Julia Robbins August 11, 2009. Objectives Clinical Significance of MRSA in Healthcare Setting...
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Transcript of Julia Robbins August 11, 2009. Objectives Clinical Significance of MRSA in Healthcare Setting...
![Page 1: Julia Robbins August 11, 2009. Objectives Clinical Significance of MRSA in Healthcare Setting Principle of assay Assay Procedure Assay Perfomance.](https://reader030.fdocuments.net/reader030/viewer/2022032607/56649ed05503460f94bdf238/html5/thumbnails/1.jpg)
Julia RobbinsAugust 11, 2009
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Objectives
Clinical Significance of MRSA in Healthcare Setting
Principle of assay
Assay Procedure
Assay Perfomance
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BD GeneOhm™ MRSA assay is a qualitative in vitro diagnostic test for the direct detection of nasal colonization by methicillin-resistant Staphylococcus aureus (MRSA) to aid in the prevention and control of MRSA infections in healthcare settings.
This rapid (within two hours) test allows for faster detection of MRSA colonization compared to culture which requires 24 to 72 hours enabling swift implementation of appropriate intervention.
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The test performed on the SmartCycler®
instrument with a nasal swab specimen from
patients at risk for colonization, utilizes
polymerase chain reaction (PCR) for the
amplification of MRSA DNA and fluorogenic
target-specific hybridization probes for the
detection of the amplified DNA.
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Following glass bead lysis, amplification of
the target, a gene sequence near the
insertion site of Staphylococcal Cassette
Chromosome mec (SCCmec) that is unique to
the methicillin-resistant strain of Staph
aureus DNA, will occur.
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Amplification of the internal control (IC), a
DNA fragment of 335-bp including a 277-bp
sequence not found in MRSA, will also take
place unless there are PCR inhibitory
substances present.
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The amplified DNA targets are
detected with molecular beacons,
hairpin-forming single-stranded
oligonucleotides labeled at one end
with a quencher and at the other end
with a fluorescent reporter dye
(fluorophore).
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For the detection of MRSA amplicons, the
molecular beacon contains the
fluorophore FAM at the 5’ end and the
non-fluorescent quencher moiety
DABCYL at the opposite end of the
oligonucleotide.
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For the detection of MRSA
amplicons, the molecular beacon
contains the fluorophore FAM at the
5’ end and the non-fluorescent
quencher moiety DABCYL at the
opposite end of the oligonucleotide.
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For the detection of the IC (internal
control) amplicons, the molecular
beacon contains the fluorophore TET at
the 5’ end and the quencher DABCYL at
the 3’ end.
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Each beacon-target hybrid fluoresces
at a wavelength characteristic of the
fluorophore used in the particular
molecular beacon. The amount of
fluorescence at any given cycle, or
following cycling, depends on the
amount of specific amplicons present
at that time.
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The SmartCycler simultaneously
monitors the fluorescence emitted by
each beacon, interprets all data and at
the end of the cycling program
provides a final result.
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Specimen Preparation/Concentration
Place swab in sample buffer tube Break swabVortex at high speedTransfer cell suspension to a lysis tubeCentrifuge at a minimum of 14,000 x g at
room temperature Discard supernatantAdd sample buffer to the lysis tube
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Lysis –DNA Extraction
Vortex, centrifuge briefly, then heat to inactivate potential inhibitors
Place lysis tube on a cooling block
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Reconstitution of Molecular Reagents
Reconstitute 1 master mix for up to 6 specimens and 2 controls
Add diluent to lyophilized master mix and transfer master mix to the reservoir of each reaction tube
Transfer lysate solution to the specimen reaction tube
Add control DNA to positive control tubeAdd sample buffer to negative control tubeCentrifuge all tubes brieflyPlace tubes on specially adapted cooling block until
ready to load
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Real-Time PCR Analysis
Insert each reaction tube into the instrument
Start run and obtain results in approximately 1 hour
No interpretation required
Internal control monitors inhibition
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Example of Test Results
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Assay PerformanceSensitivity: 93%
Specificity: 96%
Negative Predictive Value: 98%
Positive Predictive Value: 85%