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Antiviral immunity in the gut: how the intestinal epithelium and microbiota regulate infection

Antiviral immunity in the gut: how the intestinal epithelium and microbiota regulate infection
肠道抗病毒免疫:肠上皮和微生物​​群如何调节感染
批准号:
9179594
负责人:
Sara Cherry
金额:
$39.43万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2015
资助国家:
美国
项目状态:
已结题
起止时间:
2015-11-12 至 2020-10-31

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中文摘要
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英文摘要
 DESCRIPTION (provided by applicant) Enteric pathogens, which represent a major group of disease-causing agents, must overcome barrier immunity within the intestinal environment to infect a host. To counter this, the gastrointestinal tract has evolved as a physical and immunological barrier. Moreover, many enteric viruses infect intestinal epithelial cells which are both targets of and act as sentinels for infection. Increasing evidence suggests that epithelial cells sense infection directly to induce antimicrobial pathways. It is also clear that the microfloa within the intestinal tract plays a fundamental role in immunity and that imbalanced bacterial communities have detrimental consequences to immune defense. Aging animals present with immune deficiencies and an altered microbiome. Mechanistically, which microbes or microbial ligands, mediate these effects and how they impact antiviral immunity is unclear. To overcome our gap in knowledge of the molecular mechanisms that control enteric viral infection, we developed an oral model of arboviral infection using the powerful genetic model organism, Drosophila melanogaster. We found that the gut presents a high barrier to infection: young wild type flies are refractory to oral challenge with enteric viruses, while inoculation into the body cavity, which bypasses the gut, results in robust infection. Importantly, we found that the ERK pathway is activated in the intestinal epithelium by infection, and that genetic depletion of the ERK pathway only in the intestinal epithelium leads to increased infection. Furthermore, we found that the microbiota plays an important role in susceptibility to infection. In young flies, te loss of commensals in the gut led to increased permissivity to viral infection, suggesting that signals from the microbiota impact innate signaling. However, we found that older flies that present with dysbiosis are more susceptible to oral viral infection. Under these conditions ablation of the commensals protects the animals from enteric viral infection. Therefore, the microbiota, depending on its composition, can either be protective or detrimental for antiviral defenses. In this proposal we will address fundamental questions in antiviral immunity by determining the mechanisms by which the microbiota and epithelial cells control immunity in the intestine against human viruses, using a genetically tractable organism with a highly manipulable microbiome and short lifespan.
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Development and validation of antivirals against Flaviviruses
  • 批准号:
    10514328
  • 项目类别:
  • 资助金额:
    $489.76万
  • 财政年份:
    2022
  • 负责人:
    Sara Cherry
  • 依托单位:
Defining the role of microbiota-derived cyclic dinucleotides in priming antiviral immune defenses.
  • 批准号:
    10551893
  • 项目类别:
  • 资助金额:
    $40.63万
  • 财政年份:
    2020
  • 负责人:
    Sara Cherry
  • 依托单位:
Small Molecule Screening to Identify Novel Sars-CoV-2 Therapeutics
  • 批准号:
    10223018
  • 项目类别:
  • 资助金额:
    $33.6万
  • 财政年份:
    2020
  • 负责人:
    Sara Cherry
  • 依托单位:
Defining the role of microbiota-derived cyclic dinucleotides in priming antiviral immune defenses.
  • 批准号:
    10326823
  • 项目类别:
  • 资助金额:
    $40.63万
  • 财政年份:
    2020
  • 负责人:
    Sara Cherry
  • 依托单位:
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