课题基金 / 基金详情

Rationally designed probiotic approaches to combat antibiotic-associated diarrhoea:

Rationally designed probiotic approaches to combat antibiotic-associated diarrhoea:
合理设计的益生菌方法可对抗抗生素相关腹泻:
批准号:
2291269
负责人:
金额:
$0.0万
依托单位:
依托单位国家:
英国
项目类别:
Studentship
财政年份:
2019
资助国家:
英国
项目状态:
已结题
起止时间:
2019 至 --

项目摘要

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中文摘要
翻译
人类是大约100万亿个共生微生物(肠道微生物群)的家园,它们是宿主免疫和代谢的主要调节器。通过抗生素治疗破坏微生物群与抗生素相关性腹泻(AAD)和肠道感染易感性增加有关。虽然很明显,微生物群破坏导致AAD和肠道感染,但仍不清楚微生物群的哪些特定成员的丧失使宿主对AAD和肠道感染易感。在我们最近的工作中(Brown et al,Nature Comms,2017),我们已经开发出构建共生微生物合成群落的方法,以探索这些生物体如何调节宿主免疫力。该项目将以帝国的Clarke集团(http://www.imperial.ac.uk/people/thomas.clarke)为基础,并与我们的行业合作伙伴雀巢合作。我们将使用我们的新模型和方法来解决这一知识差距,为个性化,合理设计的方法铺平道路,以恢复微生物群的稳态,以对抗AAD和肠道感染。此外,它还将在令人兴奋和备受追捧的微生物群领域提供尖端培训,并提供无与伦比的行业准入。该奖学金将利用该部门世界领先的分析能力,并提高其信息学和成像能力,为微生物群失调的个性化治疗提供多窗口视图,以及对抗传染病的新方法。
英文摘要
Humans are home to approximately 100 trillion symbiotic microbes (the commensal microbiota) which are a major regulator of host immunity and metabolism. Microbiota disruption through antibiotic treatment is associated with antibiotic-associated diarrhoea (AAD) and increased susceptibility to enteric infection. While it is clear that microbiota disruption leads to AAD and enteric infection, it remains unclear as to the loss of which specific members of the microbiota renders the host susceptible to AAD and enteric infection. In our recent work (Brown et al, Nature Comms, 2017), we have developed ways to construct synthetic communities of symbiotic microbes to probe how these organisms regulate host immunity. This project will be based in the Clarke group (http://www.imperial.ac.uk/people/thomas.clarke) at Imperial and is a collaboration with our industry partner Nestlé. We will use our novel models and approaches to tackle this gap in knowledge to pave the way for personalised, rationally designed approaches to restore microbiota homeostasis to combat AAD and enteric infection. In addition it will provide cutting-edge training in the exciting and highly sought-after areas of the microbiota and provide unparalleled access to industry.This studentship will leverage the world-leading analytical capacity of the Division and advance its informatics and imaging capacity to provide a multi-window view into personalised treatments for microbiota dysbiosis, and novel ways to combat infectious disease.
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