Affiliation:
1. Infectious and Tropical Diseases Research Center, Health Research Institute, Ahvaz Jundishapur University of Medical
Sciences, Ahvaz, Iran
2. Department of Microbiology, Faculty of Medicine, Ahvaz Jundishapur University of Medical
Sciences, Ahvaz, Iran
3. Iranian Study Group on Microbial Drug Resistance, Iran
4. Clinical Microbiology Research
Center, Ilam University of Medical Sciences, Ilam, Iran
Abstract
Introduction:
Toxin–antitoxin systems (TAs) are highly conserved in Mycobacterium tuberculosis
(Mtb). The TAs role in maintaining and disseminating drug resistance in bacterial populations
has been indicated. So, we aimed to analyze the expression level of MazEF-related genes in drugsusceptible
and multidrug-resistant (MDR) Mtb isolates under isoniazid (INH) and rifampin (RIF)
stress.
Methods:
We obtained 23 Mtb isolates, including 18 MDR and 5 susceptible isolates, from the Ahvaz
Regional TB Laboratory collection. The expression levels of mazF3, mazF6, and mazF9 toxin genes,
and mazE3, mazE6, and mazE9 antitoxin genes in MDR and susceptible isolates were evaluated by
quantitative real-time PCR (qRT-PCR) after exposure to RIF and INH.
Results:
The mazF3, F6, and F9 toxin genes were overexpressed in at least two MDR isolates in the
presence of RIF and INH, in contrast to mazE antitoxin genes. More MDR isolates were induced to
overexpress mazF genes by RIF than INH (72.2% vs. 50%). Compared to the H37Rv strain and susceptible
isolates, the expression levels of mazF3,6 by RIF and mazF3,6,9 by INH were significantly
upregulated in MDR isolates (p<0.05), but no remarkable difference was detected in the expression
level of mazF9 genes by INH between these groups. In susceptible isolates, the expression levels of
mazE3,6 by RIF and mazE3,6,9 by INH were induced and enhanced significantly compared to MDR
isolates, but there was no difference between MDR and H37Rv strain.
Conclusion:
Based on the results, we propose that mazF expression under RIF/INH stress may be
associated with drug resistance in Mtb in addition to mutations, and the mazE antitoxins may be related
to enhanced susceptibility of Mtb to INH and RIF. Further experiments are needed to investigate the
exact mechanism underlying the TA system's role in drug resistance.
Funder
Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
Publisher
Bentham Science Publishers Ltd.
Subject
Microbiology (medical),Pharmacology,Molecular Medicine,General Medicine