Functional Role of the Enterococcal Polysaccharide Antigen

肠球菌多糖抗原的功能作用

基本信息

  • 批准号:
    10625496
  • 负责人:
  • 金额:
    $ 19.13万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2022
  • 资助国家:
    美国
  • 起止时间:
    2022-05-20 至 2025-04-30
  • 项目状态:
    未结题

项目摘要

Enterococci represent one of the leading causes of infections among hospitalized patients and residents of long-term care facilities. In the USA, there were over 50,000 cases of enterococcal infections in 2017, with ~10% fatality rate. The majority of infections are caused by Enterococcus faecalis and E. faecium, which include bacteremia, urinary tract and surgical sites infections, and endocarditis. E. faecalis and E. faecium display high levels of natural and acquired antibiotic resistance that severely limits the treatment options. The major component of streptococcal cell wall is the Enterococcal Polysaccharide Antigen (EPA). The recently solved structure of EPA consists of a polyrhamnose backbone decorated with a polyribitol phosphate- containing teichoic acid. While a hypothetical mechanism of EPA biosynthesis has been proposed, studies are required to test it. The goal of this application is to decipher the critical steps of EPA polyrhamnose and teichoic acid assembly. In addition, we will examine the role of EPA in binding to the enterococcal autolysins and the resistance mechanism to host antimicrobial protein expressed in the intestinal epithelial cells, ReGIIIγ. We will utilize a combination of genetic, analytical and biochemical methods to answer these questions. The enzymes of EPA biosynthetic pathway constitute promising targets for the development of novel antimicrobials to combat enterococcal infections. Thus, the proposed experiments will provide a better understanding of cell wall biogenesis in enterococci to enable the development of alternative approaches to treat drug-resistant infections. Furthermore, the proposed studies will enhance our understanding of the functions of EPA in antimicrobial resistance and persistence of enterococci in gut microbiota.
肠球菌是住院患者感染的主要原因之一

项目成果

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Konstantin V Korotkov其他文献

Konstantin V Korotkov的其他文献

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{{ truncateString('Konstantin V Korotkov', 18)}}的其他基金

Function of the type 7 secretion system in Group B Streptococcus
B 族链球菌 7 型分泌系统的功能
  • 批准号:
    10598223
  • 财政年份:
    2022
  • 资助金额:
    $ 19.13万
  • 项目类别:
Functional Role of the Enterococcal Polysaccharide Antigen
肠球菌多糖抗原的功能作用
  • 批准号:
    10527587
  • 财政年份:
    2022
  • 资助金额:
    $ 19.13万
  • 项目类别:
Novel therapeutic approaches for treatment of drug-resistant Gram-positive infections
治疗耐药革兰氏阳性菌感染的新方法
  • 批准号:
    10301362
  • 财政年份:
    2020
  • 资助金额:
    $ 19.13万
  • 项目类别:
Targeting NAD biosynthesis in Mycobacterium tuberculosis
靶向结核分枝杆菌的 NAD 生物合成
  • 批准号:
    8873087
  • 财政年份:
    2015
  • 资助金额:
    $ 19.13万
  • 项目类别:

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