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用于检测人脑脊液中脑膜炎奈瑟菌的直接聚合酶链反应检测法。

Direct PCR assay for detection of Neisseria meningitidis in human cerebrospinal fluid.

作者信息

Abdel-Salam H A

机构信息

Department of Microbiology, Faculty of Pharmacy, Zagazig University, Egypt.

出版信息

Folia Microbiol (Praha). 1999;44(6):689-94. doi: 10.1007/BF02825663.

Abstract

A PCR amplification was performed to detect Neisseria meningitidis insertion sequence 1106 (IS-1106) in the human CerebroSpinal Fluid (CSF) in cases of meningitis. The study included 27 CSF samples from suspected meningitis patients. Although the inflammatory response in most of the samples was slightly increased, the results showed that 7 (26%) and 8 (30%) CSF samples were diagnosed as meningococcal meningitis by Gram staining and by culture, respectively. The primers of the IS-1106 were used for direct diagnosis of N. meningitidis in the human spinal fluid after a minor treatment of the CSF samples. The sample was diagnosed as meningococcal meningitis, if a DNA band of about 600 bp was detected in the ethidium bromide-stained agarose gel. The 27 CSF samples were analyzed in a random manner. Of these, 18 samples including the Gram staining- and culture-positive samples were also positive in PCR amplification. However, a CSF sample, which was diagnosed to be meningococcal meningitis in culture was negative in both Gram staining and PCR analysis. The specificity of the IS-1106 primers was determined to be 95%, with 100% sensitivity in comparison to Gram staining and culture. The primers were sensitive to 10 pg or more of meningococcal DNA. In addition, the PCR amplification showed high predictive values (89 and 100%) in diagnosing meningitis in patients that were negative and positive responders when tested by culture and by Gram staining. In conclusion, the PCR amplification of IS-1106 of N. meningitidis is specific and sensitive to both culture-positive and -negative meningococcal meningitis. Hence, PCR assay is highly recommended for use in a rapid diagnosis of suspected meningitis patients.

摘要

进行聚合酶链反应(PCR)扩增以检测脑膜炎病例中人类脑脊液(CSF)中的脑膜炎奈瑟菌插入序列1106(IS-1106)。该研究纳入了27份疑似脑膜炎患者的脑脊液样本。尽管大多数样本中的炎症反应略有增加,但结果显示,分别通过革兰氏染色和培养,有7份(26%)和8份(30%)脑脊液样本被诊断为脑膜炎球菌性脑膜炎。在对脑脊液样本进行轻微处理后,使用IS-1106引物直接诊断人类脑脊液中的脑膜炎奈瑟菌。如果在溴化乙锭染色的琼脂糖凝胶中检测到约600 bp的DNA条带,则该样本被诊断为脑膜炎球菌性脑膜炎。对27份脑脊液样本进行了随机分析。其中,包括革兰氏染色和培养阳性样本在内的18份样本在PCR扩增中也呈阳性。然而,一份在培养中被诊断为脑膜炎球菌性脑膜炎的脑脊液样本在革兰氏染色和PCR分析中均为阴性。与革兰氏染色和培养相比,IS-1106引物的特异性为95%,敏感性为100%。这些引物对10 pg或更多的脑膜炎球菌DNA敏感。此外,PCR扩增在诊断培养和革兰氏染色检测为阴性和阳性反应者的患者脑膜炎时显示出较高的预测价值(89%和100%)。总之,脑膜炎奈瑟菌IS-1106的PCR扩增对培养阳性和阴性的脑膜炎球菌性脑膜炎均具有特异性和敏感性。因此,强烈推荐使用PCR检测法对疑似脑膜炎患者进行快速诊断。

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