Multiplex PCR for the simultaneous detection of Chlamydia pneumoniae, Mycoplasma pneumoniae and Legionella pneumophila in community-acquired pneumonia

被引:35
|
作者
Miyashita, N
Saito, A
Kohno, S
Yamaguchi, K
Watanabe, A
Oda, H
Kazuyama, Y
Matsushima, T
机构
[1] Kawasaki Med Sch, Dept Internal Med, Div Resp Dis, Kurashiki, Okayama 7010192, Japan
[2] Univ Ryukyus, Fac Med, Dept Internal Med 1, Okinawa 9030215, Japan
[3] Nagasaki Univ, Sch Med, Dept Internal Med 2, Nagasaki 8528523, Japan
[4] Toho Univ, Sch Med, Dept Microbiol, Tokyo 1438540, Japan
[5] Tohoku Univ, Inst Dev Aging & Canc, Dept Resp Med, Div Canc Control, Sendai, Miyagi 9808575, Japan
[6] Kagoshima Univ, Fac Med, Dept Bacteriol, Kagoshima 8908520, Japan
[7] Kitasato Otsuka Biomed Assay Lab, Kanagawa 2288555, Japan
关键词
multiplex PCR; Chlamydia pneumoniae; Mycoplasma pneumoniae; Legionella pneumophila; community-acquired pneumonia;
D O I
10.1016/j.rmed.2003.11.012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A multiplex polymerase chain reaction (PCR) was developed for the simultaneous detection of Chlamydia pneumoniae, Mycoplasma pneumoniae and Legionella pneumophila. Oligonucleotide primers for the amplification of the DNA of these three organisms were optimized for use in combination in the same reaction. PCR products were detected by the Micro-Chip Electrophoresis Analysis System. Clinical samples were obtained from 208 community-acquired pneumonia (CAP) patients who were participants in a multicenter CAP surveillance study performed at seven medical schools and their affiliate hospitals in Japan. No significant differences in the sensitivity of each primer set were observed when tested in both the multiplex and monoplex PCR assays. Our multiplex PCR was able to reliably detect 10 copies/100 mul of each of the three pathogen DNAs. Of the panel of 208 samples, 14 of 15 C. pneumoniae, 10 of 10 M. pneumoniae, eight of eight L. pneumophila and 165 of 176 negative samples were correctly identified. Eleven cases who were the multiplex PCR positive and conventional method negative were observed. The PCR findings were of possible significance in at least four of these patients. Our multiplex PCR assay could potentially be used as a diagnostic and epidemiological tool. Further prospective studies are needed to establish its clinical usefulness. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:542 / 550
页数:9
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