Anaplasma phagocytophilum induce Ixodes scapularis antifreeze glycoprotein gene e

嗜吞噬细胞无形体诱导肩胛硬蜱抗冻糖蛋白基因e

基本信息

  • 批准号:
    8578755
  • 负责人:
  • 金额:
    $ 4.21万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2011
  • 资助国家:
    美国
  • 起止时间:
    2011-03-01 至 2014-11-30
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): Ixodes scapularis ticks overwinter in the Northeast and Upper Midwest parts of United States, and transmit various human pathogens that include human anaplasmosis agent Anaplasma phagocytophilum. My preliminary data show that the presence of A. phagocytophilum in ticks increases the ability of I. scapularis to survive in the cold. I have identified an I. scapularis antifreeze glycoprotein, designated as IAFGP and demonstrate, via RNAi knockdown studies, the importance of IAFGP for the survival of ticks in a freezing environment. Transfection studies also show that IAFGP increases the viability of yeast cells subjected to low temperatures. Remarkably, I have found that A. phagocytophilum induce the expression of iafgp and thereby increase the cold tolerance of I. scapularis. These data define a molecular basis for symbiosis between A. phagocytophilum and I. scapularis. The mechanism by which A. phagocytophilum, induce iafgp expression is not understood. Therefore studies will be performed to elucidate the mechanism by which A. phagocytophilum influence vector gene expression for its own benefit as well as its vector host survival during freezing temperatures. Following are the specific aims that will be addressed to understand the mechanism: In aim 1, I will identify and characterize iafgp promoter in I. scapularis. The studies in this aim will address whether iafgp promoter is activated upon A. phagocytophilum infection. In aim 2, studies will be undertaken to characterize the role of host transcriptional activators that may be involved in iafgp promoter induction. Collectively, the proposed studies not only elucidate the molecular mechanisms of symbiotic association between A. phagocytophilum and I. scapularis ticks but also delineate a new approach to study host-pathogen interaction.
描述(由申请方提供):肩突硬蜱在美国东北部和上中西部地区越冬,并传播各种人类病原体,包括人类无形体病病原体嗜吞噬细胞无形体。我的初步数据表明,A.蜱中的嗜吞噬细胞菌增加了I.肩胛肌才能在寒冷中生存我发现了一个I。我们发现了肩胛蜱抗冻糖蛋白,命名为IAFGP,并通过RNAi敲除研究证明了IAFGP对蜱在冷冻环境中存活的重要性。转染研究还表明,IAFGP增加了酵母细胞在低温下的生存力。值得注意的是,我发现A.嗜吞噬细胞菌诱导Iafgp的表达,从而提高了I.肩胛肌这些数据为A.嗜吞噬细胞菌和I.肩胛肌研究了A.嗜吞噬细胞菌诱导IAFgp表达的机制尚不清楚。因此,将进行研究以阐明A.嗜吞噬细胞菌影响载体基因表达,以利于其自身以及其载体宿主在冷冻温度下的存活。以下是具体的目标,将致力于了解机制:在目的1,我将确定和表征iafgp启动子在I。肩胛肌本研究将探讨iafgp启动子在A.嗜吞噬细胞菌感染在目标2中,将进行研究以表征可能参与iafgp启动子诱导的宿主转录激活因子的作用。这些研究不仅阐明了A.嗜吞噬细胞菌和I.肩胛蜱,但也描绘了一个新的方法来研究宿主-病原体相互作用。

项目成果

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科研奖励数量(0)
会议论文数量(0)
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Girish Neelakanta其他文献

Girish Neelakanta的其他文献

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{{ truncateString('Girish Neelakanta', 18)}}的其他基金

Anaplasma phagocytophilum modulate tick gene expression for its survival and transmission from the vector host
嗜吞噬细胞无形体调节蜱基因表达以使其存活并从载体宿主传播
  • 批准号:
    10322351
  • 财政年份:
    2017
  • 资助金额:
    $ 4.21万
  • 项目类别:
Anaplasma phagocytophilum modulate tick gene expression for its survival and transmission from the vector host
嗜吞噬细胞无形体调节蜱基因表达以使其存活并从载体宿主传播
  • 批准号:
    10203774
  • 财政年份:
    2017
  • 资助金额:
    $ 4.21万
  • 项目类别:
Anaplasma phagocytophilum modulate tick gene expression for its survival and transmission from the vector host
嗜吞噬细胞无形体调节蜱基因表达以使其存活并从载体宿主传播
  • 批准号:
    9398343
  • 财政年份:
    2017
  • 资助金额:
    $ 4.21万
  • 项目类别:
Anaplasma phagocytophilum induce Ixodes scapularis antifreeze glycoprotein gene e
嗜吞噬细胞无形体诱导肩胛硬蜱抗冻糖蛋白基因e
  • 批准号:
    8232534
  • 财政年份:
    2011
  • 资助金额:
    $ 4.21万
  • 项目类别:
Anaplasma phagocytophilum induce Ixodes scapularis antifreeze glycoprotein gene e
嗜吞噬细胞无形体诱导肩胛硬蜱抗冻糖蛋白基因e
  • 批准号:
    8113734
  • 财政年份:
    2011
  • 资助金额:
    $ 4.21万
  • 项目类别:

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Anaplasma phagocytophilum modulate tick gene expression for its survival and transmission from the vector host
嗜吞噬细胞无形体调节蜱基因表达以使其存活并从载体宿主传播
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Anaplasma phagocytophilum modulate tick gene expression for its survival and transmission from the vector host
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嗜吞噬细胞无形体调节蜱基因表达以使其存活并从载体宿主传播
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Anaplasma phagocytophilum hijacking of host cell monoubiquitination
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