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

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.

[1]  J. G. Camp,et al.  Patterns and scales in gastrointestinal microbial ecology. , 2009, Gastroenterology.

[2]  L. Tranvik,et al.  Structure and Function of Bacterial Communities Emerging from Different Sources under Identical Conditions , 2006, Applied and Environmental Microbiology.

[3]  Kai Xue,et al.  Stochastic Assembly Leads to Alternative Communities with Distinct Functions in a Bioreactor Microbial Community , 2013, mBio.

[4]  Chih-kuan Tung,et al.  Acceleration of Emergence of Bacterial Antibiotic Resistance in Connected Microenvironments , 2011, Science.

[5]  Luke McNally,et al.  The biogeography of polymicrobial infection , 2015, Nature Reviews Microbiology.

[6]  Jessica L. Mark Welch,et al.  Systems-level analysis of microbial community organization through combinatorial labeling and spectral imaging , 2011, Proceedings of the National Academy of Sciences.

[7]  J. Choi,et al.  Defined spatial structure stabilizes a synthetic multispecies bacterial community , 2008, Proceedings of the National Academy of Sciences.

[8]  Felix J. H. Hol,et al.  The effects of chemical interactions and culture history on the colonization of structured habitats by competing bacterial populations , 2014, BMC Microbiology.

[9]  Ronn S. Friedlander,et al.  Bacterial flagella explore microscale hummocks and hollows to increase adhesion , 2013, Proceedings of the National Academy of Sciences.

[10]  R. Austin,et al.  Bacterial metapopulations in nanofabricated landscapes , 2006, Proceedings of the National Academy of Sciences.

[11]  Jamie M. Messman,et al.  Lectin-functionalized poly(glycidyl methacrylate)-block-poly(vinyldimethyl azlactone) surface scaffolds for high avidity microbial capture. , 2013, Biomacromolecules.

[12]  M. L. Simpson,et al.  Stochastic Assembly of Bacteria in Microwell Arrays Reveals the Importance of Confinement in Community Development , 2016, PloS one.

[13]  S. Retterer,et al.  Microstructured Block Copolymer Surfaces for Control of Microbe Adhesion and Aggregation , 2014, Biosensors.

[14]  M. Parsek,et al.  Going local: technologies for exploring bacterial microenvironments , 2013, Nature Reviews Microbiology.

[15]  D. Weibel,et al.  Physicochemical regulation of biofilm formation , 2011, MRS bulletin.

[16]  S. Retterer,et al.  Development of transparent microwell arrays for optical monitoring and dissection of microbial communities , 2016 .

[17]  Paul A. Wiggins,et al.  Quantitative single-cell characterization of bacterial interactions reveals type VI secretion is a double-edged sword , 2012, Proceedings of the National Academy of Sciences.

[18]  S. Okabe,et al.  Layered Structure of Bacterial and Archaeal Communities and Their In Situ Activities in Anaerobic Granules , 2007, Applied and Environmental Microbiology.

[19]  Tagbo H. R. Niepa,et al.  Microbial Nanoculture as an Artificial Microniche , 2016, Scientific Reports.

[20]  D. Goodlett,et al.  Genetically distinct pathways guide effector export through the type VI secretion system , 2014, Molecular microbiology.

[21]  F. Rombouts,et al.  Modeling of the Bacterial Growth Curve , 1990, Applied and environmental microbiology.

[22]  D. Goodlett,et al.  A type VI secretion system of Pseudomonas aeruginosa targets a toxin to bacteria. , 2010, Cell host & microbe.

[23]  G. Grundmann Spatial scales of soil bacterial diversity--the size of a clone. , 2004, FEMS microbiology ecology.

[24]  John Yin,et al.  Tools for Single-Cell Kinetic Analysis of Virus-Host Interactions , 2016, PloS one.

[25]  J. Crawford,et al.  Spatial distribution of bacterial communities and their relationships with the micro-architecture of soil. , 2003, FEMS microbiology ecology.

[26]  A. Arkin,et al.  Stochasticity, succession, and environmental perturbations in a fluidic ecosystem , 2014, Proceedings of the National Academy of Sciences.

[27]  S. Retterer,et al.  Microstencils to generate defined, multi-species patterns of bacteria. , 2015, Biomicrofluidics.