Antibiotic Resistance Patterns and a Survey of Metallo-β-Lactamase Genes Including bla-IMP and bla-VIM Types in Acinetobacter baumannii Isolated from Hospital Patients in Tehran
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E-Artikel
Titel:
Antibiotic Resistance Patterns and a Survey of Metallo-β-Lactamase Genes Including bla-IMP and bla-VIM Types in Acinetobacter baumannii Isolated from Hospital Patients in Tehran
Beschreibung:
<jats:p><b><i>Background:</i></b> Metallo-β-lactamases (MBLs) producing strains of <i>Acinetobacter baumannii</i> are serious etiological agents of hospital infections worldwide. Among the β- lactams, carbapenems are the most effective antibiotics used against <i>A. baumannii. </i>However, resistance to these drugs among clinical strains of <i>A. baumannii</i> has been increasing in recent years. In this study, the antimicrobial sensitivity patterns of <i>A. baumannii</i> strains isolated from eleven different hospitals in Tehran, Iran, and the prevalence of MBL genes (<i>bla-</i><sub><i>VIM</i></sub> and <i>bla-</i><sub><i>IMP</i></sub>) were determined. <b><i>Method:</i></b> During a period of 5 months, 176 isolates of <i>A. baumannii</i> were collected from different clinical specimens from hospitalized patients in Tehran. All isolates were confirmed by biochemical methods. The isolates were tested for antibiotic sensitivity by the Kirby-Bauer disk diffusion method. Following minimum inhibitory concentration determination, imipenem-resistant isolates were further tested for MBL production by the double disk synergy test (DDST) method. PCR assays were performed for the detection of the MBL genes <i>bla-</i><sub><i>IMP</i></sub> and <i>bla-</i><sub><i>VIM</i></sub>. <b><i>Results:</i></b> The DDST phenotypic method indicated that among the 169 imipenem-resistant isolates, 165 strains were MBL positive. The PCR assays revealed that 63 of the overall isolates (36%) carried the <i>bla-</i><sub><i>VIM</i></sub> gene and 70 strains (40%) harbored <i>bla-</i><sub><i>IMP</i></sub>. <b><i>Conclusions:</i></b> It is obvious that nosocomial infections associated with multidrug-resistant <i>Acinetobacter </i>spp. are on the rise. Therefore, the determination of antibiotic sensitivity patterns and screening for MBL production among <i>A. baumannii</i> isolates is important for controlling clinical <i>Acinetobacter</i> infections.</jats:p>