MAGPIE Project: The Structure, Biosynthesis and Assembly of the Mycobacterial Cell Envelope

MAGPIE 项目：分枝杆菌细胞包膜的结构、生物合成和组装

• 批准号: G9901077-E02/2
• 负责人: Gurdyal Besra
• 金额: $ 42.11万
• 依托单位: University of Birmingham
• 依托单位国家: 英国
• 项目类别: Research Grant
• 财政年份: 2006
• 资助国家: 英国
• 起止时间: 2006 至 无数据
• 项目状态: 已结题
• 来源: https://gtr.ukri.org/projects?ref=G9901077-E02%2F2
• 关键词: MAGPIE; Project; Structure; Biosynthesis; Assembly

Tuberculosis (TB) is a life ?threatening condition that can last for several years during which patients are debilitated and may disseminate the bacterium that causes the disease, Mycobacterium tuberculosis (Mtb). At least 30 million individuals worldwide will have died from TB in the last decade of the 20th century. In the UK the steady decline in TB cases over the whole of the last century halted in the mid 1980s and there has been alarming signs of increased numbers of cases in certain communities. The situation is compounded by the AIDS epidemic and by the emergence of Mtb strains that are resistant to virtually all the drugs that would normally be used to treat TB. It can be argued that, globally, Mtb is the single most important infectious agent affecting mankind. All bacteria have cells that, like plants, are enclosed in a cell wall. This protects the organism from its immediate environment and, fortuitously, presents an important target for drugs, like penicillin, that can be used to treat bacterial infections. However, Mtb has a distinctive cell wall that differs in composition from that of other bacteria; in particular it contains an exceptional amount of unique lipids (fats) and sugars. Although there are drugs that affect the unique Mtb cell wall, the current treatment for tuberculosis lasts 6 months and is potentially toxic to patients who often cease treatment early. Moreover, the efficacy of treatment is threatened by the emergence of drug-resistant strains of Mtb. There is therefore a great need for new and better drugs to treat TB. In this coordinated set of projects, the investigators are combining their particular expertise in analysing the Mtb cell wall to improve our understanding of these remarkable structures and the metabolic processes that are required for their assembly.Communication to the general public will be channelled through the University Press Office at Birmingham (http://www.newscentre.bham.ac.uk/office.htm) and Leciester (http://www.le.ac.uk/press/), which have established contacts in the local and national media. The MRC Co-operative Group members will also highlight there research through personal University based Web pages, which has open access. This highlights the clinical and research elements of the MRC Co-operative Group.

肺结核（TB）是一种生命吗？一种可持续数年的威胁性疾病，患者在此期间身体虚弱，并可能传播导致疾病的细菌，结核分枝杆菌（Mtb）。在20世纪的最后十年，全世界至少有3000万人死于结核病。在英国，结核病病例在整个上个世纪的稳步下降在20世纪80年代中期停止了，并且在某些社区出现了病例数量增加的惊人迹象。艾滋病的流行和结核分枝杆菌菌株的出现使这种情况更加复杂，这些菌株对通常用于治疗结核病的几乎所有药物都有抗药性。可以说，在全球范围内，结核分枝杆菌是影响人类的单一最重要的传染源。所有的细菌都有像植物一样被包围在细胞壁中的细胞。这保护了生物体免受其直接环境的影响，并且偶然地为药物提供了一个重要的靶点，如青霉素，可用于治疗细菌感染。然而，结核分枝杆菌具有独特的细胞壁，其组成与其他细菌不同;特别是它含有大量独特的脂质（脂肪）和糖。虽然有药物可以影响独特的结核杆菌细胞壁，但目前结核病的治疗持续6个月，对经常提前停止治疗的患者有潜在毒性。此外，结核分枝杆菌耐药菌株的出现威胁到治疗的功效。因此，非常需要新的和更好的药物来治疗结核病。在这一系列协调项目中，研究人员结合了他们在分析结核分枝杆菌细胞壁方面的专门知识，以提高我们对这些非凡结构及其组装所需的代谢过程的理解，将通过伯明翰大学新闻办公室（http：//www.newscentre.bham.ac.uk/office.htm）和Leciester（http：//www.le.ac.uk/press/）与公众进行沟通，这两个办公室已与当地和国家媒体建立了联系。MRC合作小组成员还将通过开放访问的个人大学网页突出研究。这突出了MRC合作组的临床和研究元素。