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Multiplex qPCR: Assay evaluation & minor troubleshooting By: R.A. Hamidjaja RIVM/Cib/LZO/RBC
Why multiplex qPCR? ,[object Object],[object Object],[object Object],[object Object],[object Object]
Work flow ,[object Object],[object Object],[object Object],[object Object],[object Object]
PCR (Polymerase chain reaction) dATP dTTP dCTP dGTP DNA Taq DNA polymerase Deoxyribonucleotide triphosphate Primers (Forward & reverse) Temperature: 95  o C = denaturing 55  o C = annealing 72  o C = elongation + 1 cycle ATCGGCTA TAGCCGAT 5’ 5’ 3’ 3’
PCR contd. 95  o C 72  o C 55  o C T: ATCGGCTA 5’ 3’ TAGCCGAT 5’ 3’ TAGCCGAT 5’ 3’ TAGCCGAT 5’ 3’ ATCGGCTA 5’ 3’ ATCGGCTA 5’ 3’ dATP TAGCCGAT 5’ 3’
qPCR (quantitative PCR) dATP dTTP dCTP dGTP DNA Taq DNA polymerase Deoxyribonucleotide triphosphate Primers (Forward & reverse) + Fluorescentlabeled probe ATCGGCTA TAGCCGAT 5’ 5’ 3’ 3’
qPCR contd. 95  o C 72  o C 55  o C T: ATCGGCTA 5’ 3’ TAGCCGAT 5’ 3’ dATP TAGCCGAT 5’ 3’ TAGCCGAT 5’ 3’ TAGCCGAT 5’ 3’ Detector
Multiplex qPCR dATP dTTP dCTP dGTP DNA Taq DNA polymerase Deoxyribonucleotide triphosphate Primers (Forward & reverse) + Fluorescent labeled probes ATCGGCTA TAGCCGAT 5’ 5’ 3’ 3’
Fluorescent label / Dye (1) Absorption of blue light Emission of red light [A] [E] 610 nm detector
Fluorescent label / Dye (2) [E] 610 nm 570 nm 530 nm
Fluorescent label / Dye (2) [E] 610 nm 570 nm 530 nm Spectral overlap
Spectral overlap ,[object Object],[object Object],[object Object],Before compensation After compensation
Data output ,[object Object],[object Object],[object Object]
Amplification curve
Cp calculations ,[object Object],[object Object],[object Object],[object Object],[object Object]
Amplification curve Cp=16 Cp=23
Problem discovery (1) ,[object Object],[object Object],[object Object],[object Object],[object Object]
Problem discovery (2) ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Amplification curve
Amplification curve
Case #1 Exp: Apr 2008 Exp: Sep 2008
Troubleshoot #1 Problem: New batch of probe is not good Apr 2008 Sep 2008 Okt 2008
Case #2 Channel 670 nm Before CC After CC
Troubleshoot #2 Non optimal dyes/label combination caused non optimal color compensation. Other possibilities: Non optimal probes concentrations Texas Red overlap CFR 590 overlap
Single  vs  Multiplex (incl. CC)
Detection limit Extraction kit limit: 25 mg tissue (20 pathogens) Extraction: 1 g tissue (100 pathogens) PCR  detection limit : 1 pathogen in 5 ul of eluted DNA 100 ul eluted DNA: 20 pathogens 1 g meat sample: 800 pathogens PCR detects: 5 pathogens in 5 ul of eluted DNA 100 ul eluted DNA: 100 pathogens 1 g meat sample: Limit  100 pathogens

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Multiplex qPCR

  • 1. Multiplex qPCR: Assay evaluation & minor troubleshooting By: R.A. Hamidjaja RIVM/Cib/LZO/RBC
  • 2.
  • 3.
  • 4. PCR (Polymerase chain reaction) dATP dTTP dCTP dGTP DNA Taq DNA polymerase Deoxyribonucleotide triphosphate Primers (Forward & reverse) Temperature: 95 o C = denaturing 55 o C = annealing 72 o C = elongation + 1 cycle ATCGGCTA TAGCCGAT 5’ 5’ 3’ 3’
  • 5. PCR contd. 95 o C 72 o C 55 o C T: ATCGGCTA 5’ 3’ TAGCCGAT 5’ 3’ TAGCCGAT 5’ 3’ TAGCCGAT 5’ 3’ ATCGGCTA 5’ 3’ ATCGGCTA 5’ 3’ dATP TAGCCGAT 5’ 3’
  • 6. qPCR (quantitative PCR) dATP dTTP dCTP dGTP DNA Taq DNA polymerase Deoxyribonucleotide triphosphate Primers (Forward & reverse) + Fluorescentlabeled probe ATCGGCTA TAGCCGAT 5’ 5’ 3’ 3’
  • 7. qPCR contd. 95 o C 72 o C 55 o C T: ATCGGCTA 5’ 3’ TAGCCGAT 5’ 3’ dATP TAGCCGAT 5’ 3’ TAGCCGAT 5’ 3’ TAGCCGAT 5’ 3’ Detector
  • 8. Multiplex qPCR dATP dTTP dCTP dGTP DNA Taq DNA polymerase Deoxyribonucleotide triphosphate Primers (Forward & reverse) + Fluorescent labeled probes ATCGGCTA TAGCCGAT 5’ 5’ 3’ 3’
  • 9. Fluorescent label / Dye (1) Absorption of blue light Emission of red light [A] [E] 610 nm detector
  • 10. Fluorescent label / Dye (2) [E] 610 nm 570 nm 530 nm
  • 11. Fluorescent label / Dye (2) [E] 610 nm 570 nm 530 nm Spectral overlap
  • 12.
  • 13.
  • 15.
  • 17.
  • 18.
  • 21. Case #1 Exp: Apr 2008 Exp: Sep 2008
  • 22. Troubleshoot #1 Problem: New batch of probe is not good Apr 2008 Sep 2008 Okt 2008
  • 23. Case #2 Channel 670 nm Before CC After CC
  • 24. Troubleshoot #2 Non optimal dyes/label combination caused non optimal color compensation. Other possibilities: Non optimal probes concentrations Texas Red overlap CFR 590 overlap
  • 25. Single vs Multiplex (incl. CC)
  • 26. Detection limit Extraction kit limit: 25 mg tissue (20 pathogens) Extraction: 1 g tissue (100 pathogens) PCR detection limit : 1 pathogen in 5 ul of eluted DNA 100 ul eluted DNA: 20 pathogens 1 g meat sample: 800 pathogens PCR detects: 5 pathogens in 5 ul of eluted DNA 100 ul eluted DNA: 100 pathogens 1 g meat sample: Limit 100 pathogens