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Rapid Identification of Mycobacterium Species with the Aid of Multiplex Polymerase Chain Reaction (PCR) From Clinical Isolates

机译:通过临床分离株的多重聚合酶链反应(PCR)快速鉴定分枝杆菌种类

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摘要

Mycobacteria are aerobic, nonspore forming, non-motile,single-cell bacteria.Of more than 40 currently recognized species of mycobacteria, Mycobacterium tuberculosis, the causative agent of human TB is the commonest pathogen for pulmonary and extra pulmonary tuberculosis cases. The other members of the Mycobacterium tuberculosis complex (MTC) or the nontubercular mycobacterium (NTM) produces similar diseases which cannot be differentiated from tuberculosis by clinical symptoms and signs. But this differentiation is important as the chemotherapy varies widely according to the strain of mycobacterium. The burden of morbidity and mortality of tuberculosis is rapidly growing worldwide, particularly with the HIV/AIDS epidemic. The strain identification of Mycobacterium remains a cumbersome, labor intensive and expensive procedure, which requires 3 to 12 weeks of time. The conventional methods of strain identification lack proper standardization and precise diagnosis. The prime objective of this study is to overcome these problems.A multiplex PCR using 3 amplicons of 165,365, and 541 base pair target sequences was done with a total number of 165 clinical isolates of suspected Koch’s patients. Strain identification was compared both by conventional methods and multiplex PCR. The results of the study show that this multiplex PCR is supposed to be less complicated, less time consuming, cost-effective and superior to the conventional methods. It is also applicable for culture negative samples where strain identification is not possible by conventional approach.
机译:分枝杆菌是有氧,无孢子形成,非运动性的单细胞细菌。在目前公认的40多种分枝杆菌结核分枝杆菌中,人结核病的病原体是肺结核和肺外结核病例的最常见病原体。结核分枝杆菌复合体(MTC)的其他成员或非结核分枝杆菌(NTM)产生的相似疾病无法通过临床症状和体征与结核病区分开。但是这种区分很重要,因为化疗根据分枝杆菌的菌株而有很大差异。在世界范围内,结核病的发病率和死亡率的负担正在迅速增长,特别是随着艾滋病毒/艾滋病的流行。分枝杆菌的菌株鉴定仍然是繁琐,费力且昂贵的过程,需要3至12周的时间。菌株鉴定的常规方法缺乏适当的标准化和精确的诊断。这项研究的主要目的是克服这些问题。使用了165,365和541个碱基对靶序列的3个扩增子进行了多重PCR,对总共165例可疑科赫患者进行了临床分离。通过常规方法和多重PCR比较了菌株鉴定。研究结果表明,这种多重PCR的复杂度较低,耗时较少,成本效益高且优于常规方法。它也适用于无法通过常规方法鉴定菌株的培养阴性样品。

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