Sharma Divakar, Bisht Deepa, Khan Asad U
Department of Biochemistry, National JALMA Institute for Leprosy and Other Mycobacterial Diseases, Tajganj, Agra 282004, India.
Medical Microbiology and Molecular Biology Laboratory, Interdisciplinary Biotechnology Unit, Aligarh Muslim University, Aligarh 202002, India.
Proteomes. 2018 May 28;6(2):26. doi: 10.3390/proteomes6020026.
is one of the deadliest human pathogen of the tuberculosis diseases. Drug resistance leads to emergence of multidrug-resistant and extremely drug resistant strains of . Apart from principal targets of resistance, many explanations have been proposed for drug resistance but some resistance mechanisms are still unknown. Recently approved line probe assay (LPA) diagnostics for detecting the resistance to first and second line drugs are unable to diagnose the drug resistance in isolates which do not have the mutations in particular genes responsible for resistance. Proteomics and bioinformatic tools emerged as direct approaches for identification and characterization of novel proteins which are directly and indirectly involved in drug resistance that could be used as potential targets in future. In future, these novel targets might reveal new mechanism of resistance and can be used in diagnostics or as drug targets.
是结核病最致命的人类病原体之一。耐药性导致了结核分枝杆菌的多重耐药和广泛耐药菌株的出现。除了主要的耐药靶点外,人们还提出了许多关于耐药性的解释,但一些耐药机制仍然未知。最近批准的用于检测一线和二线药物耐药性的线性探针分析(LPA)诊断方法,无法诊断那些在特定耐药相关基因中没有突变的结核分枝杆菌菌株的耐药性。蛋白质组学和生物信息学工具成为直接鉴定和表征直接或间接参与耐药性的新蛋白质的方法,这些新蛋白质未来可能用作潜在靶点。未来,这些新靶点可能揭示新的耐药机制,并可用于诊断或作为药物靶点。