Department of Biomedical Engineering, University of Connecticut, Storrs, CT 06269, USA.
Department of Chemical and Biomolecular Engineering, University of Connecticut, Storrs, CT 06269, USA.
Sensors (Basel). 2018 Oct 31;18(11):3700. doi: 10.3390/s18113700.
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 () 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.
准确测量活微生物的数量在微生物研究中起着至关重要的作用。由于传统的琼脂计数可见菌落的方法既耗时又不准确,因此人们一直致力于通过计数不可见的微菌落来克服这些限制。然而,在微菌落计数的研究中,没有一种方法能够显著节省时间或提供准确的结果。在这里,我们开发了一种在玻璃载玻片上的细胞培养装置,该装置能够在 0.38 毫米厚的凝胶膜上快速形成微菌落,而在细菌培养过程中不会受到营养和氧气的剥夺。我们采用相差成像设置,实现了对薄膜上大样本区域内微菌落的快速微观扫描,而无需荧光染色。以 () 为例,我们的技术能够将培养时间缩短至 5 小时内,并能自动从相差图像中对微菌落进行计数。此外,该方法的计数比传统的可见菌落计数方法更准确。由于这些优势,这种基于成像的微菌落计数技术为活微生物的定量提供了一个新的平台。