Bakaletz L O, White G J, Post J C, Ehrlich G D
Department of Otolaryngology, College of Medicine, The Ohio State University, Columbus 43210-1282, USA.
Clin Diagn Lab Immunol. 1998 Mar;5(2):219-24. doi: 10.1128/CDLI.5.2.219-224.1998.
Multiplex PCR analyses for both bacterial and viral pathogens were conducted in a blinded manner on 33 archival specimens, of known culture status, procured from chinchilla models of both single- and mixed-pathogen-induced otitis media and from a pediatric patient. These specimens had been maintained at -70 degrees C for up to 6 years. Experimental specimens evaluated included middle-ear effusions, nasopharyngeal lavage fluids and middle-ear lavage fluids from animals which were immunologically naive, sham-immunized or actively immunized with nontypeable Haemophilus influenzae antigens. Sampling times used ranged from the day of bacterial or viral challenge to 42 days after challenge. Initial PCR analyses of the 33 specimens matched the traditional culture data in 24 instances (73%), correctly identifying nontypeable H. influenzae, Moraxella catarrhalis, Streptococcus pneumoniae, or adenovirus as the causative agent. A PCR-positive signal for the microbe(s) inoculated was also obtained in four animal model specimens (12%) which were culture negative. One of two culture-negative human effusions was also PCR positive. Thus, overall, results obtained by blinded PCR were 85% concordant with traditional culture methods or correctly indicated the specific pathogen introduced in four specimens that were sterile. In no instance was a false-positive signal obtained for any of the five etiologic agents being evaluated. We conclude that the multiplex PCR analyses are rapid and accurate methodologies when they are used to retrospectively evaluate diverse archival specimens of limited volume from experimental models of otitis media.
对33份已知培养状态的存档标本进行了细菌和病毒病原体的多重PCR分析,这些标本取自单病原体和混合病原体诱导的中耳炎的栗鼠模型以及一名儿科患者。这些标本在-70摄氏度下保存了长达6年。评估的实验标本包括来自免疫未致敏、假免疫或用不可分型流感嗜血杆菌抗原主动免疫的动物的中耳积液、鼻咽灌洗液和中耳灌洗液。采样时间从细菌或病毒攻击当天到攻击后42天不等。对33份标本的初步PCR分析在24例(73%)中与传统培养数据相符,正确鉴定出不可分型流感嗜血杆菌、卡他莫拉菌、肺炎链球菌或腺病毒为病原体。在4份培养阴性的动物模型标本(12%)中也获得了接种微生物的PCR阳性信号。两份培养阴性的人类积液中有一份PCR也呈阳性。因此,总体而言,盲法PCR获得的结果与传统培养方法的一致性为85%,或者正确地指出了4份无菌标本中引入的特定病原体。在评估的5种病原体中,没有出现任何假阳性信号。我们得出结论,当多重PCR分析用于回顾性评估来自中耳炎实验模型的有限体积的各种存档标本时,它是快速且准确的方法。