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使用实时聚合酶链反应直接从阳性血培养瓶中鉴定耐甲氧西林金黄色葡萄球菌。

Use of real-time polymerase chain reaction for identification of methicillin-resistant Staphylococcus aureus directly from positive blood culture bottles.

作者信息

Stratidis John, Bia Frank J, Edberg Stephen C

机构信息

Department of Laboratory Medicine, Yale University School of Medicine, P.O. Box 208035, New Haven, CT 06520-8035, USA.

出版信息

Diagn Microbiol Infect Dis. 2007 Jun;58(2):199-202. doi: 10.1016/j.diagmicrobio.2006.12.017. Epub 2007 Mar 26.

Abstract

The utility of real-time polymerase chain reaction (RT-PCR) testing for detection of methicillin-resistant Staphylococcus aureus (MRSA) directly from positive blood culture bottles was evaluated. One hundred forty-two blood cultures showing Gram-positive cocci in clusters were detected. Each blood culture sample was tested for the presence of MRSA by PCR analysis (SmartCycler) via detection of the mecA and orfX genes. In parallel, they were plated on standard media for identification and characterization. PCR analysis directly from the blood culture bottle required a total time of 120 min (45 min for preparation and 75 min for the reaction). By comparison, conventional laboratory procedures required between 48 and 72 h. The overall test accuracy was 97% with a high positive likelihood ratio and a low negative likelihood ratio.

摘要

评估了直接从阳性血培养瓶中检测耐甲氧西林金黄色葡萄球菌(MRSA)的实时聚合酶链反应(RT-PCR)检测方法的实用性。检测到142份血培养显示革兰氏阳性球菌呈簇状。通过检测mecA和orfX基因,通过PCR分析(SmartCycler)对每份血培养样本进行MRSA检测。同时,将它们接种在标准培养基上进行鉴定和表征。直接从血培养瓶进行PCR分析总共需要120分钟(45分钟用于准备,75分钟用于反应)。相比之下,传统实验室程序需要48至72小时。总体检测准确率为97%,阳性似然比高,阴性似然比低。

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