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中文摘要
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描述(由申请人提供):蚊子利用各种策略来对抗病原体,包括病毒。pi研究的长期目标是在分子水平上阐明蚊子载体埃及伊蚊(Aedes aegypti)对一系列病毒病原体感染的免疫反应,包括那些可能被用作生物恐怖主义制剂的病原体。近年来,登革热已成为最严重的媒介传播病毒性疾病之一。登革热病毒在蚊子载体中传播的分子生物学在很大程度上是未知的,但是现在可用的基因组序列、反向遗传、转基因和功能基因组学工具为更详细地剖析蚊子的抗病毒防御系统提供了一种手段。在本建议中,我们将应用这些工具来描述Ae的含义。埃及伊蚊JAK-STAT先天免疫途径防御登革热病毒。我们已经证明蚊子利用JAK-STAT免疫途径通过基于RNAi的方法来限制登革热病毒感染。我们现在将使用基于转基因方法的更强大的方法来扩展这一发现,并更好地表征JAK-STAT途径在多个时间点和组织中对病毒感染的免疫反应。在Specific Aim 1中,我们将生成并分子表征有条件激活JAK-STAT通路的转基因蚊子系。在Specific Aim 2中,我们将研究重组激活的JAK-STAT通路的时空抗登革热活性,以更好地评估该防御系统在登革热控制策略开发中的潜在用途。
英文摘要
DESCRIPTION (provided by applicant): Mosquitoes utilize a variety of strategies to combat pathogens, including viruses. The long-term goal of the PIs research is to elucidate, at the molecular level, the immune responses of the mosquito vector Aedes aegypti to infection with a range of viral pathogens, including those that could be used as agents for bioterrorism. In recent years, dengue fever has emerged as one of the most serious vector-borne viral diseases. The molecular biology of dengue virus propagation in the mosquito vector is largely unknown, but the genome sequence, reverse genetic, transgenic and functional genomics tools that are now available provide a means of dissecting the mosquito's anti-viral defense systems in greater detail. In this proposal, we will apply these tools to characterize the implication of the Ae. aegypti JAK-STAT innate immune pathway in defense against the dengue virus. We have already showed that the mosquito is employing the JAK-STAT immune pathways to limit dengue virus infection through RNAi - based approaches. We will now use more powerful approaches, based on transgenic methodology, to expand on this finding and better characterize the JAK-STAT pathway immune responses to virus infection at multiple time points and tissues. In Specific Aim 1 we will generate and molecularly characterize the genetically modified mosquito lines that conditionally activate the JAK-STAT pathway. In Specific Aim 2 we will investigate the spatio- temporal anti-dengue activity of the recombinantly activated JAK-STAT pathway to better assess the potential use of this defense system for the development of dengue control strategies. PUBLIC HEALTH RELEVANCE: Despite the dramatic surge in dengue prevalence, surprisingly little is known about the molecular biology and genetic basis of the virus interactions with the mosquito vectors that enable transmission. This research proposal aims at the molecular characterization of the mosquito's immune defenses against virus infection that are controlled by the JAK-STAT pathway using transgenic technologies. The knowledge generated from this study can contribute to the development of control methods for dengue and other viruses such as yellow fever and West Niles viruses.
期刊论文(3)
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会议论文
DOI: 10.3390/v6114294
发表时间: 2014-11-11
期刊: Viruses
影响因子: --
作者: [Jupatanakul N, Sim S, Dimopoulos G]
通讯作者: Dimopoulos G
DOI: 10.1371/journal.pone.0135985
发表时间: 2015
期刊: PloS one
影响因子: 3.7
作者: [Bottino-Rojas V, Talyuli OA, Jupatanakul N, Sim S, Dimopoulos G, Venancio TM, Bahia AC, Sorgine MH, Oliveira PL, Paiva-Silva GO]
通讯作者: Paiva-Silva GO
DOI: 10.3390/v6114479
发表时间: 2014-11-19
期刊: Viruses
影响因子: --
作者: [Sim S, Jupatanakul N, Dimopoulos G]
通讯作者: Dimopoulos G
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:
    10182487
  • 项目类别:
  • 资助金额:
    $84.43万
  • 财政年份:
    2021
  • 负责人:
    George Dimopoulos
  • 依托单位:
海外基金