Microbial consortium

Source: Wikipedia, the free encyclopedia.

A microbial consortium or microbial community, is two or more

microbial groups living symbiotically.[1][2] Consortiums can be endosymbiotic or ectosymbiotic, or occasionally may be both. The protist Mixotricha paradoxa, itself an endosymbiont of the Mastotermes darwiniensis termite, is always found as a consortium of at least one endosymbiotic coccus, multiple ectosymbiotic species of flagellate or ciliate bacteria, and at least one species of helical Treponema bacteria that forms the basis of Mixotricha protists' locomotion.[3]

The concept of a consortium was first introduced by

land plants and for their transition from algal communities in the sea to land.[6]

Overview

bacterial filaments. h, i) Different bacterial individuals showing great varieties of shapes and morphological features.[7]

Microbes hold promising application potential to raise the efficiency of bioprocesses when dealing with substances that are resistant to decomposition.[8][9] A large number of microorganisms have been isolated based on their ability to degrade recalcitrant materials such as lignocellulose and polyurethanes.[10][11] In many cases of degradation efficiency, microbial consortia have been found superior when compared to single strains.[12] For example, novel thermophilic consortia of Brevibacillus spp. and Aneurinibacillus sp. have been isolated from the environment to enhance polymer degradation.[13]

Two approaches exist to obtain microbial consortia involving either (i) a synthetic assembly from scratch by combining several isolated strains,[14] or (ii) obtainment of complex microbial communities from environmental samples.[15] For the later, enrichment process is often used to get the desired microbial consortia.[16][17][18] For instance, a termite gut-derived consortium showing a high xylanase activity was enriched on raw wheat straw as the sole carbon source, which was able to transform lignocellulose into carboxylates under anaerobic conditions.[19]

Relatively high diversity levels are still observed despite the use of enrichment steps when working from environmental samples,[18] likely due to the high functional redundancy observed in environmental microbial communities, being a key asset of their functional stability.[20][21] This intrinsic diversity may stand as a bottleneck in attempts to move forward to practical application due to (i) potential negative correlation with efficiency,[22] (ii) real microbial cheaters whose presence has no impacts on degradation, (iii) security threats posed by the presence of known or unknown pathogens, and (iv) risks of losing the properties of interest if supported by rare taxa.[23]

Utilization of microbial consortia with less complexity, but equal efficiency, can lead to more controlled and optimized industrial processes.

lignocellulose degradation based on different metabolic functional groups.[24] Additionally, artificial selection approaches (dilution, toxicity, and heat) have been also employed to obtain bacterial consortia.[26] Among them, dilution-to-extinction has already proven its efficiency for obtaining functional microbial consortia from seawater and rumen liquor .[27][28][29] Dilution-to-extinction is expected to provide more advantages compared to conventional isolation and assembly as it (i) generates many microbial combinations ready to be screened, (ii) includes strains from the initial microbial pool that might be lost due to cultivation/isolation biases, and (iii) ensures that all microbes are physically present and interacting spontaneously.[30][23]

Examples

Microbialites

sulphate-reducing bacteria, diatoms, and microalgae.[citation needed] These microorganisms produce adhesive compounds that cement sand and join other rocky materials to form mineral "microbial mats". The mats build layer by layer, growing gradually over time.[citation needed
]

Rhizosphere

Rhizosphere microbial consortia[31]

Although various studies have shown that single microorganisms can exert beneficial effects on plants, it is increasingly evident that when a microbial consortium — two or more interacting microorganisms — is involved, additive or synergistic results can be expected. This occurs, in part, due to the fact that multiple species can perform a variety of tasks in an ecosystem like the plant root

Mycorrhizae.[31]

The diagram on the right illustrates that rhizosphere microorganisms like plant-growth-promoting bacteria (PGPB),

arbuscular mycorrhizal fungi (AMF), and fungi from the genus Trichoderma spp. can establish beneficial interactions with plants, promoting plant growth and development, increasing the plant defense system against pathogens, promoting nutrient uptake, and enhancing tolerance to different environmental stresses. Rhizosphere microorganisms can influence one another, and the resulting consortia of PGPB + PGPB (e.g., a nitrogen-fixing bacterium such as Rhizobium spp. and Pseudomonas fluorescens), AMF + PGPB, and Trichoderma + PGPB may have synergetic effects on plant growth and fitness, providing the plant with enhanced benefits to overcome biotic and abiotic stress. Dashed arrows indicate beneficial interactions between AMF and Trichoderma.[31]

Keratin degradation

Workflow of enrichment and dilution-to-extinction cultures to select simplified microbial consortia (SMC) for keratin degradation.[23]

The capacity of microbes to degrade recalcitrant materials has been extensively explored for environmental remediation and industrial production. Significant achievements have been made with single strains, but focus is now going toward the use of microbial consortia owing to their functional stability and efficiency. However, assembly of simplified microbial consortia (SMC) from complex environmental communities is still far from trivial due to large diversity and the effect of

biotic interactions.[23]

epithelial cells.[32] They are estimated to have considerable economic value after biodegradation.[33] An efficient keratinolytic microbial consortium (KMCG6) was previously enriched from an environmental sample through cultivation in keratin medium.[18] Despite reducing the microbial diversity during the enrichment process, KMCG6 still included several OTUs scattered amongst seven bacterial genera.[23]

In 2020 Kang et al., using a strategy based on enrichment and dilution-to-extinction cultures, extracted from this original consortium (KMCG6) a simplified microbial consortia (SMC) with fewer species but similar keratinolytic activity.[23] Serial dilutions were performed on a keratinolytic microbial consortium pre-enriched from a soil sample. An appropriate dilution regime (109) was selected to construct a SMC library from the enriched microbial consortium. Further sequencing analysis and keratinolytic activity assays demonstrated that obtained SMC displayed actual reduced microbial diversity, together with various taxonomic composition, and biodegradation capabilities. More importantly, several SMC possessed equivalent levels of keratinolytic efficiency compared to the initial consortium, showing that simplification can be achieved without loss of function and efficiency.[23]

As shown in the diagram on the right, the workflow for this study included four steps: (1) Enrichment for the desired traits e.g., keratinolytic activity by selection in keratin medium, where keratin is the sole carbon source. This process was evaluated by functional assessments (cell density, enzymes activity, and ratio of the residual substrate) and compositional analysis. (2) Serial dilutions were conducted to the enriched effective microbial consortia. Six dilutions were prepared, from dilution 102 to 1010 with 24 replicates. The dissimilarity between dilutions was evaluated by Euclidean distance calculation based on functional assessment criteria. (3) Library construction was done from the dilution offering the optimal dissimilarity among replicates. Dilution 109 was selected to construct the SMC library in this case. (4) Selection of the most promising SMC is based on functional and compositional characterization.[23]

Human health

Consortia are commonly found in humans, with the predominant examples being the

metagenomic evidence suggesting the species found may be enteric in origin.[34][35] As the species found appear to be well-established, have no discernible impact on human health, and are species known to form consortia when found in the gut, it is highly likely they have also formed a symbiotic consortium within the brain.[36]

Synthetic microbial consortia

chemoheterotrophic
bacterium often used in synthetic microbial consortia.

Synthetic microbial consortia (commonly called co-cultures) are multi-population systems that can contain a diverse range of microbial species, and are adjustable to serve a variety of industrial and ecological interests. For synthetic biology, consortia take the ability to engineer novel cell behaviors to a population level. Consortia are more common than not in nature, and generally prove to be more robust than monocultures.[37] Just over 7,000 species of bacteria have been cultured and identified to date. Many of the estimated 1.2 million bacteria species that remain have yet to be cultured and identified, in part due to inabilities to be cultured axenically.[38] When designing synthetic consortia, or editing naturally occurring consortia, synthetic biologists keep track of pH, temperature, initial metabolic profiles, incubation times, growth rate, and other pertinent variables.[37]

See also

Notes

  1. .
  2. ^ Mark, Martin (2009-04-27). "Happy Together… Life of the Bacterial Consortium Chlorochromatium aggregatum". Small Things Considered - The Microbe Blog. American Society for Microbiology. Archived from the original on 2009-05-01. Retrieved 2012-01-11. Consortia are assemblages of different species of microbes in physical (and sometimes intricate biochemical) contact with one another, and are implicated in biological processes ranging from sewage treatment to marine nitrogen cycling to metabolic processes within the rumen.
  3. .
  4. ^ Reinke, Johannes 1872. Ueber die anatomischen Verhältnisse einiger Arten von Gunnera L. Nachrichten von der Königl. Gesellschaft der Wissenschaften und der Georg-Augusts-Universität zu Göttingen 9: 100–108.
  5. ^ Kull, Kalevi 2010. Ecosystems are made of semiosic bonds: Consortia, umwelten, biophony and ecological codes. Biosemiotics 3(3): 347–357.
  6. PMID 26438870
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  7. doi:10.1186/s40168-018-0445-0. Material was copied from this source, which is available under a Creative Commons Attribution 4.0 International License
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    PMID 31998278. Material was copied from this source, which is available under a Creative Commons Attribution 4.0 International License
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    doi:10.3390/agronomy11020219. Material was copied from this source, which is available under a Creative Commons Attribution 4.0 International License
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  34. ^ Pennisi, Elizabeth (7 May 2020). "Meet the 'psychobiome': the gut bacteria that may alter how you think, feel, and act". Science Magazine. Retrieved 12 December 2020.
  35. ^ Rettner, Rachel (15 November 2018). "Bacteria May Live (Harmlessly) in Your Brain". livescience.com. Live Science. Retrieved 12 December 2020.
  36. ^ Roberts, R. C.; Farmer, C. B.; Walker, C. K. (6 November 2018). "The human brain microbiome; there are bacteria in our brains!". Psychiatry and Behavioral Neurobio., Univ. Of Alabama, Birmingham, Birmingham, AL. 2018 Neuroscience Meeting Planner. (Program No. 594.08). Retrieved 12 December 2020.
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