’ for the AmpC gene detection (11). Both PCRs were carried out using 10 μL of the Master Mix Red (Amplicon, Denmark), 0.5 μL of each primer, and 3 μL of the respective DNA templates, and then brought to a total volume of 25 μL by adding deionized distilled water. Reaction cycles for MefE gene included an initial 7-minute denaturation at 95 ̊C, followed by 44 cycles of: denaturation at 95 ̊C Avicenna Journal of Clinical Microbiology and Infection