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Molecular analysis of bedaquiline resistance and genetic variations in clinical isolates of multidrug and fluoroquinolones-resistant Mycobacterium tuberculosis

Authors :
Vijayalakshmi Jawaharlal Nehru
Usharani Brammacharry
S.R. Sri Ramkumar
Ameer Khusro
Maria Jose Vadakunnel
Shoba Gunasekaran
Esther David
Veeraraghavan Vishnu Priya
Reem M. Aljowaie
Saeedah Musaed Almutairi
Source :
Journal of King Saud University: Science, Vol 36, Iss 6, Pp 103226- (2024)
Publication Year :
2024
Publisher :
Elsevier, 2024.

Abstract

Background: Mycobacterium tuberculosis developing resistance to anti-tubercular therapy leads to pioneering innovative treatment protocols featuring carefully curated combinations of potent medications. The aim of this study was to analyze the frequency and pattern of fluoroquinolone (FQ) resistant mutations among the first-line drug-resistant specimens. By employing an elective sampling strategy, we deliberately focused our investigation on a targeted subset of multidrug resistant (MDR) and FQ resistant (FQR) TB cases. Method: Sputum samples from first-line drug-resistant patients were subjected to a GenoType MTBDRsl VER 2.0 assay to determine FQR. To investigate the effect of bedaquiline (BDQ) on these mutation-conferring genes (Rv0678, pepQ, and atpE), sanger sequencing was carried out on the MDR + FQR subset that was obtained. We have also conducted a computational analysis of the gene products of Rv0678 and pepQ with BDQ using molecular docking methods. Results: Eighty-three samples were observed to have FQR, and the majority of these specimens were associated with naïve and treatment failure cases. Among them, 64 isolates exhibited mutations in gyrA gene, while 19 isolates showed mutations in gyrB gene. The predominant occurrence of genetic variations, particularly in D94G and A90V, was observed within the specimens displaying resistance in gyrA gene, and the same has been confirmed by PCR-based detection. And the sequence analysis of BDQ genes among MDR + FQR subset indicated that the majority of the samples did not exhibit mutations in pepQ and atpE genes. However, only 2 samples were found to have the genetic variant G337A, which involves replacing the amino acid glutamic acid (E) at codon position 113 of Rv0678 gene with lysine (K). Conclusions: Most of the mutations were harbored in rpoB + katG + gyrA gene pattern. These findings pave the way for the development of databases and rapid diagnostic probes.

Details

Language :
English
ISSN :
10183647
Volume :
36
Issue :
6
Database :
Directory of Open Access Journals
Journal :
Journal of King Saud University: Science
Publication Type :
Academic Journal
Accession number :
edsdoj.57d66a7b8fbf4c389b1bc3444e414bba
Document Type :
article
Full Text :
https://doi.org/10.1016/j.jksus.2024.103226