Smartphone-based rapid quantification of viable bacteria by single-cell microdroplet turbidity imaging

被引:27
作者
Cui, Xiaonan [1 ,2 ,4 ]
Ren, Lihui [1 ,2 ,4 ]
Shan, Yufei [3 ]
Wang, Xixian [1 ,2 ,4 ]
Yang, Zhenlong [1 ,2 ,4 ]
Li, Chunyu [1 ,2 ,4 ]
Xu, Jian [1 ,2 ,4 ]
Ma, Bo [1 ,2 ,4 ]
机构
[1] Chinese Acad Sci, CAS Key Lab Biofuels, Single Cell Ctr, Qingdao Inst Bioenergy & Bioproc Technol, Qingdao 266101, Shandong, Peoples R China
[2] Chinese Acad Sci, Shandong Key Lab Energy Genet, Qingdao Inst Bioenergy & Bioproc Technol, Qingdao 266101, Shandong, Peoples R China
[3] Northwest A&F Univ, Yangling, Shanxi, Peoples R China
[4] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
关键词
GMD GROWTH ASSAY; DROPLET MICROFLUIDICS; FLOW-CYTOMETRY; QUANTITATIVE DETECTION; GEL MICRODROPLETS; MICROORGANISMS; SUSCEPTIBILITY; MICROBIOLOGY; CULTIVATION; ENRICHMENT;
D O I
10.1039/c8an00456k
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
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 Gramnegative 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.
引用
收藏
页码:3309 / 3316
页数:8
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