Global Health and Tropical Medicine, GHTM, Instituto de Higiene e Medicina Tropical, IHMT, Universidade Nova de Lisboa, UNL, Lisboa, Portugal.
Global Health and Tropical Medicine, GHTM, Instituto de Higiene e Medicina Tropical, IHMT, Universidade Nova de Lisboa, UNL, Lisboa, Portugal.
Infect Genet Evol. 2019 Aug;72:93-112. doi: 10.1016/j.meegid.2018.11.021. Epub 2018 Nov 30.
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.
结核病是由结核分枝杆菌引起的疾病,目前是全球单一传染病病原体导致死亡的主要原因。早期、快速、准确地鉴定结核分枝杆菌并确定药物敏感性对于该疾病的治疗和管理至关重要。结核病的诊断主要基于胸部 X 光检查、涂片显微镜检查和细菌培养。涂片显微镜检查的敏感性存在差异,主要是在人类免疫缺陷病毒(HIV)合并感染的患者中。由于结核分枝杆菌的生长缓慢,常规培养用于结核分枝杆菌的分离、鉴定和药敏试验需要数周时间。结果延迟导致潜在不适当的抗结核治疗时间延长,从而导致耐药性的出现,减少了治疗选择,并增加了治疗时间和相关成本,导致死亡率和发病率增加。出于这些原因,需要新的诊断方法来及时鉴定结核分枝杆菌并确定感染菌株的抗生素敏感性谱。分子方法提供了更高的敏感性和特异性、早期检测能力以及混合感染的检测能力。这些技术提高了周转时间、成本效益,并适用于即时检测。然而,尽管这些方法在采集样本后数小时内就能得到结果,但仍需要进行表型药敏试验来确定药物敏感性,并量化特定菌株对个体抗生素的敏感性水平。本文回顾了结核病分子诊断的历史、进展和未来前景。概述了用于检测和鉴定结核分枝杆菌及其相关疾病的一般原理、诊断价值以及分子方法的主要优点和缺点。还讨论了如何将当前的表型方法与基因型方法结合使用,以进行快速抗结核药敏试验。