Diagnosing Pulmonary Tuberculosis with the Xpert MTB/RIF Test

Standard 2 of the International Standards for Tuberculosis Care states that all patients suspected of having pulmonary TB should submit at least two sputum specimens for bacteriological examination. When possible, at least one early-morning specimen should be obtained, as sputum collected at this time has the highest yield.¹¹ The Xpert MTB/RIF assay can be applied to sputum samples or concentrated sputum sediments prepared from induced or expectorated sputa that are either acid-fast bacilli (AFB) smear positive or negative.^{6, 12, 13} The assay is intended for use with specimens from patients for whom there is clinical suspicion of pulmonary TB who have: 1) not received anti-tuberculosis therapy, 2) had < 7 days of therapy, or 3) have not received therapy in the last 60 days. Do note that it should not be used for monitoring the effects of drug therapy⁷ because bacterial DNA might persist following antimicrobial therapy.

Treat clinical specimens, including used cartridges, as if capable of transmitting infectious agents. Use proper precautions, such as wearing protective disposable gloves, laboratory coats and eye protection, and follow your institution’s safety procedures and guidelines.

1. Expectorated Sputum Samples

Note: Process only as many specimens at one time, as there are GeneXpert Dx System modules available to run the test!

1. Label each Xpert MTB/RIF cartridge with the corresponding specimen ID.
2. Transfer 1.0 ml expectorated sputum to a conical, screw-capped tube using a sterile transfer pipette. Alternatively, the entire specimen may be processed in the original leak-proof sputum collection container.
3. Add 2.0 ml Xpert MTB/RIF Sample Reagent (2:1; v/v) to the expectorated sputum using a sterile transfer pipette.
4. Replace the lid, and shake the tube vigorously 10-20 times. Alternatively, the mixture may be vortexed (30 sec).
5. Allow the tube to stand upright for 5 min at room temperature.
6. Shake the tube vigorously 10-20 times. Alternatively, use a vortex (30 sec).
7. Allow the tube to stand upright for another 10 min at room temperature.
8. Inspect the specimens: samples should be liquefied with no visible clumps of sputum.

2. Concentrated Sediments

Note: Process only as many specimens at one time as there are GeneXpert Dx System modules available to run the tests!

1. Label each Xpert MTB/RIF cartridge with the corresponding specimen ID.
2. Transfer 1.5 ml Xpert MTB/RIF Sample Reagent to a conical, screw-capped tube using a sterile transfer pipette.
3. Add at least 0.5 ml concentrated sediment to the Sample Reagent containing tube using a sterile transfer pipette.
4. Replace the lid, and shake the tube vigorously 10-20 times. Alternatively, use a vortex (30 sec).
5. Allow the tube to stand upright for 5 min at room temperature.
6. Shake the tube vigorously 10-20 times. Alternatively, use a vortex (30 sec).
7. Allow the tube to stand upright for another 10 min at room temperature.
8. Inspect the specimens: samples should be liquefied with no visible clumps of sputum.

3. Loading the Xpert MTB/RIF Cartridge

Note: Start the test within 30 minutes of adding the sample to the cartridge!

1. Check the labels on the Xpert MTB/RIF cartridge and the specimen ID.
2. Open the cartridge lid.
3. Using the sterile transfer pipette provided, aspirate the liquefied specimen into the transfer pipette until the meniscus is above the minimum mark and transfer the sample into the open port of the Xpert MTB/RIF cartridge.

Note: Dispense slowly to minimize the risk of aerosol formation!

4. Close the cartridge lid.

4. Starting the Test

Note: Before starting the test, ensure that the GeneXpert Dx System is equipped with the GX2.1 software, and the Xpert MTB/RIF assay is imported into the software! ⁹

1. Turn on the computer, and then turn on the GeneXpert Dx instrument.
2. On the Windows desktop, double-click the GeneXpert Dx shortcut icon.
3. Log on to the GeneXpert Dx System software using your user name and password.
4. In the GeneXpert Dx System window, click Create Test. The Scan Cartridge Barcode dialog box appears.
5. In the Sample ID box, scan or type the sample ID.
6. Scan the barcode on the Xpert MTB/RIF cartridge. The Create Test window appears.
7. Click Start Test, and enter your password in the dialog box that appears.
8. Open the instrument module door with the blinking green light, and load the cartridge.
9. Close the door. The test starts and the light stops blinking and remains constantly green. When the test is finished, the light turns off.
10. Wait until the system releases the door lock at the end of the run, then open the module door and remove the cartridge.
11. Dispose of used cartridges in the appropriate waste containers according to your institution’s standard practices.

5. Representative Results

Each Xpert MTB/RIF cartridge includes reagents for the detection of MTB complex and RIF resistance as well as a sample processing control (SPC) to control for adequate processing of the target bacteria and to monitor the presence of inhibitor(s) in the PCR reaction. The Probe Check Control (PCC) verifies reagent rehydration, PCR tube filling in the cartridge, probe integrity, and dye stability.⁹ The primers in the Xpert MTB/RIF assay amplify a portion of the rpoB gene containing the 81 base pair “core” region. Five differently colored fluorogenic nucleic acid hybridization probes, called molecular beacons, interrogate the entire 81-bp core.¹⁴ Each molecular beacon was designed to be so specific that it does not bind to its target if the target sequence differs from the wild-type rpoB sequence by as little as a single nucleotide substitution. Since molecular beacons fluorescence only when they are bound to their targets, i.e. wild-type rpoB sequence, the absence of any one of the five colors in the assay differentiate between the conserved wild-type sequence and mutations in the core region that are associated with RIF resistance.⁶

The SPC should be positive in a negative sample and can be negative or positive in a positive sample. The test result will be “Invalid” if the SPC is not detected in a negative test. Before the start of the PCR reaction, the GeneXpert Dx System measures the fluorescence signal from the probes to monitor bead rehydration, reaction-tube filling, probe integrity and dye stability. The PCC passes if the fluorescence signal from the probes meets the assigned acceptance criteria. The results are interpreted by the GeneXpert Dx System from measured fluorescence signals and embedded calculation algorithms and are displayed in the 結果 window⁹, as indicated below:

MTB Detected: MTB target DNA is detected; both controls, SPC and PCC, meet the assigned acceptance criteria. Lower Ct values represent a higher starting concentration of DNA template; higher Ct values represent a lower concentration of DNA template. In MTB DETECTED results “RIF Resistance DETECTED” (Figure 1A), “RIF Resistance NOT DETECTED” (Figure 1B), or “RIF Resistance INDETERMINATE” will display on a separate line.

MTB Not Detected: MTB target DNA is not detected; both controls, SPC and PCC, meet the assigned acceptance criteria (Figure 2).

Invalid: Presence or absence of MTB cannot be determined: SPC does not meet acceptance criteria, i.e. the sample was not properly processed, or PCR was inhibited (Figure 3). Note: repeat test with extra specimen!

Error: One or more of the PCC results failed (FAIL). Both MTB and SPC display NO RESULT. Note: repeat test with extra specimen! If the PCC passed (PASS), the error is caused by a system component failure.

Figure 1: MTB target DNA is detected; both controls, SPC and PCC, meet the assigned acceptance criteria. Lower Ct values represent a higher starting concentration of DNA template; higher Ct values represent a lower concentration of DNA template. In MTB DETECTED results “RIF Resistance NOT DETECTED” (Figure 1A), “RIF Resistance DETECTED” (Figure 1B), or “RIF Resistance INDETERMINATE” will display on a separate line.

Figure 1A. MTB DETECTED; RIF Resistance NOT DETECTED, i.e. only the wild-type nucleic acid sequence of the 81-bp RIF resistance-determining region (RRDR) of the rpoB gene was present.⁶ Click here to view larger figure.

Figure 1B. MTB DETECTED; RIF Resistance DETECTED. Complete drop out of Probe B (arrow), which covers the positions 513 to 517 of the RRDR of the rpoB gene.⁶ In the example, partial sequencing revealed that the rpoB gene mutation D516V was detected.⁸ Click here to view larger figure.

Figure 2. MTB target DNA was not detected; both controls, SPC and PCC, meet the assigned acceptance criteria. Click here to view larger figure.

Figure 3. Invalid test result, i.e. presence or absence of MTB cannot be determined: SPC does not meet acceptance criteria, because the sample was not properly processed, or because PCR was inhibited. Click here to view larger figure.