Detection of methicillin-resistant Staphylococcus aureus using a gold nanoparticle-based colourimetric polymerase chain reaction assay

被引:38
作者
Chan, Wai-Sing [1 ]
Tang, Bone S. F. [1 ]
Boost, Maureen V. [2 ]
Chow, Chit [3 ]
Leung, Polly H. M. [2 ]
机构
[1] Hong Kong Sanat & Hosp, Dept Pathol, Hong Kong, Hong Kong, Peoples R China
[2] Hong Kong Polytech Univ, Dept Hlth Technol & Informat, Kowloon, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, Dept Anat & Cellular Pathol, Hong Kong, Hong Kong, Peoples R China
关键词
Methicillin-resistant Staphylococcus aureus; MRSA; Gold nanoparticle; Colorimetric assay; PCR; Probe hybridization; MYCOBACTERIUM-TUBERCULOSIS; GENOMIC DNA; ESCHERICHIA-COLI; IDENTIFICATION; MRSA; PCR;
D O I
10.1016/j.bios.2013.09.027
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
We report the use of gold nanoparticles (Au NPs) for direct colourimetric polymerase chain reaction (PCR) detection of methicillin-resistant Staphylococcus aureus (MRSA) in clinical specimens. The colourimetric assay comprised of 2 Au NP probes functionalized with Staphylococcus aureus 23S rRNA- and mecA-specific oligonucleotides. In this study, 72 clinical samples were tested, which included positive blood culture (n=23), urine (n=8), respiratory samples (n=23), as well as wound swabs, pus and body fluid (n=18). Results were recorded qualitatively by direct visual examination and quantitatively by UV-vis spectrophotometry. Using conventional bacterial culture as the gold standard, the sensitivity, specificity, positive predictive value and negative predictive value of this colourimetric assay were 97.14%, 91.89%, 91.89% and 97.14%, respectively, which were comparable to that of commercial real-time PCR assays with a lower cost per reaction. Our assay also showed good agreement with bacterial culture (K=0.889). The overall detection limit was 500 ng target amplicon, which was comparable to or better than other similar Au NP biosensors. Interestingly, our data revealed the possible relationship between Au NP probe-target hybridization site and assay performance, which might provide hints for design of the Au NP biosensors for nucleic acid detection. To conclude, our study was the first report on the use of Au NP colourimetric assay for direct detection of MRSA in various types of clinical specimens. Further evaluation of the assay is needed in large-scale trials which can also allow for some modifications to streamline the procedures for routine use. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:105 / 111
页数:7
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