Triplex real-time polymerase chain reaction assay for simultaneous detection of Staphylococcus aureus and coagulase-negative staphylococci and determination of methicillin resistance directly from positive blood culture bottles

被引:48
作者
Kilic, Abdullah [1 ,2 ]
Muldrew, Kenneth L. [3 ]
Tang, Yi-Wei [4 ]
Basustaoglu, A. Celal [1 ,2 ]
机构
[1] Gulhane Mil Med Acad, Dept Microbiol & Clin Microbiol, TR-06018 Ankara, Turkey
[2] Sch Med, TR-06018 Ankara, Turkey
[3] Univ N Carolina, Mol Genet Lab, Chapel Hill Hosp, Chapel Hill, NC 27514 USA
[4] Vanderbilt Univ, Med Ctr, Mol Infect Dis Lab, Nashville, TN 37232 USA
关键词
MRSA; MSSA; MSCoNS; MRCoNS; Triplex PCR; FRAGMENT-LENGTH-POLYMORPHISM; IN-SITU HYBRIDIZATION; 16S RIBOSOMAL-RNA; RAPID DETECTION; PCR ASSAY; DIRECT IDENTIFICATION; FLUORESCENCE PCR; CLINICAL-SAMPLES; MECA GENE; TUF GENE;
D O I
10.1016/j.diagmicrobio.2009.11.010
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
We describe here a 1-step, triplex real-time polymerase chain reaction (PCR) assay for the detection and identification of staphylococci directly from signal-positive blood culture bottles containing Gram-positive cocci in clusters (GPCC). The triplex assay targeted and detected tuf, nuc, and mecA genes in a single tube and had a detection limit of 10(5) CFU/mL for each gene target. A total of 341 GPCC-positive blood culture bottles were collected between November 12, 2008, and August 11, 2009. Among them, 230 methicillin-resistant coagulase-negative staphylococci (CoNS), 54 methicillin-susceptible CoNS, 22 methicillin-resistant Staphylococcus aureus, 22 methicillin-susceptible S. aureus, and 13 nonstaphylococci species were identified by conventional methods. The results obtained by triplex assay were in agreement with those of conventional methods for tuf (99.7%), nuc (100.0%), and mecA (99.1%), respectively. The triplex assay was found to have sensitivities of 99.7%, 100%, and 99.2% and specificities of 100%, 100%, and 98.7%, respectively, for the tuf, nuc, and mecA gene targets. The triplex real-time PCR assay accurately detects and identifies staphylococci directly from positive blood cultures without nucleic acid extraction prior to amplification. (C) 2010 Elsevier Inc. All rights reserved.
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页码:349 / 355
页数:7
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