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      Prevalence of ESBL and MBL encoding genes in Acinetobacter baumannii strains isolated from patients of intensive care units (ICU)

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          Abstract

          The aim of this study was to investigate the prevalence of ESBL and MBL encoding genes among A. baumannii isolates. In this cross sectional study, 100 A. baumannii strains were isolated from ICU wards of 3 educational hospitals of Hamadan City, Iran in 2011. Phenotypic identification of the production of ESBLs and MBLs has been carried out by using E-test and DDST methods, respectively. PCR technique was used for amplification of the ESBL and MBL encoding genes, namely: CTX-M, SHV, TEM, OXA-51, VIM-Family, IMP-Family, SPM-1, SIM-1, and GIM-1. Eighty seven (87%), 95 (95%), 98 (98%) and 95 (95%) out of 100 A. baumannii isolates were resistant to imipenem, meropenem, ceftazidime and cefotaxime, respectively. Also, 99% and 7% of the isolates were MBLs and ESBLs produced phenotypically. Thirty (30%), 20 (20%) and 58 (58%) out of 100 A. baumannii isolates have been confirmed to harbor the bla VIM-family, TEM and SHV genes, respectively. Our results show no significant relationship between the detected gens with production of MBLs and ESBLs in spite of high prevalence of MBL encoding and drug resistant A. baumannii. Probably some other genes rather than what we studied are involved in phenotypic production of MBLs and ESBLs and subsequent drug resistance in Hamadan area, Iran.

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          Multiplex PCR for rapid detection of genes encoding acquired metallo-beta-lactamases.

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            Identification of Acinetobacter baumannii by detection of the blaOXA-51-like carbapenemase gene intrinsic to this species.

            bla(OXA-51-like) was sought in clinical isolates of Acinetobacter species in a multiplex PCR, which also detects bla(OXA-23-like) and class 1 integrase genes. All isolates that gave a band for bla(OXA-51-like) identified as A. baumannii. This gene was detected in each of 141 isolates of A. baumannii but not in those of 22 other Acinetobacter species.
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              New beta-lactamases in gram-negative bacteria: diversity and impact on the selection of antimicrobial therapy.

              K Bush (2001)
              Of the 340 discrete beta-lactamases that have been identified, the most important groups of enzymes that are continuing to proliferate include the plasmid-encoded cephalosporinases, the metallo-beta-lactamases, and the extended-spectrum beta-lactamases. Resistance to specific beta-lactam-containing antimicrobial agents frequently can be traced to a single beta-lactamase, but this task is becoming more difficult for the clinical microbiology laboratory. Other factors, such as multiple beta-lactamase production, transferable multidrug-resistance genes, alterations in outer-membrane porins, and possible antibiotic efflux, all may contribute to a resistance phenotype. Appreciation of these factors may help the physician make a more informed decision when choosing therapy to try to avoid selection of even more pathogenic strains.
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                Author and article information

                Contributors
                Journal
                Saudi J Biol Sci
                Saudi J Biol Sci
                Saudi Journal of Biological Sciences
                Elsevier
                1319-562X
                2213-7106
                17 January 2015
                July 2015
                17 January 2015
                : 22
                : 4
                : 424-429
                Affiliations
                [a ]Department of Microbiology, Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran
                [b ]Young Researchers and Elite Club, Sari Branch, Islamic Azad University, Sari, Iran
                [c ]Research Center for Molecular Medicine, Hamadan University of Medical Sciences, Hamadan, Iran
                [d ]Department of Microbiology, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran
                [e ]Department of Parasitology and Mycology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
                [f ]Brucellosis Research Center, Hamadan University of Medical Sciences, Hamadan, Iran
                Author notes
                [* ]Corresponding author at: Department of Microbiology, Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran. Tel.: +98 8138380267; fax: +98 8138380131. alikhani43@ 123456yahoo.com asmozafarinejad@ 123456yahoo.in
                Article
                S1319-562X(15)00005-4
                10.1016/j.sjbs.2015.01.004
                4486466
                26150748
                96b4e321-81b6-4c94-baab-dc23c107f910
                © 2015 Production and hosting by Elsevier B.V. on behalf of King Saud University.

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 7 November 2014
                : 30 December 2014
                : 10 January 2015
                Categories
                Original Article

                acinetobacter baumannii,drug resistance,mbl,esbl
                acinetobacter baumannii, drug resistance, mbl, esbl

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