Development of SYBR Green Real time PCR for identification methicillin-resistance Staphylococcus aureus (MRSA)

The increasing resistance of staphylococci to ß -lactam antibiotics has become a major clinical problem. Development of rapid and sensitive techniques for detection of MRSA is an important aim for public health. A duplex PCR were established for specific identification of methicillin-resistance Sta...

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出版年:مجلة مركز بحوث التقنيات الاحيائية
主要な著者: Noor Hashim Kareem, Majeed Arsheed Sabbah, Anas Noori Ibraheem, Al-Shayma’a Muhammad Said
フォーマット: 論文
言語:英語
出版事項: Al-Nahrain University/ Biotechnology Research Center 2013-01-01
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オンライン・アクセス:https://www.jobrc.org/index.php/jobrc/article/view/248
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author Noor Hashim Kareem
Majeed Arsheed Sabbah
Anas Noori Ibraheem
Al-Shayma’a Muhammad Said
author_facet Noor Hashim Kareem
Majeed Arsheed Sabbah
Anas Noori Ibraheem
Al-Shayma’a Muhammad Said
author_sort Noor Hashim Kareem
collection DOAJ
container_title مجلة مركز بحوث التقنيات الاحيائية
description The increasing resistance of staphylococci to ß -lactam antibiotics has become a major clinical problem. Development of rapid and sensitive techniques for detection of MRSA is an important aim for public health. A duplex PCR were established for specific identification of methicillin-resistance Staphylococcus aureus (MRSA) in clinical samples. In this work a duplex SYBR Green real time PCR was developed for rapid identification of MRSA in local methicillin-resistance S. aureus isolates. Twenty methicillin-resistance S. aureus isolates, as determined by disc diffusion method, were subjected to DNA extraction and PCR amplification. Two genes were amplified successfully, mecA (533bp) and femA (314bp), as targets for methicillin-resistance and specific identification of S. aureus, respectively using conventional PCR. Sensitivity of the duplex PCR showed that the minimum concentration of DNA that gave positive results for the two genes was 30ng/µl. In order to develop rapid and sensitive test for identification of MRSA, serial dilutions of purified DNA were amplified gradually according to their concentrations using SYBR Green real time PCR. These results indicated that the SYBR Green real time PCR can be used for identification of methicillin-resistance S. aureus (MRSA) in clinical
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spelling doaj-art-eacbddae75fa43c888280ea9433b56702025-08-20T00:20:06ZengAl-Nahrain University/ Biotechnology Research Centerمجلة مركز بحوث التقنيات الاحيائية1815-11402708-13702013-01-017110.24126/jobrc.2013.7.1.248Development of SYBR Green Real time PCR for identification methicillin-resistance Staphylococcus aureus (MRSA)Noor Hashim KareemMajeed Arsheed SabbahAnas Noori IbraheemAl-Shayma’a Muhammad Said The increasing resistance of staphylococci to ß -lactam antibiotics has become a major clinical problem. Development of rapid and sensitive techniques for detection of MRSA is an important aim for public health. A duplex PCR were established for specific identification of methicillin-resistance Staphylococcus aureus (MRSA) in clinical samples. In this work a duplex SYBR Green real time PCR was developed for rapid identification of MRSA in local methicillin-resistance S. aureus isolates. Twenty methicillin-resistance S. aureus isolates, as determined by disc diffusion method, were subjected to DNA extraction and PCR amplification. Two genes were amplified successfully, mecA (533bp) and femA (314bp), as targets for methicillin-resistance and specific identification of S. aureus, respectively using conventional PCR. Sensitivity of the duplex PCR showed that the minimum concentration of DNA that gave positive results for the two genes was 30ng/µl. In order to develop rapid and sensitive test for identification of MRSA, serial dilutions of purified DNA were amplified gradually according to their concentrations using SYBR Green real time PCR. These results indicated that the SYBR Green real time PCR can be used for identification of methicillin-resistance S. aureus (MRSA) in clinical https://www.jobrc.org/index.php/jobrc/article/view/248methicillin-resistance, Staphylococcus aureus, MRSA, PCR, mecA, femA, SYBR
spellingShingle Noor Hashim Kareem
Majeed Arsheed Sabbah
Anas Noori Ibraheem
Al-Shayma’a Muhammad Said
Development of SYBR Green Real time PCR for identification methicillin-resistance Staphylococcus aureus (MRSA)
methicillin-resistance, Staphylococcus aureus, MRSA, PCR, mecA, femA, SYBR
title Development of SYBR Green Real time PCR for identification methicillin-resistance Staphylococcus aureus (MRSA)
title_full Development of SYBR Green Real time PCR for identification methicillin-resistance Staphylococcus aureus (MRSA)
title_fullStr Development of SYBR Green Real time PCR for identification methicillin-resistance Staphylococcus aureus (MRSA)
title_full_unstemmed Development of SYBR Green Real time PCR for identification methicillin-resistance Staphylococcus aureus (MRSA)
title_short Development of SYBR Green Real time PCR for identification methicillin-resistance Staphylococcus aureus (MRSA)
title_sort development of sybr green real time pcr for identification methicillin resistance staphylococcus aureus mrsa
topic methicillin-resistance, Staphylococcus aureus, MRSA, PCR, mecA, femA, SYBR
url https://www.jobrc.org/index.php/jobrc/article/view/248
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AT anasnooriibraheem developmentofsybrgreenrealtimepcrforidentificationmethicillinresistancestaphylococcusaureusmrsa
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