Characterisation of Galleria mellonella innate immune response to Mycobacterium tuberculosis infection
大蜡螟对结核分枝杆菌感染的先天免疫反应的特征
基本信息
- 批准号:NC/W002264/1
- 负责人:
- 金额:$ 18.86万
- 依托单位:
- 依托单位国家:英国
- 项目类别:Fellowship
- 财政年份:2022
- 资助国家:英国
- 起止时间:2022 至 无数据
- 项目状态:未结题
- 来源:
- 关键词:
项目摘要
The Greater wax moth (Galleria mellonella, GM) is an insect pest of honeybee hives. However, it has been found that the caterpillar of GM can be infected in the laboratory by human bacterial pathogens. Such GM "infection models" can be used to understand how pathogens cause diseases in humans, helped by the many similarities between the insect and human immune system. GM are now being increasingly being used as an alternative to animal infection models. However, a major limitation to the more widespread use of GM-based infection models is the lack of reagents that can be used to characterise the GM immune system. Availability of such GM reagents would lead to a greater uptake of GM-based infection models and will further reduce the use of animals in research.In this exciting Fellowship, I will generate reagents, which for the first time, can distinguish the six sub-types of haemocytes (considered equivalent to white blood cells populations in humans) found in GM. These reagents will be used to characterise the immune response in a GM-Mycobacterium tuberculosis (MTB) infection model. MTB is the cause of human tuberculosis (TB) which, until the covid pandemic, was the leading worldwide cause of death due to infection. To meet the WHO goal of ending the TB epidemic by 2035, alternative infection models - like GM are urgently needed. In the work leading up to this Fellowship, I have established a GM-MTB infection model. Unlike the most widely used mouse model, granulomas - the hallmark of human TB - are produced in GM. We know that haemocytes are required for their formation. However, we do not know if only a select few or all six sub-types of GM haemocytes are needed. Knowing which sub-types are involved will enable a greater understanding of insect immunity and, in particular, the haemocyte sub-types that are involved in the response of GM to MTB. In addition, I will analyse which genes are expressed in GM caterpillars infected with MTB, allowing direct comparison with human studies. The outcome of this project will be the generation of reagents and methods that will allow a greater understanding of GM immunity, in particular, the response of larvae to MTB infection, and how close it is to the human immune response to MTB. All reagents, methods and results will be made publicly available. A successful conclusion to this project will result in a greater uptake of not only the GM-MTB infection model, but also in other GM infection models (of which there are over 65) that are currently in use.
大蜡螟(Galleria mellonella,GM)是蜜蜂蜂巢的害虫。但人们发现,转基因的毛虫在实验室中可以被人类细菌病原体感染。这种转基因“感染模型”可用于了解病原体如何在人类中引起疾病,这得益于昆虫和人类免疫系统之间的许多相似之处。转基因现在越来越多地被用作动物感染模型的替代品。然而,更广泛地使用基于转基因的感染模型的一个主要限制是缺乏可用于检测转基因免疫系统的试剂。这种转基因试剂的可用性将导致更大的吸收转基因为基础的感染模型,并将进一步减少在研究中使用的动物。在这个令人兴奋的奖学金,我将产生的试剂,这是第一次,可以区分六个亚型的血细胞(被认为相当于人类的白色血细胞群体)中发现的转基因。这些试剂将用于检测GM-结核分枝杆菌(MTB)感染模型中的免疫应答。MTB是人类结核病(TB)的病因,在新冠肺炎大流行之前,结核病是全球因感染导致死亡的主要原因。为了实现世卫组织到2035年结束结核病流行的目标,迫切需要替代感染模型,如转基因。在获得该奖学金的工作中,我建立了一个GM-MTB感染模型。与最广泛使用的小鼠模型不同,肉芽肿-人类结核病的标志-在转基因中产生。我们知道血细胞是它们形成所必需的。然而,我们不知道是否只需要选择少数或所有六种亚型的GM血细胞。了解哪些亚型参与将使更好地了解昆虫免疫,特别是血细胞亚型参与转基因对结核分枝杆菌的反应。此外,我将分析哪些基因在感染MTB的转基因毛虫中表达,从而与人类研究进行直接比较。该项目的成果将是产生试剂和方法,使人们能够更好地了解转基因免疫,特别是幼虫对结核分枝杆菌感染的反应,以及它与人类对结核分枝杆菌的免疫反应有多接近。所有试剂、方法和结果都将公开提供。该项目的成功结束将不仅导致对GM-MTB感染模型的更大吸收,而且还将导致对目前使用的其他GM感染模型(其中有超过65个)的更大吸收。
项目成果
期刊论文数量(0)
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科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Masanori Asai其他文献
Stereocontrolled synthesis of 8,11-dideoxytetrodotoxin, unnatural analogue of puffer fish toxin.
8,11-双脱氧河豚毒素的立体控制合成,河豚毒素的非天然类似物。
- DOI:
- 发表时间:
2004 - 期刊:
- 影响因子:5.2
- 作者:
T. Nishikawa;D. Urabe;Kazumasa Yoshida;T. Iwabuchi;Masanori Asai;M. Isobe - 通讯作者:
M. Isobe
Design, synthesis, and structure-activity relationship study of a novel class of ORL1 receptor antagonists based on N-biarylmethyl spiropiperidine.
基于N-联芳甲基螺哌啶的一类新型ORL1受体拮抗剂的设计、合成和构效关系研究。
- DOI:
- 发表时间:
2008 - 期刊:
- 影响因子:2.7
- 作者:
T. Yoshizumi;H. Miyazoe;H. Ito;Tomohiro Tsujita;Hirobumi Takahashi;Masanori Asai;S. Ozaki;H. Ohta;O. Okamoto - 通讯作者:
O. Okamoto
Optimization of benzimidazole series as opioid receptor-like 1 (ORL1) antagonists: SAR study directed toward improvement of selectivity over hERG activity.
苯并咪唑系列作为阿片类受体样 1 (ORL1) 拮抗剂的优化:SAR 研究旨在提高 hERG 活性的选择性。
- DOI:
- 发表时间:
2009 - 期刊:
- 影响因子:2.7
- 作者:
Kensuke Kobayashi;Tetsuya Kato;I. Yamamoto;A. Shimizu;Sayaka Mizutani;Masanori Asai;H. Kawamoto;S. Ito;T. Yoshizumi;M. Hirayama;S. Ozaki;H. Ohta;O. Okamoto - 通讯作者:
O. Okamoto
Asymmetric total synthesis of 11-deoxytetrodotoxin, a naturally occurring congener.
11-脱氧河豚毒素(一种天然同源物)的不对称全合成。
- DOI:
10.1021/ja0265153 - 发表时间:
2002 - 期刊:
- 影响因子:15
- 作者:
T. Nishikawa;Masanori Asai;M. Isobe - 通讯作者:
M. Isobe
An anatomical malleus-to-footplate prosthesis for ossicular chain reconstruction
- DOI:
10.1016/s0194-5998(97)80107-6 - 发表时间:
1997-08-01 - 期刊:
- 影响因子:
- 作者:
Masanori Asai;Richard Goode - 通讯作者:
Richard Goode
Masanori Asai的其他文献
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