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Hemocyte Transcriptome and Immunity in Aedes aegypti

Hemocyte Transcriptome and Immunity in Aedes aegypti
埃及伊蚊的血细胞转录组和免疫
批准号:
7379916
负责人:
BRUCE MARTIN CHRISTENSEN
金额:
$34.65万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-02-15 至 2011-01-31

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中文摘要
翻译
蚊的先天免疫反应是控制媒介与病原体相互作用的主要因素; 因此,它是载体能力的主要决定因素。蚊子和其他昆虫的先天免疫力 利用细胞和体液成分来应对入侵的病原体,但体液方面的研究 先天免疫的研究占主导地位,主要强调抗菌肽(AMP)的鉴定, 参与其生产的信号通路。对血细胞和细胞的重视要少得多。 免疫反应,但最近的数据清楚地证实,细胞反应可能在清除微生物方面发挥关键作用, 病原体通过吞噬作用、黑化作用或通过两种过程的组合。在所需的数据中有一个空白, 准确定义调控过程,血细胞产生的效应分子,以及这些细胞和细胞因子的作用。 产品在先天免疫中发挥作用。同样清楚的是,AMP是针对免疫缺陷病毒的先天免疫应答中的重要因素。 入侵微生物,但目前尚不清楚细胞和AMP为基础的体液反应如何协同作用,以清除 微生物感染我们相信,研究一个基因或一小部分基因, 对于确定蚊子先天遗传中无疑存在的复杂相互关系, 免疫反应。因此,为了开创更全面的研究先天免疫的实验方法, 蚊子,我们开发了一个大型表达序列标签(EST)数据集,从埃及伊蚊免疫激活 血细胞和互补的基于谷胱甘肽的微阵列作为基底来评估蚊子细胞,以及 体液免疫反应本文提出的研究的一般假设是, 免疫应答是一个高度复杂的过程网络,其采用不同的,但不相互排斥的, 吞噬和黑化反应,与AMP一致,以清除血淋巴中的细菌感染, 被感染的蚊子为了验证这一假设,我们将使用蚊子Ae。埃及和一些细菌物种, (1)高通量分子方法来分析基因转录和识别不同的模式, 噬菌作用和黑化的抗菌反应,(2)利用微阵列分析评估转录谱 与不同细菌物种(致病性和引起反应的能力不同)有关的变化, 为了更好地剖析影响细胞免疫的机制,以及(3)采用微阵列分析,合成肽, RNAi方法和表型评估,以更好地确定AMP的作用,并选择未知基因,在 先天免疫所有来自微阵列分析的数据,包括所使用的实验方案,将由 在包含我们的血细胞EST数据的交互式网站上公开。
英文摘要
The mosquito innate immune response is a major factor governing the interaction between vector and pathogen; consequently, it is a primary determinant of vector competence. Innate immunity in mosquitoes and other insects employs both cellular and humoral components in response to invading pathogens, but studies of the humoral aspects of innate immunity have dominated, with a primary emphasis on the identification of antimicrobial peptides (AMPs) and the signaling pathways involved in their production. Far less emphasis has been placed on hemocytes and cellular immune responses, but recent data clearly verify that cellular responses likely play a critical role in clearing microbial pathogens by phagocytosis, melanization, or by both processes in combination. There is a void in the data required to accurately define regulatory processes, hemocyte-produced effector molecules, and the role these cells and cell products play in innate immunity. It also is clear that AMPs are significant factors in innate immune responses against invading microbes, but it is not known how cellular and AMP-based humoral responses function in concert to clear microbial infections. We believe that a reductionist approach, that studies one gene, or a small set of genes, in relation to a phenotype, has limitations for determining the complex interrelationships that undoubtedly exist in mosquito innate immune responses. Therefore, in order to initate more holistic experimental approaches for studying innate immunity in mosquitoes, we developed a large expressed sequence tag (EST) data set from Aedes aegypti immune-activated hemocytes and complementary oligonucleotide-based microarrays as substrates to evaluate mosquito cellular, as well as humoral, immune responses. The general hypothesis for the research proposed herein is that mosquito innate immune responses are a highly complex network of processes that employ the distinct, but not mutually exclusive, responses of phagocytosis and melanization, in concert with AMPs, to clear bacteria infections from the hemolymph of infected mosquitoes. To test this hypothesis, we will use the mosquito Ae. aegypti and a number of bacteria species in (1) high-throughput molecular approaches to profile gene transcription and to identify distinct patterns underlying the anti-bacterial responses of phagocytosis and melanization, (2) utilize microarray analyses to assess transcription profile changes in relation to different bacterial species (that vary in their pathogenicity and ability to elicit a response) in order to better dissect mechanisms influencing cellular immunity, and (3) employ microarray analyses, synthetic peptides, RNAi methodologies, and phenotype evaluations to better define the role AMPs, and select unknown genes, play in innate immunity. All data resulting from microarray analyses, including experimental protocols used, will be made publicly available on the interactive website that contains our hemocyte EST data.
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Mosquito-parasite interactions and filariasis transmission in Papua New Guinea
  • 批准号:
    8261118
  • 项目类别:
  • 资助金额:
    $6.13万
  • 财政年份:
    2010
  • 负责人:
    BRUCE MARTIN CHRISTENSEN
  • 依托单位:
Mosquito-parasite interactions and filariasis transmission in Papua New Guinea
  • 批准号:
    8080937
  • 项目类别:
  • 资助金额:
    $5.52万
  • 财政年份:
    2010
  • 负责人:
    BRUCE MARTIN CHRISTENSEN
  • 依托单位:
Mosquito-parasite interactions and filariasis transmission in Papua New Guinea
  • 批准号:
    7852770
  • 项目类别:
  • 资助金额:
    $7.34万
  • 财政年份:
    2010
  • 负责人:
    BRUCE MARTIN CHRISTENSEN
  • 依托单位:
Hemocyte Transcriptome and Immunity in Aedes aegypti
  • 批准号:
    7763198
  • 项目类别:
  • 资助金额:
    $34.3万
  • 财政年份:
    2006
  • 负责人:
    BRUCE MARTIN CHRISTENSEN
  • 依托单位:
海外基金