Medical
Sara Amini; Amir Hossein Omidi; Hamed Afkhami; Hoda Sabati; Amin Mohsenzadeh; Atyieh Soleymani; Mohammad Ali Zonobian; Negin Ghanbarnejad; Mohammad Reza Mohammadi
Abstract
Staphylococcus aureus is one of the most common infectious bacterial species and one of the agents of community-acquired infections (CAIs) and hospital-acquired infections (HAIs). Aminoglycosides are potent antibactericidal agents often used together with Beta Lactams or Glycopeptides, especially in ...
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Staphylococcus aureus is one of the most common infectious bacterial species and one of the agents of community-acquired infections (CAIs) and hospital-acquired infections (HAIs). Aminoglycosides are potent antibactericidal agents often used together with Beta Lactams or Glycopeptides, especially in treating Staphylococcal endocarditis. The present research aimed to determine the frequency of the aac (6 ́)-le-aph (2 ́ ́) gene that encodes Aminoglycoside modifying enzymes using PCR on clinical isolates of S. aureus. 115 clinical isolates of S. aureus were collected at educational hospitals in Karaj during 12 months. They were first identified by using standard biochemical and laboratory methods and, following CLSI principles and procedures, antibiotic sensitivity patterns of all isolates were obtained using the disc diffusion method. Moreover, using agar dilution, the minimum inhibitory concentration was determined using the antibiotic powder Gentamycin. Finally, gene frequency was measured by employing PCR. The highest levels of resistance to Aminoglycosides were observed in Kanamycin (47.8%), Gentamycin (46.9%), and Tobramycin (46.9%), and Doxycycline and Ciprofloxacin with 50.4 and 49.5 percent respectively, were the non-Aminoglycoside antibiotics to which the highest levels of resistance were exhibited. The frequency of the aac (6 ́)-le-aph (2 ́ ́) gene was 39.1 percent. Rapid and timely detection of resistant strains seems to be necessary in selecting suitable treatment options and in preventing the spread of resistance. Furthermore, rapid identification of genes that encode AME enzymes using PCR enjoys special advantages such as high levels of precision and speed.
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