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Submitted: 16 Nov 2019
Accepted: 10 Dec 2019
ePublished: 31 Dec 2019
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Avicenna J Clin Microbiol Infect. 2019;6(4): 100-105.
doi: 10.34172/ajcmi.2019.18
  Abstract View: 1145
  PDF Download: 714
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Original Article

Molecular Typing of ccrB Gene in Methicillin-resistant Staphylococcus aureus by Restriction Fragment Length Polymorphism

Fatemeh Noorbakhsh 1* ORCID logo, Parvaneh Atayifar 1, Shohreh Zare Karizi 2

1 Department of Microbiology, Biological Science College, Varamin-Pishva Branch, Islamic Azad University, VaraminPishva, Iran
2 Department of Genetics, Biological Science College, Varamin-Pishva Branch, Islamic Azad University, Varamin-Pishva, Iran
*Corresponding Author: *Corresponding author: Fatemeh Noorbakhsh, Ph.D. Department of Microbiology, Islamic Azad University, Varamin-Pishva Branch, Varamin, Iran, P.O. BOX: 33817-74895, Tel: 09122043654, Email: , Email: niloofar_noorbakhsh@yahoo.com

Abstract

Background: Staphylococcus aureus is one of the most important pathogens acquired from the hospital and community. Increasing the resistance of S. aureus to antibiotics is a major health concentration, and thus the study of antibiotic resistance in S. aureus is very important. The aim of this study is to determine the typing of methicillin-resistant S. aureus (MRSA) in the region of the ccrB gene by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP).

Methods: One hundred and six S. aureus were isolated from urine, blood, sputum, wound, and the trachea of patients hospitalized in Tehran during (March-April) 2016. Antibiotic susceptibility test was done by the disk diffusion method according to the Clinical and Laboratory Standards Institute (CLSI). In addition, molecular typing for staphylococcal cassette chromosome mec (Sccmec) type I-V was performed in MRSA isolates, followed by conducting PCR-RFLP by restriction enzymes BsmI and HinfI in the ccrB gene area.

Results: PCR and typing showed that type II SCCmec was 40% (n=20), followed by types III (28, 56%), IVc (12, 24%), I (11, 22%), V (9, 18%) IVa (7, 14%), and IVb (5, 10%). However, SCCmec type IVd was not observed in the isolates. Finally, after the amplification of ccrB gene and RFLP, all isolates the same as the typing method represented types I, II, III, IVa, IVb, and IVc while no type V was detected by this method.

Conclusions: The results of this study demonstrated that SCCmec (type I-IV) can be detected by PCR-RFLP in the ccrB gene, but this method identified no type V SCCmec in MRSA

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