Suppr超能文献

测量单克隆细菌群体内单细胞对抗生素的敏感性。

Measuring single-cell susceptibility to antibiotics within monoclonal bacterial populations.

作者信息

Le Quellec Lena, Aristov Andrey, Gutiérrez Ramos Salomé, Amselem Gabriel, Bos Julia, Baharoglu Zeynep, Mazel Didier, Baroud Charles N

机构信息

Institut Pasteur, Université Paris Cité, Physical Microfluidics and Bioengineering, Paris, France.

LadHyX, CNRS, Ecole Polytechnique, Institut Polytechnique de Paris, Palaiseau, France.

出版信息

PLoS One. 2024 Aug 1;19(8):e0303630. doi: 10.1371/journal.pone.0303630. eCollection 2024.

Abstract

The emergence of new resistant bacterial strains is a worldwide challenge. A resistant bacterial population can emerge from a single cell that acquires resistance or persistence. Hence, new ways of tackling the mechanism of antibiotic response, such as single cell studies are required. It is necessary to see what happens at the single cell level, in order to understand what happens at the population level. To date, linking the heterogeneity of single-cell susceptibility to the population-scale response to antibiotics remains challenging due to the trade-offs between the resolution and the field of view. Here we present a platform that measures the ability of individual E. coli cells to form small colonies at different ciprofloxacin concentrations, by using anchored microfluidic drops and an image and data analysis pipelines. The microfluidic results are benchmarked against classical microbiology measurements of antibiotic susceptibility, showing an agreement between the pooled microfluidic chip and replated bulk measurements. Further, the experimental likelihood of a single cell to form a colony is used to provide a probabilistic antibiotic susceptibility curve. In addition to the probabilistic viewpoint, the microfluidic format enables the characterization of morphological features over time for a large number of individual cells. This pipeline can be used to compare the response of different bacterial strains to antibiotics with different action mechanisms.

摘要

新型耐药菌株的出现是一个全球性挑战。耐药细菌群体可能源自单个获得耐药性或持续性的细胞。因此,需要新的方法来研究抗生素反应机制,比如单细胞研究。有必要了解单细胞水平上发生了什么,以便理解群体水平上发生了什么。迄今为止,由于分辨率和视野之间的权衡,将单细胞敏感性的异质性与群体规模的抗生素反应联系起来仍然具有挑战性。在此,我们展示了一个平台,该平台通过使用锚定微流控液滴以及图像和数据分析流程,来测量单个大肠杆菌细胞在不同环丙沙星浓度下形成小菌落的能力。微流控结果与经典的抗生素敏感性微生物学测量结果进行了对比,结果表明微流控芯片汇总数据与再平板接种的大量样本测量结果一致。此外,利用单个细胞形成菌落的实验概率来提供概率性抗生素敏感性曲线。除了概率视角外,微流控形式还能够对大量单个细胞随时间变化的形态特征进行表征。该流程可用于比较不同细菌菌株对具有不同作用机制的抗生素的反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0515/11293721/eaaa6d73f1f5/pone.0303630.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