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Soil-on-chip: a review

Published on August 26th 2020

In this review, the progress in the field of so-called soil-on-chip systems will be discussed, including some of the most exciting applications already available to this date and some promising areas of research for the future. Soil is a complex environment consisting of minerals, water, gases, organic matter, microorganisms, and plant roots. 

All these elements are interconnected in such ways that their interactions shape a heterogeneous yet balanced environment under constant changes. 

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The challenge to studying this system comes from the fact that, as of today, no direct techniques allow its analysis without fundamental alterations of its properties, and no model has been able to recreate and control the spatiotemporal variations required for a reliable simulation of its environmental conditions. A webinar with further information on the topic is available below.

The potential solution to many of the obstacles that microbial ecology faces in soil research can be found in microfluidics. Not only is the scale of soil structures in the range of application, but also, the reduced quantities of reagents needed, transparency, and the specifically tailored approaches offered by microfluidic systems are valuable advantages that make them fit for this purpose. If interested in this topic, further information can be found in the reviews from [1] and [2].

Reproducing heterogeneity in soil-on-chip models

From a structural point of view, the soil is a complex configuration of microaggregates and pores. The microaggregates consist of different types of particles, minerals, or organic matter particles. These microaggregates are held together in macroaggregates by combining electrostatic forces and organic structures such as fungal hyphae and roots [3]. 

Therefore, it can be stated that the main characteristic of soil is its heterogeneity, which is effective at many levels, and that it can be simulated in different ways with microfluidic models, depending on the focus of the study.

soil on chip microbial commmunities
Fig. 1: Structure and components of the soil, including organic and inorganic matter [3].

Physical heterogeneity

From a physical point of view, the soil has many obstacles and barriers that prevent the free circulation and dispersal of substances and microorganisms. To better understand the transport of entities through the soil medium, an intricate topography of channel pillars and walls of different shapes and sizes can be achieved through microfluidics. 

 

This environment is especially interesting for the research of auto-propelled particles, that is, active matter [4]. The specific requirements of a particular type of soil can be tailored according to actual samples taken from the soil thanks to microfabrication techniques like soft lithography [5] and PDMS casting [6], which allows complex structures without compromising reproducibility.

Soil-on-Chip
Fig. 2: Different topographies achieved in microfluidic chips to mimic soil physical structure. A) generated particle pattern of varying shape and size [6], B) Intersection of channels (Voronoi tessellations) [5], C) Pore replication [3].

Introduction to soil-on-chip systems

Chemical heterogeneity

As stated before, soil composition is far from constant, and a wide variety exists of the materials that make up the aggregates and other substances present in the form of gradients and flows. Most of these substances are essential biological resources such as water, nitrogen, carbon dioxide, and oxygen, varying continuously depending on external conditions.

 

In this regard, microfluidic devices can produce similar gradients through the use of agar blocks (with the drawback of increased opacity) and hydrogels to achieve controlled release or controlling the flow through the use of tree-shaped channel flows,  pressure balance (OB1) or membranes [7]. 

Soil-on-Chip_Microfluidics_Innovation center
Fig. 3: Chemical gradients generated with flow control. A) Membranes, B) Tree shaped channel flows and C) Pressure balance [7].

Biological heterogeneity

Soil organisms mainly refer to bacteria and fungi, even though plants and some animals, especially nematodes, must also be considered for a complete system analysis. Traditionally, the culture of microorganisms is focused on a single species to which the physical and chemical requirements of the device are adapted. Nonetheless, in the case of soil-dwelling microorganisms, those requirements also include the presence of another particular set of species that share synergistic metabolism paths or communication, that is, quorum sensing [8]. 

 

A better understanding of these effects is one of the aims of soil-on-chip systems, so the idea of co-cultivation of several species has been explored through different methods. On the one hand, the option of Individual cultures, in which each cell is confined in its permeable chamber, is explored on isolation chips [9]. 

The cells and populations are not connected but can access the same medium and the products others generate. On the other hand, a similar microfluidic concept is based on the circulation of each species through different channels but being close together, only divided by membranes [10].

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Fig. 4: Microfluidic chips that allow the indirect contact of different species in the same environment. A) Isolation chips [9] B) Separation by membranes [10].

Study of interactions in soil-on-chip models

All the previous types of heterogeneity can be interlinked to combine their effects. These direct interactions between elements of the environment are critical to a more realistic characterization, even including more complex organisms like the roots of plants [11] and nematodes [12]. 

A general approach to analyzing direct interactions uses droplet-based microfluidics, where each droplet is an isolated and complete environment [13]. Depending on its elements, a different stage of development will be reached according to the interactions and relations established. 


This technique is beneficial in detecting symbiotic relations [14] as only the direct contact of both species will trigger their proliferation. It is also worth noting that the droplet format provides some advantages, namely, the simultaneous parallel performance of many experiments, sorting droplets depending on the outcome, and more accessible screening and handling. 

Alternatively, single-cell trapping also allows direct contact with the present elements and the analysis of possible interactions in a static, isolated environment [15].

Microfluidic approaches for direct interaction of multiple elements
Fig. 5: Microfluidic approaches for direct interaction of multiple elements. A) Droplet-based microfluidics, B) Cell trapping [16].

Applications of soil-on-chip microfluidic devices

On top of research to understand the soil ecosystem, further applications can be envisaged for soil-on-chip systems. These are derived from the advantage of a controlled environment where every significant parameter can be adjusted accordingly, and previously nonculturable species can be maintained in culture.

Bioremediation

Soil is an environment susceptible to pollution, but as opposed to water or air, the medium is primarily static, and a thorough detoxification implies its fundamental alteration. A more environmentally friendly and viable option to avoid radical intervention in the ecosystem comes from the possibility of using microorganisms to metabolize the present toxic substances. However, for this process to be successful, the suitable species must be in adequate amounts to access the pollutant and additional resources required for the metabolic pathway. 

 

Natural systems hardly meet these conditions and usually have to be optimized. Consequently, reliable soil models suggest to offer the most efficient solution. Conveniently, there are many soil microorganisms, especially bacteria and fungi [17], capable of degrading substances hazardous to the environment, such as crude oil [18], pesticides, and heavy metals [19].

Soil-on-Chip 6
Fig. 6: Schematic representation of bioremediation of soil. After the inoculation of organisms and nutrients, air is injected to promote expansion and in some cases, the partial retrieval of substances [20].

Biofilms on soil-on-chip

Soil-on-Chip_Microfluidics 7
Fig. 7: Biofilm life cycle and dispersion. Free and the embedded phases are shown [23].

Under the right conditions, microorganisms can associate themselves with supracellular structures known as biofilms, which consist of communities of cells embedded in extracellular polymeric substrates.

The main interest of these structures comes from the fact that the collective behavior of microorganisms can change significantly compared to their free-moving state. Therefore, the substances they produce change, and their survival resources change.

 

This effect can be further enhanced by associating different species that complement each other inside the biofilm, granting protection against environmental changes and increasing the community’s overall viability.

Microfluidic approaches have successfully formed biofilm for aquatic [21] and marine bacteria [22]. In the case of soil, even if microorganisms are often found in biofilms, microfluidic research is still relatively recent [23]. 

A better understanding of biofilm formation mechanisms could lead to the culture of many new soil species, which could have critical applications such as bioremediation or the discovery of novel pharmaceutical compounds [24].

Conclusion

In short, the study of soil tries to answer many questions that could be answered through microfluidics. Even if some notable advances have been made, most of the research has been done in recent years, and the proper development of the field has yet to come. Moreover, given the complexity of soil, we are far from a reliable single device that can mimic soil completely. 

However, different models adapted for a few specific aspects of this multifaceted environment are being developed. The slow progress of research on this topic can also be linked to the low availability of soil-on-chip devices nowadays, so these new tools will significantly benefit the field by giving access to the required apparatus to a broader audience.

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Soil-on-chip review done thanks to the support of the ActiveMatter 

H2020-MSCA-ITN-2018-Action “Innovative Training Networks”, Grant agreement number: 812780

Author: Jesús Manuel Antúnez Domínguez, PhD candidate
Contact: jesus.dominguez@microfluidic.fr

Jesus Mantunez Dominguez
References
  1. C. E. Stanley, G. Grossmann, X. CasadevallI Solvas, and A. J. DeMello, “Soil-on-a-Chip: Microfluidic platforms for environmental organismal studies,” Lab Chip, vol. 16, no. 2, pp. 228–241, 2016.
  2. K. Aleklett, E. T. Kiers, P. Ohlsson, T. S. Shimizu, V. E. Caldas, and E. C. Hammer, “Build your own soil: Exploring microfluidics to create microbial habitat structures,” ISME J., vol. 12, no. 2, pp. 312–319, 2018.
  3. R. L. Wilpiszeski et al., “Soil Aggregate Microbial Communities: Towards Understanding Microbiome Interactions at Biologically Relevant Scales,” Appl. Environ. Microbiol., vol. 85, no. 14, pp. 1–18, 2019.
  4. S. Makarchuk, V. C. Braz, N. A. M. Araújo, L. Ciric, and G. Volpe, “Enhanced propagation of motile bacteria on surfaces due to forward scattering,” Nat. Commun., vol. 10, no. 1, 2019.
  5. M. Wu, F. Xiao, R. M. Johnson-Paben, S. T. Retterer, X. Yin, and K. B. Neeves, “Single- and two-phase flow in microfluidic porous media analogs based on Voronoi tessellation,” Lab Chip, vol. 12, no. 2, pp. 253–261, 2012.
  6. J. Deng et al., “Synergistic effects of soil microstructure and bacterial EPS on drying rate in emulated soil micromodels,” Soil Biol. Biochem., vol. 83, no. December, pp. 116–124, 2015.
  7. X. Wang, Z. Liu, and Y. Pang, “Concentration gradient generation methods based on microfluidic systems,” RSC Adv., vol. 7, no. 48, pp. 29966–29984, 2017.
  8. M. Whiteley, S. P. Diggle, E. P. Greenberg, and E. O. Wilson, “Bacterial quorum sensing: the progress and promise of an emerging research area Main text Humans have provided descriptions of the natural history of animals for millennia. Apart from basic anatomy and physiology, it was also noted that a number of animal,” Nature, vol. 551, no. 7680, pp. 313–320, 2017.
  9. D. Nichols et al., “Use of ichip for high-throughput in situ cultivation of “uncultivable microbial species,” Appl. Environ. Microbiol., vol. 76, no. 8, pp. 2445–2450, 2010.
  10. A. Burmeister et al., “A microfluidic co-cultivation platform to investigate microbial interactions at defined microenvironments,” Lab Chip, vol. 19, no. 1, pp. 98–110, 2019.
  11. H. Massalha, E. Korenblum, S. Malitsky, O. H. Shapiro, and A. Aharoni, “Live imaging of root-bacteria interactions in a microfluidics setup,” Proc. Natl. Acad. Sci. U. S. A., vol. 114, no. 17, pp. 4549–4554, 2017.
  12. A. Parashar and S. Pandey, “Plant-in-chip: Microfluidic system for studying root growth and pathogenic interactions in Arabidopsis,” Appl. Phys. Lett., vol. 98, no. 26, pp. 1–4, 2011.
  13. L. Boitard, D. Cottinet, N. Bremond, J. Baudry, and J. Bibette, “Growing microbes in millifluidic droplets,” Eng. Life Sci., vol. 15, no. 3, pp. 318–326, 2015.
  14. J. Park, A. Kerner, M. A. Burns, and X. N. Lin, “Microdroplet-enabled highly parallel co-cultivation of microbial communities,” PLoS One, vol. 6, no. 2, 2011.
  15. S. Hong, Q. Pan, and L. P. Lee, “Single-cell level co-culture platform for intercellular communication,” Integr. Biol., vol. 4, no. 4, pp. 374–380, 2012.
  16. S. G. Hays, W. G. Patrick, M. Ziesack, N. Oxman, and P. A. Silver, “Better together: Engineering and application of microbial symbioses,” Curr. Opin. Biotechnol., vol. 36, pp. 40–49, 2015.
  17. V. Kumar, M. Kumar, and R. Prasad, “Microbial action on hydrocarbons,” Microb. Action Hydrocarb., no. January 2018, pp. 1–667, 2019.
  18. A. A. Burghal, N. M. J. A. Abu-Mejdad, and W. H. Al-Tamimi, “Mycodegradation of Crude Oil by Fungal Species Isolated from Petroleum Contaminated Soil,” Int. J. Innov. Res. Sci. Mon. Peer Rev. Journal), vol. 5, no. 2, pp. 1517–1524, 2016.
  19. S. J. Edwards and B. V. Kjellerup, “Applications of biofilms in bioremediation and biotransformation of persistent organic pollutants, pharmaceuticals / personal care products, and heavy metals,” Appl. Microbiol. Biotechnol., vol. 97, no. 23, pp. 9909–9921, 2013.
  20. B. Antizar-Ladislao, “Bioremediation: Working with bacteria,” Elements, vol. 6, no. 6, pp. 389–394, 2010.
  21. J. Kim, H. D. Park, and S. Chung, “Microfluidic approaches to bacterial biofilm formation,” Molecules, vol. 17, no. 8, pp. 9818–9834, 2012.
  22. Y. Yawata, J. Nguyen, R. Stocker, and R. Rusconi, “Microfluidic studies of biofilm formation in dynamic environments,” J. Bacteriol., vol. 198, no. 19, pp. 2589–2595, 2016.
  23. P. Cai et al., “Soil biofilms: microbial interactions, challenges, and advanced techniques for ex-situ characterization,” Soil Ecol. Lett., vol. 1, no. 3–4, pp. 85–93, 2019.
  24. E. J. Stewart, “Growing unculturable bacteria,” J. Bacteriol., vol. 194, no. 16, pp. 4151–4160, 2012.

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