Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/21533
Title: Detection of methicillin-resistant Staphylococcus aureus using a gold nanoparticle-based colourimetric polymerase chain reaction assay
Authors: Chan, WS
Tang, BSF
Boost, MV
Chow, C
Leung, PHM 
Keywords: Colorimetric assay
Gold nanoparticle
Methicillin-resistant Staphylococcus aureus
MRSA
PCR
Probe hybridization
Issue Date: 2014
Publisher: Elsevier
Source: Biosensors and bioelectronics, 2014, v. 53, p. 105-111 How to cite?
Journal: Biosensors and bioelectronics 
Abstract: 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 (κ=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.
URI: http://hdl.handle.net/10397/21533
ISSN: 0956-5663
EISSN: 1873-4235
DOI: 10.1016/j.bios.2013.09.027
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