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Real-time PCR detection of Mycoplasma pneumoniae in respiratory specimens
被引:23
|作者:
Schmitt, Bryan H.
[1
]
Sloan, Lynne M.
[1
]
Patel, Robin
[1
,2
]
机构:
[1] Mayo Clin, Div Clin Microbiol, Dept Lab Med & Pathol, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Med, Div Infect Dis, Rochester, MN 55905 USA
关键词:
Mycoplasma;
PCR;
pneumoniae;
DIAGNOSIS;
INFECTION;
ASSAYS;
D O I:
10.1016/j.diagmicrobio.2013.07.016
中图分类号:
R51 [传染病];
学科分类号:
100401 ;
摘要:
A real-time PCR assay targeting the phosphotransferase system I gene (ptsI) of Mycoplasma pneumoniae was compared to 2 commercially available PCR assays targeting the P1 cytadhesion gene (the LightMix (R) Kit Mycoplasma pneumoniae [TIB MOLBIOL, Adelphia, NJ, USA] and M. pneumoniae Analyte Specific Reagent [Focus Diagnostics, Cypress, CA, USA] assays) and to a PCR assay targeting the M. pneumoniae repetitive element, RepMP1. Thirty previously positive specimens including 15 throat swab, 10 bronchoalveolar lavage, and 5 sputum specimens, all tested positive with the ptsI and M. pneumoniae ASR assays. Among the previously positive specimens, 14/15 throat swab, 9/10 bronchoalveolar lavage, and 4/5 sputum specimens tested positive with the LightMix (R) Kit Mycoplasma pneumoniae assay and 13/15 throat swab, 10/10 bronchoalveolar lavage, and 4/5 sputum specimens tested positive with the RepMP1 assay. Forty previously negative clinical specimens tested negative using the ptsI assay. A PCR assay targeting M. pneumoniae ptsI performs equivalently to assays targeting the P1 cytadhesion gene or RepMP1. (C) 2013 Elsevier Inc. All rights reserved.
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页码:202 / 205
页数:4
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