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微孔阵列平台内微生物群落发育的组装与追踪

Assembly and Tracking of Microbial Community Development within a Microwell Array Platform.

作者信息

Timm Andrea C, Halsted Michelle C, Wilmoth Jared L, Retterer Scott T

机构信息

Biosciences Division, Oak Ridge National Laboratory.

Bredesen Center for Interdisciplinary Research and Graduate Education, University of Tennessee.

出版信息

J Vis Exp. 2017 Jun 6(124):55701. doi: 10.3791/55701.

Abstract

The development of microbial communities depends on a combination of complex deterministic and stochastic factors that can dramatically alter the spatial distribution and activities of community members. We have developed a microwell array platform that can be used to rapidly assemble and track thousands of bacterial communities in parallel. This protocol highlights the utility of the platform and describes its use for optically monitoring the development of simple, two-member communities within an ensemble of arrays within the platform. This demonstration uses two mutants of Pseudomonas aeruginosa, part of a series of mutants developed to study Type VI secretion pathogenicity. Chromosomal inserts of either mCherry or GFP genes facilitate the constitutive expression of fluorescent proteins with distinct emission wavelengths that can be used to monitor community member abundance and location within each microwell. This protocol describes a detailed method for assembling mixtures of bacteria into the wells of the array and using time-lapse fluorescence imaging and quantitative image analysis to measure the relative growth of each member population over time. The seeding and assembly of the microwell platform, the imaging procedures necessary for the quantitative analysis of microbial communities within the array, and the methods that can be used to reveal interactions between microbial species area all discussed.

摘要

微生物群落的发展取决于复杂的确定性因素和随机因素的组合,这些因素可显著改变群落成员的空间分布和活动。我们开发了一种微孔阵列平台,可用于并行快速组装和追踪数千个细菌群落。本方案突出了该平台的实用性,并描述了其用于光学监测平台内阵列集合中简单的双成员群落发展的用途。本演示使用铜绿假单胞菌的两个突变体,这是为研究VI型分泌致病性而开发的一系列突变体的一部分。mCherry或GFP基因的染色体插入促进了具有不同发射波长的荧光蛋白的组成型表达,可用于监测每个微孔内群落成员的丰度和位置。本方案描述了将细菌混合物组装到阵列孔中,并使用延时荧光成像和定量图像分析来测量每个成员群体随时间的相对生长的详细方法。还讨论了微孔平台的接种和组装、阵列内微生物群落定量分析所需的成像程序,以及可用于揭示微生物物种间相互作用的方法。

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