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- Publisher Website: 10.1128/JCM.00488-13
- Scopus: eid_2-s2.0-84882786765
- PMID: 23784133
- WOS: WOS:000323214200010
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Article: Evaluation Of The Lightcycler Methicillin-resistant Staphylococcus Aureus (mrsa) Advanced Test For Detection Of Mrsa Nasal Colonication
Title | Evaluation Of The Lightcycler Methicillin-resistant Staphylococcus Aureus (mrsa) Advanced Test For Detection Of Mrsa Nasal Colonication |
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Authors | |
Issue Date | 2013 |
Publisher | American Society for Microbiology. The Journal's web site is located at http://jcm.asm.org/ |
Citation | Journal of Clinical Microbiology, 2013, v. 51 n. 9, p. 2869-2874 How to Cite? |
Abstract | 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 (bioMérieux) 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 (Tm) values (57.0 to 62.0°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 Tm values of 55°C, providing overall sensitivity and specificity values of 83.3% and 99%, respectively. Among isolates with Tm values of 55°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 Tm values of 55°C and not in those with typical Tm values. It is conceivable that those SNPs were located inside the target region of the proprietary hybridization probes, which resulted in a Tm 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. Copyright © 2013, American Society for Microbiology. All Rights Reserved. |
Persistent Identifier | http://hdl.handle.net/10722/191432 |
ISSN | 2023 Impact Factor: 6.1 2023 SCImago Journal Rankings: 1.653 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Yam, WC | - |
dc.contributor.author | Siu, GKH | - |
dc.contributor.author | Ho, PL | - |
dc.contributor.author | NG, TK | - |
dc.contributor.author | Que, TL | - |
dc.contributor.author | Yip, KT | - |
dc.contributor.author | FOK, CP | - |
dc.contributor.author | Chen, JHK | - |
dc.contributor.author | Cheng, VCC | - |
dc.contributor.author | Yuen, KY | - |
dc.date.accessioned | 2013-10-15T06:59:31Z | - |
dc.date.available | 2013-10-15T06:59:31Z | - |
dc.date.issued | 2013 | - |
dc.identifier.citation | Journal of Clinical Microbiology, 2013, v. 51 n. 9, p. 2869-2874 | - |
dc.identifier.issn | 0095-1137 | - |
dc.identifier.uri | http://hdl.handle.net/10722/191432 | - |
dc.description.abstract | 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 (bioMérieux) 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 (Tm) values (57.0 to 62.0°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 Tm values of 55°C, providing overall sensitivity and specificity values of 83.3% and 99%, respectively. Among isolates with Tm values of 55°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 Tm values of 55°C and not in those with typical Tm values. It is conceivable that those SNPs were located inside the target region of the proprietary hybridization probes, which resulted in a Tm 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. Copyright © 2013, American Society for Microbiology. All Rights Reserved. | - |
dc.language | eng | - |
dc.publisher | American Society for Microbiology. The Journal's web site is located at http://jcm.asm.org/ | - |
dc.relation.ispartof | Journal of Clinical Microbiology | - |
dc.rights | Journal of Clinical Microbiology. Copyright © American Society for Microbiology. | - |
dc.title | Evaluation Of The Lightcycler Methicillin-resistant Staphylococcus Aureus (mrsa) Advanced Test For Detection Of Mrsa Nasal Colonication | - |
dc.type | Article | - |
dc.identifier.email | Yam, WC: wcyam@hkucc.hku.hk | - |
dc.identifier.email | Siu, GKH: gilman06@hkucc.hku.hk | - |
dc.identifier.email | Ho, PL: plho@hkucc.hku.hk | - |
dc.identifier.email | Chen, JHK: jonchk@hku.hk | - |
dc.identifier.email | Cheng, VCC: vcccheng@hkucc.hku.hk | - |
dc.identifier.email | Yuen, KY: kyyuen@hkucc.hku.hk | - |
dc.identifier.authority | Yam, WC=rp00313 | - |
dc.identifier.authority | Ho, PL=rp00406 | - |
dc.identifier.authority | Yuen, KY=rp00366 | - |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1128/JCM.00488-13 | - |
dc.identifier.pmid | 23784133 | - |
dc.identifier.pmcid | PMC3754679 | - |
dc.identifier.scopus | eid_2-s2.0-84882786765 | - |
dc.identifier.hkuros | 225739 | - |
dc.identifier.volume | 51 | - |
dc.identifier.issue | 9 | - |
dc.identifier.spage | 2869 | - |
dc.identifier.epage | 2874 | - |
dc.identifier.isi | WOS:000323214200010 | - |
dc.publisher.place | United States | - |
dc.identifier.issnl | 0095-1137 | - |