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中文摘要
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描述(申请人提供):冈比亚按蚊转基因和高通量基因组技术的最新进展使其成为研究宿主-寄生虫相互作用和天然免疫的强大模式生物。此外,按蚊传播人类最严重的疾病之一疟疾。缺乏有效的疫苗、寄生虫对药物的抗药性以及蚊子对杀虫剂的抗药性加剧了疾病的扩大,因此迫切需要制定新的新的控制战略。基于阻断媒介蚊子中疟原虫生命周期的控制策略将需要了解蚊子-寄生虫相互作用所涉及的分子机制。蚊子的先天免疫系统能够杀死大量的疟疾寄生虫。摄入受疟疾感染的血液会激活先天免疫反应,从而极大地杀灭中肠内的疟原虫。这些免疫反应的特定激发子、它们调节的免疫途径以及它们在寄生虫不同阶段的杀原虫活性尚不清楚。这项应用将利用全基因组微阵列来全面剖析全身和中肠对与疟疾感染血液相关的不同成分(激发子)的特定转录反应,然后评估这些反应对疟原虫发育的影响。这些分析将阐明蚊子感染反应生理学的重要方面,并提供有关抗疟原虫免疫反应调节的信息。它将为制定疟疾控制战略提供利用蚊子先天免疫系统的基线评估。
英文摘要
DESCRIPTION (provided by applicant): Recent advances in Anopheles gambiae transgenic and high throughput genomic technologies have rendered it a powerful model organism for the study of host - parasite interactions and innate immunity. In addition, Anopheline mosquitoes transmit one of the most serious diseases of mankind, malaria. The lack of effective vaccines, the development of parasite resistance to drugs and mosquito resistance to insecticides contribute to the expansion of the disease and have thereby created an acute need for the development of additional novel control strategies. Control strategies based on the blocking of Plasmodium's lifecycle in the vector mosquito will require the understanding of the molecular mechanisms implicated in mosquito - parasite interactions. The mosquito's innate immune system is capable of killing large numbers of malaria parasites. Ingestion of malaria infected blood results in the activation of innate immune responses that contribute significantly to the killing of Plasmodia in the midgut. The specific elicitors of these immune responses, the immune pathways they regulate and their plasmodiocidal activity on the different stages of the parasite are as yet unknown. This application will utilize a full genome microarray for a comprehensive dissection of the systemic and midgut specific transcript responses to the different components (elicitors) that are associated with malaria infected blood and then assess the impact of these responses on Plasmodium development. These analyses will elucidate important aspects of the mosquito's infection responsive physiology and provide information on the regulation of antiplasmodial immune response. It will provide baseline assessment on the utilization of the mosquito's innate immune system for the development of malaria control strategies.
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Impact of gene-drive systems for population modification on malaria vector mosquitoes
  • 批准号:
    10658710
  • 项目类别:
  • 资助金额:
    $109.21万
  • 财政年份:
    2023
  • 负责人:
    George Dimopoulos
  • 依托单位:
Complete Plasmodium falciparum infection cycle model
  • 批准号:
    10592599
  • 项目类别:
  • 资助金额:
    $20.47万
  • 财政年份:
    2022
  • 负责人:
    George Dimopoulos
  • 依托单位:
Mosquito SAMSP1 and SAMSP2 influence the initial stage of Plasmodium infection of mice
  • 批准号:
    10589090
  • 项目类别:
  • 资助金额:
    $80.78万
  • 财政年份:
    2021
  • 负责人:
    George Dimopoulos
  • 依托单位:
Mosquito SAMSP1 and SAMSP2 influence the initial stage of Plasmodium infection of mice
  • 批准号:
    10393036
  • 项目类别:
  • 资助金额:
    $81.95万
  • 财政年份:
    2021
  • 负责人:
    George Dimopoulos
  • 依托单位:
海外基金