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Detection of Mycobacterium tuberculosis directly from sputum specimens & phenotypic drug resistance pattern of M tuberculosis isolates from suspected tuberculosis patients in Chennai

机译:直接从金奈痰标本中检测结核分枝杆菌和疑似结核病患者的结核分枝杆菌的表型耐药模式

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Background & objectives: mRNAis more rapidly destroyed in cells than rRNA or genomic DNA, an assay targeting bacterial mRNA would provide a better guide to mycobacterial viability than amplification tests directed at DNA or rRNA targets. This study was carried out to standardize reverse transcriptase PCR (RT-PCR) targeting 85B gene for the rapid detection of viable Mycobacterium tuberculosis from sputum specimens of suspected TB patients at Chennai, South India and to detect MDR-TB circulating in this population.Methods'. Sputum samples from clinically suspected tuberculosis patients (n=301) and 78 controls were included in the study. The sputum samples were collected in sterile diethyl pyrocarbonate (DEPC) treated containers and transported in ice to the laboratory within 2 h to prevent degradation of RNA. RT-PCR targeting 85B gene, mycobacterial culture and phenotypic drug susceptibility testing for the first line drugs streptomycin (S), isoniazid (H), rifampicin (R), ethambutol (E) and pyrazinamide (Z) were performed by BACTEC microMGIT culture system for all the sputum specimens.Results'. All the 78 controls were negative for culture and RT-PCR. Among the 301 sputum specimens from patients, 231 (76.8%) were RT-PCR positive and 70 (23.2%) were negative. There were 166 M. tuberculosis isolates, of which 11 (2.9%) were MDR-TB, 33 (8.7%) were polyresistant, 31 (8.2%) were monoresistant and 91 (30.2%) were sensitive to all five first line anti-tuberculous drugs by phenotypic drug susceptibility testing. Monoresistance was higher with Z [20 (20.8%)], followed by S [6 (3%)].Interpretation & conclusions'. RT-PCR targeting 85B gene of M. tuberculosis was a specific, rapid, reliable technique to detect the M. tuberculosis directly from sputum specimens. Our results showed that 2.9 per cent of M. tuberculosis isolates in the study population of Chennai were MDR.
机译:背景与目的:与rRNA或基因组DNA相比,mRNA在细胞中的破坏速度更快,一种针对细菌mRNA的检测方法将比针对DNA或rRNA靶标的扩增试验提供更好的分枝杆菌生存能力指南。这项研究的目的是标准化针对85B基因的逆转录酶PCR(RT-PCR),以从印度南部金奈的疑似TB患者的痰标本中快速检测有活力的结核分枝杆菌,并检测该人群中循环的MDR-TB。 '。研究包括来自临床疑似结核病患者(n = 301)和78名对照的痰液样本。痰标本收集在无菌的焦碳酸二乙酯(DEPC)处理过的容器中,并在冰中2小时内运送到实验室,以防止RNA降解。通过BACTEC microMGIT培养系统对一线药物链霉素(S),异烟肼(H),利福平(R),乙胺丁醇(E)和吡嗪酰胺(Z)进行靶向85B基因的RT-PCR,分枝杆菌培养和表型药敏试验所有痰标本。所有的78个对照培养和RT-PCR均为阴性。在301例患者的痰标本中,RT-PCR阳性231例(76.8%),阴性70例(23.2%)。有166株结核分枝杆菌,其中耐多药结核病11株(2.9%),多药耐药33株(8.7%),单药耐药31株(8.2%),对所有五种一线抗药性敏感的91株(30.2%)。结核药物通过表型药敏试验。 Z的单电阻更高[20(20.8%)],S的单电阻更高[6(3%)]。解释和结论。靶向结核分枝杆菌85B基因的RT-PCR是一种直接从痰液标本中检测结核分枝杆菌的特异性,快速,可靠的技术。我们的结果表明,在钦奈研究人群中,结核分枝杆菌中有2.9%是MDR。

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