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DESCRIPTION (provided by applicant): Chlamydia are Gram-negative bacterial pathogens that infect a wide range of hosts and cause various diseases, including preventable blindness in developing countries, sexually transmitted disease and pneumonia. Chlamydia replicate intracellularly in a membrane-bound compartment that potentially serves as a protector shield against immune surveillance but also acts as a "platform" to exchange factors with the host cell. Despite the primary importance of Chlamydia as a human pathogen, little is known about the bacterial and host factors involved in the infection process. This paucity of knowledge is mainly due to the fact that Chlamydia is not a genetically tractable organism and to the difficulty of conducting genetic approaches in the mammalian host. We propose to conduct a genome-wide siRNA screen in order to identify and characterize human host factors involved in post-invasion events of Chlamydia trachomatis infection. We have demonstrated the feasibility of the approach on a subset of the genome and we propose to extend the approach to the entire human genome (Aim#1). Since RNAi treatment has been shown to be associated with the unintended silencing of genes displaying limited sequence homology with the targeted gene, we will perform a systematic validation procedure of the candidates to unambiguously establish a functional relationship between the knock-down of the targeted gene and the observed phenotype (Aim#2). Finally, we will conduct secondary assays to identify and characterize Chlamydia specific candidates involved in post-invasion events of C. trachomatis intracellular development (Aim#3). Overall, this developmental proposal is likely to provide new insights in Chlamydia pathogenesis and to generate the required preliminary results for future funding application(s) related to the characterization of known and/or novel pathway(s) involved in C. trachomatis infection. PUBLIC HEALTH RELEVANCE: Chlamydia are obligate intracellular bacterial pathogens responsible for various diseases such as trachoma, sexually transmitted disease and pneumoniae. We study how Chlamydia hijack cellular components to successfully replicate and disseminate inside the host. We focus on dissecting the cellular mechanism(s) invloved in the infection process by identifying the host factors required for Chlamydia development. The identification of these factors may help design new therapeutic treatments.
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DOI: 10.1371/journal.pone.0057090
发表时间: 2013
期刊: PloS one
影响因子: 3.7
作者: [Agaisse H, Derré I]
通讯作者: Derré I
The Effects of Sex Hormones on Chlamydia Infection
  • 批准号:
    10190235
  • 项目类别:
  • 资助金额:
    $20.26万
  • 财政年份:
    2021
  • 负责人:
    ISABELLE DERRE
  • 依托单位:
The Effects of Sex Hormones on Chlamydia Infection
  • 批准号:
    10395583
  • 项目类别:
  • 资助金额:
    $25.41万
  • 财政年份:
    2021
  • 负责人:
    ISABELLE DERRE
  • 依托单位:
Host-pathogen interactions controlling Chlamydia developmental cycle
  • 批准号:
    10456920
  • 项目类别:
  • 资助金额:
    $47.97万
  • 财政年份:
    2021
  • 负责人:
    ISABELLE DERRE
  • 依托单位:
The Effects of Sex Hormones on Chlamydia Infection
  • 批准号:
    10596516
  • 项目类别:
  • 资助金额:
    $23.11万
  • 财政年份:
    2021
  • 负责人:
    ISABELLE DERRE
  • 依托单位:
国内基金
海外基金
Epac1/2通过蛋白酶体调控中性粒细胞NETosis和Apoptosis在急性肺损伤中的作用研究
  • 批准号:
    LBY21H010001
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2020
  • 负责人:
    郑绪阳
  • 依托单位:
基于Apoptosis/Ferroptosis双重激活效应的天然产物AlbiziabiosideA的抗肿瘤作用机制研究及其结构改造
  • 批准号:
    81703335
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    20.0万元
  • 批准年份:
    2017
  • 负责人:
    卫高菲
  • 依托单位:
双肝移植后Apoptosis和pyroptosis在移植物萎缩差异中的作用和供受者免疫微环境变化研究
  • 批准号:
    81670594
  • 项目类别:
    面上项目
  • 资助金额:
    58.0万元
  • 批准年份:
    2016
  • 负责人:
    陈昊
  • 依托单位:
Serp-2 调控apoptosis和pyroptosis 对肝脏缺血再灌注损伤的保护作用研究
  • 批准号:
    81470791
  • 项目类别:
    面上项目
  • 资助金额:
    73.0万元
  • 批准年份:
    2014
  • 负责人:
    董家鸿
  • 依托单位: