Ramirez J A, Ahkee S, Tolentino A, Miller R D, Summersgill J T
Department of Medicine, University of Louisville, School of Medicine, KY, USA.
Diagn Microbiol Infect Dis. 1996 Jan;24(1):7-14. doi: 10.1016/0732-8893(95)00254-5.
Diagnosis of Mycoplasma pneumoniae and Chlamydia pneumoniae lower respiratory infections using DNA amplification by polymerase chain reaction (PCR) on throat swab specimens has been reported. In this study we determined the sensitivity of the detection of Legionella pneumophila in simulated throat swab specimens by PCR. Next, we compared the sensitivity and specificity of a single throat swab PCR with the current tests for diagnosis of Legionella spp., M. pneumoniae, and C. pneumoniae in patients with lower respiratory tract infections. Patients' work-up included: (a) throat swab specimen for Legionella spp., M. pneumoniae, and C. pneumoniae PCR; (b) throat swab specimen for C. pneumoniae culture; (c) sputum specimen for L. pneumophila direct fluorescent antibody and culture; (d) urine specimen for L. pneumophila serogroup 1 antigen detection; and (e) serum specimen for L. pneumophila, M. pneumoniae, and C. pneumoniae acute and convalescent antibody titers. A total of 155 patients with lower respiratory infection were enrolled in this prospective study. Throat swab PCR was positive for Legionella spp. in five of the six patients with legionellosis, indicating the presence of this organism in the oropharynx of patients with Legionnaires disease. Mycoplasma pneumoniae PCR was positive in eight of the nine patients with mycoplasma infection. Chlamydia pneumoniae PCR was positive in the two patients with C. pneumoniae infection. None of the other 138 patients with negative PCR had other positive confirmatory tests for respiratory infection by these three organisms (100% specificity). PCR was able to detect 15 of the 17 infected (88.2%). Results of this investigation indicate that PCR on a single throat swab specimen is a rapid, sensitive, and specific test that may greatly simplify the diagnosis of lower respiratory infection caused by Legionella spp., Mycoplasma pneumoniae, or C. pneumoniae.
已有报道称,通过聚合酶链反应(PCR)对咽拭子标本进行DNA扩增来诊断肺炎支原体和肺炎衣原体引起的下呼吸道感染。在本研究中,我们通过PCR测定了模拟咽拭子标本中嗜肺军团菌的检测灵敏度。接下来,我们比较了单份咽拭子PCR与目前用于诊断下呼吸道感染患者中军团菌属、肺炎支原体和肺炎衣原体的检测方法的灵敏度和特异性。患者的检查包括:(a)用于军团菌属、肺炎支原体和肺炎衣原体PCR的咽拭子标本;(b)用于肺炎衣原体培养的咽拭子标本;(c)用于嗜肺军团菌直接荧光抗体和培养的痰标本;(d)用于嗜肺军团菌血清群1抗原检测的尿液标本;以及(e)用于嗜肺军团菌、肺炎支原体和肺炎衣原体急性期和恢复期抗体滴度检测的血清标本。共有155名下呼吸道感染患者纳入了这项前瞻性研究。在6例军团菌病患者中的5例中,咽拭子PCR检测军团菌属呈阳性,表明军团菌病患者的口咽部存在该病原体。9例支原体感染患者中的8例肺炎支原体PCR检测呈阳性。2例肺炎衣原体感染患者的肺炎衣原体PCR检测呈阳性。其他138例PCR检测阴性的患者均未通过这三种病原体的其他阳性确诊试验(特异性为100%)。PCR能够检测出17例感染者中的15例(88.2%)。本调查结果表明,单份咽拭子标本的PCR是一种快速、灵敏且特异的检测方法,可极大地简化由军团菌属、肺炎支原体或肺炎衣原体引起的下呼吸道感染的诊断。