Single-Cell Center, CAS Key Laboratory of Biofuels and Shandong Key Laboratory of Energy Genetics, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao, Shandong, 266101, China.
Analyst. 2018 Jul 9;143(14):3309-3316. doi: 10.1039/c8an00456k.
Standard plate count (SPC) has been recognized as the golden standard for the quantification of viable bacteria. However, SPC usually takes one to several days to grow individual cells into a visible colony, which greatly hampers its application in rapid bacteria enumeration. Here we present a microdroplet turbidity imaging based digital standard plate count (dSPC) method to overcome this hurdle. Instead of cultivating on agar plates, bacteria are encapsulated in monodisperse microdroplets for single-cell cultivation. Proliferation of the encapsulated bacterial cell produced a detectable change in microdroplet turbidity, which allowed, after just a few bacterial doubling cycles (i.e., a few hours), enumeration of viable bacteria by visible-light imaging. Furthermore, a dSPC platform integrating a power-free droplet generator with smartphone-based turbidity imaging was established. As proof-of-concept demonstrations, a series of Gram-negative bacteria (Escherichia coli) and Gram-positive bacteria (Bacillus subtilis) samples were quantified via the smartphone dSPC accurately within 6 hours, representing a detection sensitivity of 100 CFU ml-1 and at least 3 times faster. In addition, Enterobacter sakazakii (E. sakazakii) in infant milk powder as a real sample was enumerated within 6 hours, in contrast to the 24 hours needed in traditional SPC. Results with high accuracy and reproducibility were achieved, with no difference in counts found between dSPC and SPC. By enabling label-free, rapid, portable and low-cost enumeration and cultivation of viable bacteria onsite, smartphone dSPC forms the basis for a temporally and geographically trackable network for surveying live microbes globally where every citizen with a cellphone can contribute anytime and anywhere.
标准平板计数(SPC)已被公认为定量活菌的黄金标准。然而,SPC 通常需要一到几天的时间才能使单个细胞生长成可见的菌落,这极大地限制了其在快速细菌计数中的应用。在这里,我们提出了一种基于微滴浊度成像的数字标准平板计数(dSPC)方法来克服这一障碍。细菌不是在琼脂平板上培养,而是封装在单分散的微滴中进行单细胞培养。被包裹的细菌细胞的增殖会导致微滴浊度的可检测变化,仅经过几个细菌倍增周期(即几个小时),就可以通过可见光成像来计数活菌。此外,建立了一个集成无电源微滴发生器和基于智能手机的浊度成像的 dSPC 平台。作为概念验证演示,通过智能手机 dSPC 准确地在 6 小时内对一系列革兰氏阴性菌(大肠杆菌)和革兰氏阳性菌(枯草芽孢杆菌)样本进行定量,检测灵敏度为 100 CFU ml-1,至少快 3 倍。此外,在婴儿奶粉中的肠杆菌 sakazakii(E. sakazakii)作为实际样本,在 6 小时内进行了计数,而传统 SPC 需要 24 小时。结果具有高准确性和重现性,dSPC 和 SPC 之间的计数没有差异。智能手机 dSPC 能够实现无标记、快速、便携和低成本的活菌计数和培养,为在全球范围内对活体微生物进行可追溯的调查提供了基础,每个拥有手机的公民都可以随时随地进行贡献。