2018Jundishapur Journal of MicrobiologyOpen access

The Effect of Ubiquitin Like Protein-Proteasome System on the Drug Resistance of Isoniazid Mono-Resistant Mycobacterium tuberculosis

Shuai Zhang, Shun Wen Zhang, Jiang Wu, Jie Zhang, Dong Jiang, Hui Zhu, Fang C. Wu, Wan jiang Zhang

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Abstract

: Tuberculosis (TB) is one of the most widespread and lethal infectious diseases worldwide. The emergence of drug-resistant TB has hampered effective TB treatment and control. Prokaryotic ubiquitin-like Protein-Proteasome System (PPS) contributes to the survival of Mycobacterium tuberculosis in the host. However, whether PPS effects drug resistance of isoniazid mono-resistant Mycobacterium tuberculosis (INH-MTB) is still unknown. This study aimed at exploring the effect of PPS on drug resistance of INH-MTB strain. In this study, over-expression of strains and deletion of mutant strains were constructed using electroporation. The researchers identified these constructed strains by Quantitative Reverse Transcription Polymerase Chain Reaction (RT-qPCR) or PCR. The Minimum Inhibitory Concentration (MIC) of isoniazid in INH-MTB strain and its derivative PPS mutant strains were determined using the Resazurin micro-titre assay. The MIC of isoniazid was 8 µg/mL higher in INH-MTB with Pup over-expression strain than that in INH-MTB. The MIC of isoniazid was 4.82 µg/mL, 4.98 µg/mL, 4.99 µg/mL, and 4.9 µg/mL lower in INH-MTB with deletion of Pup, Dop, PafA or Mpa strains than that in INH-MTB, respectively. The differences had statistical significance (P < 0.05). The MIC of isoniazid was 1.03 µg/mL higher in INH-MTB with PafA over-expression strain than that in INH-MTB. The MIC of isoniazid was 1.03 µg/mL and 0.68 µg/mL lower in INH-MTB with Dop, Mpa over-expression strains than that in INH-MTB, respectively. The differences had no statistical significance (P > 0.05). These results show that PPS effects the drug resistance of the INH-MTB strain.

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: Tuberculosis (TB) is one of the most widespread and lethal infectious diseases worldwide. The emergence of drug-resistant TB has hampered effective TB treatment and control. Prokaryotic ubiquitin-like Protein-Proteasome System (PPS) contributes to the survival of Mycobacterium tuberculosis in the host. However, whether PPS effects drug resistance of isoniazid mono-resistant Mycobacterium tuberculosis (INH-MTB) is still unknown. This study aimed at exploring the effect of PPS on drug resistance of INH-MTB strain. In this study, over-expression of strains and deletion of mutant strains were constructed using electroporation. The researchers identified these constructed strains by Quantitative Reverse Transcription Polymerase Chain Reaction (RT-qPCR) or PCR. The Minimum Inhibitory Concentration (MIC) of isoniazid in INH-MTB strain and its derivative PPS mutant strains were determined using the Resazurin micro-titre assay. The MIC of isoniazid was 8 µg/mL higher in INH-MTB with Pup over-expression strain than that in INH-MTB. The MIC of isoniazid was 4.82 µg/mL, 4.98 µg/mL, 4.99 µg/mL, and 4.9 µg/mL lower in INH-MTB with deletion of Pup, Dop, PafA or Mpa strains than that in INH-MTB, respectively. The differences had statistical significance (P < 0.05). The MIC of isoniazid was 1.03 µg/mL higher in INH-MTB with PafA over-expression strain than that in INH-MTB. The MIC of isoniazid was 1.03 µg/mL and 0.68 µg/mL lower in INH-MTB with Dop, Mpa over-expression strains than that in INH-MTB, respectively. The differences had no statistical significance (P > 0.05). These results show that PPS effects the drug resistance of the INH-MTB strain.

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Available abstract

: Tuberculosis (TB) is one of the most widespread and lethal infectious diseases worldwide. The emergence of drug-resistant TB has hampered effective TB treatment and control. Prokaryotic ubiquitin-like Protein-Proteasome System (PPS) contributes to the survival of Mycobacterium tuberculosis in the host. However, whether PPS effects drug resistance of isoniazid mono-resistant Mycobacterium tuberculosis (INH-MTB) is still unknown. This study aimed at exploring the effect of PPS on drug resistance of INH-MTB strain. In this study, over-expression of strains and deletion of mutant strains were constructed using electroporation. The researchers identified these constructed strains by Quantitative Reverse Transcription Polymerase Chain Reaction (RT-qPCR) or PCR. The Minimum Inhibitory Concentration (MIC) of isoniazid in INH-MTB strain and its derivative PPS mutant strains were determined using the Resazurin micro-titre assay. The MIC of isoniazid was 8 µg/mL higher in INH-MTB with Pup over-expression strain than that in INH-MTB. The MIC of isoniazid was 4.82 µg/mL, 4.98 µg/mL, 4.99 µg/mL, and 4.9 µg/mL lower in INH-MTB with deletion of Pup, Dop, PafA or Mpa strains than that in INH-MTB, respectively. The differences had statistical significance (P < 0.05). The MIC of isoniazid was 1.03 µg/mL higher in INH-MTB with PafA over-expression strain than that in INH-MTB. The MIC of isoniazid was 1.03 µg/mL and 0.68 µg/mL lower in INH-MTB with Dop, Mpa over-expression strains than that in INH-MTB, respectively. The differences had no statistical significance (P > 0.05). These results show that PPS effects the drug resistance of the INH-MTB strain.

Key concepts: Isoniazid, Mycobacterium tuberculosis, Microbiology, Tuberculosis, Drug resistance, Rifampicin, Medicine, Virology

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