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Journal of Ecology & Natural Resources Research Article 23 min read

Environmental and Ecological Impact of Soil Microorganisms in Plant Sciences

Das K*, Das SC and Aminuzzaman FM
* Corresponding author
ISSN: 2578-4994  10.23880/jenr-16000273  Received: March 11, 2022  Published: April 07, 2022
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Keywords
Ecology Environment Plant Sciences Soil Microorganisms
Abstract

The field of environmental and microbial ecology is undergoing a revolution, having ramifications in microbiology, ecology, and ecosystem research. The tremendous accumulation of molecular data is revealing a vast diversity of microbial groups, as well as unique microbial functions. Plants are part of a varied ecosystem in their natural habitat, which includes numerous and different microorganisms in the soil. Some of these microbes, such as mycorrhizal fungi and nitrogen-fixing symbiotic bacteria, have long been known to improve plant performance through enhancing mineral nutrition. A substantial quantity of data on the structure and dynamics of plant microbiota, as well as the functional capacities of isolated community members, is currently available. The adoption of appropriate delivery techniques and formulations, as well as smart, knowledge-driven microbe selection, is required. Plant-microbe interactions may now be studied in greater depth thanks to modern biotechnology. In this review, we look at the interaction between the soil, the host, and the microbial population, as well as their involvement in plant sciences, to see what we can learn about the ecosystem function of plants and symbiotic microorganisms, which will help us to improve agricultural techniques.

Introduction

Several studies have shown that soil microorganisms and plant–microbe interactions can improve environmental quality and reduce global warming. Soil microbial community composition changes between compartments and levels, posing a serious problem in soil ecology. Microbes, especially plant growth-promoting microorganisms, are vital in agriculture (PGPMs). The following three mechanisms contribute to plant growth - (i) PGPMs that operate as biofertilizers (like nitrogen-fixing bacteria and phosphate- solubilizing bacteria) help plants absorb nutrients [1], (ii) Phytostimulators (microbes that produce phytohormones, including Azospirillum) can directly stimulate plant development [2, 3], (iii) Plants are protected from phytopathogens by biological control agents (Trichoderma, Pseudomonas, and Bacillus) [4–6].

However, as a metaorganism, plants have only lately been identified as having their own specific and intertwined microbiome [7]. A plant’s ecology is influenced by interactions with microbes that live in or on the plant. In ecosystem functioning, the roles of both plants and their accompanying microorganisms have been recognized, but the specific mechanisms are still unclear. Being unable to move, plants have co-evolved with microorganisms, which have resulted in a variety of processes that influence the outcome of their interactions [8]. In Ciccazzo’s work [9], a certain bacterial population is selected by a plant species. The long-term effects of soil microbes on a plant species’ coexistence are defined by changes in the plant’s relative performance in response to changes in the microbial composition [10, 11]. A variety of volatile compounds can be produced by plant growth-promoting rhizobacteria (PGPR), and these compounds are specific to bacterial species and other closely related species [12, 13, 14]. Some of these bacterial volatiles can boost plant development, decrease disease- stimulating induced systemic resistance (ISR), or antagonize phytopathogens [15], nematodes, or insects [16, 17]. In this review, we will explore understanding the environmental and ecological impacts of soil microorganisms which will help farmers improve their methods while also helping us to appreciate the significance of microbial communities in plant biology.

Environmental Impact of Soil Microorganisms

Some soil microorganisms known as mycorrhiza, as well as plant-associated bacteria (rhizospheric or endophytic), can help their plant hosts with nutrient supply, which is vital not only for optimal plant development in normal conditions, but also for plant survival in hostile settings [18]. Endophytic bacteria can support plant growth through a variety of mechanisms, including biological nitrogen fixation, tolerance, and the existence of pollutant degradation pathways. The biomass obtained from those plants and soil microbes can be a valuable resource for producing bio-energy as alternative fuels such as biodiesel, bioethanol, or biogas, which are thought to slow down global warming. As a result, it’s possible that this occurred as part of the compatible reaction during mycorrhization. During times of world change, mycorrhiza may be useful in overcoming xenobiotic or environmental stress [18, 19].

Furthermore, knowing changes in ecosystem environmental characteristics is important on a worldwide basis. On the one hand, more precise understanding would aid in improved environmental management and the protection of environmental structures, reducing damages such as soil contamination and erosion in ecosystems subjected to pollution, drought, or other environmental stressors. Locally, sustainable usage of environmental species is required for a balanced economic and ecological growth, especially in light of global warming. In recent years, subsidies for research in both ecosystems have been substantially decreased, exacerbating the problems of providing incentives to conserve environmental quality and assure functional microbial behaviour [18, 19]. With such a powerful impact on the environment, it is critical to better understand the mechanisms involved in order to control it. The impact of environmental management on soil microorganisms is critical for improving our understanding of how to maintain such ecosystems’ quality. Moreover, soil structure is a part of the environment’s ecology, and it can be changed by the following factors:

  • Plant community structure and vegetation cover are readily damaged and difficult to recover.
  • Humus and/or nutrients, particularly P (Phosphorus), are frequently low in soils.
  • Nutrients and organic matter in the soil are frequently depleted and quickly lost.
  • There are temperature extremes that are seasonal and/or diurnal.
  • Precipitation is usually strong and erosive, and it falls in short bursts.
  • There is a chance of strong winds and bushfires, among other things.

Scientists conducted two long-term trials in a Mediterranean habitat, demonstrating that inoculation with indigenous soil microorganisms improved not only plant establishment but also soil fertility and environmental quality [20]. Soil nitrogen (N) content, organic matter, and hydrostable soil aggregates have all grown as a result of this symbiosis, as has nutrient transfer among plant species associated with natural succession. The introduction of target indigenous plant species in conjunction with a managed community of microbial systems was found to be a successful approach for assisting the recovery of low vegetative habitats. The diversity of soil microbe species relevant to the setting of the current project is first discussed in this chapter, followed by a review of the proposed mechanisms of soil structure formation [21]. Microbial symbioses provide a biofertilizing and environmental stability role because colonized plants are better able to receive nutrients and tolerate environmental challenges. In the ecosystem, colonized plants’ greater uptake of soil minerals means that fertilizer treatments can be reduced significantly while crop yields remain comparable or even higher.

Ecological Impact of Potential Soil Microorganisms

Plants have evolved to include a diverse range of microorganisms that play critical functions in plant growth and health. A substantial quantity of data on the structure and dynamics of plant microbiota, as well as the functional capacities of isolated community members, is currently available (Figure 1). There is a pressing need to put microbial innovations into practice, both because of the intriguing functional potential of plant microbiota and because of existing crop production issues [22]. Plants actively recruit microorganisms from the soil/rhizosphere, the phyllosphere, the anthosphere (the external environment of flowers), the spermosphere (the exterior of germinated seed), and the carposphere (the external environment of fruit) [23]. The majority of root microbiota is horizontally transported, meaning it comes from the soil environment, which comprises a varied range of microorganisms dominated by Acidobacteria, Verrucomicrobia, Bacteroidetes, Proteobacteria, Planctomycetes, and Actinobacteria. Bacteria can also be spread vertically via seeds. Seeds are also a major source of microorganisms, which grow in the developing plant’s roots [24, 25]. Plants provide unique ecological niches for soil microbes, which invade the rhizosphere, roots, and to a degree above ground sections [26]. Similarly, Kawasaki, et al. [27] reported that the Brachypodium distachyon (a model for wheat) rhizosphere was dominated by Burkholderiales, Sphingobacteriales and Xanthomonadales, while the bulk soil was dominated by the order Bacillales. Organic acids, amino acids, fatty acids, phenolics, plant growth regulators, nucleotides, sugars, putrescine, sterols, and vitamins, as well as other root exudates, have been shown to impact microbial composition near roots [28].

However, above-ground plant tissues such as vegetative foliar parts, leaves, and floral parts provide distinct settings for endophyte and epiphyte diversities, although the ecology of endosphere and phyllosphere bacteria differs significantly [29]. As a result, different microorganisms are found in the endosphere and phyllosphere at the genus and species level, such as Pseudomonas, Sphingomonas, Frigoribacterium, Curtobacterium, Bacillus, Enterobacter, Acinetobacter, Erwinia, Citrobacter, Pantoea, and Methylobacterium as predominant genera [30, 31]. Wallace, et al. [32] investigated the maize leaf microbiome across 300 different maize lines and discovered that sphingomonads and methylobacteria were the most common species. They also discovered that environmental conditions influenced the phyllosphere’s microbial composition. Pseudomonas and Enterobacteriaceae were found to be the most common taxa in apple flowers, according to Steven, et al. [33]. Pseudomonas was also reported to be the most prevalent genus in various investigations on apple, almond, grapefruit, tobacco, and pumpkin blossoms [34]. Seed-associated bacteria have only lately been studied, with Proteobacteria, Actinobacteria, Bacteroidetes, and Firmicutes being the most common [35, 36]. Seed microbiotas have a connection to soil microbiota, as well as those of flowers and fruits [37, 38].

Functions and Factors Affecting Microorganisms

The term “core plant microbiome” refers to microorganisms that are intimately connected with a particular plant species or genotype regardless of soil or environmental circumstances [39]. A variety of biotic and abiotic variables determine the microbial composition of any plant organ. External environmental conditions such as climate, pathogen presence, and human practices [40] influence microbiota of above- and below-ground plant parts, whereas soil pH, salinity, soil type, soil structure, soil moisture, and soil organic matter and exudates [41] are most relevant for belowground plant parts (Table 1). Beneficial, neutral, and harmful microbes make up the plant microbiome. Plant growth-promoting bacteria (PGPB) can enhance plant growth in a number of ways, both directly and indirectly. Auxin, cytokinin, and gibberellin are phytohormones produced by certain PGPB that affect plant growth by modifying endogenous hormone levels in interaction with a plant. Furthermore, some PGPB can secrete an enzyme called 1-aminocyclopro pane-1-carboxylate (ACC) deaminase, which lowers ethylene levels in the plant. Pseudomonas spp., Arthrobacter spp., Bacillus spp., and other bacteria have been found to boost plant development by producing ACC deaminase [42] (Table 1).

Phytotoxic chemicals, proteins, and phytohormones produced by some bacteria can induce illness symptoms. Pseudomonas syringae, for example, is a well-known plant pathogen with a wide host range that includes tomato, tobacco, olive, and green bean. Erwinia amylovora is another well- known pathogenic bacterium that causes fire blight in fruit trees and ornamental plants. Many significant crop diseases, such as potato and banana, are linked to Xanthomonas species, Ralstonia solanacearum, and Xylella fastidiosa [43]. In terms of above- and below-ground ecological diversity in a terrestrial ecosystem, global temperature change can have an impact on plant ecology. The terrestrial plant community affects the microbial ecology of the soil, which can lead to changes in ecosystem function. Plant species cohabitation can be governed by resource partitioning and sharing of soil resources. Root symbionts have been discovered to improve nutrient uptake efficiency and let the host to persist in low- nutrient environments, thereby contributing directly to the competitive exclusion of other plants [44].

Soil is a complex ecosystem that hosts bacteria, fungus, protists, and animals, despite the fact that plant physiologists sometimes see it as only a source of nutrients for plants [45]. Plants engage in a wide range of interactions with these soil- dwelling creatures, spanning the entire ecological spectrum (competitive, exploitative, neutral, commensal, mutualistic) (Figure 1). Most interaction investigations in modern plant science have focused on reducing pathogenic impacts such herbivory and infection [46] or reducing abiotic stress conditions [47, 48].

Sl. No.Organisms involvedType of
interaction
Compounds/
mechanisms involved
FindingsReferences
1Moniliophthora roreri
and
Trichoderma
harzianum
Phytopathogen–
endophyte
T39 butenolide,
harzianolide,
sorbicillinol
Compounds dependent on the
phytopathogen
presence and were spatially localized
in the
interaction zone.
[49]
2Trichoderma
atroviride and
Arabidopsis sp.
Endophyte–
plant
Indole acetic acid-
related indoles
Plant root colonization promotes
growth and
enhances systemic disease resistance
in the
plant by endophytes.
[50]
3Xylella fastidiosa and
Methylobacterium
mesophilicum
Phytopathogen–
endophyte
Hydroxamate typeGenes related to energy production,
stress,
transport, and motility were
upregulated in the
phytopathogen, but genes related to
growth
were downregulated.
[51]
4Burkholderia gladioli,
B. seminalis, and
orchid
Phytopathogen–
endophyte–
plant
Extracellular
polysaccharides;
altering hormone
metabolism
By using extracellular polysaccharides
and by
altering hormone metabolism, the
endophyte
strain probably interacts with the
plant, as was
suggested by genomic analysis.
[52]
5Bradyrhizobium
diazoefficiens and
Aeschynomene
afraspera
Symbiont–plantC35 hopanoidsC35 hopanoids are essential for
symbiosis and
are related to evasion of plant defense,
utilization
of host photosynthates, and nitrogen
fixation.
[53]
6Stachybotrys elegans
and Rhizoctonia solani
Mycoparasite–
host
Trichothecenes and
atranones
Mycoparasite-induced alterations in
Rhizoctonia
solani metabolism, growth, and
development
by the production of mycotoxins. The
biosynthesis of many antimicrobial
compounds
by R. solani was downregulated.
[54]
7Candida albicans
and Pseudomonas
aeruginosa
Microbial
community
Quorum sensingThe Pseudomonas aeruginosa QS
system may
block the yeast-to-hypha transition or
activate
the hypha-to-yeast reversion of
Candida
albicans. Farnesol produced by C.
albicans
downregulates the QS system of P.
aeruginosa.
[55]
8Vibrio fischeri and
fishes or
squids
Symbiont–fishQuorum sensingIn symbiotic association with fishes
and squids,
the auto-inducer molecule reaches a
threshold
and luminescence genes are activated.
[56]
9Rhizobium
leguminosarum
and plants
Symbiont–fishQuorum sensingThe quorum-sensing system in these
bacteria is
related to different functions:
nodulation efficiency,
growth inhibition, nitrogen fixation,
and plasmid transfer.
[57]
10Xanthomonas or
Xylella and
grapevines or citrus
Pathogen–hostQuorum sensingQuorum-sensing signaling molecules
control
the expression of virulence factor as
well a s
biofilm formation.
[42]
11Pantoea stewartii and
Zea mays
Pathogen–hostQuorum sensingQuorum-sensing mutants of Pantoea
stewartii
were not able to disperse and migrate
in the
vasculature, consequently decreasing
the
disease.
[58]
12Pseudomonas syringae
and
tabacco and bean
Phytopathogen–
plant
Quorum sensingQuorum-sensing system allows this
bacterium
to control motility and
exopolysaccharide synthesis
essential on biofilm formation and
leaves
colonization.
[59]
13Streptomyces
coelicolor and
other Actinomycetes
spp.
Microbial
community
Prodiginines,
ctinorhodins,
coelichelins, acyl-
desferrioxamines,
and other compounds
The 227 compounds differentially
produced in
the interactions were unique.
[60]
14Aspergillus nidulans
and Streptomyces
rapamycinicus
Microbial
community
Aromatic polyketidesActivation of fungal secondary
metabolite
genes that were otherwise silent led
physical
interaction between the
microorganisms. The
actinomycete triggered alterations in
fungal
histone acetylation.
[61]
15Pseudomonas sp.Microbial
community
Pyoverdines
(siderophore)
Pyoverdines act as signaling
molecules, activating
a cascade that results in the
production
of several virulence factors. It is
essential to
infection and biofilm formation.
[62]
16Burkholderia sp.,
Rhizopus sp., and rice
Symbiont
phytopathogen
plant
Rhizoxin, bongkrekic
acid,
enacyloxins
In the absence of the endosymbiont
the fungus
does not form spores. The phytotoxin
rhizoxin
is the causal agent of rice seedling
blight produced
by the endosymbiont; fungus induces
the growth of the endosymbiont.
[63]
17Vibrio sp. and diverse
marine bacteria
strains
Microbial
community
N,N-bis-(2,3-
Dihydroxybenzoyl)
-Oserylserine:exogenous
siderophore
Siderophores and iron-regulated
outer membrane
proteins produced by marine bacteria
and other species only in the presence
of exogenous
siderophores.
[64]

Table 1: Recent Studies of Microbial Interaction.

Figure 1: Interactions among plants, microbes, and soil with the microbial activity.
Click to enlarge
Figure 1: Interactions among plants, microbes, and soil with the microbial activity.

Soil Improvement for the Plant with Microorganisms

To be genuinely effective in an agricultural setting, proposed growth-promoting strains must be shown to be able to be re-inoculated onto plants, colonize the rhizospheric niche successfully, and then mediate nutrient mobilization that improves plant development. Plant–microbe interaction assays can be used to examine prospective strains for their capacity to stimulate plant growth and nutrient absorption (Figure 1) [65]. Plant growth stimulation by microbial mobilization of alternative nitrogen sources has also been reported, as evidenced by greater yield in plants treated with bacterial strains [66, 67]. Sustainable agriculture has grown in popularity in recent years, necessitating new technology advancements to limit the usage of environmentally hazardous chemical fertilizers and pesticides. Several research have focused on plant probiotics as an alternative soil fertilization source; their application in agriculture enhances nutrient availability and conserves field management while causing no harmful consequences [68] (Table 2).

Many biogeochemical processes are mediated by soil microflora, with some species influencing organic matter and soil pollutant biodegradation (rhizoremediators) as well as abiotic stress tolerance [69, 70]. Environmental pollution levels have continuously increased in tandem with industrial growth. Efforts to restore polluted soil have been made, however traditional hazardous chemical treatment approaches are both excessively expensive and damaging to soil microbiota [71]. Furthermore, Cadmium, chromium, copper, lead, mercury, nickel, zinc, and other heavy metals are the most common inorganic pollutants [72]. To rehabilitate polluted soil, however, an environmentally beneficial and low-cost method has been used. Plant species capable of collecting heavy metals are used in phytoremediation for area recovery. The plant’s ability to tolerate huge concentrations of pollutants without compromising its biomass is a limiting factor for this technique’s success [73].

Sl. No.Microbial AgentsNutrient CyclingSoil Structure
1Microflora (fungi, bacteria,
actinomycetes)
Catabolize organic matter;
mineralize and immobilize
nutrients.
Produce organic compounds that bind
aggregates; hyphae entangle particles
onto aggregates.
2Microfauna (Acarina, Collembola)Regulate bacterial and fungal
populations; alter nutrient
turnover.
May affect aggregate structure
through interactions with microflora
3Mesofauna (Acarina, Collembola,
enchytraeids)
Regulate fungal and microfaunal
populations; alter nutrient
turnover; fragment plant residues.
Produce fecal pellets; create biopores;
promote humification.
4Macrofauna (isopods, centipedes,
millipedes, earthworms, etc.)
Fragment plant residues;
stimulate microbial activity.
Mix organic and mineral particles;
redistribute organic matter and micro-
organisms; create biopores; promote
humification; produce fecal pellets.

Table 2: Influences of soil biota on soil processes in ecosystems [70].

Also Metal-tolerant microorganisms, particularly PGPR, have been examined for their ability to bioaccumulate metals in contaminated settings, which improves metal uptake and stimulates plant development. The major mechanism of bioremediation is microbe-plant association, which leads to soil purification and plant development [74].

Future Development of Application in Plant Microbe Interaction

Understanding the connections between plants and microbes, as well as microbes and microbes, will be useful in the future as a regulating microbiome for reducing disease incidence and increasing gross plant yield. In the future, a well-studied plant-microbe alliance could assist enhance crop output at a low cost, potentially leading to another “Green Revolution.” Since people began to farm and were no longer nomads, plants have been an important element of our diet. Since then, the globe has been faced with the constant issue of feeding an ever-increasing population. Microbes’ role in plant-microbe interactions has been extensively researched during the last decade [75, 76]. Extensive research suggests that utilizing beneficial bacteria is a superior long-term strategy for increasing crop productivity, which will play a key role in disease transmission and management [77]. Transcriptomics, proteomics, and metabolomics, as well as bioinformatics, have all been used extensively in plant abiotic stress research [78]. The proteomics approach has been widely used to analyze plant protein profiles in response to abiotic challenges, which could lead to the development of new stress tolerance strategies [79]. Another technique for studying the collection of metabolites found in microbial communities is microbial metabolomics [80]. Infections and their emergence have posed a serious danger to food security, agricultural practices, and the conservation of food species, and understanding the emergence of new pathogens and their significance has become a key job [81].

Conclusion

Plant microbiota and their interactions are extremely complex, and a variety of factors influence how communities form and function. Plant-associated microbes have a big impact on the health and performance of their hosts. Attempts to use beneficial bacteria in the field, on the other hand, have failed to reliably boost crops. Plant-symbiotic microbial community interactions, ecological repercussions of plant- associated microorganisms, and plant-microbial metabolic dynamics are all poorly understood at the moment. More light will be shed on the intricacy of the metabolic potentials of soil microbial communities and their value to the soil ecosystem as DNA-sequencing tools evolve and become more accessible to various working groups. The introduction of genomic techniques has greatly aided our understanding of plant-bacterial interactions, yet genomic approaches are still insufficient to fully explain plant-pathogen interactions. The effect of these alterations on soil biology is still unknown and needs to be investigated further. The fundamental question is still how the impact on taxonomic groups relates to implications on soil microbial communities’ functional capacities.

Moreover, Plants rely on the metabolic activities of soil microbes to gain access to refractory soil-borne nutrients. Given the environmental harm caused by existing fertilization processes, optimizing plant–microbe nutritional interactions is a current research goal for more sustainable agriculture systems. The mechanisms driving the formation of the plant microbiome and its modification in response to plant nutritional status, on the other hand, are exceedingly complicated and difficult to predict. This understanding could help to guide the extremely promising techniques to using microorganisms for more sustainable plant nutrition in a mechanistic way. However, there is still a huge gap in understanding when it comes to a sound theory of plant– microbe interactions.

Acknowledgements

We would like to express our gratitude to the management of MEDWIN PUBLISHERS for inviting us to write the Mini Review and providing the support for the publications.

Conflict of Interest

The authors declare no conflict of interest.

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Cite this article

BibTeX
APA
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@article{das2022,
  title   = {Environmental and Ecological Impact of Soil Microorganisms in
Plant Sciences},
  author  = {Das K, Das SC and Aminuzzaman FM},
  journal = {Journal of Ecology & Natural Resources},
  year    = {2022},
  volume  = {6},
  number  = {2},
  doi     = {10.23880/jenr-16000273}
}
Das K, Das SC and Aminuzzaman FM (2022). Environmental and Ecological Impact of Soil Microorganisms in
Plant Sciences. Journal of Ecology & Natural Resources, 6(2). https://doi.org/10.23880/jenr-16000273
TY  - JOUR
TI  - Environmental and Ecological Impact of Soil Microorganisms in
Plant Sciences
AU  - Das K, Das SC and Aminuzzaman FM
JO  - Journal of Ecology & Natural Resources
PY  - 2022
VL  - 6
IS  - 2
DO  - 10.23880/jenr-16000273
ER  -