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Patterns and profiles of drug resistance-conferring mutations in Mycobacterium tuberculosis genotypes isolated from tuberculosis-suspected attendees of spiritual holy water sites in Northwest Ethiopia

Bibliographic Data

ID22070576
AuthorsMelese Abate Reta (0000-0003-1301-4746, Woldia University, corresponding author), Nontuthuko Excellent Maningi (0000-0001-5089-7678, University of KwaZulu-Natal), P Bernard Fourie (0000-0002-1630-3554, University of Pretoria)
Year2024
Volume12
Pages1356826-1356826
Publication date2024-03-19
Open AccessYes
TypeARTICLE
VenueFrontiers in Public Health (JOURNAL)
Journal identifiersISSN: 2296-2565 • E-ISSN: 2296-2565
PublisherFrontiers Media SA (PUBLISHER • CH)
DOI10.3389/fpubh.2024.1356826
PMID38566794
OpenAlexW4392966890
LanguageEN
References cited60

Purpose This study examined the patterns and frequency of genetic changes responsible for resistance to first-line (rifampicin and isoniazid), fluoroquinolones, and second-line injectable drugs in drug-resistant Mycobacterium tuberculosis (MTB) isolated from culture-positive pulmonary tuberculosis (PTB) symptomatic attendees of spiritual holy water sites (HWSs) in the Amhara region. Patients and methods From June 2019 to March 2020, a cross-sectional study was carried out. A total of 122 culture-positive MTB isolates from PTB-suspected attendees of HWSs in the Amhara region were evaluated for their drug resistance profiles, and characterized gene mutations conferring resistance to rifampicin (RIF), isoniazid (INH), fluoroquinolones (FLQs), and second-line injectable drugs (SLIDs) using GenoType®MTBDR plus VER2.0 and GenoType®MTBDR sl VER2.0. Drug-resistant MTB isolates were Spoligotyped following the manufacturer’s protocol. Results Genetic changes (mutations) responsible for resistance to RIF, INH, and FLQs were identified in 15/122 (12.3%), 20/122 (16.4%), and 5/20 (25%) of MTB isolates, respectively. In RIF-resistant, rpo B/Ser 531 Lue ( n = 12, 80%) was most frequent followed by His 526 Tyr (6.7%). Amongst INH-resistant isolates, kat G/Ser 315 Thr1 ( n = 19, 95%) was the most frequent. Of 15 MDR-TB, the majority ( n = 12, 80%) isolates had mutations at both rpo B/Ser 531 Leu and kat G/Ser 315 Thr1. All 20 INH and/or RIF-resistant isolates were tested with the MTBDR sl VER 2.0, yielding 5 FLQs-resistant isolates with gene mutations at rpo B/Ser 531 Lue, kat G/Ser 315 Thr1, and gyr A/Asp 94 Ala genes. Of 20 Spoligotyped drug-resistant MTB isolates, the majority ( n = 11, 55%) and 6 (30%) were SIT149/T3-ETH and SIT21/CAS1-Kili sublineages, respectively; and they were any INH-resistant (mono-hetero/multi-). Of 15 RIF-resistant (RR/MDR-TB) isolates, 7 were SIT149/T3-ETH, while 6 were SIT21/CAS1-Kili sublineages. FLQ resistance was detected in four SIT21/CAS1-Kili lineages. Conclusion In the current study, the most common gene mutations responsible for resistance to INH, RIF, and FLQs were identified. SIT149/T3-ETH and SIT21/CAS1-Kili constitute the majority of drug-resistant TB (DR-TB) isolates. To further understand the complete spectrum of genetic changes/mutations and related genotypes, a sequencing technology is warranted

Antibiotics · Biology · Drug resistance · Gene · Genotype · Isoniazid · Mycobacterium tuberculosis · Pathology · Rifampicin · Tuberculosis · Infectious Diseases and Tuberculosis · Medicine · Mycobacterium research and diagnosis · Tuberculosis Research and Epidemiology · Genetics · Microbiology · Virology

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Highly citedNo
Open DOIOpen Access
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