Using next generation sequencing to reveal human impact on aquatic reservoirs of antibiotic resistant bacteria at the catchment scale

使用下一代测序揭示人类对流域规模的抗生素耐药细菌水库的影响

• 批准号: NE/M01133X/1
• 负责人: Andrew Singer
• 金额: $ 18.83万
• 依托单位: NERC CEH (Up to 30.11.2019)
• 依托单位国家: 英国
• 项目类别: Research Grant
• 财政年份: 2015
• 资助国家: 英国
• 起止时间: 2015 至 无数据
• 项目状态: 已结题
• 来源: https://gtr.ukri.org/projects?ref=NE%2FM01133X%2F1
• 关键词: Using; next; generation; sequencing; reveal

The threat of antibiotic resistance has been compared to that posed by climate change and global terrorism by the Chief medical Officer Dame Sally Davies. Bacterial resistance to antibiotics has existed for hundreds of millions of years, as it evolved to combat antibiotics produced by bacteria and fungi. Resistance is conferred either by mutation or by uptake of DNA from other bacteria which may not even be closely related. This horizontal resistance gene transfer is one of the most important issues facing the fight against infection in the clinic. Novel resistance genes that are taken up by clinical pathogens originate in environmental bacteria, and once in human pathogens or even harmless commensal bacteria, will be selected for by clinical use of antibiotics. However, little is known about the conditions under or locations in which these genes are mobilised into human associated bacteria, or what the human exposure routes for transmission of these resistance genes are. Increasing evidence suggests that the use of antibiotics in agriculture contributes to the increase in resistance seen in the clinic, however much less research has focused on evolution of resistance in farm animals than in humans so less evidence is available. Even less is known regarding reservoirs of resistant bacteria in the natural environment, particularly locations heavily polluted by human or animal waste. 11 billion litres of waste water are discharged into UK rivers every day; critically much of this treatment does not significantly reduce numbers of resistant bacteria. Millions of tons of animal faecal wastes are spread to agricultural land every year, providing additional inputs of resistant organisms into the wider environment. Our previous work has shown that the use of a marker gene, which is predictive of levels of antibiotic resistance genes in sediments, varies by up to 1000 times between clean and dirty sediments. Our data also shows that waste water treatment plants are responsible for the majority of this effect (about 50%), and 30% is associated with diffuse pollution from land adjacent to the river. Other data generated by the consortium suggests that there are real human exposure risks to these environmental reservoirs of resistant organisms, with several million exposure events occurring each year in England and Wales through recreational use of coastal waters alone.This project will, for the first time, use cutting edge high through put DNA sequencing technologies and computational analyses to increase our understanding of the human activities that drive increased levels of antibiotic resistant bacteria across the River Thames catchment. Abundance and identity of over 3000 different resistance genes will be determined at 40 sampling sites, in triplicate at three time points over one year, to capture impacts of seasonality and flow. We will also measure a range of antibiotic residues, metals and nutrients. We will use graphical information system data on waste water treatment plant type, size and location and land use throughout the catchment. Together this data will be used to produce a model which will reveal the main drivers of resistance gene abundance and diversity at the catchment scale. We will also identify novel molecular markers associated with different sources of pollution that can be used as source tracking targets. We aim to analyse the effects of specific mitigation strategies that are able to reduce levels of resistant bacteria, this will enable estimates of reduction in resistance levels that can inform policy and regulatory targets.A translational tool will be developed for surveillance of the most important marker genes identified from the DNA sequence analyses and modelling work. This will be an affordable test that will help identify key factors for human health risk assessment.

首席医疗官Dame Sally Davies将抗生素耐药性的威胁与气候变化和全球恐怖主义所造成的威胁进行了比较。细菌对抗生素的耐药性已经存在了数亿年，因为它进化到对抗细菌和真菌产生的抗生素。耐药性是通过突变或从其他细菌中摄取DNA而产生的，这些细菌甚至可能不密切相关。这种水平抗性基因转移是临床上对抗感染所面临的最重要的问题之一。被临床病原体摄取的新的耐药基因来源于环境细菌，一旦进入人类病原体甚至无害的肠道细菌，将被临床使用的抗生素所选择。然而，人们对这些基因被动员到人类相关细菌中的条件或位置知之甚少，也不知道这些耐药基因传播的人类暴露途径是什么。越来越多的证据表明，在农业中使用抗生素有助于增加在临床上看到的耐药性，但更少的研究集中在农场动物的耐药性的演变比在人类，所以更少的证据是可用的。关于自然环境中耐药细菌的储存库，特别是被人类或动物废物严重污染的地方，所知更少。每天有110亿升废水排入英国河流;关键是这种处理并没有显着减少耐药细菌的数量。每年有数百万吨的动物粪便散布到农业用地上，为更广泛的环境提供了额外的抗性生物。我们以前的工作表明，使用标记基因，这是预测沉积物中的抗生素耐药性基因的水平，变化高达1000倍之间的清洁和肮脏的沉积物。我们的数据还表明，废水处理厂是造成这种影响的主要原因（约50%），30%与河流附近土地的扩散污染有关。该联盟产生的其他数据表明，人类接触这些耐药生物的环境水库存在真实的风险，仅在英格兰和威尔士，每年就有数百万起接触事件发生在沿海沃茨的娱乐使用中。使用尖端的高通量DNA测序技术和计算分析，以增加我们对人类活动的理解，泰晤士河流域的抗生素耐药性细菌水平上升。将在40个采样点确定3000多个不同抗性基因的突变和身份，在一年内的三个时间点重复三次，以捕获季节性和流量的影响。我们还将测量一系列抗生素残留物、金属和营养素。我们将使用有关污水处理厂类型、规模和位置以及整个集水区土地使用的图形信息系统数据。这些数据将被用来建立一个模型，揭示集水区抗性基因丰度和多样性的主要驱动因素。我们还将确定与不同污染源相关的新型分子标记，这些标记可用作源跟踪目标。我们的目标是分析能够降低耐药细菌水平的特定缓解策略的影响，这将能够估计耐药水平的降低，从而为政策和监管目标提供信息。将开发一种翻译工具来监测从DNA序列分析和建模工作中识别的最重要的标记基因。这将是一个负担得起的测试，将有助于确定人类健康风险评估的关键因素。

项目成果

Functional metagenomic libraries generated from anthropogenically impacted environments reveal importance of metabolic genes in biocide and antibiotic resistance.

• DOI: 10.1016/j.crmicr.2023.100184
• 发表时间: 2023
• 期刊: CURRENT RESEARCH IN MICROBIAL SCIENCES
• 作者: Murray, Aimee K.;Zhang, Lihong;Snape, Jason;Gaze, William H.
• 通讯作者: Gaze, William H.

Novel Insights into Selection for Antibiotic Resistance in Complex Microbial Communities.

• DOI: 10.1128/mbio.00969-18
• 发表时间: 2018-07-24
• 期刊: mBio
• 影响因子: 6.4
• 作者: Murray AK;Zhang L;Yin X;Zhang T;Buckling A;Snape J;Gaze WH
• 通讯作者: Gaze WH

Gene duplication drives genome expansion in a major lineage of Thaumarchaeota.

• DOI: 10.1038/s41467-020-19132-x
• 发表时间: 2020-10-30
• 期刊: Nature communications
• 影响因子: 16.6
• 作者: Sheridan PO;Raguideau S;Quince C;Holden J;Zhang L;Thames Consortium;Williams TA;Gubry-Rangin C
• 通讯作者: Gubry-Rangin C