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解读代谢途径:治疗靶点的藏宝图。

Deciphering metabolic pathways: A treasure map to therapeutic targets.

作者信息

Prajapat Brijesh, Sharma Ankita, Kumar Sunil, Sharma Dixit

机构信息

Department of Animal Sciences, School of Life Sciences, Central University of Himachal Pradesh, District Kangra, Himachal Pradesh, India, 176206.

Dr. Ambedkar Centre of Excellence, Central University of Himachal Pradesh, District Kangra, Himachal Pradesh, 176215, India.

出版信息

Biotechnol Notes. 2024 Nov 23;6:1-9. doi: 10.1016/j.biotno.2024.11.006. eCollection 2025.

DOI:10.1016/j.biotno.2024.11.006
PMID:39722831
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11667008/
Abstract

Indian tick typhus is an infectious disease caused by intracellular gram-negative bacteria (). 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 (). A comprehensive analysis revealed 163 proteins implicated in 18 unique metabolic pathways of . 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, , metabolism, transport, gene expression and regulation, antimicrobial resistance, cell signalling and proteolysis. Further, 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.

摘要

印度蜱传斑疹伤寒是一种由细胞内革兰氏阴性细菌引起的传染病。该细菌通过受感染蜱虫的叮咬传播给人类,有时也可通过虱子、跳蚤或螨虫传播。这种疾病局限于某些地区,病例较少,但在过去十年中,它在印度不同地区再度出现,病例数量众多。对细菌病原体基因组成的深入了解可以从它们的代谢途径中获得。在当前的研究中,发现18种代谢途径是该病原体所特有的。全面分析揭示了163种蛋白质与该病原体的18种独特代谢途径有关。据报道,140种蛋白质对细菌的生存至关重要,46种具有毒性,10种参与抗性,这可能会增强细菌的致病性。对独特代谢途径蛋白质的功能分析表明,存在大量的质粒接合转移TrbL/VirB6、短链脂肪酸激酶、信号转导反应调节受体和IV型转运系统结构域的成分。根据预测的结构域,这些蛋白质被分为六大类,即代谢、转运、基因表达与调控、抗微生物抗性、细胞信号传导和蛋白水解。此外,分析表明,88种蛋白质是合适的治疗靶点,它们与宿主蛋白质没有同源性。43种蛋白质在DrugBank数据库中有匹配结果,表明它们具有可成药的特性,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情况,并着手开发成功治疗印度蜱传斑疹伤寒的疗法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4193/11667008/7dc3a2b3c75e/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4193/11667008/bc305f90bfea/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4193/11667008/65c4369ba5b2/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4193/11667008/5116be065b5a/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4193/11667008/7dc3a2b3c75e/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4193/11667008/bc305f90bfea/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4193/11667008/65c4369ba5b2/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4193/11667008/5116be065b5a/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4193/11667008/7dc3a2b3c75e/gr4.jpg

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