Identification of Genes Encoded Toxin-Antitoxin System in Mycobacterium Tuberculosis Strains from Clinical Sample
- Authors: Sundaram K.1, Kagithakara Vajravelu L.2, Velayutham R.3, Mohan U.4
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Affiliations:
- Department of Microbiology,, SRM Medical College Hospital and Research Centre
- Department of Microbiology, SRM Medical College Hospital and Research Centre
- Department of Natural Products, National Institute of Pharmaceutical Education and Research
- Department of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research
- Issue: Vol 24, No 8 (2024)
- Section: Medicine
- URL: https://vietnamjournal.ru/1871-5265/article/view/645767
- DOI: https://doi.org/10.2174/0118715265274164240117104534
- ID: 645767
Cite item
Full Text
Abstract
Background:The toxin-antitoxin system is a genetic element that is highly present in Mycobacterium tuberculosis (MTB), the causative agent of tuberculosis. The toxin-antitoxin sys-tem comprises toxin protein and antitoxin protein or non-encoded RNA interacting with each other and inhibiting toxin activity. M. Tuberculosis has more classes of TA loci than non-tubercle bacilli and other microbes, including VapBC, HigBA, MazEF, ParDE, RelBE, MbcTA, PemIK, DarTG, MenTA, one tripartite type II TAC chaperone system, and hypothetical proteins.
Aims:The study aims to demonstrate the genes encoded toxin-antitoxin system in mycobacterium tuberculosis strains from clinical samples.
Materials and Methods:The pulmonary and extra-pulmonary tuberculosis clinical samples were collected, and smear microscopy (Ziehl-Neelsen staining) was performed for the detection of high bacilli (3+) count, followed by nucleic acid amplification assay. Bacterial culture and growth assay, genomic DNA extraction, and polymerase chain reaction were also carried out.
Results:The positive PTB and EPTB samples were determined by 3+ in microscopy smear [20], and the total count of tubercle bacilli determined by NAAT assay was 8.0×1005 in sputum and 1.3×1004 CFU/ml in tissue abscess. Moreover, the genomic DNA was extracted from culture, and the amplification of Rv1044 and Rv1045 genes in 624 and 412 base pairs (between 600-700 and 400-500 in ladder), respectively, in the H37Rv and clinical samples was observed.
Conclusion:It has been found that Rv1044 and Rv1045 are hypothetical proteins with 624 and 882 base pairs belonging to the AbiEi/AbiEii family of toxin-antitoxin loci. Moreover, the signifi-cant identification of TA-encoded loci genes may allow for the investigation of multidrug-resistant and extensively drug-resistant tuberculosis.
About the authors
Karthikeyan Sundaram
Department of Microbiology,, SRM Medical College Hospital and Research Centre
Author for correspondence.
Email: info@benthamscience.net
Leela Kagithakara Vajravelu
Department of Microbiology, SRM Medical College Hospital and Research Centre
Email: info@benthamscience.net
Ravichandiran Velayutham
Department of Natural Products, National Institute of Pharmaceutical Education and Research
Email: info@benthamscience.net
Utpal Mohan
Department of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research
Email: info@benthamscience.net
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