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应用 PNA-FISH 快速检测变形杆菌属引起的尿路感染。

Rapid detection of urinary tract infections caused by Proteus spp. using PNA-FISH.

机构信息

IBB-Institute for Biotechnology and Bioengineering, Centre of Biological Engineering, Universidade do Minho, Campus de Gualtar, 4710-057, Braga, Portugal.

出版信息

Eur J Clin Microbiol Infect Dis. 2013 Jun;32(6):781-6. doi: 10.1007/s10096-012-1808-2. Epub 2013 Jan 4.

DOI:10.1007/s10096-012-1808-2
PMID:23288291
Abstract

We developed a fluorescence in situ hybridization (FISH) method for the rapid detection of Proteus spp. in urine, using a novel peptide nucleic acid (PNA) probe. Testing on 137 urine samples from patients with urinary tract infections has shown specificity and sensitivity values of 98 % (95 % CI, 93.2-99.7) and 100 % (95 % CI, 80,8-100), respectively, when compared with CHROMagar Orientation medium. Results indicate that PNA-FISH is a reliable alternative to traditional culture methods and can reduce the diagnosis time to approximately 2 h.

摘要

我们开发了一种使用新型肽核酸 (PNA) 探针的荧光原位杂交 (FISH) 方法,用于快速检测尿液中的变形菌属。对 137 份尿路感染患者的尿液样本进行检测,与 CHROMagar Orientation 培养基相比,该方法的特异性和灵敏度分别为 98%(95%CI,93.2-99.7)和 100%(95%CI,80.8-100)。结果表明,PNA-FISH 是传统培养方法的可靠替代方法,可将诊断时间缩短至约 2 小时。

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2
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3
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4
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