大肠杆菌双重性方向博士职位

PhD Studentship: The Double Life of E. Coli as Benign Commensal and Deadly Pathogen: the COHORT-Microbiome Study

University of Oxford · 英国 · Oxford

原帖优先:申请材料、截止时间与资格以原帖和学校官方说明为准。

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研究内容
本项目旨在通过长读长测序和生物信息学方法,结合纵向粪便样本和临床数据,研究大肠杆菌作为人类肠道共生菌与致病菌的双重角色及其定植动态和感染风险。
申请条件
原文未说明具体学历及专业硬性门槛,仅指出项目适合热衷于在干湿实验室发展技能并具有雄心壮志的学生。
待遇
提供最低涵盖本土学费的资助,并最高可支持国际学生(需获得 NDM 奖学金)。
申请方式
截止日期为 2026 年 12 月 1 日,申请详情请参阅官方说明。
材料清单
  • 原文未说明

由 gemini-2.5-flash-lite 生成,博士岗判定置信度 100%。

结构化信息

截止
(Europe/London) 剩 52 天
学科
免疫与微生物学
合同类型
雇佣合同
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内容更新
导师
Susanna Dunachie
来源
jobs.ac.uk(英国博士项目及学术招聘) · 最近核对 2026-10-09
详情核验
判定依据(原文摘录)
  • 这是一项博士培养岗位
    PhD Studentship: The Double Life of E. Coli as Benign Commensal and Deadly Pathogen: the COHORT-Microbiome Study
  • 支持国际申请者资金
    Funding Maximum: International student (subject to gaining an NDM studentship)
原文

Location: John Radcliffe Hospital

Background

Escherichia coli is a common and usually benign constituent of the human gut microbiome but is also a leading cause of urinary tract and bloodstream infection associated with substantial morbidity and mortality. We have shown that despite there being many thousands of known sequence types of E. coli , just four cause ~50% of bloodstream infections in England. Despite intensive genomic surveillance of invasive E. coli isolates (e.g. from bloodstream infections), comparatively little is known about the molecular epidemiology of commensal strains. We want to find out whether these strains are better at causing invasive disease (i.e. more pathogenic) or simply have more opportunities to do so because they are better at colonising and persisting in the gut.

Project overview

This project will form part of a unique study being run in collaboration with the Oxford Vaccine Group and Ellison Institute of technology. The COHORT study (PI Prof Susanna Dunachie) seeks to understand immunological responses to E. coli in patients across a spectrum from health to disease. COHORT-Microbiome will add longitudinal faecal sampling to investigate longitudinal microbiome profiles in this same group of participants.

The student will generate unique, high-quality genomic datasets using long-read sequencing facilities available within our unit. They will then link these with highly granular clinical metadata from electronic healthcare records. Using recently developed bioinformatic methodologies for strain deconvolution in long-read metagenomic samples, they will generate unprecedented insights into the colonisation dynamics of E. coli in patients at risk of invasive disease and compare this to healthy controls. The student will then use this data to explore the association between the ecology of E. coli in the context of the wider microbiome and future infection risk.

The student will have the opportunity to test specific hypothesis arising from COHORT-Microbiome in the lab by performing in vitro studies to investigate in more detail the interaction between strain colonisation dynamics, microbiome background and antibiotic exposure. We anticipate that there will also be opportunities for further collaborative work to perform a joint exploratory analysis of the combined microbiome and immunological datasets.

Ultimately the insights generated from this project will help to shape our understanding of the ecology of an important human pathogen and inform the design of much needed interventions to reduce the burden of disease associated with it. The project would suit an ambitious student who is keen to develop skills across both the wet and dry labs and work within an inter-disciplinary team to apply these to an important clinical problem.

Funding Details

Funding Minimum: Home fees student

Funding Maximum: International student (subject to gaining an NDM studentship) Please see details below

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