Proteomic analysis of sensitive and multi drug resistant Mycobacterium tuberculosis strains
- Authors: Yari S.1, Tasbiti A.H.1, Ghanei M.1,2, Shokrgozar M.A.3, Vaziri B.4, Mahdian R.5, Yari F.6, Bahrmand A.1
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Affiliations:
- Tuberculosis Department
- Chemical Injury Research Center
- National Cell Bank of Iran
- Protein Chemistry Unit, Biotechnology Research Center
- Molecular Medicine Dept, Biotechnology Research Center
- Blood Transfusion Research Center
- Issue: Vol 85, No 3 (2016)
- Pages: 350-358
- Section: Experimental Articles
- URL: https://bakhtiniada.ru/0026-2617/article/view/162638
- DOI: https://doi.org/10.1134/S0026261716030164
- ID: 162638
Cite item
Abstract
Multidrug-resistant tuberculosis (MDR-TB) is caused by bacteria that are resistant to the most effective anti TB drugs (Isoniazid and Rifampicin) with or without resistance to other drugs. Novel intervention strategies to eliminate this disease based on finding proteins can be used for designing new drugs or new and reliable kits for diagnosis. The aim of this study was to compare the protein profile of MDR-TB with sensitive isolates. Two-dimensional gel electrophoresis (2DE) along with mass spectrometry is a powerful and effective tool to identification and characterization of Mycobacterium tuberculosis. Two-dimensional gel electrophoresis and matrix assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry was used for diagnosis and comparison of proteins. We identified 14 protein spots in MDR-TB isolates that 2DE analysis showed these spots absent in M. tuberculosis sensitive isolates (Rv1876, Rv0379, Rv0147, Rv2031c, Rv3597c, Rv1886c, MT0493, Rv0440, Rv3614c, Rv1626, Rv0443, Rv0475, Rv3057 and unknown protein. The results showed 22 protein spots which were up regulated (or expressed) by the MDR-TB isolates, (Rv1240, Rv3028c, Rv2971, Rv2114c, Rv3311, Rv3699, Rv1023, Rv1308, Rv3774, Rv0831c, Rv2890c, Rv1392, Rv0719, Rv0054, Rv3418c, Rv0462, Rv2215, Rv2986c, Rv3248c and Rv1908c)). Two up regulated protein spots were identified in sensitive isolate (Rv1133c and Rv0685). These data will provide valuable clues in further investigation for suitable TB rapid tests or drug targets against drug resistant and sensitive of M. tuberculosis.
Keywords
About the authors
Shamsi Yari
Tuberculosis Department
Email: tbchemistry@gmail.com
Iran, Islamic Republic of, Tehran
Alireza Hadizadeh Tasbiti
Tuberculosis Department
Email: tbchemistry@gmail.com
Iran, Islamic Republic of, Tehran
Mostafa Ghanei
Tuberculosis Department; Chemical Injury Research Center
Email: tbchemistry@gmail.com
Iran, Islamic Republic of, Tehran; Tehran
Mohammad Ali Shokrgozar
National Cell Bank of Iran
Email: tbchemistry@gmail.com
Iran, Islamic Republic of, Tehran
Behrouz Vaziri
Protein Chemistry Unit, Biotechnology Research Center
Email: tbchemistry@gmail.com
Iran, Islamic Republic of, Tehran
Reza Mahdian
Molecular Medicine Dept, Biotechnology Research Center
Email: tbchemistry@gmail.com
Iran, Islamic Republic of, Tehran
Fatemeh Yari
Blood Transfusion Research Center
Email: tbchemistry@gmail.com
Iran, Islamic Republic of, Tehran
Ahmadreza Bahrmand
Tuberculosis Department
Author for correspondence.
Email: tbchemistry@gmail.com
Iran, Islamic Republic of, Tehran
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