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Monitoring Microbiological Response to Antituberculosis Therapy by Real-Time PCR

Received: 19 October 2014    Accepted: 6 November 2014    Published: 19 January 2015
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Abstract

Background: M. tuberculosis grows slowly and requires several weeks to detect in clinical specimens using standard culture techniques. Messenger RNA is more rapidly destroyed in cells than rRNA or genomic DNA, assays that target mycobacterial mRNA better reflect mycobacterial viability. Therefore we evaluated performance of mRNA for monitoring response to antituberculosis therapy using Real-Time PCR. Methods: Sputum specimens from 29 tuberculosis patients confirmed by positive culture were included in this study. Sputum specimens were collected before therapy, at 1st week, 4th week, 8th week and 16th week after initiating antituberculosis therapy to evaluate acid-fast bacilli (AFB), culture and mRNA level. Results: All 29 specimens were positive for culture and mRNA before initiating tuberculosis chemotherapy. Within 29 samples confirmed by positive culture, only 22 (75.9%) patients were positive by AFB. After 8 and 16 weeks of therapy, 27 (93.1%) and 28 (96.5%) were negative by culture, 26 (89.6%) and 28 (96.5%) were negative results for mRNA, and 15 (51.7%) and 29 (100%) were negative results for AFB. Conclusion: Rapidly decline of mRNA level correlated with rapid culture clearance after anti-tuberculosis therapy.

Published in American Journal of Clinical and Experimental Medicine (Volume 3, Issue 1)
DOI 10.11648/j.ajcem.20150301.11
Page(s) 1-5
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

M. tuberculosis, mRNA, Real-Time PCR

References
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Cite This Article
  • APA Style

    Yadi Yasir, Ressy Dwiyanti, Muhammad Sabir, Andini Febrianty, Ahmad Adhyka, et al. (2015). Monitoring Microbiological Response to Antituberculosis Therapy by Real-Time PCR. American Journal of Clinical and Experimental Medicine, 3(1), 1-5. https://doi.org/10.11648/j.ajcem.20150301.11

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    ACS Style

    Yadi Yasir; Ressy Dwiyanti; Muhammad Sabir; Andini Febrianty; Ahmad Adhyka, et al. Monitoring Microbiological Response to Antituberculosis Therapy by Real-Time PCR. Am. J. Clin. Exp. Med. 2015, 3(1), 1-5. doi: 10.11648/j.ajcem.20150301.11

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    AMA Style

    Yadi Yasir, Ressy Dwiyanti, Muhammad Sabir, Andini Febrianty, Ahmad Adhyka, et al. Monitoring Microbiological Response to Antituberculosis Therapy by Real-Time PCR. Am J Clin Exp Med. 2015;3(1):1-5. doi: 10.11648/j.ajcem.20150301.11

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  • @article{10.11648/j.ajcem.20150301.11,
      author = {Yadi Yasir and Ressy Dwiyanti and Muhammad Sabir and Andini Febrianty and Ahmad Adhyka and Nur Indah Purnamasari and Muhammad Reza Primaguna and Nataniel Tandirogang and Masyhudi Amir and Syamsu Rijal and Rosdiana Natzir and SutjiPratiwi Rahardjo and Mochammad Hatta},
      title = {Monitoring Microbiological Response to Antituberculosis Therapy by Real-Time PCR},
      journal = {American Journal of Clinical and Experimental Medicine},
      volume = {3},
      number = {1},
      pages = {1-5},
      doi = {10.11648/j.ajcem.20150301.11},
      url = {https://doi.org/10.11648/j.ajcem.20150301.11},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajcem.20150301.11},
      abstract = {Background: M. tuberculosis grows slowly and requires several weeks to detect in clinical specimens using standard culture techniques. Messenger RNA is more rapidly destroyed in cells than rRNA or genomic DNA, assays that target mycobacterial mRNA better reflect mycobacterial viability. Therefore we evaluated performance of mRNA for monitoring response to antituberculosis therapy using Real-Time PCR. Methods: Sputum specimens from 29 tuberculosis patients confirmed by positive culture were included in this study. Sputum specimens were collected before therapy, at 1st week, 4th week, 8th week and 16th week after initiating antituberculosis therapy to evaluate acid-fast bacilli (AFB), culture and mRNA level. Results: All 29 specimens were positive for culture and mRNA before initiating tuberculosis chemotherapy. Within 29 samples confirmed by positive culture, only 22 (75.9%) patients were positive by AFB. After 8 and 16 weeks of therapy, 27 (93.1%) and 28 (96.5%) were negative by culture, 26 (89.6%) and 28 (96.5%) were negative results for mRNA, and 15 (51.7%) and 29 (100%) were negative results for AFB. Conclusion: Rapidly decline of mRNA level correlated with rapid culture clearance after anti-tuberculosis therapy.},
     year = {2015}
    }
    

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  • TY  - JOUR
    T1  - Monitoring Microbiological Response to Antituberculosis Therapy by Real-Time PCR
    AU  - Yadi Yasir
    AU  - Ressy Dwiyanti
    AU  - Muhammad Sabir
    AU  - Andini Febrianty
    AU  - Ahmad Adhyka
    AU  - Nur Indah Purnamasari
    AU  - Muhammad Reza Primaguna
    AU  - Nataniel Tandirogang
    AU  - Masyhudi Amir
    AU  - Syamsu Rijal
    AU  - Rosdiana Natzir
    AU  - SutjiPratiwi Rahardjo
    AU  - Mochammad Hatta
    Y1  - 2015/01/19
    PY  - 2015
    N1  - https://doi.org/10.11648/j.ajcem.20150301.11
    DO  - 10.11648/j.ajcem.20150301.11
    T2  - American Journal of Clinical and Experimental Medicine
    JF  - American Journal of Clinical and Experimental Medicine
    JO  - American Journal of Clinical and Experimental Medicine
    SP  - 1
    EP  - 5
    PB  - Science Publishing Group
    SN  - 2330-8133
    UR  - https://doi.org/10.11648/j.ajcem.20150301.11
    AB  - Background: M. tuberculosis grows slowly and requires several weeks to detect in clinical specimens using standard culture techniques. Messenger RNA is more rapidly destroyed in cells than rRNA or genomic DNA, assays that target mycobacterial mRNA better reflect mycobacterial viability. Therefore we evaluated performance of mRNA for monitoring response to antituberculosis therapy using Real-Time PCR. Methods: Sputum specimens from 29 tuberculosis patients confirmed by positive culture were included in this study. Sputum specimens were collected before therapy, at 1st week, 4th week, 8th week and 16th week after initiating antituberculosis therapy to evaluate acid-fast bacilli (AFB), culture and mRNA level. Results: All 29 specimens were positive for culture and mRNA before initiating tuberculosis chemotherapy. Within 29 samples confirmed by positive culture, only 22 (75.9%) patients were positive by AFB. After 8 and 16 weeks of therapy, 27 (93.1%) and 28 (96.5%) were negative by culture, 26 (89.6%) and 28 (96.5%) were negative results for mRNA, and 15 (51.7%) and 29 (100%) were negative results for AFB. Conclusion: Rapidly decline of mRNA level correlated with rapid culture clearance after anti-tuberculosis therapy.
    VL  - 3
    IS  - 1
    ER  - 

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Author Information
  • Molecular Biology and Immunology Laboratory for Infectious Diseases, Faculty of Medicine, Hasanuddin University, Makassar,Indonesia; Department of Microbiology, Faculty of Medicine, Tadulako University, Palu, Indonesia

  • Molecular Biology and Immunology Laboratory for Infectious Diseases, Faculty of Medicine, Hasanuddin University, Makassar,Indonesia; Department of Microbiology, Faculty of Medicine, Tadulako University, Palu, Indonesia

  • Molecular Biology and Immunology Laboratory for Infectious Diseases, Faculty of Medicine, Hasanuddin University, Makassar,Indonesia; Department of Microbiology, Faculty of Medicine, Tadulako University, Palu, Indonesia

  • Molecular Biology and Immunology Laboratory for Infectious Diseases, Faculty of Medicine, Hasanuddin University, Makassar,Indonesia; Department of Microbiology, Faculty of Medicine, Tadulako University, Palu, Indonesia

  • Molecular Biology and Immunology Laboratory for Infectious Diseases, Faculty of Medicine, Hasanuddin University, Makassar,Indonesia; Department of Microbiology, Faculty of Medicine, Tadulako University, Palu, Indonesia

  • Department of Microbiology, Faculty of Medicine, Haluoleo University, Kendari, Indonesia

  • Molecular Biology and Immunology Laboratory for Infectious Diseases, Faculty of Medicine, Hasanuddin University, Makassar,Indonesia; Department of Microbiology, Faculty of Medicine, Haluoleo University, Kendari, Indonesia

  • Department Microbiology, Faculty of Medicine, Mulawarman University, Samarinda, Indonesia

  • Department Microbiology, Faculty of Medicine, Mulawarman University, Samarinda, Indonesia

  • Department of Histology, Faculty of Medicine, Muslim University of Indonesia, Makassar, Indonesia

  • Department of Biochemistry, Faculty of Medicine, Hasanuddin University, Makassar, Indonesia

  • Department of Otorhinolaryngology, Faculty of Medicine, Hasanuddin University, Makassar, Indonesia

  • Molecular Biology and Immunology Laboratory for Infectious Diseases, Faculty of Medicine, Hasanuddin University, Makassar,Indonesia

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