Identification of the respiratory tract infection due to methicillin-resistant Staphylococcus aureus by TaqMan real-time PCR

Q4 Biochemistry, Genetics and Molecular Biology Medical Journal of Cell Biology Pub Date : 2021-06-01 DOI:10.2478/acb-2021-0012
Sabah Saad Abdulsahib
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Abstract

Abstract The methicillin-resistant Staphylococcus aureus (MRSA) is a significant human pathogenic bacterium that is endemic within hospitals around the world. The identification and inspection of MRSA in clinical samples is quite helpful both in advising individual patients about the required care and in tracking these species. The goal of this study was to present a modern, faster, and more accurate diagnostic technique to operate on the real-time duplex PCR applicable to S. aureus/MRSA monitoring in Iraqi patients. For this reason, the S. aureus-specific nuc gene sequence and the mecA gene sequence were checked simultaneously. To estimate the assay efficiency, a set of six target strains, 34 non-target strains, and 296 clinical specimens were used. The findings obtained from the diagnosis of a total of 296 isolates based on phenotypic characteristics and biochemical tests showed that 146 (49.32%) were classified as individuals with respiratory tract infections of S. aureus with a total male to female ratio of 1.47, and 142 isolates demonstrated methicillin resistance. 142 MRSA isolates were investigated in the molecular analysis, all MRSA isolates had positive results for the nuc gene and 138 isolates were positive for the mecA gene. The current real-time PCR assay has 97% sensitivity, 100% specificity, and 98% accuracy. Running title: Identification of the MRSA by real time PCR
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TaqMan实时PCR检测耐甲氧西林金黄色葡萄球菌呼吸道感染
摘要耐甲氧西林金黄色葡萄球菌(MRSA)是一种重要的人类病原菌,在世界各地的医院中流行。临床样本中MRSA的识别和检查对建议个别患者所需的护理和追踪这些物种都很有帮助。本研究的目的是提供一种现代、快速、更准确的诊断技术,用于实时双链PCR,适用于伊拉克患者的金黄色葡萄球菌/MRSA监测。因此,同时检查金黄色葡萄球菌特异性nuc基因序列和mecA基因序列。为了估计测定效率,使用了一组6个靶菌株、34个非靶菌株和296个临床样本。根据表型特征和生化测试对296个分离株的诊断结果显示,146个(49.32%)分离株被归类为金黄色葡萄球菌呼吸道感染个体,男女比例为1.47,142个分离株表现出对甲氧西林的耐药性。对142株耐甲氧西林金黄色葡萄球菌(MRSA)分离株进行了分子分析,所有MRSA分离株的nuc基因检测结果均为阳性,138株的mecA基因检测结果为阳性。目前的实时PCR检测具有97%的灵敏度、100%的特异性和98%的准确度。运行标题:通过实时PCR鉴定耐甲氧西林金黄色葡萄球菌
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来源期刊
Medical Journal of Cell Biology
Medical Journal of Cell Biology Biochemistry, Genetics and Molecular Biology-Cell Biology
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