The Application of Real-Time PCR in the Diagnosis of ...trishul.sci.gu.edu.au/courses/2711bbs/lecture_13.pdf · in the Diagnosis of Infectious Disease ... • Taq DNA polymerase has

The Application of Real-Time PCR

in the Diagnosis of Infectious Disease

The Application of Real-Time PCR

in the Diagnosis of Infectious Disease

T.P.Sloots Clinical Virology Research Unit, RCH, & Microbiology, QHPS.

Why should we use PCR?Why should we use PCR?

• Very sensitive (1 copy – 10 copies of DNA)

• Can detect organisms that cannot be isolated

• Rapid (TAT = < 24 hrs)

• Very sensitive (1 copy – 10 copies of DNA)

• Can detect organisms that cannot be isolated

• Rapid (TAT = < 24 hrs)

Disadvantages of PCRDisadvantages of PCR

• Technically demanding

• Can be expensive

• Risk of contamination

• Need rigid QC

• Technically demanding

• Can be expensive

• Risk of contamination

• Need rigid QC

PCRPCRPCRPCR

real-timereal-time real-timerealreal--timetime

integrated systemamplifies & detects

constant monitoringfluorescent probes

rapid cycling times

quantitative

low contamination risk

assay design

PCRPCR

fast turn-around

sealed system

• Microtitre plate format, sealed system• Processes 96 samples in 2½ hours• Real-time - amplification and detection • Quantitative results• Uses a fluorogenic probe, with reporter & quencher dyes• Taq DNA polymerase has 5’-3’ exonuclease activity

ABI 7700

real-timereal-time real-time

TaqManTaqManhardwarehardware

ABI Biosystems

real-timereal-timerealreal--timetime

TaqManTaqMan

real-time

Amplicon

FRET

Amplicon

Emission

EXTENSION

ANNEALING

Excitation

5’-3’ exonuclease

Reporter

Quencher

• Real-time detection

• Quantitative results • Hybridization probes• Can detect 2 targets simultaneously

• Uses capillaries (10-20ul)

• 32 samples / 60 minutes

• Sealed system – contamination free

• Real-time detection

• Quantitative results • Hybridization probes• Can detect 2 targets simultaneously

• Uses capillaries (10-20ul)

• 32 samples / 60 minutes

• Sealed system – contamination free


LightCyclerLightCyclerHardware


LightCyclerLightCyclerHardwareHardware

FRET (Fluorescence Resonance Energy Transfer)

using adjacent hybridization probes

FRET (Fluorescence Resonance Energy Transfer) FRET (Fluorescence Resonance Energy Transfer)

using adjacent hybridization probes using adjacent hybridization probes

FITC

Red 640

P Phosphate

FRET Emission

P

Excitation

Amplicon


LightCyclerLightCyclerFRETFRET

real-timereal-timereal-time

LightCyclerLightCyclerOperation

DenaturationDenaturation

95oC

FRET Emission

P

ExcitationTm

55oC

Primer/Probe AnnealingPrimer/Probe Annealing

FluorimeterReading

FluorimeterReading

72oC

Primer ExtensionPrimer Extension

• Detection of Infectious Disease agents

• Target Characterisation

• Determining Microbial Load (quantitation)

• Detection of Infectious Disease agents

• Target Characterisation

• Determining Microbial Load (quantitation)


LightCyclerLightCyclerApplications

Routine Use

HSV-1 & HSV-2JCV & BKVPneumocystis cariniiNeisseria meningitidisNeisseria gonorrhoeaVZVToxoplasma gondiiBordetella pertussis

Validation

Influenza ARSV

CMV (quantitative)

Under Development

Enterovirus (group)16S Bacterial rRNAFlu/RSV multiplex


LightCyclerLightCyclerApplications

62 (23%) were culture positive, confirmed by antigen detection with MoAb (27= HSV-1, 35= HSV-2).

113 (42%) were LC-PCR positive following extraction of VTM using a glass fibre column (Qiagen).

51 were LC-PCR positive and culture negative. All these were confirmed as HSV by sequencing.

1 culture + / PCR - specimen. Was negative by repeat culture, and remained negative by “in house” PCR using different primers


LightCyclerLightCyclerHSV PCR

266 swabs from multiple sites were collected in VTM for HSV culture.

Characterisation of HSV by melting curve Characterisation of HSV by melting curve

DNA pol

HSV

HSV-1

HSV-2

mismatch

Hybridisation probes (to HSV-1)

no mismatchAmplicon


LightCyclerLightCyclerApplication

Primers commonto HSV 1 & 2

HSV 2 HSV 1

Melting Curve Analysis

HSV 1

HSV 2

55oC

HSV 1

HSV 2

73oC

HSV 1

HSV 2

67oC

real-timereal-timereal-timerealreal--timetime

PCR quantitationPCR quantitation

Microbial load testingMicrobial load testing

• For commensal organisms determine a “normal” microbial load. Elevated level determines infection.

• Detect active infection by increasing load

• Detect anti-viral drug resistance (CMV, HSV)

0.5

1.5

2.5

0 10 20 30 40 50 60 70

Cycles

F2

/F1

NEG

10

100

1000

10000

100000

1000000



Threshold Cycle

Microbial Load Testing

0

10

20

30

40

50

1 2 3 4 5 6

Concentration log 10

Th

resh

old

Cycl

e

0.5

1.5

2.5

0 10 20 30 40 50 60 70

Cycles

F2

/F1

Test Sample

Threshold

Threshold Cycle

Threshold Cycle = 35Load = 103.8 copies/ml

PRACTICAL APPLICATIONPRACTICAL APPLICATION



Monitoring CMV disease in transplant patients, particularly Bone Marrow Transplant recipients.

1. Early detection of disease progression to apply appropriate drug therapy

2. Detect ganciclovir drug resistance

0

1000

2000

3000

4000

5000

6000

7000

8000

Sampling Time (Wks)

40

30

20

10

0

AntigenemiaPositive cells

per 200,000 cells


per 200,000 cells

geno

me

copi

es

q-PCR

1 2 3 4 5 6 7 8 9 10 11

Ganciclovir

BMT PATIENT 1BMT PATIENT 11 2 3 4 5 6 7 8 9 10 11

ROCHE PCR

“in house” PCR

Antigenemia


realreal--time PCRtime PCRViral LoadViral Load

0

1000

2000

3000

4000

5000

6000

7000

8000

q-PCR

1 2 3 4 5 6 7 8 9 10 11 12 13

80

60

40

20

0

Ganciclovir

Foscarnet

BMT PATIENT 2BMT PATIENT 2

Sampling Time (Wks)


per 200,000 cells


per 200,000 cells

geno

me

copi

es

1 2 3 4 5 6 7 8 9 10 11 12 13

ROCHE PCR

“in house” PCR

real-timereal-timerealreal--time PCRtime PCR

Viral LoadViral Load


SummarySummary

DISADVANTAGES OF REAL-TIME PCRDISADVANTAGES OF REAL-TIME PCR

Current technology has limited capacity for multiplexing. Simultaneous detection of 2 targets is the limit.

Development of protocols needs high level of technical skill and/or support. (Requires R&D capacity and capital)

High capital equipment costs ($ 50,000 -160,000).

ADVANTAGES OF REAL-TIME PCRADVANTAGES OF REAL-TIME PCR

Rapid cycling times (1 hour)High sample throughput (~200 samples/day)Low contamination risk (sealed reactions)Very sensitive (3pg or 1 genome eq of DNA)Broad dynamic range (10 - 1010 copies)Reproducible (CV < 2.0 %)Allows for quantitation of resultsSoftware driven operationNo more expensive than “in house” PCR ($15/test)


Summary Summary

PCR DetectionPCR Detection

• TaqMan and LC utilse probes

• Non-specific reactions with probe may occur

• Number of chromophors is limited

• Alternative detection technologies

- molecular beacons

- multiple arrays (gene chip)

Amplicon

molecular beaconsmolecular beacons

A

B

C

FRET

real-timereal-time real-timerealreal--timetime

Reporter

Non-fluorescent Quencher

Excitation

ANNEALING

Molecular BeaconsMolecular Beacons

APPLICATIONSAPPLICATIONS

• Detection of amplification products (real time, end-point)

• Multicolour beacons detect multiple targets (8)

• Better detection of single point mutation

• Drug resistance analysis

• Non-PCR hybridisation analysis (in situ labeling)

Multiple DNA ArraysMultiple DNA Arrays

Use of Multiple Arrays involves 5 steps

• Preparation of array containing capture probes

• Isolation, purification and labeling of test sample DNA

• Hybridisation of test sample DNA to capture array

• Detection of captured DNA hybrids

• Data analysis

The Application of Real-Time PCR in the Diagnosis of ...trishul.sci.gu.edu.au/courses/2711bbs/lecture_13.pdf · in the Diagnosis of Infectious Disease ... • Taq DNA polymerase has

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