Exploring host-gut microbial genetic and immune interactions using twins
Exploring host-gut microbial genetic and immune interactions using twins
批准号:
MR/N01183X/1
负责人:
Tim Spector
金额:
$102.41万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2016
资助国家:
英国
项目状态:
已结题
起止时间:
2016 至 --
中文摘要
微生物对维持健康的免疫系统至关重要,也是我们饮食和健康之间的纽带。我们大约有100万亿个肠道微生物,其数量是人类细胞数量的10倍,是基因数量的100倍。这些微生物产生多种酶、化学物质、荷尔蒙和维生素,可能会与我们的身体相互作用。我们肠道微生物的变化与许多人类疾病有关,包括肥胖、结肠炎、过敏和自闭症。直到最近,由于基因测序,我们才能够对它们进行适当的研究,并意识到绝大多数对我们无害,许多是有益的。肠道微生物的研究特别令人兴奋,因为我们知道我们可以通过手术、药物、益生菌和饮食改变它们的组成。通过这种方式,我们可能会通过微生物操作改变许多疾病。我们目前正经历着西方世界过敏的流行,以及许多自身免疫性疾病的增加,这可能与我们肠道微生物的异常和最近的变化有关。我们的微生物和我们的身体之间的主要交流方式是通过肠道内的免疫细胞。这项研究旨在提供有关我们肠道内的人类免疫细胞与栖息在我们肠道中的数万亿微生物之间相互作用的重要信息。最近,我们发现在人类粪便中发现的微生物在不同个体之间存在巨大差异,其中一些差异是由于我们人类基因的差异。然而,粪便中的微生物并不一定代表肠壁中微生物的丰度或功能,这可能对宿主健康有更大的影响。我们缺乏有关肠壁微生物和宿主细胞反应之间关系的重要信息,如果我们要推进这一令人兴奋的领域,就需要这些信息。该项目将提供100对同卵双胞胎肠道壁微生物和宿主细胞反应的宝贵资源数据库。使用双胞胎的好处是,这让我们能够确定与年龄、早期家庭环境以及重要的人类遗传学无关的影响。我们最近表明,我们自己的基因决定了哪些种类的细菌在我们的肠道中繁殖,这些细菌在人与人之间存在显着差异。双胞胎志愿者的年龄将超过40岁,没有任何重大疾病,他们将接受正常的结肠镜检查。我们已经试行了我们的志愿者,发现超过60%的人热衷于参与。在手术过程中,我们将在肠道的3个不同部位进行活组织检查和刷检,直到小肠末端。这将使我们能够测试每个地点的不同微生物物种,以及最重要的微生物如何与人类免疫基因(通过基因表达水平衡量)和免疫系统的其他标记相互作用。由于微生物很少单独工作,也很少探索相关物种,我们将研究具有类似功能的微生物网络,并将其构建到我们的资源中。该资源将使该领域的其他科学家能够寻找潜在的有趣的基因和微生物,并探索它们各自的功能。它还将使科学家能够比较粪便中的微生物结果,并预测肠道和人类免疫系统内的影响。最后,我们将进行一些初步研究,以测试将人类免疫相关微生物移植到不育小鼠身上的效果,这将测试这些微生物是否直接影响免疫系统。最终目标将是找到帮助我们免疫系统的关键微生物,并开发通过饮食或其他方法增加它们的数量或功能的方法。这项研究有可能对许多疾病和医学领域产生巨大影响,涉及衰老、饮食和免疫系统。我们有来自世界各地的学者的支持信,他们将从这项工作中受益。
英文摘要
Microbes are crucial in maintaining a healthy immune system and are the link between our diet and health. We have around 100 trillion gut microbes that outnumber our human cells ten to one and our genes 100 to one. The microbes produce a wide range of enzymes, chemicals, hormones and vitamins that can potentially interact with our bodies. Alterations to our gut microbes have been implicated in many human diseases ranging from obesity, colitis, allergy and autism. Only recently thanks to genetic sequencing have we been able to study them properly and realise that the vast majority are not harmful to us and many are beneficial. Study of the gut microbes is particularly exciting because we know that we can alter their composition through surgery, drugs, probiotics and diet. In this way we could potentially alter many diseases via microbial manipulation. We are currently experiencing an epidemic of allergies in the western world as well as increases in many autoimmune diseases and this could be related to abnormalities and recent changes in our gut microbes. The main method of communication between our microbes and our body is via the immune cells in the gut lining.This is a study designed to provide vital information about the interactions between our human immune cells in our gut lining and the trillions of microbes that inhabit our gut. Recently we have discovered that the microbes found in our stools vary enormously between individuals and that some of this variation is due to differences in our human genes. However microbes in the stool do not necessarily represent the abundance or functions of the microbes in the gut wall, which may have even greater effect on host health. We lack vital information on the relationship between microbes in the gut wall and our host cellular responses which we need if we are to progress this exciting field. This project will provide a valuable resource database of microbes in the gut wall and the cellular responses of the host in 100 pairs of identical twins. The benefit of using twins is that this allows us to determine effects which are independent of age, early family environment and importantly human genetics. We have recently shown that our own genes determine which species of bacteria proliferate in our guts which vary markedly between people. Twin volunteers will be aged over 40 without any major diseases and will undergo a normal screening colonoscopy. We have already piloted our volunteers and found over 60% keen to participate. During the procedure we will obtain biopsies and brushings at 3 different sites in the bowel, going up to the end of the small intestine. This will allow us to test the different microbe species at each site and how the most important ones interact with the human immune genes (measured by levels of gene expression) and other markers of the immune system. As microbes rarely work alone as well as exploring the associated species we will look at the networks of microbes that have similar functions and build this into our resource. The resource will enable other scientists in the field to look up potentially interesting genes and microbes and explore their respective functions. It will also allow scientists to compare microbe results from stools and predict the effects seen within the gut and the human immune system. Finally, we will do some pilot studies to test the effects of transplanting immune related microbes from humans into sterile mice which will test if the microbes are directly affecting the immune system. The ultimate aim will be to find the key microbes that help our immune system and develop ways to increase their numbers or their function through diet or other methods. The study has the potential to have enormous impact across many diseases and fields of medicine involving ageing, diet and the immune system. We have support letters from a wide range of academics across the world who would benefit from this work.
期刊论文(9)
专著(0)
科研奖励(0)
会议论文
登录
查看更多内容
DOI:
10.3390/microorganisms7010017
发表时间:
2019-01-01
期刊:
MICROORGANISMS
影响因子:
4.5
作者:
[Bowyer, Ruth C. E., Jackson, Matthew A., Steves, Claire J.]
通讯作者:
Steves, Claire J.
DOI:
10.1016/j.chom.2016.04.017
发表时间:
2016-05-11
期刊:
Cell host & microbe
影响因子:
30.3
作者:
[Goodrich JK, Davenport ER, Beaumont M, Jackson MA, Knight R, Ober C, Spector TD, Bell JT, Clark AG, Ley RE]
通讯作者:
Ley RE
DOI:
10.1136/gutjnl-2020-323877
发表时间:
2021-09
期刊:
Gut
影响因子:
24.5
作者:
[Asnicar F, Leeming ER, Dimidi E, Mazidi M, Franks PW, Al Khatib H, Valdes AM, Davies R, Bakker E, Francis L, Chan A, Gibson R, Hadjigeorgiou G, Wolf J, Spector TD, Segata N, Berry SE]
通讯作者:
Berry SE
DOI:
10.1038/s41591-020-0934-0
发表时间:
2020-06
期刊:
Nature medicine
影响因子:
82.9
作者:
[Berry SE, Valdes AM, Drew DA, Asnicar F, Mazidi M, Wolf J, Capdevila J, Hadjigeorgiou G, Davies R, Al Khatib H, Bonnett C, Ganesh S, Bakker E, Hart D, Mangino M, Merino J, Linenberg I, Wyatt P, Ordovas JM, Gardner CD, Delahanty LM, Chan AT, Segata N, Franks PW, Spector TD]
通讯作者:
Spector TD
DOI:
10.1186/s40168-018-0455-y
发表时间:
2018-04-25
期刊:
Microbiome
影响因子:
15.5
作者:
[Bowyer RCE, Jackson MA, Pallister T, Skinner J, Spector TD, Welch AA, Steves CJ]
通讯作者:
Steves CJ
共 6 条
Diet-induced Arrangement of the gut Microbiome for improvement of Cardiometabolic health
-
批准号:MR/N030125/1
-
项目类别:Research Grant
-
资助金额:$21.38万
-
财政年份:2016
-
负责人:Tim Spector
-
依托单位:
A systems based approach to integrating genetic and longitudinal omics data to support diagnosis and prediction of common chronic disease
-
批准号:MR/M004422/1
-
项目类别:Research Grant
-
资助金额:$232.71万
-
财政年份:2015
-
负责人:Tim Spector
-
依托单位:
The growth hormone pathway and the genetic control of height and weight
-
批准号:G20234/2
-
项目类别:Research Grant
-
资助金额:$16.11万
-
财政年份:2006
-
负责人:Tim Spector
-
依托单位:
国内基金
海外基金
登录
查看更多内容
lncRNA-HOST2—USP15—VGLL4轴促进乳腺癌肝转移的机制研究
-
批准号:82073204
-
项目类别:面上项目
-
资助金额:55.0万元
-
批准年份:2020
-
负责人:房林
-
依托单位:
新鉴定PA-X“host-shutoff”功能区调控H7N9禽流感病毒毒力的机制
-
批准号:32072832
-
项目类别:面上项目
-
资助金额:58.0万元
-
批准年份:2020
-
负责人:胡娇
-
依托单位:
能量代谢触发植入干细胞和损伤视网膜细胞Graft-to Host细胞间通讯/物质交换及命运转变的机制
-
批准号:31930068
-
项目类别:重点项目
-
资助金额:298.0万元
-
批准年份:2019
-
负责人:徐海伟
-
依托单位:
溶液加工型多层磷光器件的组装与性能优化
-
批准号:51573183
-
项目类别:面上项目
-
资助金额:64.0万元
-
批准年份:2015
-
负责人:丁军桥
-
依托单位:
Intronic miR-944联合Host gene p63在肺鳞癌中的作用机制及其诊断价值研究
-
批准号:81572275
-
项目类别:面上项目
-
资助金额:65.0万元
-
批准年份:2015
-
负责人:邢凌霄
-
依托单位:
长链非编码RNA HOST2在卵巢癌发生与转移中作用的研究
-
批准号:81172472
-
项目类别:面上项目
-
资助金额:68.0万元
-
批准年份:2011
-
负责人:刘善荣
-
依托单位:
基于虚拟化平台支持HOST-SWAPPING机制的内存管理模型研究
-
批准号:60970125
-
项目类别:面上项目
-
资助金额:32.0万元
-
批准年份:2009
-
负责人:陈文智
-
依托单位:
多盘科单殖吸虫宿主特异性及其与无尾两栖类宿主协同进化关系研究
-
批准号:30960049
-
项目类别:地区科学基金项目
-
资助金额:23.0万元
-
批准年份:2009
-
负责人:范丽仙
-
依托单位:
Jagged2high CD11bhigh 调节性树突状细胞防治cGVHD的实验研究
-
批准号:30972790
-
项目类别:面上项目
-
资助金额:28.0万元
-
批准年份:2009
-
负责人:杜欣
-
依托单位:
遍历理论和加性组合及其相关课题
-
批准号:10871186
-
项目类别:面上项目
-
资助金额:23.0万元
-
批准年份:2008
-
负责人:邵松
-
依托单位: