破译立克次体新陈代谢途径:治疗目标的藏宝图

Brijesh Prajapat , Ankita Sharma , Sunil Kumar , Dixit Sharma
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引用次数: 0

摘要

印度蜱斑疹伤寒是一种由细胞内革兰氏阴性细菌康氏立克次体引起的传染病。这种细菌通过受感染的蜱虫叮咬传播给人类,有时也通过虱子、跳蚤或螨虫传播。这种疾病局限于一些病例很少的地区,但在过去十年中,它在印度不同地区重新出现了大量病例。对细菌病原体基因组成的了解可以从它们的代谢途径中得到。在目前的研究中,发现18种代谢途径是病原体(conorii)所特有的。综合分析发现了163个蛋白与18个独特的代谢途径有关。据报道,140种蛋白质是细菌生存所必需的,46种被发现是有毒的,10种被发现参与耐药性,可以增强细菌的发病机制。独特代谢途径蛋白的功能分析显示,质粒偶联转移TrbL/VirB6、脂肪酸激酶短链、信号转导反应调节受体和IV型转运体系统域成分丰富。根据预测结构域,将这些蛋白分为六大类,即代谢、转运、基因表达和调控、抗微生物耐药性、细胞信号传导和蛋白水解。此外,计算机分析显示88个蛋白与宿主蛋白不同源,是合适的治疗靶点。这43种蛋白质在DrugBank数据库中显示出它们的可药物性,其余45种蛋白质被归类为需要进一步验证的新型药物靶点。这项研究将有助于更好地了解病原体的生存,并着手开发成功的治疗方法来管理印度蜱虫斑疹伤寒。
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Deciphering Rickettsia conorii metabolic pathways: A treasure map to therapeutic targets
Indian tick typhus is an infectious disease caused by intracellular gram-negative bacteria Rickettsia conorii (R. conorii). The bacterium is transmitted to humans through bite of infected ticks and sometimes by lice, fleas or mites. The disease is restricted to some areas with few cases but in last decade it is re-emerging with large number of cases from different areas of India. The insight in to genetic makeup of bacterial pathogens can be derived from their metabolic pathways. In the current study 18 metabolic pathways were found to be unique to the pathogen (R. conorii). A comprehensive analysis revealed 163 proteins implicated in 18 unique metabolic pathways of R. conorii. 140 proteins were reported to be essential for the bacterial survival, 46 were found virulent and 10 were found involved in resistance which can enhance the bacterial pathogenesis. The functional analysis of unique metabolic pathway proteins showed the abundance of plasmid conjugal transfer TrbL/VirB6, aliphatic acid kinase short chain, signal transduction response regulator receiver and components of type IV transporter system domains. The proteins were classified into six broad categories on the basis of predicted domains, i.e., metabolism, transport, gene expression and regulation, antimicrobial resistance, cell signalling and proteolysis. Further, in silico analysis showed that 88 proteins were suitable therapeutic targets which do not showed homology with host proteins. The 43 proteins showed hits with the DrugBank database showing their druggable nature and remaining 45 proteins were classified as novel drug targets that require further validation. The study will help to provide the better understanding of pathogens survival and embark on the development of successful therapies for the management of Indian tick typhus.
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