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Advances in the molecular diagnosis of tuberculosis: From probes to genomes

机译:结核病分子诊断的进展:从探针到基因组

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Tuberculosis, disease caused by Mycobacterium tuberculosis, is currently the leading cause of death by a single infectious agent worldwide. Early, rapid and accurate identification of M. tuberculosis and the determination of drug susceptibility is essential for the treatment and management of this disease. Tuberculosis diagnosis is mainly based on chest radiography, smear microscopy and bacteriological culture. Smear microscopy has variable sensitivity, mainly in patients co-infected with the human immunodeficiency virus (HIV). Conventional culture for M. tuberculosis isolation, identification and drug susceptibility testing requires several weeks owning to the slow growth of M. tuberculosis. The delay in the time to results drives the prolongation of potentially inappropriate antituberculosis therapy contributing to the emergence of drug resistance, reducing treatment options and increasing treatment duration and associated costs, resulting in increased mortality and morbidity. For these reasons, novel diagnostic methods are need for timely identification of M. tuberculosis and determination of the antibiotic susceptibility profile of the infecting strain. Molecular methods offer enhanced sensitivity and specificity, early detection and the capacity to detect mixed infections. These technologies have improved turnaround time, cost effectiveness and are amenable for point-of-care testing. However, although these methods produce results within hours from sample collection, the phenotypic susceptibility testing is still needed for the determination of drug susceptibility and quantify the susceptibility levels of a given strain towards individual antibiotics. This review presents the history, advances and forthcoming promises in the molecular diagnosis of tuberculosis. An overview on the general principles, diagnostic value and the main advantages and disadvantages of the molecular methods used for the detection and identification of M. tuberculosis and its associated disease, is provided. It will be also discussed how the current phenotypic methods should be used in combination with the genotypic methods for rapid antituberculosis susceptibility testing.
机译:结核病,由结核分枝杆菌引起的疾病,目前是全世界单一传染病的致病原因。早期,快速准确地鉴定结核病和药物易感性的测定对于这种疾病的治疗和管理至关重要。结核病诊断主要基于胸部射线照相,涂片显微镜和细菌培养。涂片显微镜具有可变敏感性,主要是与人类免疫缺陷病毒(HIV)共同感染的患者。结核分离,鉴定和药物易感性试验的常规培养物需要几周的肺结核增长缓慢。结果的延迟驱动潜在不恰当的抗尿素症治疗的延长,这会导致耐药性,减少治疗方案和增加治疗持续时间以及相关成本,导致死亡率和发病率增加。出于这些原因,新的诊断方法需要及时鉴定M.结核分枝杆菌和感染菌株的抗生素敏感性曲线的测定。分子方法提供增强的敏感性和特异性,早期检测和检测混合感染的能力。这些技术提高了周转时间,成本效益,并且适用于护理点测试。然而,尽管这些方法在样品收集后几小时产生了结果,但仍需要测定药物敏感性的表型易感性测试,并量化给定菌株对个体抗生素的敏感性水平。本次审查提出了历史,进展和即将举行的结核病分子诊断的承诺。提供了一般原理,诊断价值和用于检测和鉴定型结核病及其相关疾病的分子方法的主要原理,诊断价值和主要优点及缺点。还将讨论当前的表型方法如何与基因型方法结合使用,以便快速抗核分辨率易感测试。

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