Wang Yajuan, Kong Fanrong, Yang Yonghong, Gilbert Gwendolyn L
Beijing Children's Hospital, Affiliated to Capital Medical University, Beijing, People's Republic of China.
Pediatr Pulmonol. 2008 Feb;43(2):150-9. doi: 10.1002/ppul.20749.
To develop and evaluate a novel method for simultaneous identification of 12 potential bacterial pathogens in children with community-acquired pneumonia.
A multiplex PCR-based reverse line blot (mPCR/RLB) assay was developed, to identify 12 respiratory bacterial pathogens, namely Staphylococcus aureus, Streptococcus pneumoniae, Streptococcus pyogenes, Moraxella catarrhalis, Haemophilus influenzae, Haemophilus influenzae type b, Bordetella pertussis, Klebsiella pneumoniae, Legionella pneumophila, Mycobacterium tuberculosis, Chlamydia pneumoniae, Mycoplasma pneumoniae, and single (uniplex) PCRs were used for S. pneumoniae and H. influenzae only. In a preliminary evaluation, we compared the results of mPCR/RLB with those of single (uniplex) PCRs and culture of nasopharyngeal aspirates (NPAs) from 100 children under 5 years, admitted to Beijing Children's Hospital between October 2004 and May 2005, with pneumonia.
Reference strains and clinical isolates of all 12 target species were correctly identified by mPCR/RLB. Potential pathogens were isolated from one blood culture and 26% of respiratory cultures. One or more pathogens were identified in 70% of respiratory specimens--by mPCR/RLB in 63%, uPCR only in another 3%, culture only in 2%, and culture plus uPCR in 2%. The species most commonly identified were S. pneumoniae (54%) and H. influenzae (38%, including type b, 4%). Cultures were not performed for B. pertussis, M. tuberculosis, C. pneumoniae or M. pneumoniae but each was identified by mPCR/RLB in between one and four specimens. Two or more potential pathogens were identified in 35% of specimens. Ten of 14 S. pneumoniae isolates belonged to serotypes represented in the 11-valent pneumococcal conjugate vaccine.
The mPCR/RLB assay is a sensitive tool for identification of respiratory pathogens, including mixed infections and bacteria requiring special culture methods.
开发并评估一种同时鉴定社区获得性肺炎患儿12种潜在病原菌的新方法。
开发了一种基于多重PCR的反向线杂交(mPCR/RLB)检测法,以鉴定12种呼吸道病原菌,即金黄色葡萄球菌、肺炎链球菌、化脓性链球菌、卡他莫拉菌、流感嗜血杆菌、b型流感嗜血杆菌、百日咳博德特氏菌、肺炎克雷伯菌、嗜肺军团菌、结核分枝杆菌、肺炎衣原体、肺炎支原体,仅对肺炎链球菌和流感嗜血杆菌使用单一(单重)PCR。在初步评估中,我们将mPCR/RLB的结果与2004年10月至2005年5月间入住北京儿童医院的100名5岁以下肺炎患儿的单一(单重)PCR结果以及鼻咽抽吸物(NPA)培养结果进行了比较。
mPCR/RLB正确鉴定了所有12种目标菌种的参考菌株和临床分离株。从1份血培养和26%的呼吸道培养物中分离出潜在病原菌。在70%的呼吸道标本中鉴定出一种或多种病原菌——mPCR/RLB鉴定出63%,仅单重PCR鉴定出另外3%,仅培养鉴定出2%,培养加单重PCR鉴定出2%。最常鉴定出的菌种是肺炎链球菌(54%)和流感嗜血杆菌(38%,包括b型,4%)。未对百日咳博德特氏菌、结核分枝杆菌、肺炎衣原体或肺炎支原体进行培养,但每种菌在1至4份标本中通过mPCR/RLB被鉴定出来。35%的标本中鉴定出两种或更多潜在病原菌。14株肺炎链球菌分离株中有10株属于11价肺炎球菌结合疫苗中包含的血清型。
mPCR/RLB检测法是鉴定呼吸道病原菌的敏感工具,包括混合感染和需要特殊培养方法的细菌。