Evaluation of the LightCycler Methicillin-Resistant Staphylococcus aureus (MRSA) Advanced Test for Detection of MRSA Nasal Colonization

被引:15
|
作者
Yam, W. C. [1 ]
Siu, Gilman K. H. [1 ]
Ho, P. L. [1 ]
Ng, T. K. [2 ]
Que, T. L. [3 ]
Yip, K. T. [3 ]
Fok, Cathie P. K. [3 ]
Chen, Jonathan H. K. [1 ]
Cheng, Vincent C. C. [1 ]
Yuen, K. Y. [1 ]
机构
[1] Univ Hong Kong, Li Ka Shing Fac Med, Dept Microbiol, Queen Mary Hosp, Hong Kong, Hong Kong, Peoples R China
[2] Princess Margaret Hosp, Dept Pathol, Hong Kong, Hong Kong, Peoples R China
[3] Tuen Mun Hosp, Dept Clin Pathol, Hong Kong, Hong Kong, Peoples R China
关键词
REAL-TIME PCR; COAGULASE-NEGATIVE STAPHYLOCOCCI; HONG-KONG; CLINICAL-SAMPLES; RAPID DETECTION; MOLECULAR EPIDEMIOLOGY; BLOOD CULTURES; ASSAY; IDENTIFICATION; INFECTIONS;
D O I
10.1128/JCM.00488-13
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Rapid detection of methicillin-resistant Staphylococcus aureus (MRSA) nasal colonization is crucial for the prevention and control of MRSA infections in health care settings. The LightCycler MRSA Advanced Test (Roche Diagnostics) is a commercially available real-time PCR assay for direct detection of MRSA nasal colonization by targeting of the staphylococcal cassette chromosome mec (SCCmec)-orfX junction. The diagnostic performance of the assay was compared with that of ChromID MRSA agar (bioMerieux) culture and an in-house duplex real-time PCR assay. Among 1,246 nasal swab specimens collected from 2 general hospitals in Hong Kong, 174 (14%) were considered true positive for MRSA. Chromogenic culture and the in-house real-time PCR assay identified 147 (84.5%) and 133 (76.4%) true-positive cases with specificities of 100% and 98.6%, respectively. Based on the target melting temperature (T-m) values (57.0 to 62.0 degrees C) defined by the manufacturer, the LightCycler MRSA Advanced Test identified only 85 (48.9%) true-positive specimens. Interestingly, an additional 60 (34.5%) true-positive specimens were detected despite atypical T-m values of 55 degrees C, providing overall sensitivity and specificity values of 83.3% and 99%, respectively. Among isolates with T-m values of 55 degrees C, most were typed as clonal complex 45 (CC45). By sequence analysis of the SCCmec-orfX junction, characteristic single-nucleotide polymorphisms (SNPs) were identified only in isolates with T-m values of 55 degrees C and not in those with typical T-m values. It is conceivable that those SNPs were located inside the target region of the proprietary hybridization probes, which resulted in a T-m shift in the melting curve analysis. Our study highlights the importance of a global evaluation of commercial kits so that the interpretation algorithm covers different lineages of MRSA clones prevalent in various geographical regions.
引用
收藏
页码:2869 / 2874
页数:6
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