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宏基因组学在尿路感染的诊断和靶向治疗中的应用。

Metagenomics in diagnosis and improved targeted treatment of UTI.

机构信息

Norwich Medical School, University of East Anglia, Norwich, UK.

Florida Hospital Celebration Health, Celebration, FL, USA.

出版信息

World J Urol. 2020 Jan;38(1):35-43. doi: 10.1007/s00345-019-02731-9. Epub 2019 Apr 3.

Abstract

INTRODUCTION

The genomic revolution has transformed our understanding of urinary tract infection. There has been a paradigm shift from the dogmatic statement that urine is sterile in healthy people, as we are becoming forever more familiar with the knowledge that bacterial communities exist within the urinary tracts of healthy people. Metagenomics can investigate the broad populations of microbial communities, analysing all the DNA present within a sample, providing comprehensive data regarding the state of the microenvironment of a patient's urinary tract. This permits medical practitioners to more accurately target organisms that may be responsible for disease-a form of 'precision medicine'.

METHODS AND RESULTS

This paper is derived from an extensive review and analysis of the available literature on the topic of metagenomic sequencing in urological science, using the PubMed search engine. The search yielded a total of 406 results, and manual selection of appropriate papers was subsequently performed. Only one randomised clinical trial comparing metagenomic sequencing to standard culture and sensitivity in the arena of urinary tract infection was found.

CONCLUSION

Out of this process, this paper explores the limitations of traditional methods of culture and sensitivity and delves into the recent studies involving new high-throughput genomic technologies in urological basic and clinical research, demonstrating the advances made in the urinary microbiome in its entire spectrum of pathogens and the first attempts of clinical implementation in several areas of urology. Finally, this paper discusses the challenges that must be overcome for such technology to become widely used in clinical practice.

摘要

简介

基因组学革命改变了我们对尿路感染的认识。从健康人群的尿液无菌这一教条式的陈述,我们已经发生了范式转变,因为我们越来越熟悉细菌群落存在于健康人群的尿路这一知识。宏基因组学可以研究广泛的微生物群落群体,分析样本中存在的所有 DNA,提供有关患者尿路微环境状态的全面数据。这使得医疗从业者能够更准确地针对可能导致疾病的生物体,这是一种“精准医学”。

方法和结果

本文源自对主题为尿科学中宏基因组测序的相关文献的广泛综述和分析,使用 PubMed 搜索引擎。该搜索共产生了 406 个结果,随后进行了适当论文的手动选择。仅发现了一项将宏基因组测序与尿路感染领域的标准培养和药敏比较的随机临床试验。

结论

通过这一过程,本文探讨了传统培养和药敏方法的局限性,并深入研究了涉及泌尿科基础和临床研究中新的高通量基因组技术的最新研究,展示了尿路微生物组在其所有病原体谱中的进展,以及在泌尿科多个领域首次尝试临床应用。最后,本文讨论了必须克服的挑战,以使该技术在临床实践中得到广泛应用。

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