首页> 外文期刊>Journal of Infection >Use of polymerase chain reaction (PCR) and DNA probe hybridization to determine the Gram reaction of the infecting bacterium in the intraocular fluids of patients with endophthalmitis.
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Use of polymerase chain reaction (PCR) and DNA probe hybridization to determine the Gram reaction of the infecting bacterium in the intraocular fluids of patients with endophthalmitis.

机译:使用聚合酶链反应(PCR)和DNA探针杂交来确定眼内炎患者眼内液中感染细菌的革兰氏反应。

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OBJECTIVES: To evaluate polymerase chain reaction (PCR) combined with DNA probe hybridization to determine the Gram reaction of the bacterium in intraocular specimens from patients with infectious endophthalmitis. METHODS: Fifty-seven intraocular specimens - 17 aqueous humor (AH) and 40 vitreous fluid (VF) - from 55 patients with clinically diagnosed infectious endophthalmitis and 25 control intraocular specimens from non-infectious ocular disorders (10 AH and 15 VF) were evaluated by microscopy, culture and PCR-DNA probe hybridization to detect the Gram reaction of the bacterium. RESULTS: PCR-DNA probe hybridization was specific and sensitive to detect 30 fg of both gram-positive and gram-negative bacterial DNA. None of the controls showed bacteria by microscopy, culture or PCR. Of the 57 intraocular specimens, conventional microbiological methods could detect a bacterial aetiology in 32 (56.1%), while PCR-DNA probe hybridization could detect 52 (91.2%) specimens. This difference was statistically significant (P= 0.003). In bacteriologically positive specimens, there was absolute correlation of the Gram reaction between the results of smear and culture methods and PCR-DNA probe hybridization. Of the 25 bacteriologically negative specimens, 20 (80%) were positive by PCR-DNA probe hybridization, of which seven (35%) were gram-positive, 12 (60%) gram-negative and one (5%) positive by both. Results of PCR on AH and VF were not significantly different. CONCLUSION: PCR and DNA probe hybridization to determine the Gram reaction of the bacterium in intraocular fluids is a specific and sensitive method in the diagnosis of bacterial endophthalmitis. AH is an ideal specimen for PCR, since its collection is a simple and safe office procedure. Copyright 2000 The British Infection Society.
机译:目的:评估聚合酶链反应(PCR)与DNA探针杂交技术,以确定感染性眼内炎患者眼内标本中细菌的革兰氏反应。方法:评估了55例眼内标本-17房水(AH)和40眼玻璃体液(VF)-评估了55例临床诊断为感染性眼内炎的患者和25例非感染性眼部疾病的对照眼内标本(10 AH和15 VF)通过显微镜,培养和PCR-DNA探针杂交来检测细菌的革兰氏反应。结果:PCR-DNA探针杂交具有特异性和灵敏性,可检测30 fg革兰氏阳性和革兰氏阴性细菌DNA。对照都没有通过显微镜,培养或PCR显示细菌。在57个眼内标本中,传统的微生物学方法可以检测32个(56.1%)的细菌病因,而PCR-DNA探针杂交可以检测52个(91.2%)的标本。这种差异具有统计学意义(P = 0.003)。在细菌学阳性标本中,涂片和培养方法与PCR-DNA探针杂交结果之间的革兰氏反应具有绝对的相关性。在25个细菌学阴性样本中,通过PCR-DNA探针杂交呈阳性的有20个(80%),其中革兰氏阳性的有7个(35%),革兰氏阴性的有12个(60%),革兰氏阴性的一个(5%) 。 AH和VF的PCR结果没有显着差异。结论:PCR和DNA探针杂交测定眼内液中细菌的革兰氏反应是诊断细菌性眼内炎的一种特异性和灵敏的方法。 AH是PCR的理想标本,因为它的收集是一种简单且安全的办公程序。版权所有2000英国感染学会。

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