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Digital Rapid Accurate and Label-Free Enumeration of Viable Microorganisms Enabled by Custom-Built On-Glass-Slide Culturing Device and Microscopic Scanning

机译:通过定制的玻璃载玻片培养装置和显微扫描实现了活菌的数字化快速准确和无标签计数

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摘要

Accurately measuring the number of viable microorganisms plays an essential role in microbiological studies. Since the conventional agar method of enumerating visible colonies is time-consuming and not accurate, efforts have been made towards overcoming these limitations by counting the invisible micro-colonies. However, none of studies on micro-colony counting was able to save significant time or provide accurate results. Herein, we developed an on-glass-slide cell culture device that enables rapid formation of micro-colonies on a 0.38 mm-thick gel film without suffering from nutrient and oxygen deprivation during bacteria culturing. Employing a phase contrast imaging setup, we achieved rapid microscopic scanning of micro-colonies within a large sample area on the thin film without the need of fluorescent staining. Using Escherichia coli (E. coli) as a demonstration, our technique was able to shorten the culturing time to within 5 h and automatically enumerate the micro-colonies from the phase contrast images. Moreover, this method delivered more accurate counts than the conventional visible colony counting methods. Due to these advantages, this imaging-based micro-colony enumeration technique provides a new platform for the quantification of viable microorganisms.
机译:准确测量存活微生物的数量在微生物研究中起着至关重要的作用。由于枚举可见菌落的常规琼脂方法耗时且不准确,因此已努力通过计算不可见的微菌落来克服这些限制。但是,有关小菌落计数的研究均无法节省大量时间或提供准确的结果。本文中,我们开发了一种玻璃载玻片细胞培养装置,该装置可在0.38毫米厚的凝胶膜上快速形成微菌落,而不会在细菌培养过程中遭受营养和氧气剥夺的情况。利用相衬成像设置,我们无需进行荧光染色即可在薄膜上大样本区域内实现对显微菌落的快速显微扫描。以大肠埃希氏菌(E. coli)为例,我们的技术能够将培养时间缩短至5小时以内,并从相衬图像中自动枚举微菌落。而且,该方法比常规的可见菌落计数方法提供了更准确的计数。由于这些优点,这种基于成像的微菌落枚举技术为定量活微生物提供了一个新平台。

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