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VOLUME 24 , ISSUE 1 ( January-June, 2022 ) > List of Articles

Original Article

Comparison of TrueNat polymerase chain reaction and mycobacterium growth indicator tube culture in the diagnosis of pulmonary and extrapulmonary tuberculosis

Poornima Mankara Valsan, J Sudarasana

Keywords : Diagnosis of tuberculosis, mycobacterium growth indicator tube, TrueNat mycobacterium tuberculosis polymerase chain reaction

Citation Information : Valsan PM, Sudarasana J. Comparison of TrueNat polymerase chain reaction and mycobacterium growth indicator tube culture in the diagnosis of pulmonary and extrapulmonary tuberculosis. 2022; 24 (1):21-25.

DOI: 10.4103/jacm.jacm_6_22

License: CC BY-NC 4.0

Published Online: 11-07-2022

Copyright Statement:  Copyright © 2022; Wolters Kluwer India Pvt. Ltd.


Abstract

Many diagnostic tests are available for tuberculosis (TB), from light microscopy, fluorescent microscopy, solid culture, liquid culture (Mycobacterium growth indicator tube [MGIT] culture) to molecular methods. The turnaround time and sensitivity of these tests vary depending on the procedure and principle involved. Based on this background, we compared the results of TrueNat Mycobacterium TB (MTB) Polymerase chain reaction (PCR) and MGIT culture in different clinical samples. A retrospective study was conducted in a tertiary care Hospital Kozhikode, Kerala from December 2018 to October 2021. A total of 431 samples (342 extrapulmonary and 119 pulmonary) were received in the laboratory for both TrueNat MTB PCR and MGIT culture. The samples sent for a single test and/or inadequate volume of samples for both tests were excluded from the study. In extrapulmonary samples, TrueNat MTB PCR and MGIT culture were positive for 31 (9%) samples. MGIT culture was positive in 48 (14%). Seventeen samples (5%) were positive only by MGIT culture. The sensitivity and specificity of PCR in extrapulmonary TB samples are 65% and 70%, respectively. Eighteen pulmonary samples (15%) were positive by both TrueNat PCR & MGIT culture. MGIT culture was positive in 20 (17%) pulmonary samples. Two pulmonary samples were positive by MGIT culture only. The sensitivity and specificity of PCR in pulmonary samples are 90% and 96%, respectively. Accurate diagnosis followed by prompt treatment is vital for the elimination of TB from our country by 2025. PCR is found to be a very rapid method in the early diagnosis of TB. However, culture still remains the gold standard test for the diagnosis.


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  1. World Health Organization. Global Tuberculosis Report 2020. Geneva: World Health Organization; 2020.
  2. World Health Organization. Global Tuberculosis Report 2021. Geneva: World Health Organization; 2021.
  3. Purohit M, Mustafa T. Laboratory diagnosis of extra-pulmonary tuberculosis (EPTB) in resource-constrained setting: State of the art, challenges and the need. J Clin Diagn Res 2015;9:E01-6.
  4. Campelo TA, Cardoso de Sousa PR, Nogueira LL, Frota CC, Zuquim Antas PR. Revisiting the methods for detecting Mycobacterium tuberculosis: What has the new millennium brought thus far? Access Microbiol 2021;3:000245.
  5. Global Laboratory Initiative Advancing TB Diagnosis. Mycobacteriology Laboratory Manual. 1st ed. Global Laboratory Initiative a Working Group of the Stop TB Partnership; 2014.
  6. Mangayarkarasi V, Sneka P, Sujith R, Jayaprakash. Ergonomic diagnostic tool based on chip mini RT PCR for diagnosis of pulmonary and extra pulmonary tuberculosis. J Pure Appl Microbiol 2019;13:1185-90.
  7. India TB report 2020, National Tuberculosis Elimination Program Anual report, Central Tb division, Ministry of Health and Family Welfare, New Delhi.
  8. Tortoli E, Russo C, Piersimoni C, Mazzola E, Dal Monte P, Pascarella M, et al. Clinical validation of Xpert MTB/RIF for the diagnosis of extrapulmonary tuberculosis. Eur Respir J 2012;40:442-7.
  9. Cheng VC, Yam WC, Hung IF, Woo PC, Lau SK, Tang BS, et al. Clinical evaluation of the polymerase chain reaction for the rapid diagnosis of tuberculosis. J Clin Pathol 2004;57:281-5.
  10. WHO. The Use of Liquid Medium for Culture and DST. Geneva: World Health Organization; 2007.
  11. Jose RA, Gopal K, Johnson AS, Samuel JA, Abraham SS, Goswami T, et al. Evaluation of TrueNat MTB/RIF test in comparison with microscopy and culture for diagnosis of extrapulmonary tuberculosis in a tertiary care centre. J Clin Diagn Res 2021;15:DC05-9.
  12. Thangavelu K, Jamir I, Ellappan K, Krishnakumariamma K, Gopichand P, Sindhusuta D, et al. Comparison of MGIT 960 with Lowenstein Jensen Media for recovery of mycobacteria from extrapulmonary specimens in Southern India. J Clin Diagn Res 2021;15:DC01-4.
  13. Pfyffer GE, Welscher HM, Kissling P, Cieslak C, Casal MJ, Gutierrez J, et al. Comparison of the mycobacteria growth indicator tube (MGIT) with radiometric and solid culture for recovery of acid-fast bacilli. J Clin Microbiol 1997;35:364-8.
  14. Hillemann D, Richter E, Rüsch-Gerdes S. Use of the BACTEC mycobacteria growth indicator tube 960 automated system for recovery of mycobacteria from 9,558 extrapulmonary specimens, including urine samples. J Clin Microbiol 2006;44:4014-7.
  15. Sastry A, Bhat S. Essential of Medical Microbiology. 2nd ed. New Delhi: Jaypee Publication; 2018. p. 281.
  16. van Zyl-Smit RN, Binder A, Meldau R, Mishra H, Semple PL, Theron G, et al. Comparison of quantitative techniques including Xpert MTB/RIF to evaluate mycobacterial burden. PLoS One 2011;6:e28815.
  17. Kumar P, Bhardwaj P. Diagnosis of pulmonary tuberculosis with cartridge based nucleic acid amplification test and light emitting diode fluorescent microscopy: A comparative study. Int J Adv Med 2019;6:1580-83.
  18. Gomathi NS, Singh M, Singh UB, Myneedu VP, Chauhan DS, Sarin R, et al. Multicentric validation of indigenous molecular test TrueNat™ MTB for detection of Mycobacterium tuberculosis in sputum samples from presumptive pulmonary tuberculosis patients in comparison with reference standards. Indian J Med Res 2020;152:378-85.
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