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首页> 外文期刊>Journal of Clinical Microbiology >Direct Identification of Staphylococcus aureus from Positive Blood Culture Bottles
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Direct Identification of Staphylococcus aureus from Positive Blood Culture Bottles

机译:从阳性血培养瓶中直接鉴定金黄色葡萄球菌

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Fluorescence in situ hybridization (FISH) using peptide nucleic acid (PNA) probes targeting Staphylococcus aureus 16S rRNA is a novel method for direct identification of S. aureus from positive blood culture bottles. The test (S. aureus PNA FISH) is performed on smears made directly from positive blood culture bottles with gram-positive cocci in clusters (GPCC) and provides results within 2.5 h. A blinded comparison of S. aureus PNA FISH with standard identification methods was performed in collaboration with eight clinical microbiology laboratories. A total of 564 routine blood culture bottles positive for GPCC recovered from both aerobic and anaerobic media from three different manufacturers (ESP, BACTEC, and BacT/Alert) were included in the study. The sensitivity and specificity of S. aureus PNA FISH were 100% (57 of 57) and 99.2% (116 of 117), respectively, with 174 GPCC-positive ESP blood culture bottles, 98.5% (67 of 68) and 98.5% (129 of 131), respectively, with 200 GPCC-positive BACTEC blood culture bottles, and 100% (74 of 74) and 99.1% (115 of 116), respectively, with 190 GPCC-positive BacT/Alert blood culture bottles. It is concluded that S. aureus PNA FISH performs well with commonly used continuously monitoring blood culture systems.
机译:靶向金黄色葡萄球菌 16S rRNA的肽核酸(PNA)探针进行荧光原位杂交(FISH)是一种直接鉴定 S的新方法。阳性血液培养瓶中的金黄色葡萄球菌。该测试(金黄色葡萄球菌PNA FISH)是在直接从阳性血液培养瓶中制成的涂片中进行革兰氏阳性球菌成群(GPCC)涂片,并在2.5小时内得出结果。 S的盲目比较。与八个临床微生物学实验室合作,采用标准鉴定方法对金黄色葡萄球菌进行了PNA FISH。从三个不同制造商(ESP,BACTEC和BacT / Alert)的需氧和厌氧培养基中回收的共564个常规GPCC阳性血培养瓶被纳入研究。 S的敏感性和特异性。金黄色葡萄球菌的PNA FISH分别为100%(57/57)和99.2%(116/117),其中有174个GPCC阳性ESP血培养瓶,分别为98.5%(68/67)和98.5%(129/131) )分别使用200个GPCC阳性BACTEC血液培养瓶,以及100%(74个74)和99.1%(115个116),以及190个GPCC阳性BacT / Alert血液培养瓶。结论是 S。金黄色葡萄球菌PNA FISH在常用的连续监测血液培养系统中表现良好。

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