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Biofilm Forming Ability and Spa Gene Polymorphism in Methicillin Resistant Staphylococcus aureus Clinical Isolates in North of Iran

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Abstract

Spa typing has been shown to function as a genetic marker for Staphylococcus aureus outbreak investigations and epidemiological studies. This study was aimed to investigate biofilm formation capacity and spa gene polymorphism in methicillin resistant S. aureus (MRSA) strains isolated from clinical samples. A total of 102 S. aureus isolated during 2016, were analyzed for methicillin resistance and biofilm formation using phenotypic assays and PCR-based detection of associated genes. The polymorphic region of the spa gene was amplified by PCR using specific primers and subsequently in MRSA strains the amplified products were sequenced and spa types determined by using the spa database website. Out of 102 S. aureus, 41 isolates (40.2%) recognized as MRSA in phenotypic and genotypic investigations. In phenotypic assay, biofilm forming ability was detected in 71 isolates. The frequency of icaA and fnbA in test isolate were 53.9 and 65.7% respectively. Amplification of polymorphic region of the spa gene in all 102 tested isolates resulted in eight size fragments ranged between 168–336 bp. In MRSA strains thirteen distinct spa types with 5–12 repeats were observed. The most frequent types of spa were t030, t037, t325, t421, t937, t1814 and t084. spa types t2421, t1814, t359 and t2617 identified for the first time in Iran. The present results showed high biofilm formation capacity and great diversity of variable region of spa gene in MRSA strains and confirmed that, spa typing provides valuable information on the epidemiologic features and discrimination of this bacterium.

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Authors and Affiliations

  1. Department of Biology, Faculty of Science, Rasht Branch, Islamic Azad University, Rasht, Iran

    L. Asadpour

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  1. L. Asadpour
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Asadpour, L. Biofilm Forming Ability and Spa Gene Polymorphism in Methicillin Resistant Staphylococcus aureus Clinical Isolates in North of Iran. Mol. Genet. Microbiol. Virol. 33, 55–59 (2018). https://doi.org/10.3103/S0891416818010032

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  • DOI: https://doi.org/10.3103/S0891416818010032

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