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Genotype mtbdrsl line probe assay

Manufactured by Hain Lifescience
Sourced in Germany

The Genotype MTBDRsl/Line probe assay is a molecular diagnostic tool used for the rapid detection of drug resistance in Mycobacterium tuberculosis (TB) isolates. It is designed to identify genetic mutations associated with resistance to second-line anti-TB drugs, including fluoroquinolones and injectable agents.

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2 protocols using genotype mtbdrsl line probe assay

1

Evaluating Second-line Drug Resistance in Rifampicin-resistant TB

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Two sputum samples from patients with presumptive pulmonary tuberculosis were collected. The sputa of patients with rifampicin resistance tuberculosis detected by GeneXpert MTB/RIF (Cepheid, Sunnyvale, CA, USA) were further analysed for second-line drug resistance using the Genotype MTBDRsl/Line probe assay (Hain Life Science GmbH, Nehren, Germany). The GeneXpert MTB/RIF and Genotype MTBDRsl/Line probe assay tests were carried out according to the manufacturer’s instructions [13 , 14 ]. The line probe assay is a deoxyribonucleic acid (DNA) strip-based test determining Mycobacterium tuberculosis drug-resistant strains. It identifies resistance due to mutations in gyrA (from codon 85–96) and gyrB (from codon 536–541) [2 (link)] genes for fluoroquinolone (levofloxacin or moxifloxacin), the rrs gene’s (nucleic acid position 1401, 1402 and 1484) and the eis gene’s promoter region (from − 37 to − 2 nucleotides upstream) for detection of resistance to the second-line injectable anti-TB drugs (kanamycin, amikacin or capreomycin) used during the earlier years of the study period. Mutations are detected by either the binding of amplicons to probes targeting the most commonly occurring mutations (MUT probes); or by the lack of hybridisation (i.e. lack of binding) of the amplicons to the corresponding WT probes [13 ].
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2

Evaluating MDR-TB Treatment Eligibility

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Potential participants were identified from the community health centers where, within the TB Program, patients evaluated (due to poor treatment response, treatment failure, etc. in TB episode) or confirmed of MDR-TB were treated. Patients newly registered to initiate MDR-TB treatment were asked to participate. Eligible participants consisted of adults with smear-positive pulmonary MDR-TB, confirmed as isoniazid and rifampicin-resistant by GenoType MTBDRplus Line Probe Assay (Hain Lifescience GmbH, Nehren, Germany) and fluoroquinolone-susceptible by GenoType MTBDRsl Line Probe Assay (Hain Lifescience GmbH, Nehren, Germany). Exclusion criteria included: poorly controlled diabetes mellitus (HbA1c >9%), concurrent use of known QTprolonging drugs, known glucose-6-phosphate dehydrogenase deficiency, current pregnancy, or breastfeeding, anticipated surgical intervention for pulmonary TB treatment, among others. 14
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