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Identification of mutations in rpoB, pncA, embB, and ubiA genes among drug-resistant Mycobacterium tuberculosis clinical isolates from Iran

Bakhtiyariniya, Pejman and Khosravi, Azar Dokht and Hashemzadeh, Mohammad and Savari, Mohammad (2022) Identification of mutations in rpoB, pncA, embB, and ubiA genes among drug-resistant Mycobacterium tuberculosis clinical isolates from Iran. ACTA MICROBIOLOGICA ET IMMUNOLOGICA HUNGARICA, 69 (2). pp. 150-157. ISSN 1217-8950

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Abstract

Mycobacterium tuberculosis resistant to effective first-line drugs (FLDs) has challenged national and global tuberculosis control programs. This study aimed to identify mutations in 4 genes related to rifampin, pyrazinamide, and ethambutol resistance among clinical isolates of M. tuberculosis from southwestern Iran. After drug susceptibility testing of 6620 M. tuberculosis clinical isolates by proportional method, a total of 24 FLD-resistant strains were included in the study. Fragments of rpoB, pncA, embB, and ubiA genes were amplified and sequenced to mine the mutations by pairwise alignment with the corresponding M. tuberculosis H37Rv genes. Phenotypic resistance to rifampin, isoniazid, and ethambutol was detected in 67, 54, and 33% (n 5 16, 13, and 8) of the isolates, respectively. Of rifampin-resistant isolates, 31% (5/16) were mono-resistant, and 56% (9/16) were multidrug-resistant (MDR). In 100% of rifampin-resistant isolates, mutations were found in the rifampin resistancedetermining region (RRDR) of the rpoB, with S450L substitution being the most common, especially in MDRs (77.8%, 7/9). Resistance-conferring mutations in pncA were present in 12.5% (3/24) of FLD-resistant isolates. The embB and ubiA mutations were found in 62.5 and 12.5% (5/8 and 1/8) of ethambutol-resistant isolates, respectively, of which the embB D354A was the most common substitution (37.5%, 3/8). Sixteen distinct mutations were identified, one of which was novel. The sequence analysis of the RRDR segment was the best way to detect rifampin resistance. The rpoB S450L substitution could be a helpful molecular marker to predict MDR. In other genes, no mutation was identified as a reliable marker.

Item Type: Article
Additional Information: Funding Agency and Grant Number: Ahvaz Jundishapur University of Medical Sciences (AJUMS), Ahvaz, Iran [OG-9903] Funding text: This work was financially supported by the Ahvaz Jundishapur University of Medical Sciences (AJUMS), Ahvaz, Iran (grant No: OG-9903). It was conducted at the Infectious and Tropical Diseases Research Center of AJUMS. We sincerely appreciate the staff of the Regional Tuberculosis Reference Laboratory of Khuzestan province for providing the isolates, the staff of the Infectious and Tropical Diseases Research Center, and the Department of Microbiology to provide the necessary equipment and an appropriate atmosphere for experiments.
Uncontrolled Keywords: MUTATIONS; EVOLUTION; DATABASE; immunology; diagnosis; Drug Resistance; Mycobacterium tuberculosis; Pulmonary tuberculosis; HIGH-LEVEL; eMBB; rpoB; rifampicin resistance; rpoB gene; pyrazinamide resistance; pncA; ETHAMBUTOL RESISTANCE;
Subjects: Q Science / természettudomány > QR Microbiology / mikrobiológia
SWORD Depositor: MTMT SWORD
Depositing User: MTMT SWORD
Date Deposited: 07 Aug 2023 07:29
Last Modified: 07 Aug 2023 07:29
URI: http://real.mtak.hu/id/eprint/170989

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