Ursi D, Ieven M, Van Bever H P, Goossens H
Department of Microbiology, University Hospital Antwerp, Edegem, Belgium.
Mol Cell Probes. 1998 Aug;12(4):235-8. doi: 10.1006/mcpr.1998.0180.
For the detection of Chlamydia pneumoniae by polymerase chain reaction (PCR) in respiratory samples, an internal control was constructed to monitor the efficiency of amplification in each reaction. The internal control was designed in a way that the same primer pair can be used to amplify the internal control and target DNA. Nasopharyngeal aspirates of children suffering from asthma (> 2 years of age; 24 patients) or bronchiolitis (< 2 years of age; 47 patients) were analysed for the presence of C. pneumoniae, using the internal control in each amplification reaction. Two specimens from asthma patients, both children of 8 years old, were positive for C. pneumoniae. The number of cases studied is too small to draw conclusions regarding the incidence of C. pneumoniae in different age categories in children.
为了通过聚合酶链反应(PCR)检测呼吸道样本中的肺炎衣原体,构建了一个内部对照来监测每个反应中的扩增效率。内部对照的设计方式是,同一对引物可用于扩增内部对照和靶DNA。利用每个扩增反应中的内部对照,分析了患有哮喘(>2岁;24例患者)或细支气管炎(<2岁;47例患者)儿童的鼻咽抽吸物中肺炎衣原体的存在情况。来自哮喘患者的两份标本,均为8岁儿童,肺炎衣原体检测呈阳性。所研究的病例数量太少,无法就儿童不同年龄组中肺炎衣原体的发病率得出结论。