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PACE 2C Genetic probe screening for C. Trachomatis & N. Gonorrhoeae in Endocervical and Male urethral specimens Heidi Philips and Michael S. Joseph.

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Presentation on theme: "PACE 2C Genetic probe screening for C. Trachomatis & N. Gonorrhoeae in Endocervical and Male urethral specimens Heidi Philips and Michael S. Joseph."— Presentation transcript:

1 PACE 2C Genetic probe screening for C. Trachomatis & N. Gonorrhoeae in Endocervical and Male urethral specimens Heidi Philips and Michael S. Joseph

2 Outline  Biological background on Chlamydia Trachomatis and Neisseria Gonorrhoeae  Flow chart  Biology of the PACE 2C  Assay Applications  Assay Components  Interpretation of the assay  Biological background on Chlamydia Trachomatis and Neisseria Gonorrhoeae  Flow chart  Biology of the PACE 2C  Assay Applications  Assay Components  Interpretation of the assay

3 Why test for this disease?  Gonorrhea in the US, nearly 392,200 cases  Public health measures requires surveillance by monitoring and screening as a preventative and allocation of public funds.  Gonorrhea in the US, nearly 392,200 cases  Public health measures requires surveillance by monitoring and screening as a preventative and allocation of public funds.

4 Background: Neisseria Gonorrhoeae  Gonorrhea is a very common sexually transmitted disease (STD).  The disease is caused by the gonococcus bacteria that can multiply and grow in moist, warm areas of the body.  In women, gonorrhea can infect the cervix (opening to the uterus, or womb), uterus, and fallopian tube.  It can also infect the urethra (urine canal) in men and women, as well as the mouth, throat, and rectum.  Gonorrhea can be treated and cured by antibiotics.  Gonorrhea is a very common sexually transmitted disease (STD).  The disease is caused by the gonococcus bacteria that can multiply and grow in moist, warm areas of the body.  In women, gonorrhea can infect the cervix (opening to the uterus, or womb), uterus, and fallopian tube.  It can also infect the urethra (urine canal) in men and women, as well as the mouth, throat, and rectum.  Gonorrhea can be treated and cured by antibiotics.

5 Background: Chlamydia Trachomatis  Chlamydia is caused by the bacterium Chlamydia trachomatis.  It persists at body sites that are inaccessible to phagocytes, T-cells, and B-cells.  Endemic trachoma leads to blindness, whereas inclusion conjunctivitis is associated with the sexually transmitted form and does not lead to blindness.  The surface of chlamydia does not contain proteins that are distinctive enough to induce a full immune response.  The organism is also extremely temperature sensitive and must be refrigerated at 4 C as soon as a sample is obtained.  Chlamydia is caused by the bacterium Chlamydia trachomatis.  It persists at body sites that are inaccessible to phagocytes, T-cells, and B-cells.  Endemic trachoma leads to blindness, whereas inclusion conjunctivitis is associated with the sexually transmitted form and does not lead to blindness.  The surface of chlamydia does not contain proteins that are distinctive enough to induce a full immune response.  The organism is also extremely temperature sensitive and must be refrigerated at 4 C as soon as a sample is obtained.

6 What is PACE 2C Assay?  Probe Activated Chemiluminescent Enhancement 2C  Direct Genetic probe  DNA-RNA hybridization  With Chemiluminescent probe  Acridinium ester  Direct assay with qualitative results  Probe Activated Chemiluminescent Enhancement 2C  Direct Genetic probe  DNA-RNA hybridization  With Chemiluminescent probe  Acridinium ester  Direct assay with qualitative results

7 Steps in PACE One swab, one tube, two test convince. 1.Sample Preparation 2.Hybridization -incubation 3.Separation -incubation -magnetic separation 4. Detection One swab, one tube, two test convince. 1.Sample Preparation 2.Hybridization -incubation 3.Separation -incubation -magnetic separation 4. Detection

8 Flow Chart Obtain Sample Reagent Preparation Sample Preparation Hybridization Separation Detection Reconstitute Primer - Samples must be obtained using the PACE Specimen Collection Kits. - All reagents aside from the probe reagent must reach room temperature prior to use. -The solid phase must be reconstituted in the selection reagent prior to use. - Sample must reach room temperature prior to use. -Temperature dependent - Incubation - Forceful wash - Incubation - Magnetic separation unit - Chemiluminescent probes - Leader Illuminometer

9 What makes it attractive  PACE 2C is a qualitative assay for both C. Trachomatis and N. Gonorrheae.  Detects rRNA of the bacteria  Initial screening  High specificity of DNA Probe  Enhanced by targeting rRNA, which is highly abundant w/o amplification  Free from false negative, due to amplification inhibition.  Hybridization protocol with addition of Chemiluminescent label detection.  PACE 2C is a qualitative assay for both C. Trachomatis and N. Gonorrheae.  Detects rRNA of the bacteria  Initial screening  High specificity of DNA Probe  Enhanced by targeting rRNA, which is highly abundant w/o amplification  Free from false negative, due to amplification inhibition.  Hybridization protocol with addition of Chemiluminescent label detection.

10 What makes it attractive cont.  Cost-effective, do not need amplification  Increased efficiency and lower costs by testing CT and GC from single specimen  Simple workflow  high tolerance for various specimen quality  Cost-effective, do not need amplification  Increased efficiency and lower costs by testing CT and GC from single specimen  Simple workflow  high tolerance for various specimen quality

11 Samples  Endocervical for female and male urethral swab specimens collected with the Gen-Probe PACE Specimen Collection Kits

12 Samples cont.  The kit consists of single tube assay  There is no transfer sample from collection container to assay tube.  Avoiding transportation of sample  But once in the specimen collection kit,it can last for 7 days.  The kit consists of single tube assay  There is no transfer sample from collection container to assay tube.  Avoiding transportation of sample  But once in the specimen collection kit,it can last for 7 days.

13 Additional Products & Reagents  GEN-PROBE® PACE Specimen Collection Kits  GEN-PROBE® Detection Reagent Kit  GEN-PROBE® Leader® Luminometer  GEN-PROBE® Magnetic Separation Unit  Vortex Mixer  Covered water bath (60°±1° C)  Micropipettes (100 µL)  Pipettes capable of delivering 1-25 mL  Absorbent paper  GEN-PROBE® PACE Specimen Collection Kits  GEN-PROBE® Detection Reagent Kit  GEN-PROBE® Leader® Luminometer  GEN-PROBE® Magnetic Separation Unit  Vortex Mixer  Covered water bath (60°±1° C)  Micropipettes (100 µL)  Pipettes capable of delivering 1-25 mL  Absorbent paper

14 Economics of the PACE 2C  Luminometer $29,550  Separation Unit $450  PACE 2A kit $1000  100 test per kit  Specimen Collection Kit $500  50 tubes per kit  Luminometer $29,550  Separation Unit $450  PACE 2A kit $1000  100 test per kit  Specimen Collection Kit $500  50 tubes per kit

15 Sample Limitations  ONLY sampled from the endocervical area and the male urethra.  Performance with other samples has not been tested.  Only to be used with swabs transported and stored in the GEN-PROBE transport medium.  Transport and store sample at 2º-25º until use if before 7 days.  If longer storage is needed prepare sample for freezing at -20º to -70ºC.  ONLY sampled from the endocervical area and the male urethra.  Performance with other samples has not been tested.  Only to be used with swabs transported and stored in the GEN-PROBE transport medium.  Transport and store sample at 2º-25º until use if before 7 days.  If longer storage is needed prepare sample for freezing at -20º to -70ºC.

16 Detection Scheme  Specificity  rapid DNA probe test which utilizes the nucleic acid hybridization to screen for the presence of Chlamydia trachomatis and/or Neisseria gonorrhoeae  System uses single-stranded DNA probes with chemiluminescent labels  complementary to the ribosomal RNA of the target organism.  Specificity  rapid DNA probe test which utilizes the nucleic acid hybridization to screen for the presence of Chlamydia trachomatis and/or Neisseria gonorrhoeae  System uses single-stranded DNA probes with chemiluminescent labels  complementary to the ribosomal RNA of the target organism.

17 Target Capture  Magnetic particles (1  m in diameter), with synthetic oligonucleotides/ antibody specific/ charge specific for target nucleic acid are bound to the surface  The beads are used to capture target nucleic acid  target nucleic acid is the DNA/rRNA probe  Magnetic particles (1  m in diameter), with synthetic oligonucleotides/ antibody specific/ charge specific for target nucleic acid are bound to the surface  The beads are used to capture target nucleic acid  target nucleic acid is the DNA/rRNA probe

18 Detection  It confers specificity because the relationship between the DNA/rRNA hybrid molecule and the magnetic bead  It is selective because a minimal amount of non amplified rRNA is need to have quantifiable amount.  It confers specificity because the relationship between the DNA/rRNA hybrid molecule and the magnetic bead  It is selective because a minimal amount of non amplified rRNA is need to have quantifiable amount.

19 Detection: specificity cont.  Specificity- complementary base pairing - Precise hybridization conditions - Lyophilized probe The use of single-strand DNA probes with chemiluminescent labels that are complementary to the ribosomal RNA of the target organism allows the DNA probes to combine with the rRNA of the target organism to form stable DNA:RNA hybrids.  Specificity- complementary base pairing - Precise hybridization conditions - Lyophilized probe The use of single-strand DNA probes with chemiluminescent labels that are complementary to the ribosomal RNA of the target organism allows the DNA probes to combine with the rRNA of the target organism to form stable DNA:RNA hybrids.

20 Wash/ Separation  Washing/ Separation – Labeled DNA:RNA hybrids are separated and removed from the non-hybridized probes.  Incubation with separation suspension buffer  Magnetic separation with stringent/ forceful washes  Washing/ Separation – Labeled DNA:RNA hybrids are separated and removed from the non-hybridized probes.  Incubation with separation suspension buffer  Magnetic separation with stringent/ forceful washes

21 Visualization  The luminometer measures the amount of chemiluminescent emission from reactive patient samples (PACE assays)  light emitted from these reactions is detected by a photomultiplier tube  It is converted into a digital signal  The final measurable signal is directly proportional to the number of photons released by the respective reaction.  The luminometer measures the amount of chemiluminescent emission from reactive patient samples (PACE assays)  light emitted from these reactions is detected by a photomultiplier tube  It is converted into a digital signal  The final measurable signal is directly proportional to the number of photons released by the respective reaction.

22 Visualization: chemiluminescence  Acridinium ester made pre-attached to the probe.  The probe binds to the target rRNA of the bacterium.  Selection reagent is added which will hydrolyze acridinium ester of the single stranded probe.  However, the probes that have hybridized DNA/rRNA probe, the acridinium ester is protected in the double helix of the DNA RNA probe.  Detection reagent is added and no light is emitted from the ss probes, because the acradidium ester has been hydrolyzed.  In the hybridized probe, the acradidium ester is protected and can emit light, and the light can be quantified in the luminometer as Relative Light Unites.  Acridinium ester made pre-attached to the probe.  The probe binds to the target rRNA of the bacterium.  Selection reagent is added which will hydrolyze acridinium ester of the single stranded probe.  However, the probes that have hybridized DNA/rRNA probe, the acridinium ester is protected in the double helix of the DNA RNA probe.  Detection reagent is added and no light is emitted from the ss probes, because the acradidium ester has been hydrolyzed.  In the hybridized probe, the acradidium ester is protected and can emit light, and the light can be quantified in the luminometer as Relative Light Unites.

23 Sensitivity  Relatively large number of organisms in a typical sample collected in swab. No amplification is need  Targeting of rRNA  Background Reduction -Separation- Forceful washing: Angle wash to front sides of tube with the appearance of foam head to ensure adequate wash procedure.  Relatively large number of organisms in a typical sample collected in swab. No amplification is need  Targeting of rRNA  Background Reduction -Separation- Forceful washing: Angle wash to front sides of tube with the appearance of foam head to ensure adequate wash procedure.

24 Controls The Negative Reference and Positive Controls provided, control for the PACE 2C assay ONLY.  Negative Reference control- Non-infectious nucleic acid in a buffered solution containing <5% detergent. Provides a measure of the assay background and is used to calculate the run cut-off.  Chlamydia trachomatis Positive Control- Non- infectious C. trachomatis nucleic acid in a buffered solution containing <5% detergent  Neisseria gonorrhoeae Positive Control- Non- infectious N. gonorrhoeae nucleic acid in a buffered solution containing <5% detergent The Negative Reference and Positive Controls provided, control for the PACE 2C assay ONLY.  Negative Reference control- Non-infectious nucleic acid in a buffered solution containing <5% detergent. Provides a measure of the assay background and is used to calculate the run cut-off.  Chlamydia trachomatis Positive Control- Non- infectious C. trachomatis nucleic acid in a buffered solution containing <5% detergent  Neisseria gonorrhoeae Positive Control- Non- infectious N. gonorrhoeae nucleic acid in a buffered solution containing <5% detergent

25 Results calculation:  Result is calculated based on the difference the Response Light Units of the specimen and the mean of the negative reference.  Mean of the Negative Reference =  (65 RLU + 71 RLU + 80 RLU)/3 = 72 RLU  Assigned Cut-off = 300 RLU  Calculated Cut-off = 300 RLU + 72 RLU = 372 RLU Negative  Specimen Response = 900 RLU Positive  The limit RLU = 600 to 3200  Result is calculated based on the difference the Response Light Units of the specimen and the mean of the negative reference.  Mean of the Negative Reference =  (65 RLU + 71 RLU + 80 RLU)/3 = 72 RLU  Assigned Cut-off = 300 RLU  Calculated Cut-off = 300 RLU + 72 RLU = 372 RLU Negative  Specimen Response = 900 RLU Positive  The limit RLU = 600 to 3200

26 Interpretation  A negative test does not exclude the possibility that the numbers of C. trachomatis and/or N. gonorrhoeae organisms may be below the level of detection of the assay.  Second test is required  Lack of forceful washing may result in false positive  A negative test does not exclude the possibility that the numbers of C. trachomatis and/or N. gonorrhoeae organisms may be below the level of detection of the assay.  Second test is required  Lack of forceful washing may result in false positive

27 Detection Cont. C. trachomatisN. gonorrhoeae Sample Positive Control Positive Control Number of Replicates Mean Response (RLU) Standard Deviation (RLU) Coefficient of Variance 5.6% 5.1% C. trachomatisN. gonorrhoeae Sample Positive Control Positive Control Number of Replicates Mean Response (RLU) Standard Deviation (RLU) Coefficient of Variance 5.6% 5.1%

28 Critical Parameters  Hybridization and separation temperature - Temperature Dependent - Uniform equilibration of reaction tubes needed  Background Reduction -Separation- Forceful washing: Angle wash to front sides of tube with the appearance of foam head to ensure adequate wash procedure.  Hybridization and separation temperature - Temperature Dependent - Uniform equilibration of reaction tubes needed  Background Reduction -Separation- Forceful washing: Angle wash to front sides of tube with the appearance of foam head to ensure adequate wash procedure.

29 Conclusion  Results form the PACE 2C system should be used in conjunction with other data. This is a screening test only.  Detection is based on luminometer RLU unites  Positive RLU  Negative 372 or less  Results form the PACE 2C system should be used in conjunction with other data. This is a screening test only.  Detection is based on luminometer RLU unites  Positive RLU  Negative 372 or less

30 Reference 1.http://www.gen-probe.com/prod_serv/std_pace.asp 2.http://www.4woman.gov/faq/stdgonor.htm 3.Iwen, P.C., Walker, P.A., Warren, K.L., Kelly, D.M., Hinrichs, S.H., and Linder, J. Evaluation of Nucleic Acid-Based Test (PACE 2C) for Simultaneous Detection of Chlamydia trachomatis and Neisseria gonorrhoeae in Endocervical Specimens. 1995, Journal of Clinical Microbiology, Vol. 33, No.10; http://www.gen-probe.com/prod_serv/std_pace.asp 2.http://www.4woman.gov/faq/stdgonor.htm 3.Iwen, P.C., Walker, P.A., Warren, K.L., Kelly, D.M., Hinrichs, S.H., and Linder, J. Evaluation of Nucleic Acid-Based Test (PACE 2C) for Simultaneous Detection of Chlamydia trachomatis and Neisseria gonorrhoeae in Endocervical Specimens. 1995, Journal of Clinical Microbiology, Vol. 33, No.10;


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