NEC05836 The environmental REsistome: confluence of Human and Animal Biota in antibiotic resistance spread (REHAB)

NEC05836 环境 REsistome:人类和动物生物群在抗生素耐药性传播中的汇合 (REHAB)

基本信息

  • 批准号:
    NE/N019660/1
  • 负责人:
  • 金额:
    $ 24.63万
  • 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
  • 起止时间:
    2016 至 无数据
  • 项目状态:
    已结题

项目摘要

OVERALL STUDY AIMWe do not fully understand how important types (species) of bacteria and packages of genetic material (genes) coding for antibiotic resistance move between humans, animals and the environment, or where, how and why antibiotic resistance emerges. This study aims to look in detail at the genetic level at bacteria in farm animals, human/animal sewage, sewage treatment works and rivers, to work out the complex network of transmission of important antibiotic-resistant bacteria and antibiotic resistance genes. We will use this information to work out how best to slow down the spread of antibiotic resistance between humans, livestock and the environment. STUDY BACKGROUND AND AIMS IN MORE DETAILInfections are one of the most common causes of ill-health in human and animal medicine, and are caused by a range of different micro-organisms, including viruses and bacteria. Amongst bacteria, there are some species, or types, of bacteria, which can live harmlessly in human and animal intestines, sewage, and rivers, but can also cause disease in humans and animals if they get into the wrong body space, such as the bloodstream or urine. Examples of these bacteria include E. coli, and other similar organisms, which belong to a family of bacteria called "Enterobacteriaceae".It has generally been possible to treat infections caused by bacteria using several classes of medicines, known as antibiotics. Different antibiotics kill bacteria in different ways: for example, they can switch off critical chemical processes that the bacteria need to survive, or they can break down the outer shell of the bacteria. In response to the use of antibiotics, bacteria have changed over time, finding ways to alter their structure so that antibiotics no longer have a target to act on, or by producing substances that break down the antibiotic before it has a chance to kill the bacteria. These changes to the bacteria's genetic code, so that they are no longer killed by an antibiotic, create antibiotic resistance. Bacteria can also acquire packages of genes that cause antibiotic resistance from other surrounding bacteria. This is known as horizontal gene transfer. Through these mechanisms, members of the Enterobacteriaceae family of bacteria have developed antibiotic resistance to a number of different antibiotics over a short period of time. In some cases we are no longer able to treat these infections with the antibiotics we have available. Studying antibiotic resistance and horizontal gene transfer in bacteria found in humans, animals and the environment is difficult because we cannot directly see how bacteria and their genetic material move between them. However, new "Next Generation Sequencing" (NGS) technologies allow scientists to look in great detail at the genetic code of large numbers of bacteria. Comparing this information across bacteria which have been living in the different parts of the environment (e.g. sewage treatment works, rivers) and in human and animal sewage allows us to see how bacteria have evolved to become resistant to antibiotics, and how resistance genes have been shared between them. This study will use NGS technologies to look at the genetic code of large numbers of Enterobacteriaceae bacteria found in humans, animals (pigs, sheep and poultry), sewage (pre-, during and post-treatment), and rivers. These different groups/areas will be sampled in different seasons of one calendar year to determine how antibiotic resistance genes move around between these locations and over time, and what factors might influence this movement. We will also be investigating whether various chemicals and nutrients in the water may be affecting how quickly horizontal gene transfer occurs. Understanding this is essential to work out how we might intervene more effectively to slow the spread of antibiotic resistance genes and bacteria, and keep our antibiotic medicines useful.
总体研究目标我们并不完全了解重要的细菌类型(种类)和编码抗生素耐药性的遗传物质(基因)包在人类、动物和环境之间如何移动,或者抗生素耐药性在何处、如何以及为何出现。本研究旨在详细研究农场动物、人类/动物污水、污水处理厂和河流中细菌的基因水平,以弄清楚重要的抗生素耐药细菌和抗生素耐药基因的复杂传播网络。我们将利用这些信息来研究如何最好地减缓抗生素耐药性在人类、牲畜和环境之间的传播。更详细的研究背景和目标感染是人类和动物医学​​中健康不良的最常见原因之一,由一系列不同的微生物引起,包括病毒和细菌。在细菌中,有一些种类或类型的细菌可以无害地生活在人类和动物的肠道、污水和河流中,但如果它们进入错误的身体空间,也可能引起人类和动物的疾病,例如血液或尿液。这些细菌的例子包括大肠杆菌和其他类似的生物体,它们属于称为“肠杆菌科”的细菌家族。通常可以使用几类称为抗生素的药物来治疗由细菌引起的感染。不同的抗生素以不同的方式杀死细菌:例如,它们可以关闭细菌生存所需的关键化学过程,或者可以分解细菌的外壳。为了应对抗生素的使用,细菌随着时间的推移而发生变化,找到改变其结构的方法,使抗生素不再有作用的目标,或者通过产生在抗生素有机会杀死细菌之前分解抗生素的物质。细菌遗传密码的这些变化使它们不再被抗生素杀死,从而产生了抗生素耐药性。细菌还可以获得导致周围其他细菌产生抗生素耐药性的基因包。这称为水平基因转移。通过这些机制,肠杆菌科细菌的成员在短时间内对多种不同的抗生素产生了抗生素耐药性。在某些情况下,我们不再能够使用现有的抗生素来治疗这些感染。研究人类、动物和环境中细菌的抗生素耐药性和水平基因转移很困难,因为我们无法直接看到细菌及其遗传物质如何在它们之间移动。然而,新的“下一代测序”(NGS)技术使科学家能够详细研究大量细菌的遗传密码。通过比较生活在环境不同部分(例如污水处理厂、河流)以及人类和动物污水中的细菌的这些信息,我们可以了解细菌是如何进化到对抗生素产生耐药性的,以及耐药基因是如何变化的。他们之间共享。这项研究将利用 NGS 技术来研究人类、动物(猪、羊和家禽)、污水(处理前、处理中和处理后)和河流中发现的大量肠杆菌科细菌的遗传密码。这些不同的群体/区域将在一个日历年的不同季节进行采样,以确定抗生素抗性基因如何在这些地点之间以及随着时间的推移而移动,以及哪些因素可能影响这种移动。我们还将调查水中的各种化学物质和营养物质是否可能影响水平基因转移发生的速度。了解这一点对于我们如何更有效地进行干预以减缓抗生素抗性基因和细菌的传播并保持抗生素药物的有效性至关重要。

项目成果

期刊论文数量(10)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
MOESM2 of The impact of sequencing depth on the inferred taxonomic composition and AMR gene content of metagenomic samples
MOESM2 测序深度对宏基因组样本推断分类组成和 AMR 基因含量的影响
  • DOI:
    http://dx.10.6084/m9.figshare.10049006
  • 发表时间:
    2019
  • 期刊:
  • 影响因子:
    0
  • 作者:
    H. Gweon
  • 通讯作者:
    H. Gweon
The impact of sequencing depth on the inferred taxonomic composition and AMR gene content of metagenomic samples.
测序深度对宏基因组样本推断的分类组成和 AMR 基因含量的影响。
  • DOI:
    http://dx.10.1186/s40793-019-0347-1
  • 发表时间:
    2019
  • 期刊:
  • 影响因子:
    7.9
  • 作者:
    Gweon HS
  • 通讯作者:
    Gweon HS
The impact of sequencing depth on the inferred taxonomic composition and AMR gene content of metagenomic samples
测序深度对宏基因组样本推断分类组成和AMR基因含量的影响
  • DOI:
    http://dx.10.1101/593301
  • 发表时间:
    2019
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Gweon H
  • 通讯作者:
    Gweon H
Systematic Review of Wastewater Surveillance of Antimicrobial Resistance in Human Populations
人类抗生素耐药性废水监测的系统评价
  • DOI:
    http://dx.10.20944/preprints202010.0267.v2
  • 发表时间:
    2021
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Chau K
  • 通讯作者:
    Chau K
Wastewater Surveillance of Antimicrobial Resistance in Human Populations: A Systematic Review
人类抗生素耐药性的废水监测:系统评价
  • DOI:
    10.20944/preprints202010.0267.v1
  • 发表时间:
    2020-10-13
  • 期刊:
  • 影响因子:
    0
  • 作者:
    K. Chau;L. Barker;N. Sims;B. Kasprzyk;E. Budgell;E. Harriss;D. Crook;D. Read;S. Walker;N. Stoesser
  • 通讯作者:
    N. Stoesser
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Daniel Read其他文献

Journal of Experimental Psychology : Learning , Memory , and Cognition DRIFT : An Analysis of Outcome Framing in Intertemporal Choice
实验心理学杂志:学习、记忆和认知漂移:跨期选择结果框架的分析
Journal of Experimental Psychology : Learning , Memory , and Cognition Tradeoffs Between Sequences : Weighing Accumulated Outcomes Against Outcome-Adjusted Delays
实验心理学杂志:学习、记忆和认知序列之间的权衡:权衡累积结果与结果调整延迟
  • DOI:
    10.1007/s10683-020-09695-3
  • 发表时间:
    2024-09-13
  • 期刊:
  • 影响因子:
    2.3
  • 作者:
    Daniel Read;M. Scholten
  • 通讯作者:
    M. Scholten
Legitimating innovation through category positioning: a case study of The Hundred cricket competition
通过品类定位使创新合法化:百强板球比赛案例研究
Limitations in artificial spin ice path selectivity: the challenges beyond topological control
人工自旋冰路径选择性的局限性:拓扑控制之外的挑战
  • DOI:
    10.1088/1367-2630/17/1/013054
  • 发表时间:
    2015-01-27
  • 期刊:
  • 影响因子:
    3.3
  • 作者:
    S. Walton;K. Zeissler;D. M. Burn;S. Ladak;Daniel Read;T. Tyliszczak;Lesley F. Cohen;W. Branford
  • 通讯作者:
    W. Branford
The Efficacy of Different Methods for Informing the Public About the Range Dependency of Magnetic Fields from High Voltage Power Lines
向公众通报高压输电线磁场范围依赖性的不同方法的功效
  • DOI:
    10.1111/j.1539-6924.1998.tb00373.x
  • 发表时间:
    1998-10-01
  • 期刊:
  • 影响因子:
    3.8
  • 作者:
    Daniel Read;M. G. Morgan
  • 通讯作者:
    M. G. Morgan

Daniel Read的其他文献

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{{ truncateString('Daniel Read', 18)}}的其他基金

MICRO-CYCLE: Unravelling the role of microbial genomic traits in organic matter cycling and molecular composition along the river continuum
微循环:揭示微生物基因组特征在河流连续体有机物循环和分子组成中的作用
  • 批准号:
    NE/Z000173/1
  • 财政年份:
    2024
  • 资助金额:
    $ 24.63万
  • 项目类别:
    Research Grant
BBSRC Institute Strategic Programme: Decoding Biodiversity (DECODE) - Partner Grant
BBSRC 研究所战略计划:解码生物多样性 (DECODE) - 合作伙伴资助
  • 批准号:
    BB/X020037/1
  • 财政年份:
    2023
  • 资助金额:
    $ 24.63万
  • 项目类别:
    Research Grant
PAthways of Chemicals Into Freshwaters and their ecological ImpaCts (PACIFIC)
化学品进入淡水的途径及其生态影响(太平洋)
  • 批准号:
    NE/X015947/1
  • 财政年份:
    2022
  • 资助金额:
    $ 24.63万
  • 项目类别:
    Research Grant
Unlocking wetland ecologies and agriculture in prehistory through sulphur isotopes.
通过硫同位素解锁史前时期的湿地生态和农业。
  • 批准号:
    NE/W000814/1
  • 财政年份:
    2022
  • 资助金额:
    $ 24.63万
  • 项目类别:
    Research Grant
NSF: Molecular Engineering of Polymers for Processing Performance and Properties
NSF:聚合物分子工程的加工性能和特性
  • 批准号:
    EP/D06631X/1
  • 财政年份:
    2007
  • 资助金额:
    $ 24.63万
  • 项目类别:
    Research Grant

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Impact of Urban Environmental Factors on Momentary Subjective Wellbeing (SWB) using Smartphone-Based Experience Sampling Methods
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  • 批准号:
    2750689
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    2025
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    Studentship
Collaborative Research: BoCP-Implementation: Quantifying the response of biodiverse freshwater ecosystems to abrupt and progressive environmental change
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  • 批准号:
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    2024
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    $ 24.63万
  • 项目类别:
    Standard Grant
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