Species Specific Detection of Methicillin-resistant Staphylococcus aureus (MRSA) by Multiplex PCR

Introduction: Staphylococcus aureus is one of the pathogens that is a major agent of infectious diseases. So detection, control and treatment of this pathogen is very important. The objective of this study is setting up a fast method to detect methicillin resistant Staphylococcus aureus (MRSA) for b...

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Main Authors: Mehdi Haseli, Ali Ramazani, Alireza Khaleghi Khorram, Laleh Mehrad
Format: Article
Language:fas
Published: Isfahan University of Medical Sciences 2013-01-01
Series:مجله دانشکده پزشکی اصفهان
Online Access:http://jims.mui.ac.ir/index.php/jims/article/view/2175
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author Mehdi Haseli
Ali Ramazani
Alireza Khaleghi Khorram
Laleh Mehrad
author_facet Mehdi Haseli
Ali Ramazani
Alireza Khaleghi Khorram
Laleh Mehrad
author_sort Mehdi Haseli
collection DOAJ
description Introduction: Staphylococcus aureus is one of the pathogens that is a major agent of infectious diseases. So detection, control and treatment of this pathogen is very important. The objective of this study is setting up a fast method to detect methicillin resistant Staphylococcus aureus (MRSA) for better management of diseases related to this pathogen. Materials and methods: In this study 225 sample collected form staff of University hospitals of Zanjan province. After detection and confirmation of bacteria by conventional and biochemical methods, antimicrobial susceptibility was tested by disk diffusion (Kirby-Bauer) method. After DNA extraction by boiling and phenol – chloroform method, Sa442, mecA and femA genes were detected by multiplex PCR and PCR products were analyzed by electrophoresis (70V, 30 min) in gels composed of 1.5% (w/v) agarose stained with SyberGreen. Result: 208 out of 225 samples made colony in bacterial culture medium. 203/208 isolates were gram positive; 201/208 isolates were catalase positive and 71/208 isolates were coagulase positive. Most of the isolates were resistant to oxacillin and penicillin. By optimization of PCR conditions, Sa442, mecA and femA genes were detected by multiplex PCR simultaneously in single reaction tube. Discussion: Multiplex PCR can detect rapidly and selectively methicillin resistant Staphylococcus aureus in comparison with disk diffusion method.
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spelling doaj.art-d68c53e8010a49b8822e731b657e045d2023-09-03T02:11:05ZfasIsfahan University of Medical Sciencesمجله دانشکده پزشکی اصفهان1027-75951735-854X2013-01-01302131199Species Specific Detection of Methicillin-resistant Staphylococcus aureus (MRSA) by Multiplex PCRMehdi Haseli0Ali Ramazani1Alireza Khaleghi Khorram2Laleh Mehrad3PharmD Student, Department of Biotechnology, School of Pharmacy, Zanjan University of Medical Sciences, Zanjan, IranAssistant Professor, Department of Biotechnology, School of Pharmacy, Zanjan University of Medical Sciences, Zanjan, IranDepartment of Microbiology, School of Medicine, Zanjan University of Medical Sciences, Zanjan, IranMSc Student, Department of Microbiology, Islamic Azad University, Science and Research Branch, Arak, IranIntroduction: Staphylococcus aureus is one of the pathogens that is a major agent of infectious diseases. So detection, control and treatment of this pathogen is very important. The objective of this study is setting up a fast method to detect methicillin resistant Staphylococcus aureus (MRSA) for better management of diseases related to this pathogen. Materials and methods: In this study 225 sample collected form staff of University hospitals of Zanjan province. After detection and confirmation of bacteria by conventional and biochemical methods, antimicrobial susceptibility was tested by disk diffusion (Kirby-Bauer) method. After DNA extraction by boiling and phenol – chloroform method, Sa442, mecA and femA genes were detected by multiplex PCR and PCR products were analyzed by electrophoresis (70V, 30 min) in gels composed of 1.5% (w/v) agarose stained with SyberGreen. Result: 208 out of 225 samples made colony in bacterial culture medium. 203/208 isolates were gram positive; 201/208 isolates were catalase positive and 71/208 isolates were coagulase positive. Most of the isolates were resistant to oxacillin and penicillin. By optimization of PCR conditions, Sa442, mecA and femA genes were detected by multiplex PCR simultaneously in single reaction tube. Discussion: Multiplex PCR can detect rapidly and selectively methicillin resistant Staphylococcus aureus in comparison with disk diffusion method.http://jims.mui.ac.ir/index.php/jims/article/view/2175
spellingShingle Mehdi Haseli
Ali Ramazani
Alireza Khaleghi Khorram
Laleh Mehrad
Species Specific Detection of Methicillin-resistant Staphylococcus aureus (MRSA) by Multiplex PCR
مجله دانشکده پزشکی اصفهان
title Species Specific Detection of Methicillin-resistant Staphylococcus aureus (MRSA) by Multiplex PCR
title_full Species Specific Detection of Methicillin-resistant Staphylococcus aureus (MRSA) by Multiplex PCR
title_fullStr Species Specific Detection of Methicillin-resistant Staphylococcus aureus (MRSA) by Multiplex PCR
title_full_unstemmed Species Specific Detection of Methicillin-resistant Staphylococcus aureus (MRSA) by Multiplex PCR
title_short Species Specific Detection of Methicillin-resistant Staphylococcus aureus (MRSA) by Multiplex PCR
title_sort species specific detection of methicillin resistant staphylococcus aureus mrsa by multiplex pcr
url http://jims.mui.ac.ir/index.php/jims/article/view/2175
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AT alirezakhaleghikhorram speciesspecificdetectionofmethicillinresistantstaphylococcusaureusmrsabymultiplexpcr
AT lalehmehrad speciesspecificdetectionofmethicillinresistantstaphylococcusaureusmrsabymultiplexpcr