High-throughput phenotyping of cell-to-cell interactions in gel microdroplet pico-cultures

被引:26
|
作者
Ohan, Juliette [1 ,3 ]
Pelle, Benjamin [1 ]
Nath, Pulak [2 ]
Huang, J-H [1 ]
Hovde, Blake [1 ]
Vuyisich, Momchilo [1 ]
Dichosa, Armand E. K. [1 ]
Starkenburg, Shawn R. [1 ,4 ]
机构
[1] Los Alamos Natl Lab, Biosci Div, Los Alamos, NM 87545 USA
[2] Los Alamos Natl Lab, Phys Div, Los Alamos, NM 87545 USA
[3] Oregon State Univ, Dept Microbiol, Corvallis, OR 97330 USA
[4] New Mexico Consortium, Los Alamos, NM 87544 USA
关键词
algae; emulsion; encapsulation; flow cytometry; high-throughput; microdroplet; microfluidics; picoculture; ENCAPSULATION; MICROALGAE; DROPLETS; GROWTH; FLOW;
D O I
10.2144/btn-2018-0124
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Microbiomes exert significant influence on our planet's ecology. Elucidating the identities of individual microbes within these communities and how they interact is a vital research imperative. Using traditional plating and culturing methods, it is impractical to assess even a small fraction of the interactions that exist within microbial communities. To address this technology gap, we integrated gel microdroplet technology with microfluidics to generate millions of microdroplet cultures (MDs) that sequester individual cells for phenotyping MDs, facilitating rapid analysis and viable recovery using flow cytometry. Herein, we describe a validated high-throughput phenotyping pipeline that elucidates cell-to-cell interactions for millions of combinations of microorganisms. Through iterative co-culturing of an algae and a pool of environmentally sourced microbes, we successfully isolated bacteria that improved algal growth. METHOD SUMMARY A high-throughput method to identify cell-to-cell interactions within complex microbial communities was designed and validated. This platform integrates gel microdroplet and microfluidic technologies with flow cytometry to enable the identification and recovery of viable cells with specific phenotypes.
引用
收藏
页码:218 / 224
页数:7
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