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多重聚合酶链反应用于同时检测中耳积液中四种细菌的应用。

Use of multiplex PCR for simultaneous detection of four bacterial species in middle ear effusions.

作者信息

Hendolin P H, Markkanen A, Ylikoski J, Wahlfors J J

机构信息

AIV-Institute, University of Kuopio, Finland.

出版信息

J Clin Microbiol. 1997 Nov;35(11):2854-8. doi: 10.1128/jcm.35.11.2854-2858.1997.

Abstract

A multiplex PCR procedure was developed for the simultaneous detection of Alloiococcus otitidis, Haemophilus influenzae, Moraxella catarrhalis, and Streptococcus pneumoniae in middle ear effusions (MEEs) from patients with chronic otitis media with effusion. The bacterial 16S rRNA gene was chosen as the target, and the procedure used one common lower primer and four species-specific upper primers. The reaction was optimized by changing the primer concentrations to yield equal amounts of amplification products. The specificity of the reaction was verified with various bacterial species found in the nasopharynx. The performance of the procedure was examined with 25 MEE specimens, and the results were compared to those obtained by conventional culture methods. A detection level of 10 bacterial cells/reaction for each of the study organisms was achieved. By conventional culture methods, 8 (32%) of the specimens showed growth of one of the study organisms. In contrast, 21 (84%) of the specimens tested positive by the multiplex PCR. None of the culture-positive specimens were PCR negative, whereas three (12%) of the PCR-positive specimens tested positive for two of the four study organisms. Thus, the multiplex PCR method improves the detection rate significantly compared to that of the conventional culture method.

摘要

开发了一种多重PCR方法,用于同时检测来自慢性分泌性中耳炎患者中耳积液(MEE)中的耳炎差异球菌、流感嗜血杆菌、卡他莫拉菌和肺炎链球菌。选择细菌16S rRNA基因作为靶标,该方法使用一个通用的下游引物和四个物种特异性的上游引物。通过改变引物浓度优化反应,以产生等量的扩增产物。用在鼻咽部发现的各种细菌物种验证反应的特异性。用25份MEE标本检测该方法的性能,并将结果与通过传统培养方法获得的结果进行比较。对于每种研究生物体,实现了每个反应10个细菌细胞的检测水平。通过传统培养方法,8份(32%)标本显示出一种研究生物体的生长。相比之下,21份(84%)标本通过多重PCR检测呈阳性。所有培养阳性的标本均无PCR阴性,而3份(12%)PCR阳性标本对四种研究生物体中的两种检测呈阳性。因此,与传统培养方法相比,多重PCR方法显著提高了检测率。

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