Suppr超能文献

基于快速电化学的无PCR微生物定量分析及直接从微生物载量或种类未知的血液和尿液中进行抗菌药敏分析

Rapid Electrochemical-Based PCR-Less Microbial Quantification and Antimicrobial Susceptibility Profiling Directly From Blood and Urine With Unknown Microbial Load or Species.

作者信息

Chen Jade, Navarro Eduardo, Nuñez Eliseo, Gau Vincent

机构信息

GeneFluidics, Irwindale, CA, United States.

出版信息

Front Bioeng Biotechnol. 2021 Sep 16;9:744198. doi: 10.3389/fbioe.2021.744198. eCollection 2021.

Abstract

Novel molecular platforms are available for identifying (ID) the causative agents of microbial infections and generating antimicrobial susceptibility testing (AST) profiles, which can inform the suitable course of treatment. Many methods claim to perform AST in minutes or hours, often ignoring the need for time-consuming steps such as enrichment cultures and isolation of pure cultures. In clinical microbiology laboratories, an infectious microbial must first be cultured (overnight to days) and identified at the species level, followed by a subsequent AST with an additional turnaround time of 12-48 h due to the need for regrowth of the organism in the absence and presence of relevant antibiotics. Here, we present an electrochemical-based direct-from-specimen ID/AST method for reporting directly from unprocessed urine and blood in hours. In a limit of detection study of 0.5-ml whole blood samples for point-of-care and pediatric applications, 16.7% (4/24) of samples contrived at 2 CFU/ml and 100% (24/24) of samples contrived at 6 CFU/ml were reported positive in 6.5 h, indicating a limit of detection of 6 CFU/ml. In a separate direct-from-specimen AST study, the categorical susceptibility was reported correctly for blinded susceptible, intermediate, resistant, and polymicrobial contrived specimens in 4 h.

摘要

新型分子平台可用于识别微生物感染的病原体并生成抗菌药物敏感性测试(AST)结果,从而为合适的治疗方案提供依据。许多方法声称能在数分钟或数小时内完成AST,却常常忽略了富集培养和纯培养物分离等耗时步骤的必要性。在临床微生物学实验室中,感染性微生物必须首先进行培养(过夜至数天)并鉴定到种水平,随后进行AST,由于需要在有无相关抗生素的情况下让微生物再次生长,这又需要额外12 - 48小时的周转时间。在此,我们展示了一种基于电化学的直接从样本进行识别/ AST的方法,可在数小时内直接从未经处理的尿液和血液中报告结果。在针对即时护理和儿科应用的0.5毫升全血样本的检测限研究中,接种量为2 CFU/毫升的样本中有16.7%(4/24)、接种量为6 CFU/毫升的样本中有100%(24/24)在6.5小时内报告为阳性,表明检测限为6 CFU/毫升。在另一项直接从样本进行AST的研究中,对于盲法设置的敏感、中介、耐药和多微生物样本,在4小时内正确报告了分类敏感性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db66/8481646/ee60adf75d1d/fbioe-09-744198-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验