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Novel Therapeutic Approach to Invasive Group A Streptococcal Disease

Novel Therapeutic Approach to Invasive Group A Streptococcal Disease
侵袭性 A 组链球菌疾病的新治疗方法
批准号:
10546470
负责人:
Michael G. Caparon
金额:
$19.56万
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
项目状态:
已结题
起止时间:
2022-01-05 至 2024-12-31

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英文摘要
ABSTRACT Microbial-derived Short Chain Fatty Acids (SCFAs) have emerged as important mediators of “Disease Tolerance,” a process that seeks to limit collateral damage to host tissues that accompanies immune responses. SCFAs are the principle end-products of the metabolism of the Gram-positive pathogen Streptococcus pyogenes which can cause several severe invasive diseases that are notoriously difficult to treat due to extensive and rapid tissue destruction that limits perfusion of antibiotics to the site of bacterial multiplication. For the most severe manifestations, in particular necrotizing fasciitis, lesions expand to involve additional tissue at a rapid rate that can approach several cm per hour. This necessitates multiple rounds of aggressive and disfiguring surgical interventions, including debridement, fasciotomy and even amputation of limbs and this lack of therapeutic options results in high mortality. An important gap in our treatment arsenal is the lack of therapies to mitigate tissue damage during severe invasive disease, which would improve the efficacy of antibiotic treatment to promote clearance of the infection. The goal of this study is to explore proof-of-principle that therapeutic manipulation of streptococcal pyruvate metabolism can provide a viable strategy for mitigation of tissue damage to improve treatment outcomes of severe, invasive S. pyogenes disease. This concept builds upon our preliminary data that suggests S. pyogenes employs its several alternative pathways for pyruvate reduction to actively manipulate the host’s “Disease Tolerance” response to promote its ability to infect diverse host niches. Disease tolerance is the process the host employs to balance pathogen growth against the collateral damage to host tissues that accompanies immune responses, known as Growth/Damage Balance. Through identification of host cells and relevant signaling pathways that control disease tolerance, a therapeutic approach that targets microbial metabolic and host cell signaling pathways can reduce damage to tissue to improve the ability of antibiotics to clear infections.
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会议论文
Central carbon flux controls growth/damage balance for Streptococcus pyogenes.
中央碳通量控制化脓链球菌的生长/损害平衡。
DOI: 10.1371/journal.ppat.1011481
发表时间: 2023-06
期刊: PLoS pathogens
影响因子: 6.7
作者: []
通讯作者:
Novel Therapeutic Approach to Invasive Group A Streptococcal Disease
  • 批准号:
    10452033
  • 项目类别:
  • 资助金额:
    $23.63万
  • 财政年份:
    2022
  • 负责人:
    Michael G. Caparon
  • 依托单位:
Characterization of assembly factors for type IV secretion systems
  • 批准号:
    10435561
  • 项目类别:
  • 资助金额:
    $25.42万
  • 财政年份:
    2021
  • 负责人:
    Michael G. Caparon
  • 依托单位:
GmPcides: Componds that disarm antibiotic resistance in multiple gram-positive pathogens
  • 批准号:
    10577811
  • 项目类别:
  • 资助金额:
    $39.0万
  • 财政年份:
    2021
  • 负责人:
    Michael G. Caparon
  • 依托单位:
GmPcides: Componds that disarm antibiotic resistance in multiple gram-positive pathogens
  • 批准号:
    10162829
  • 项目类别:
  • 资助金额:
    $37.38万
  • 财政年份:
    2021
  • 负责人:
    Michael G. Caparon
  • 依托单位:
国内基金
海外基金
具有抗癌活性的天然产物金霉酸(Aureolic acids)全合成与选择性构建2-脱氧糖苷键
  • 批准号:
    22007039
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    24.0万元
  • 批准年份:
    2020
  • 负责人:
    王黎明
  • 依托单位:
海洋放线菌来源聚酮类化合物Pteridic acids生物合成机制研究
手性Lewis Acids催化的分子内串联1,5-氢迁移/环合反应及其在构建结构多样性手性含氮杂环化合物中的应用
对空气稳定的新型的有机金属Lewis Acids催化剂制备、表征与应用研究
  • 批准号:
    21172061
  • 项目类别:
    面上项目
  • 资助金额:
    30.0万元
  • 批准年份:
    2011
  • 负责人:
    许新华
  • 依托单位: