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Modulation of beta-lactam resistance in methicillin-resistant Staphylococcus aureus by catechin gallates

Modulation of beta-lactam resistance in methicillin-resistant Staphylococcus aureus by catechin gallates
儿茶素没食子酸酯对耐甲氧西林金黄色葡萄球菌的β-内酰胺耐药性的调节
批准号:
G0600004/1
负责人:
Peter Taylor
金额:
$38.34万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2007
资助国家:
英国
项目状态:
已结题
起止时间:
2007 至 --

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中文摘要
翻译
从20世纪30年代开始,抗菌药物被引入医疗实践,并在20世纪40年代初随着青霉素的大规模生产而以惊人的方式继续下去,这使人们相信传染病是可以控制并最终被掌握的。然而,最初人们普遍乐观地认为抗生素将把严重的传染病驱逐到地球上。历史的垃圾箱?已经被证明是不成熟的;感染仍然是全世界第二大死亡原因,也是发展中国家的主要杀手。未能战胜感染威胁的原因很多,也很复杂,但抗生素耐药性的出现对我们抗击感染的能力产生了巨大影响。每当一种新的抗生素被引入,耐药性总是随之而来。细菌很快就找到了对抗这种生存威胁的方法,并发展出了将抗性基因传递给其他细菌的方法。这种获得性抗生素耐药性是多重耐药菌株出现的原因。称为超级细菌?通过媒体?这在医院里很常见,在社区获得性感染中也越来越常见。其中典型的是耐甲氧西林金黄色葡萄球菌,它已成为英国和其他地方医院的持久和常见的永久居民。虽然它仍然对一些昂贵的抗生素敏感,但有充分理由担心这种情况可能不会持续下去,在这种情况下,MRSA感染将变得无法治愈。我们一直在研究如何逆转MRSA的抗生素耐药性,使其对甲氧西林和苯氧西林等廉价抗生素再次敏感。这些抗生素阻止细菌形成它们赖以生存的硬壁?MRSA通过改变其壁的方式颠覆了这一作用。我们发现茶中的一种成分叫做?心电图?干扰MRSA的破坏机制,使细菌对甲氧西林敏感。因此,心电图可能与奥西林联合使用,以恢复抗生素敏感性。不幸的是,心电图在体内会迅速分解,但我们已经改变了它的化学性质,使其不易分解,我们还以其他方式修改了这种化合物,以增加其作为治疗药物的吸引力。我们现在希望更好地了解心电图是如何对抗MRSA的。我们知道它可以插入细菌膜中,因为对所涉及过程的深入了解将使我们能够改进最有前途的化合物,并使它们更接近临床应用。
英文摘要
The introduction of antibacterial drugs into medical practice, which began in the 1930s and continued in spectacular fashion with the mass production of penicillin in the early 1940s gave rise to the belief that infectious diseases could be controlled and, eventually, mastered. However, the initial widespread optimism that antibiotics would banish serious infectious disease to the ?dustbin of history? has proven to be premature; infections remain the second leading cause of mortality worldwide and the major killer in the developing world. The reasons for the failure to defeat the threat from infection are many and complex but the emergence of antibiotic resistance has had an enormous impact on our ability to combat infection. Whenever a new antibiotic has been introduced, resistance has always followed. Bacteria have quickly found the means to counteract this threat to their survival and have developed ways to pass on their resistance genes to other bacteria. This acquired antibiotic resistance is responsible for the emergence of multi-resistant strains ? called ?superbugs? by the media ? that are now commonplace in hospitals and increasingly found in community acquired infections. Typical of these is MRSA, which has become a persistent and common permanent inhabitant of hospitals in the United Kingdom and elsewhere. While it is still sensitive to a few expensive antibiotics, there are well-founded fears that this may not last, in which case MRSA infections will become untreatable. We have been researching ways to reverse antibiotic resistance in MRSA, making it again sensitive to inexpensive antibiotics such as methicillin and oxacillin. These antibiotics prevent bacteria from making the rigid wall that they need to survive ? MRSA subverts this action by altering the way it makes its wall. We have found that a component of tea called ?ECg? interferes with the MRSA subverting machinery and converts the bacteria to methicillin sensitivity. Thus, ECg might be used in combination with oxacillin to restore antibiotic sensitivity. Unfortunately, ECg is rapidly broken down in the body but we have changed its chemical nature to make it resistant to breakdown and we have modified the compound in other ways to increase its attraction as a therapeutic. We now wish to understand better how ECg works against MRSA ? we know it inserts into the bacterial membrane - as deeper understanding of the processes involved will enable us to refine our most promising compounds and bring them closer to clinical use.
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[SurgeryNet] Epilepsy surgery induced brain network changes: relation to patient outcomes
  • 批准号:
    MR/T04294X/1
  • 项目类别:
    Fellowship
  • 资助金额:
    $105.33万
  • 财政年份:
    2021
  • 负责人:
    Peter Taylor
  • 依托单位:
Biocatalytic Approaches to the Synthetic Manipulation of Silicones
  • 批准号:
    EP/S013660/1
  • 项目类别:
    Research Grant
  • 资助金额:
    $4.34万
  • 财政年份:
    2019
  • 负责人:
    Peter Taylor
  • 依托单位:
Molecular mechanisms of enterobacterial resistance to complement
  • 批准号:
    MR/R009937/1
  • 项目类别:
    Research Grant
  • 资助金额:
    $98.46万
  • 财政年份:
    2018
  • 负责人:
    Peter Taylor
  • 依托单位:
Treatment of multi-drug-resistant Gram-negative bacterial infections using capsule depolymerases
  • 批准号:
    MR/N012542/1
  • 项目类别:
    Research Grant
  • 资助金额:
    $48.8万
  • 财政年份:
    2016
  • 负责人:
    Peter Taylor
  • 依托单位:
国内基金
海外基金
人附睾蛋白4靶向调控TGF beta-smad轴加剧克罗恩病相关肠纤维化进程的作用机制研究
AP2B通过WNT/BETA-CATENIN调控颅骨元件成骨活性差异的 分子机制研究
  • 批准号:
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2025
  • 负责人:
    孙贤杰
  • 依托单位:
TGF-beta通路通过降低自噬-基因组稳定性介导胶质母细胞瘤间质亚型替莫唑胺耐药的机制研究
  • 批准号:
    82303919
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    30万元
  • 批准年份:
    2023
  • 负责人:
    陈鹭跃
  • 依托单位: