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首页> 外文期刊>Journal of Clinical Microbiology >Quantitative Detection of Staphylococcus aureus and Enterococcus faecalis DNA in Blood To Diagnose Bacteremia in Patients in the Intensive Care Unit
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Quantitative Detection of Staphylococcus aureus and Enterococcus faecalis DNA in Blood To Diagnose Bacteremia in Patients in the Intensive Care Unit

机译:定量检测血液中的金黄色葡萄球菌和粪肠球菌DNA,以诊断重症监护病房的细菌血症

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摘要

Direct detection of bacterial DNA in blood offers a fast alternative to blood culture and is presumably unaffected by the prior use of antibiotics. We evaluated the performance of two real-time PCR assays for the quantitative detection of Staphylococcus aureus bacteremia and for Enterococcus faecalis bacteremia directly in blood samples, without prior cultivation. Whole-blood samples for PCR were obtained simultaneously with blood cultures from patients admitted to the intensive care unit of our hospital. After the extraction of DNA from 200 μl of blood, real-time PCR was performed for the specific detection and quantification of S. aureus and E. faecalis DNA. The sensitivity for bacteremia of the S. aureus PCR was 75% and that of the E. faecalis PCR was 73%, and both tests had high specificity values (93 and 96%, respectively). PCR amplification reactions were positive for S. aureus for 10 (7%) blood samples with negative blood cultures, and 7 (4%) PCR reactions were positive for E. faecalis. The majority of these PCR results were likely (50%) or possibly (42%) related to infection with the specific microorganism, based on clinical data and radiological and microbiological investigations. PCR results were concordant for 95% of paired whole-blood samples, and blood culture results were concordant for 97% of the paired samples. We conclude that the detection of S. aureus and E. faecalis DNA in blood by real-time PCR enables a rapid diagnosis of bacteremia and that a positive DNAemia is related to proven or possible infection with the specific microorganism in the majority of patients with negative blood cultures.
机译:直接检测血液中的细菌DNA提供了一种快速的血液培养方法,并且不受先前使用抗生素的影响。我们评估了两种实时PCR检测方法的性能,这些方法无需直接培养即可直接定量检测血样中金黄色葡萄球菌菌血症和粪肠球菌菌血症的数量。从我院重症监护病房住院的患者中同时采集全血样本进行PCR和血液培养。从200μl血液中提取DNA后,进行实时PCR进行 S的特异性检测和定量。金黄色 E。粪便DNA S对菌血症的敏感性。金黄色葡萄球菌的PCR率为75%,而 E的为75%。粪便的PCR率为73%,两种测试的特异性值都很高(分别为93%和96%)。 PCR扩增反应对 S呈阳性。金黄色葡萄球菌对10个(7%)血液培养阴性的血液样本进行了检测,而7个(4%)PCR反应对 E呈阳性。粪便。根据临床数据以及放射学和微生物学调查,这些PCR结果大多数可能与特定微生物感染有关(50%)或可能与42%有关。 95%配对全血样本的PCR结果一致,而97%配对血样的血液培养结果一致。我们得出结论,检测到 S。金黄色 E。通过实时PCR检测粪便中的粪便DNA可以快速诊断菌血症,并且在大多数血液培养阴性的患者中,阳性的DNAemia与特定微生物的已证实或可能的感染有关。

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