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Microbiome

The microbiome refers to the collective community of microorganisms—such as bacteria, archaea, fungi, viruses, and protozoa—and their associated genetic material (collectively known as the metagenome) that inhabit a specific environmental niche, including the human body and other ecosystems.^[1]^[2] In the context of human health, the microbiome encompasses trillions of microbial cells, estimated at 10 to 100 trillion, primarily residing in symbiotic or commensal relationships with the host.^[2]^[3] The human microbiome is distributed across diverse body sites, with the gut harboring the most abundant and diverse microbial population, followed by the skin, oral cavity, respiratory tract, and urogenital tract.^[2]^[4] These microbial communities vary in composition based on factors such as age, diet, lifestyle, geography, and health status, contributing to individual variability often described as a personalized microbial fingerprint.^[5]^[6] The Human Microbiome Project (HMP), initiated by the National Institutes of Health (NIH) in 2007 as part of the NIH Roadmap for Medical Research, systematically characterized the microbiome's structure, function, and dynamics through metagenomic sequencing of over 200 healthy volunteers across multiple body sites.^[4]^[3] This effort generated comprehensive reference datasets, including the Human Microbiome Project Data Portal, which have accelerated global research into microbial ecology and host-microbe interactions.^[4]^[7] Functionally, the microbiome is integral to host physiology, aiding in nutrient metabolism, vitamin synthesis (such as vitamins K and B), breakdown of complex carbohydrates, and modulation of the immune system to maintain homeostasis and tolerance.^[8]^[9] It also serves as a barrier against pathogenic invasions by competing for resources and producing antimicrobial compounds.^[1] Disruptions in microbial balance, termed dysbiosis, have been associated with a range of conditions, including inflammatory bowel disease, obesity, diabetes, allergies, and neurological disorders like Parkinson's disease.^[8]^[10] Emerging research highlights the microbiome's influence on drug metabolism, response to therapies, and even mental health via the gut-brain axis, underscoring its potential as a therapeutic target through interventions like probiotics, prebiotics, and fecal microbiota transplantation.^[11]^[12]

Background

Definitions

The microbiome encompasses the collective microorganisms—including bacteria, archaea, fungi, viruses, and protists—residing in a particular environment, along with their genomic material (collectively termed the metagenome), the ecological interactions among these microbes, and the surrounding habitat conditions that influence their dynamics.^[13] This definition, analogous to a biome in ecology, emphasizes not just the microbial community but also its functional and structural elements, such as gene expression and environmental metadata, which are often studied through metagenomic sequencing.^[2] The term originated in the late 1980s but gained prominence in the 2000s with advances in high-throughput sequencing, shifting from a focus on isolated microbes to integrated ecosystem-like analyses.^[14] A key distinction exists between the microbiome and the microbiota, where the latter refers solely to the assemblage of living microorganisms themselves in a defined environment, excluding their genetic content and habitat details.^[13] Similarly, the holobiont describes the host organism integrated with its associated microbiome, viewing them as a unified ecological unit that functions interdependently, as seen in host-microbe symbioses across plants, animals, and humans.^[15] These terms highlight the microbiome's broader scope, incorporating both biotic and abiotic factors that shape microbial persistence and activity. Central to microbiome research are the concepts of dysbiosis and eubiosis, which denote deviations from or maintenance of a balanced microbial state, respectively.^[16] Eubiosis represents a healthy equilibrium, characterized by high microbial diversity and stable functional contributions, such as in the human gut where Firmicutes and Bacteroidetes dominate to support digestion and immune homeostasis.^[16] In contrast, dysbiosis involves an imbalance, often with reduced diversity or overgrowth of opportunistic pathogens, as observed in marine environments polluted by antibiotics leading to algal bloom disruptions or in plant rhizospheres affected by soil salinization, impairing nutrient cycling.^[16] These states underscore the microbiome's role in environmental stability, with dysbiosis frequently linked to broader ecological or health perturbations.^[17]

History

The study of the microbiome traces its origins to the 17th century, when Dutch microscopist Antonie van Leeuwenhoek first observed microorganisms, including bacteria and protozoa, in samples such as dental plaque and pond water, describing them as "animalcules" in letters to the Royal Society starting in 1676.^[18] These early observations laid the groundwork for recognizing microbial life within and around hosts, though without the ecological context that would later define microbiome research. By the 19th century, Louis Pasteur's experiments in the 1860s established the germ theory of disease, demonstrating that specific microorganisms cause fermentation, putrefaction, and infections, shifting perceptions from spontaneous generation to microbial agency in biological processes.^[19] In the early 20th century, attention turned to the beneficial roles of microbes, particularly in digestion. Russian immunologist Élie Metchnikoff, working at the Pasteur Institute, proposed in 1907 that certain lactic acid bacteria in fermented milk could replace harmful gut flora, promoting health and longevity by reducing intestinal toxins—a foundational idea for probiotics that emphasized microbial communities' influence on host physiology.^[20] During the 1970s and 1980s, microbiology increasingly adopted ecological perspectives, influenced by advances like Carl Woese's 1977 development of 16S rRNA sequencing for phylogenetic classification, which enabled the study of unculturable microbes and their communities in natural environments, fostering the view of microbes as integral to ecosystems rather than isolated pathogens.^[11] The term "microbiome," derived from "micro" (small) and "biome" (a living community), was first defined in 1988 by J.M. Whipps and colleagues as "a characteristic microbial community occupying a reasonably well-defined habitat which has distinct physio-chemical properties," originally applied to rhizosphere ecology but encompassing microbes, their interactions, and environmental influences.^[21] Though coined then, the concept gained traction in the 2000s amid rising interest in host-associated communities. Post-2000 advancements in metagenomics propelled the field forward. J. Craig Venter's Global Ocean Sampling Expedition (2003–2007) produced the first large-scale metagenomic dataset, sequencing over 6 billion base pairs from marine microbes and revealing vast uncultured diversity.^[22] In 2006, Steven Gill and colleagues reported the first comprehensive metagenomic analysis of the human distal gut microbiome, sequencing 78 million base pairs from two individuals and identifying an estimated 100 times more microbial genes than in the human genome, highlighting functions in metabolism and nutrient processing.^[23] The U.S. National Institutes of Health launched the Human Microbiome Project in 2007 with $115 million over five years to characterize microbial communities across healthy human body sites, generating reference genomes and fostering standardized approaches.^[24] By 2010, the Earth Microbiome Project initiated a global, crowd-sourced effort to catalog microbial diversity across environments using standardized sequencing, amassing terabases of data to explore ecological patterns.^[25] In the 2010s, integration with systems biology emerged, as seen in the Integrative Human Microbiome Project (2014–2019), which linked microbial dynamics to host health outcomes through longitudinal studies and multi-omics integration.^[26]

Composition

Microbiota

The microbiota refers to the assemblage of microorganisms, including bacteria, archaea, fungi, viruses, and protists, that inhabit a particular environment and collectively form the living component of the microbiome. Bacteria overwhelmingly dominate the microbiota in terms of both diversity and abundance across various ecosystems, with key phyla such as Firmicutes and Bacteroidetes frequently comprising a substantial proportion of bacterial communities.^[14] Archaea, though less abundant, include methanogenic species like those in the genus Methanobrevibacter, which contribute to metabolic processes such as methane production. Fungi, represented by genera like Candida, along with viruses—predominantly bacteriophages that infect bacterial hosts—and protists, constitute smaller but functionally significant fractions of the microbiota.^[27]^[28] The abundance of microbiota is influenced by environmental factors, leading to varying biomass estimates; for instance, the human body hosts approximately 3.8 × 10^{13} bacterial cells compared to about 3.0 × 10^{13} human cells, highlighting the scale of microbial presence relative to host cells in such systems.^[29] Spatial distribution plays a critical role in microbial abundance and organization, with many microbiota members existing in structured biofilms—adherent, matrix-embedded communities that enhance resilience and resource sharing—contrasted against planktonic forms that remain free-floating and more susceptible to environmental fluctuations. These distributions affect overall microbial density and interactions within the microbiome.^[30] Diversity within the microbiota is quantified using metrics such as alpha diversity, which assesses species richness and evenness within a single sample, often via the Shannon index that accounts for both the number of taxa and their relative abundances. Beta diversity, in contrast, measures compositional variation between samples, capturing differences in microbial community structure across environments. In general settings like soil or aquatic systems, high alpha diversity might reflect hundreds of bacterial species per sample, while beta diversity reveals shifts driven by factors like pH or nutrient availability. Viability in the microbiota extends beyond active growth, encompassing states like the viable but non-culturable (VBNC) condition, where bacteria remain metabolically active and potentially virulent but fail to form colonies on standard media due to stress responses. Additionally, spore-forming bacteria, such as those in the Firmicutes phylum (e.g., Clostridium species), enter dormant states via endospore formation to survive adverse conditions, allowing persistence and eventual reactivation in favorable environments. These mechanisms underscore the adaptive resilience of microbiota components.^[31]^[32]

Microbial Networks

Microbial networks represent the intricate web of structural and functional interconnections among microorganisms within a microbiome, where individual microbes interact through various relational dynamics that influence community assembly and function. These networks emerge from the collective behaviors of microbiota, which serve as the foundational nodes, linked by edges representing positive or negative associations derived from ecological processes. Understanding these networks is crucial for elucidating how microbial communities maintain diversity and respond to environmental changes.^[33] Network types in microbial communities encompass mutualistic, competitive, and commensal interactions that shape resource utilization and population dynamics. Mutualistic interactions, such as syntrophy, involve microbes exchanging metabolic byproducts to enable nutrient sharing, as seen in anaerobic consortia where one species ferments compounds that another oxidizes for energy. Competitive interactions often manifest through mechanisms like antibiotic production, where microbes inhibit rivals to secure niche space, promoting coexistence via negative feedback in diverse assemblages. Commensal interactions occur when one microbe benefits from another's activity without affecting it, such as through the passive utilization of excreted metabolites, contributing to neutral stability in polymicrobial environments.^[33]^[34] Modeling approaches for microbial networks frequently employ co-occurrence analyses to infer interactions from abundance data, constructing correlation-based graphs using metrics like Pearson or Spearman coefficients to identify significant associations. These graphs reveal community structure by highlighting modules of co-occurring taxa, with keystone species identified through network centrality measures such as betweenness or degree centrality, indicating microbes that disproportionately influence overall connectivity and stability. For instance, keystone taxa often act as hubs that facilitate information flow or resource transfer across the network, as demonstrated in soil and gut microbiomes where their removal disrupts community integrity. Spatial organization within microbial networks is governed by physical proximity and signaling, prominently in biofilms where quorum sensing coordinates collective behaviors via autoinducers—diffusible molecules that accumulate to threshold levels, triggering gene expression for matrix production and adhesion. Horizontal gene transfer further interconnects networks through mechanisms like conjugation, involving direct plasmid exchange via cell-to-cell contact, and transformation, the uptake of free DNA, enhancing adaptive potential in dense communities. Trophic cascades propagate effects across network levels, where changes in one microbe's abundance alter downstream consumers and decomposers, structuring food web-like dependencies in microbial ecosystems.^[35]^[36] Stability factors in microbial networks are underpinned by resilience to perturbations, quantified through metrics like network modularity—which measures the density of intra-module connections versus inter-module links—and overall connectivity, where higher modularity buffers against species loss by compartmentalizing impacts. Resilient networks exhibit robust connectivity that maintains function despite disturbances, such as antibiotic exposure, as evidenced in bacterial communities where modular structures preserve metabolic pathways. These properties ensure community persistence, with connectivity acting as a key determinant of recovery dynamics in fluctuating environments.^[33]^[37]

Host-Microbe Coevolution

Host-microbe coevolution encompasses the reciprocal genetic changes between host organisms and their microbial partners, driven by shared evolutionary pressures that foster symbiotic associations.^[38] This dynamic integrates the host genome with microbial genomes, treating the combined entity as a unit of selection under the hologenome concept.^[38] Mechanisms include vertical transmission, where beneficial microbes are inherited directly from parents, as seen in maternal transfer to mammalian offspring, promoting tight linkage between host and microbial lineages. Horizontal acquisition from environmental sources introduces variability, allowing hosts to assemble diverse microbiomes while exposing them to potential mismatches in evolutionary trajectories. Selection pressures, such as host immune responses and nutrient dependencies, further refine these associations by favoring microbes that enhance host survival and reproduction. Genomic evidence underscores these processes, particularly through signatures of reductive evolution in obligate symbionts. In aphids, the endosymbiont Buchnera aphidicola displays a drastically reduced genome of approximately 618 kb, a 65–74% shrinkage from its free-living ancestor, with conservation of genes for essential amino acid biosynthesis that aphids cannot produce independently.^[39] This reduction, ongoing since the symbiosis began around 200 million years ago, reflects coevolutionary streamlining where the bacterium relies on the host for replication and protection in exchange for nutritional provisioning. The hologenome theory formalizes this interdependence, proposing that the holobiont—the host plus its microbiota—evolves as an integrated unit, with microbial variation contributing to host adaptability via mechanisms like horizontal gene transfer and microbial acquisition.^[38] These coevolutionary patterns operate across expansive timescales, from primordial events to contemporary shifts. The most ancient example is the endosymbiotic origin of mitochondria, where an alphaproteobacterium was engulfed by a proto-eukaryotic host roughly 1.5 billion years ago, leading to gene transfer and integration that powered eukaryotic diversification.^[40] On shorter scales, diet-driven microbiome adaptations in herbivores illustrate rapid coevolution; independent transitions to herbivory in mammals have converged on microbial consortia capable of degrading plant cell walls, with functional gene repertoires for fiber fermentation appearing across lineages separated by millions of years. Illustrative cases highlight symbiosis establishment and refinement. The coral-algal mutualism emerged over 210 million years ago during the late Triassic, as evidenced by fossilized skeletons showing photosymbiotic associations that enabled reef-building scleractinian corals to colonize oligotrophic seas through algal nutrient translocation.^[41] In humans, the evolution of lactase persistence—a dominant allele allowing adult dairy consumption—correlates with microbiome structuring, where host genotypes influence microbial strains like Bifidobacterium that metabolize lactose, indicating a coevolutionary feedback that supported pastoralist expansions.^[42] Recent metagenomic studies as of 2023 highlight accelerated coevolution in response to environmental stressors like climate change and antibiotic use, further emphasizing the dynamic nature of host-microbe interactions.^[43]

Types

Human Microbiome

The human microbiome encompasses the collective microbial communities residing across various body sites, including the gut, skin, oral cavity, vagina, and respiratory tract, each characterized by distinct compositions and densities that contribute to host physiology. These communities consist primarily of bacteria, with smaller contributions from archaea, fungi, and viruses, and exhibit high inter-individual variability even among healthy adults. Studies from the Human Microbiome Project (HMP), conducted between 2007 and 2013, analyzed samples from 242 healthy individuals across 18 body sites, revealing that while a small core set of microbial taxa is shared, the overall diversity is shaped by site-specific niches and environmental factors.^[44] The gut harbors the largest and most dense microbial population, estimated at approximately 10^14 bacterial cells, predominantly from the phyla Firmicutes and Bacteroidetes, which together comprise over 90% of the community in healthy adults.30504-3)^[44] In contrast, the skin microbiome is sparser and varies by region, with Actinobacteria (including Cutibacterium acnes, formerly Propionibacterium acnes) dominating sebaceous areas, while moist sites favor Proteobacteria and dry areas Firmicutes. The oral cavity supports a highly diverse community of over 700 bacterial species, dominated by Streptococcus species in saliva and plaque, reflecting its role as a transitional environment. The vaginal microbiome in reproductive-age women is typically dominated by Lactobacillus species, which maintain an acidic environment, though community state types can vary. The respiratory tract, particularly the upper airways, hosts lower biomass communities enriched in Streptococcus and Prevotella, with diversity decreasing toward the lungs. Variability in the human microbiome is influenced by multiple factors, including age, diet, geography, and lifestyle. During infancy, the gut microbiome undergoes rapid colonization starting at birth, initially dominated by facultative anaerobes like Enterobacteriaceae and shifting toward anaerobic Bifidobacterium and Bacteroides by weaning, establishing adult-like stability by age three.00157-3) Dietary patterns significantly modulate composition; for instance, high-fiber diets promote increases in Bifidobacterium and other short-chain fatty acid producers, while high-fat, low-fiber Western diets favor Bacteroides dominance. Geographic and cultural differences are evident, with rural populations like the Hadza hunter-gatherers exhibiting greater gut diversity and higher Prevotella abundance compared to urban Western cohorts, reflecting subsistence-based variations. Lifestyle factors, such as antibiotic use, profoundly disrupt communities by reducing alpha-diversity and altering ratios of key phyla, with recovery taking months to years. Metagenomic analyses from the HMP and related efforts, including the MetaHIT consortium, have cataloged approximately 3.3 million non-redundant microbial genes in the gut alone, vastly expanding the functional potential beyond the human genome.^[45] A notable discovery is the existence of gut enterotypes—stable community clusters defined by dominant genera: Bacteroides (carbohydrate metabolism-focused), Prevotella (fiber degradation-oriented), and Ruminococcus (mucin utilization-specialized)—which are robust across populations and independent of host metadata like age or body mass index. These enterotypes highlight the modular nature of microbial ecosystems. Regarding disease associations, altered microbiome profiles are linked to conditions such as obesity, where lower overall diversity and shifts toward higher Firmicutes to Bacteroidetes ratios have been observed in affected individuals compared to lean controls. Similar dysbioses appear in inflammatory bowel disease and type 2 diabetes, underscoring the microbiome's role in metabolic health, though causality remains under investigation.

Animal Microbiome

The animal microbiome refers to the diverse communities of microorganisms inhabiting non-human animals, varying widely across taxa to support ecological adaptations and physiological needs. These microbiomes often exhibit higher functional diversity in herbivores than in carnivores or omnivores, reflecting specialized metabolic capabilities such as nutrient extraction from complex diets.^[46] Across phyla, archaeal components like methanogens are prevalent in over 175 species spanning eight animal classes, contributing to hydrogen metabolism and energy production in anaerobic environments.^[47] Host diet and evolutionary history independently modulate aspects of this diversity, with phylogenetic relatedness preserving core taxa while dietary niches drive compositional shifts.^[48] In insects, the endosymbiont Wolbachia dominates arthropod microbiomes, manipulating reproduction via mechanisms like cytoplasmic incompatibility to enhance vertical transmission and influence host speciation, as seen in diverse species including mosquitoes and beetles.^[49] Fish gut microbiomes adapt to osmoregulatory demands, with salinity changes during seawater transfer altering bacterial profiles in the intestine to support ion absorption and epithelial integrity, exemplified in species like Atlantic salmon.^[50] In mammals, ruminants such as cows host methanogenic archaea in the rumen that scavenge hydrogen during cellulose fermentation, enabling efficient lignocellulose breakdown and contributing to global methane emissions.^[51] Environmental factors profoundly shape animal microbiomes. Dietary transitions, such as carnivore-to-herbivore shifts, increase alpha diversity and enrich pathways for plant polymer degradation, as observed in convergent evolutions like pandas.^[52] Habitat influences, including social structures like bee hives, foster distinct microbial reservoirs; exposure to semi-natural environments restores gut community balance disrupted by stressors such as pesticides.^[53] Symbiosis types further diversify these communities, with chemosynthetic mutualisms in deep-sea vent tubeworms involving sulfur-oxidizing bacteria that fix carbon in the absence of sunlight, sustaining host nutrition in extreme conditions.^[54] Prominent examples highlight microbiome functionality. Termite guts feature protist-bacterial consortia, including spirochetes and flagellates, that hydrolyze lignocellulose through coordinated glycoside hydrolases, achieving near-complete wood degradation.^[55] Coral holobionts integrate Symbiodinium dinoflagellates with bacterial associates for photosynthetic energy transfer and nutrient recycling, bolstering resilience against environmental perturbations.^[56] Microbiomes also inform conservation strategies for threatened species. In amphibians, skin communities provide resistance to chytridiomycosis by producing antifungal metabolites that inhibit Batrachochytrium dendrobatidis, with probiotic interventions enhancing survival in declining populations like mountain yellow-legged frogs.^[57]

Plant Microbiome

The plant microbiome encompasses the diverse communities of microorganisms associated with plant tissues and surfaces, playing essential roles in nutrient acquisition, pathogen defense, and stress tolerance. These microbial assemblages are primarily bacteria, fungi, and viruses that colonize specific plant compartments, influencing overall plant health and productivity. Unlike transient soil microbes, plant-associated communities are shaped by host exudates and selective pressures, forming stable interactions that enhance plant resilience in varying environments.^[58] Key compartments of the plant microbiome include the rhizosphere, phyllosphere, and endosphere. The rhizosphere, the soil-root interface, is enriched with organic compounds from root exudates, fostering high microbial densities and diversity, particularly dominated by Proteobacteria such as Pseudomonas and Burkholderia.^[59] The phyllosphere, encompassing leaf surfaces and aerial parts, experiences greater exposure to atmospheric fluctuations and UV radiation, resulting in communities often led by epiphytic bacteria like Pseudomonas and Sphingomonas, alongside fungi adapted to oligotrophic conditions.^[60] In contrast, the endosphere—internal plant tissues like roots and shoots—hosts lower-diversity microbiomes due to stringent host barriers, featuring beneficial endophytes that colonize vascular systems without causing disease.^[61] The composition of the plant microbiome varies by compartment but predominantly includes bacteria, with notable examples like Rhizobium species that form symbiotic nodules in legume roots for nitrogen fixation, converting atmospheric N2 into plant-usable forms.^[62] Fungi, such as arbuscular mycorrhizal species including Glomus, extend hyphal networks to improve phosphorus and water uptake, while viruses modulate bacterial and fungal populations, sometimes enhancing host fitness through lysogenic cycles.^[62] These components collectively form a holobiont, where plant-specific symbioses, like those between legumes and Rhizobium, illustrate coevolutionary adaptations for mutual benefit.^[63] Several factors influence plant microbiome assembly and function. Soil type, particularly pH, modulates bacterial recruitment; for instance, neutral to alkaline soils promote Actinobacteria, while acidic conditions favor Acidobacteria and certain mycorrhizal fungi.^[64] Plant genotype exerts selective pressure, as seen in Arabidopsis thaliana where immune receptors like PRRs shape root-associated bacterial communities by recognizing microbial patterns.^[65] Climate variables, such as drought, drive shifts toward resilient taxa; drought-stressed plants recruit microbiomes enriched in drought-tolerant bacteria like those in the Actinobacteria phylum, aiding survival through osmoprotectant production.^[66] Central to the plant microbiome's ecological role are key processes like nutrient cycling, where microbes facilitate the solubilization and mineralization of essential elements. For example, Bacillus species solubilize insoluble phosphates via organic acid secretion, increasing bioavailability and supporting plant growth in phosphorus-limited soils.^[67] This process, often coupled with nitrogen fixation by diazotrophs, underscores the microbiome's contribution to efficient resource use, enhancing plant vigor without external inputs.^[58]

Marine Microbiome

The marine microbiome encompasses the diverse communities of microorganisms inhabiting oceanic environments, including free-living populations in the water column and those associated with marine hosts. In the photic zone of oligotrophic ocean gyres, bacterioplankton communities are numerically dominated by the cyanobacterium Prochlorococcus and the alphaproteobacterium SAR11 clade, which together account for over half of the identifiable genome equivalents and maintain a combined global population of approximately 2.7 × 10²⁸ cells.^[68] These organisms drive primary production and heterotrophic respiration, respectively, sustaining the base of marine food webs. A key dynamic in these communities is the viral shunt, where lytic phages infect and lyse about 20% of marine bacteria daily, releasing cellular contents that recycle nutrients like carbon and phosphorus back into dissolved organic matter, thereby preventing transfer to higher trophic levels and enhancing microbial loop efficiency.^[69]^[70] Host-associated marine microbiomes exhibit specialized compositions adapted to symbiotic roles. In sponges, the candidate phylum Poribacteria forms a predominant component of the microbiome, nearly exclusively associated with these hosts and contributing to nutrient cycling through complex carbohydrate degradation pathways.^[71] Coral microbiomes, meanwhile, undergo shifts involving increased abundance of Vibrionaceae, such as Vibrio coralliilyticus, during thermal stress-induced bleaching, exacerbating tissue damage and symbiont expulsion.^[72]^[73] In fish, gill microbiomes support osmoregulation, with taxa like Gillisia (a member of Flavobacteriaceae) identified among novel species in marine and aquatic vertebrate communities, potentially aiding ionic balance in saline environments.^[74]^[75] Global patterns in the marine microbiome reflect environmental gradients and connectivity. Microbial diversity increases with depth, peaking in the mesopelagic zone due to stable conditions and diverse organic substrates that support higher functional redundancy in carbon processing.^[76] Ocean currents facilitate microbial dispersal, homogenizing communities across basins while introducing variability through water mass mixing, as seen in distinct bacterial assemblages in Arctic surface versus Pacific inflows.^[77]^[78] These patterns link to ocean productivity via the microbial loop and carbon pump, where heterotrophic bacteria convert dissolved organic carbon into refractory forms sequestered in the deep ocean, amplifying the efficiency of biological carbon export.^[79]^[80] The Tara Oceans expedition (2009–2013) illuminated these dynamics through metagenomic sampling, cataloging approximately 40 million previously undescribed microbial genes and highlighting plastid contributions from eukaryotic algae to prokaryotic-like functions in global plankton networks.^[81]^[82]

Functions

Metabolic Roles

Microbiomes play pivotal roles in driving biochemical transformations and nutrient cycling across diverse environments, enabling the breakdown of complex substrates and the generation of essential compounds for host organisms and ecosystems. Through metabolic processes such as fermentation, fixation of atmospheric gases, and redox reactions, microbial communities facilitate energy extraction and resource availability, influencing everything from host nutrition to planetary-scale element flows.^[83] Core metabolic processes within microbiomes include fermentation, where gut bacteria anaerobically degrade undigested carbohydrates to produce short-chain fatty acids (SCFAs) like acetate, propionate, and butyrate, which serve as energy sources for host epithelial cells in the human intestine.^[84] Nitrogen fixation, a key anabolic process, is exemplified by symbiotic Rhizobia bacteria in plant root nodules, converting atmospheric dinitrogen into ammonia via the nitrogenase enzyme complex, as represented by the reaction:

\ce{N2 + 8H+ + 8e- -> 2NH3 + H2}

This process supplies bioavailable nitrogen for plant growth and soil fertility.^[85] Sulfur cycling, particularly sulfate reduction in anoxic sediments, involves dissimilatory sulfate-reducing bacteria (e.g., Desulfovibrio spp.) that respire sulfate to sulfide, coupling organic matter oxidation to sulfur reduction and influencing carbon burial in marine environments.^[86] Microbial energy harvest encompasses both anaerobic respiration and oxygenic photosynthesis. In oxygen-limited settings, denitrifying bacteria perform anaerobic respiration by reducing nitrate to dinitrogen gas, as in the overall process \ce{NO3- -> N2}, which mitigates nitrate accumulation and recycles nitrogen in aquatic systems.^[87] In contrast, cyanobacterial microbiomes in aquatic habitats conduct oxygenic photosynthesis, using photosystems I and II to split water and produce oxygen while fixing carbon dioxide into biomass, a foundational process for primary productivity.^[88] Cross-feeding enhances metabolic efficiency in microbiomes through metabolite exchange, such as Bacteroides species degrading complex polysaccharides into simple sugars that Firmicutes then ferment into SCFAs, promoting community stability and resource utilization in the gut.^[89] On a global scale, these activities underpin biogeochemical cycles; for instance, marine microbial communities, including phytoplankton and cyanobacteria, generate approximately 50% of Earth's atmospheric oxygen through photosynthesis, sustaining aerobic life and regulating climate.^[90]

Protective and Immune Functions

The microbiome provides critical protection against pathogenic invasion through mechanisms such as competitive exclusion, where resident microbes occupy ecological niches and deplete essential nutrients, thereby limiting pathogen colonization.^[91] For instance, diverse gut microbial communities block iron acquisition by pathogens like Salmonella enterica, enhancing host resistance to infection.^[91] Additionally, bacteriocin production by commensal bacteria directly antagonizes invaders; Lactococcus lactis synthesizes nisin, a lantibiotic that disrupts Gram-positive pathogen membranes, contributing to colonization resistance in the gut.^[92] Biofilm formation by host-associated microbes further acts as a physical barrier, encapsulating communities and restricting pathogen adhesion and penetration in mucosal surfaces.^[93] Microbial communities also modulate host immunity to bolster defenses. Lipopolysaccharide (LPS) from Gram-negative bacteria activates Toll-like receptors (TLRs) on immune cells, priming innate responses and promoting epithelial barrier integrity without inducing excessive inflammation.^[94] Microbial metabolites, such as short-chain fatty acids (SCFAs) produced via fermentation, further influence adaptive immunity by promoting differentiation of regulatory T cells (Tregs), which suppress overzealous responses and maintain tolerance.^[95] These SCFAs, including butyrate, enhance Treg function through histone deacetylase inhibition, linking metabolic outputs to immune homeostasis.^[95] Specific examples illustrate these protective roles. In the gut, intact microbiota prevents Salmonella Typhimurium colonization by outcompeting it for tetrathionate and producing antimicrobial compounds, reducing infection severity in animal models.^[96] On the skin, Staphylococcus epidermidis inhibits Staphylococcus aureus through its serine protease Esp, which degrades biofilm components and limits nasal and cutaneous colonization. Dysbiosis disrupts these protections, increasing pathogen susceptibility. Antibiotic-induced depletion of commensals allows Clostridioides difficile overgrowth, as reduced microbial diversity fails to restore colonization resistance, leading to recurrent infections in approximately 20–35% of cases.^[97]

Developmental and Structural Roles

The microbiome plays a crucial role in host ontogeny, particularly in the development of the gastrointestinal tract. Studies using germ-free animal models, such as mice raised without microbial exposure, demonstrate stunted growth and altered intestinal morphology, including shorter small intestines and reduced villus length compared to conventionally raised counterparts.^[98] These observations highlight the necessity of microbial colonization for proper intestinal expansion and vascularization during early development. Furthermore, microbial signals promote epithelial maturation in the gut by inducing differentiation of enterocytes and goblet cells, thereby establishing a functional mucosal barrier essential for host physiology.^[99] Beyond the gut, the microbiome influences broader structural aspects of host physiology. In mammals, gut bacteria regulate bone density through modulation of estrogen metabolism; for instance, microbial production of β-glucuronidase deconjugates estrogens, enhancing their bioavailability and thereby supporting osteoblast activity and preventing bone loss.^[100] Similarly, the microbiome contributes to neural development via the gut-brain axis, where bacterial metabolites and signals transmitted through the vagus nerve influence neurogenesis and myelination in regions like the hippocampus.^[101] This vagal signaling pathway mediates microbiota effects on brain structure, underscoring the interconnectedness of microbial communities with host nervous system maturation.^[102] Illustrative examples from non-mammalian hosts further illustrate these developmental dependencies. In the freshwater polyp Hydra vulgaris, regeneration of body structures following injury relies on the resident microbiome, as germ-free individuals exhibit impaired tissue reformation due to disrupted signaling pathways that require bacterial cues for stem cell proliferation and patterning.^[103] In plants, rhizobacteria such as Pseudomonas species shape root architecture by altering auxin gradients, promoting lateral root formation and elongation to optimize nutrient foraging in soil.^[104] These interactions demonstrate conserved mechanisms across taxa where microbes guide morphological adaptations. Long-term structural influences extend to epigenetic regulation, where microbial metabolites induce heritable changes in host gene expression. For example, butyrate produced by gut bacteria acts as a histone deacetylase inhibitor, increasing histone acetylation at promoter regions and thereby enhancing expression of genes involved in epithelial integrity and neural plasticity.^[105] Such modifications can persist across generations, linking early microbial colonization to enduring impacts on host morphology and physiology.^[106]

Interactions

Microbe-Microbe Interactions

Microbe-microbe interactions encompass a range of molecular and ecological processes that govern community structure and dynamics within microbial consortia, including signaling, competition, cooperation, and predation. These interactions enable bacteria to sense population density, compete for resources, exchange metabolites, and engage in predatory behaviors, all without involving host organisms. Such processes are fundamental to the stability and function of microbiomes in diverse environments. Signaling between microbes often occurs through quorum sensing, a cell-density-dependent communication system prevalent in Gram-negative bacteria. In this mechanism, cells produce and release autoinducer molecules, such as acyl-homoserine lactones (AHLs), which accumulate extracellularly and trigger gene expression changes once a threshold concentration is reached. For instance, AHLs like N-(3-oxohexanoyl)-L-homoserine lactone in Vibrio fischeri bind to LuxR-type receptors, activating transcription of bioluminescence genes as a coordinated response. This seminal discovery of the LuxR-LuxI family highlighted how QS coordinates behaviors like virulence factor production in pathogens such as Pseudomonas aeruginosa. Toxin-antitoxin (TA) systems represent another signaling modality, where stable toxins are neutralized by labile antitoxins under normal conditions, but antitoxin degradation during stress activates the toxin to induce dormancy or programmed cell death, facilitating persistence in fluctuating microbial environments. These type II TA modules, widespread across bacterial genomes, modulate interactions by enabling subpopulations to survive competitive pressures from phages or antibiotics. Resource competition among microbes frequently manifests as chemical warfare through antibiotic production, where bacteria secrete compounds to inhibit rivals while resisting their own toxins. For example, Paenibacillus polymyxa produces colistin, a cationic peptide that disrupts lipid A in the outer membranes of competing Gram-negative bacteria, providing a selective advantage in polymicrobial niches like soil. This strategy is part of broader interference competition, where antimicrobial biosynthesis genes are upregulated in response to competitor cues, as seen in streptomycetes that sense peptidoglycan fragments from lysed cells to induce antibiotic output. Complementing this, the phage-bacteria arms race drives evolutionary dynamics, with bacteria deploying CRISPR-Cas systems for adaptive immunity against viral invaders. In CRISPR-Cas type I and II systems, spacer sequences derived from prior phage infections are integrated into CRISPR arrays, enabling Cas proteins to cleave matching viral DNA during reinfection; this was first demonstrated in Streptococcus thermophilus, where CRISPR acquisition conferred resistance to virulent phages, illustrating a molecular "memory" that counters phage propagation in dense communities. Cooperative interactions, conversely, promote mutualism through cross-feeding networks, where microbes exchange metabolic byproducts to enhance collective fitness. In biofilms, amino acid cross-feeding is common, with prototrophic bacteria overproducing essential amino acids like leucine that auxotrophic neighbors scavenge, stabilizing diverse consortia under nutrient limitation. Computational models of Escherichia coli microcolonies show that such exchanges evolve pervasively in spatially structured environments, increasing genotypic diversity by up to 73% under low diffusion rates and modest production costs. Syntrophic consortia exemplify advanced cooperation, particularly in anaerobic methane oxidation, where anaerobic methanotrophic archaea (ANME) partner with sulfate-reducing bacteria (SRB) like Desulfosarcina species. ANME oxidize methane to release electrons, which SRB use for sulfate reduction, forming stable aggregates in marine sediments; single-cell genomics revealed these partnerships involve direct interspecies electron transfer, sustaining energy flow in otherwise thermodynamically unfavorable reactions. Predator-prey dynamics further shape microbial communities, with predatory bacteria like Bdellovibrio bacteriovorus targeting Gram-negative prey through contact-dependent invasion. Bdellovibrio cells attach to prey via type IV pili, breach the outer membrane using a sheathed apparatus, and enter the periplasm to elongate and divide while consuming host resources, lysing the prey bdelloplast upon completion. This intraperiplasmic predation, first observed in the 1960s, reduces prey populations by orders of magnitude in model systems and is modulated by motility and chemotaxis toward damaged cells. These interactions collectively form the basis of microbial networks, where emergent properties arise from balanced antagonism and synergy.

Host-Microbe Interactions

Host-microbe interactions encompass a complex array of bidirectional signaling mechanisms that enable symbiotic relationships, colonization, and mutual physiological adaptations between microbial communities and their hosts. These exchanges involve the recognition of microbial components by host immune sensors, microbial adhesion and effector molecules that interface with host cells, and dynamic feedback loops influenced by environmental factors such as diet. Additionally, multi-omics approaches reveal how co-metabolites produced through joint host-microbial pathways contribute to overall homeostasis. Such interactions are fundamental to maintaining barrier integrity and modulating host responses across diverse ecosystems like the gut, skin, and mucosal surfaces. Hosts detect microbial presence primarily through pattern recognition receptors (PRRs), which initiate innate immune signaling. For instance, NOD-like receptors (NLRs), such as NOD1 and NOD2, are cytosolic PRRs that sense specific motifs in bacterial peptidoglycan, a key cell wall component, triggering inflammatory responses like NF-κB activation and cytokine production to limit pathogen invasion. In the gut, microbial signals prompt the host epithelium to produce a protective mucus layer, composed mainly of mucins, which physically separates microbes from host cells while fostering a niche for commensals; studies show that segmented filamentous bacteria and other microbiota members stimulate goblet cell differentiation and mucin secretion via pathways involving Th17 cells. This mucus barrier not only prevents overgrowth but also allows selective microbial access, illustrating the host's adaptive response to microbial density. Microbes, in turn, employ specialized structures and proteins to colonize host surfaces and modulate host physiology. Adhesins, such as fimbriae or pili on bacteria like enterotoxigenic Escherichia coli, mediate attachment to host epithelial receptors, facilitating biofilm formation and persistent colonization in the intestines. Effector proteins further influence host immunity; for example, cholera toxin from Vibrio cholerae enters host cells via receptor-mediated endocytosis, elevating cAMP levels that suppress T-cell activation and promote immune evasion, thereby enhancing bacterial survival during infection. These microbial strategies ensure stable host association while altering local immune environments. Feedback loops between hosts and microbes amplify these interactions, with host factors shaping microbial composition and vice versa. Dietary components, particularly fiber, profoundly influence the gut microbiome by serving as substrates for fermentation; indigestible polysaccharides are broken down by bacteria like Bifidobacterium species into short-chain fatty acids, which in turn select for fiber-degrading taxa and reinforce mucosal integrity. Reciprocally, certain microbes can alter host behavior to favor transmission; Toxoplasma gondii infection in rodents disrupts amygdala function, converting innate fear of cat odors into attraction, likely through dopamine pathway manipulation, increasing predation risk and parasite dissemination. Multi-omics analyses, especially metabolomics, highlight co-metabolites as key mediators of host-microbe crosstalk. Tryptophan, sourced from host diet, is metabolized by gut bacteria such as Clostridium species into indoles like indole-3-propionic acid via the kynurenine pathway, which activates host aryl hydrocarbon receptors to promote intestinal barrier function and immune tolerance. These microbial-derived indoles exemplify how host-microbe metabolic partnerships yield bioactive compounds that regulate inflammation and epithelial repair, underscoring the integrated nature of these interactions.

Assessment Methods

Sampling and Cultivation Techniques

Sampling strategies for microbiomes vary by environmental niche to ensure representative collection while minimizing contamination. For human-associated microbiomes, swabbing is commonly used for skin surfaces, involving sterile swabs moistened with saline or buffer to capture superficial microbial communities, followed by immediate placement in transport media to prevent degradation.^[107] In the gut, biopsies obtained via endoscopy provide direct access to mucosal-associated communities, though this invasive method is limited to clinical settings and requires careful handling to avoid host tissue contamination.^[108] For soil microbiomes, coring or augering at specific depths (e.g., 0-20 cm) allows profiling of vertical stratification, with composite sampling from multiple points reducing spatial variability; contamination control involves using autoclaved tools and gloves to exclude airborne microbes.^[109] Marine microbiomes are typically sampled through filtration of seawater volumes (e.g., 1-10 L) using 0.22 μm pore-size filters to concentrate planktonic cells, with depth profiling via Niskin bottles on research vessels to capture gradients in the water column.^[110] Across all strategies, aseptic techniques, such as working in laminar flow hoods and using negative controls, are essential to distinguish true microbial signals from contaminants.^[108] Cultivation techniques aim to grow viable microbes for functional studies, starting with classical plating on nutrient agar or selective media tailored to niche conditions, such as anaerobic chambers with reducing agents for gut anaerobes like Bacteroides species.^[111] Co-culture systems, where multiple species are grown together in shared media, mimic symbiotic interactions and have enabled isolation of fastidious organisms dependent on cross-feeding metabolites.^[111] For uncultivable microbes, microfluidic devices facilitate high-throughput screening by encapsulating single cells in droplets with nutrients, allowing growth under controlled microenvironments and recovery of rare taxa.^[112] A major challenge in cultivation is the Great Plate Count Anomaly, where only about 1% of environmental microbes form colonies on standard media due to unmet physiological requirements like specific signaling molecules or consortia effects.^[113] Innovations like the iChip device address this by embedding cells in agarose plugs within a semi-permeable membrane, enabling in situ diffusion of nutrients from the native environment during incubation, which has increased recovery rates up to 300-fold for soil and aquatic microbes.^[114] Preservation methods are crucial for maintaining microbial integrity post-sampling, with snap-freezing at -80°C in glycerol (10-20%) stocks preserving viability for culturing over months to years, particularly for gut and soil samples.^[115] For molecular analyses, stabilizers like RNAlater or bead-beating buffers lyse cells and protect DNA/RNA from nucleases, allowing room-temperature storage for up to two weeks without significant community shifts.^[116] These techniques ensure downstream reproducibility while accounting for niche-specific sensitivities, such as desiccation in skin swabs.^[115]

Molecular and Sequencing Approaches

Molecular approaches for characterizing microbiomes rely on high-throughput sequencing technologies to analyze genetic material directly from environmental samples, enabling the identification of microbial diversity without cultivation. These methods target specific genetic markers or entire community DNA to reveal taxonomic composition and functional potential. In diverse ecosystems, including the human gut, soil, and oceans, such techniques have uncovered vast uncultured diversity, including rare taxa that influence nutrient cycling and host health.^[117] Metagenomics, a cornerstone of microbiome analysis, involves sequencing total DNA from samples to profile community structure and function. Amplicon sequencing of the 16S rRNA gene, particularly the V3-V4 hypervariable regions, provides taxonomic resolution at the genus or species level by amplifying and sequencing this conserved bacterial marker, allowing relative abundance estimates of dominant phyla like Firmicutes and Bacteroidetes in human gut samples or Proteobacteria in ocean waters.^[118]^[4] Shotgun metagenomics, in contrast, sequences all DNA fragments randomly, capturing the entire community's genetic content for de novo assembly into contigs and bins, often yielding metagenome-assembled genomes (MAGs) that represent near-complete microbial genomes; for instance, global surveys have recovered over 40,000 high-quality MAGs spanning thousands of genera, revealing novel lineages adapted to various niches from human-associated to environmental.^[119] These approaches integrate with sampling to provide a holistic view of microbiome composition, though they require careful handling of PCR biases in amplicon methods.^[120] Functional profiling extends beyond taxonomy to assess active processes through multi-omics layers. Metatranscriptomics sequences community RNA to identify expressed genes, highlighting metabolic pathways like short-chain fatty acid production in human gut microbiomes or nitrogen fixation in soil and oligotrophic waters, where transcript abundances correlate with environmental gradients.^[121] Metaproteomics analyzes proteins via mass spectrometry to quantify enzymatic activities, such as those involved in organic matter degradation in soil communities or pathogen resistance in host-associated microbiomes, providing direct evidence of trophic interactions.^[122] Metabolomics, often using liquid chromatography-mass spectrometry (LC-MS), detects small molecules like amino acids and lipids excreted by microbes, elucidating chemical exchanges in plant root or coral-associated microbiomes where host-symbiont metabolite overlaps indicate mutualistic roles.^[123] Together, these methods link genetic potential to realized function in dynamic environments.^[124] Bioinformatic pipelines process raw sequencing data to generate interpretable insights. Sequences from 16S amplicons are typically clustered into operational taxonomic units (OTUs) at 97% similarity threshold to account for sequencing errors and intraspecies variation, reducing noise while preserving diversity estimates in complex assemblages.^[125] Taxonomic assignment compares OTUs to reference databases like SILVA, which curates aligned 16S/18S rRNA sequences from diverse environments, enabling precise classification of prokaryotes and eukaryotes with up to 99% accuracy for well-represented taxa. Functional prediction tools such as PICRUSt infer metagenomic content from 16S data by mapping OTUs to reference genomes annotated with KEGG pathways, predicting abundances of genes for processes like sulfate reduction in anoxic sediments, though accuracy depends on database coverage for specific strains. Recent advances have enhanced resolution and throughput in microbiome studies. Long-read sequencing platforms like PacBio generate continuous reads exceeding 10 kb, improving strain-level differentiation in diverse communities by resolving repetitive regions missed by short-read methods; applications since 2015 have reconstructed complete operons in human and environmental samples, identifying strain variants with distinct adaptive traits.^[120] Single-cell genomics isolates and sequences individual microbial cells, bypassing assembly challenges in low-abundance populations; this approach has revealed unique genomic features in uncultured microbes, such as novel biosynthetic gene clusters, achieving high genome recovery rates in complex samples like soils and sediments.^[126] These innovations continue to expand the catalog of microbial genomes, facilitating finer-scale ecological interpretations.

Applications

Medical and Therapeutic Uses

The medical and therapeutic applications of microbiome research have advanced significantly, leveraging the gut microbiota's role in human health to develop targeted interventions for various conditions. Probiotics, defined as live microorganisms that confer health benefits when administered in adequate amounts, and prebiotics, non-digestible fibers that promote beneficial microbial growth, represent foundational therapies. For instance, strains such as Lactobacillus plantarum and Bifidobacterium infantis have shown efficacy in alleviating symptoms of irritable bowel syndrome (IBS), including abdominal pain and bloating, through randomized controlled trials demonstrating improved quality of life scores.^[127]^[128] The U.S. Food and Drug Administration (FDA) has granted Generally Recognized as Safe (GRAS) status to several Lactobacillus strains, such as L. rhamnosus CBT LR5, for use in food products aimed at supporting digestive health, though specific health claims for IBS remain limited due to variable evidence across strains.^[129] Prebiotics like inulin and fructooligosaccharides (FOS) selectively stimulate Bifidobacterium growth, significantly increasing their populations in the gut in clinical studies, which correlates with reduced inflammation markers in IBS patients; however, the FDA has not approved prebiotic-specific health claims, classifying them primarily as dietary fibers.^[130]^[131] Fecal microbiota transplantation (FMT), involving the transfer of donor stool to restore microbial balance, has emerged as a highly effective treatment for recurrent Clostridioides difficile infection (CDI), with cure rates of 80-90% after a single administration via colonoscopy or enema, as established in multiple randomized trials.^[132]^[133] The American Gastroenterological Association (AGA) endorsed FMT in 2013 guidelines for patients failing standard antibiotic therapy, recommending it as a first-line option for recurrent CDI based on sustained response rates exceeding 90% in real-world data.^[134] Emerging applications include inflammatory bowel disease (IBD), where FMT has induced remission in approximately 30-40% of ulcerative colitis cases in various trials, including phase II studies, by modulating immune responses and microbial diversity, though results for IBS remain inconsistent and not routinely recommended.^[134]^[135]^[136] Phage therapy, utilizing bacteriophages to selectively target pathogenic bacteria, offers a precise alternative to broad-spectrum antibiotics, particularly for multidrug-resistant (MDR) infections. Since the 2010s, clinical trials have demonstrated success in treating MDR Pseudomonas aeruginosa and Acinetobacter baumannii infections, with resolution rates of 70-80% in compassionate-use cases involving intravenous or topical phage administration, without significant adverse effects.^[137]^[138] For example, a 2019 case at the University of California San Diego reported successful treatment of a cystic fibrosis patient with disseminated Mycobacterium abscessus infection using a personalized triple-phage cocktail, highlighting the therapy's adaptability to bacterial resistance profiles.^[139] Ongoing phase II/III studies since 2020 continue to evaluate phages against MDR urinary tract and wound infections, emphasizing their low immunogenicity and specificity.^[140]^[141] Microbiome-based diagnostics harness gut microbial signatures as non-invasive biomarkers for disease detection and personalized medicine. Fecal microbiome profiling has identified consistent dysbiosis patterns, such as elevated Fusobacterium nucleatum and reduced Faecalibacterium prausnitzii, in colorectal cancer (CRC) patients, enabling machine learning models with 85-90% accuracy for early-stage detection in validation cohorts.^[142]^[143] These signatures outperform traditional fecal immunochemical tests in some studies by distinguishing precancerous adenomas from healthy controls.^[144] In personalized medicine, microbiome typing—assessing individual microbial compositions—guides pharmacomicrobiomics, predicting drug responses like reduced efficacy of levodopa in Parkinson's patients due to Eggerthella lenta metabolism, with tailored probiotics improving outcomes in 60% of cases.^[145]^[146] This approach integrates with precision oncology, where baseline microbiome assessments inform immunotherapy success rates.^[147] Despite these advances, microbiome therapies face significant challenges, including regulatory hurdles and technical limitations. The FDA classifies FMT and live biotherapeutic products as investigational drugs under biologics regulations, requiring phase III trials for approval, which has delayed widespread adoption beyond CDI; only two FMT products, Rebyota and Vowst, received approval in 2022-2023 for CDI recurrence prevention. As of 2025, advancements include AI models for optimizing donor-recipient matching in FMT and breakthrough therapy designations for novel microbiome modulators.^[148]^[149]^[150]^[151] Engraftment issues, where transplanted microbes fail to persist (success rates dropping to 50-70% long-term), stem from donor-recipient mismatches and host immune barriers, necessitating improved screening and delivery methods like encapsulated formulations.^[152]^[153] Additionally, variability in microbiome responses across populations complicates standardization, underscoring the need for robust clinical frameworks.^[154]

Agricultural and Environmental Uses

In agriculture, microbial inoculants such as plant growth-promoting rhizobacteria (PGPR), including Azospirillum brasilense, enhance crop yields by facilitating nitrogen fixation, hormone production, and nutrient uptake, leading to 1–1.5-fold increases in maize productivity under tropical conditions.^[155] These bacteria colonize plant roots and improve soil fertility, allowing for reduced application of synthetic fertilizers by up to 25% while maintaining or boosting yields in crops like wheat and sugarcane.^[156] Biofertilizers based on nitrogen-fixing diazotrophs, such as Azotobacter chroococcum and Rhizobium species, further support sustainable farming by converting atmospheric nitrogen into plant-available forms, potentially decreasing synthetic nitrogen inputs by 20–30% in systems like cotton and common bean cultivation.^[157] Microbial consortia play a key role in bioremediation, where bacteria like Pseudomonas species degrade environmental pollutants. For instance, Pseudomonas strains efficiently break down petroleum hydrocarbons in oil spills through enzymatic oxidation, accelerating natural attenuation in contaminated marine and soil ecosystems.^[158] Similarly, Pseudomonas stutzeri and other consortia target polychlorinated biphenyls (PCBs) via dechlorination and mineralization pathways, enabling the remediation of persistent organic pollutants in sediments and soils.^[159] In animal husbandry, probiotics and feed additives modulate the rumen microbiome to curb greenhouse gas emissions. Trials in the 2020s using seaweed supplements like Asparagopsis taxiformis in grazing beef cattle achieved an average 37.7% reduction in enteric methane emissions without affecting animal weight gain or health.^[160] Conservation efforts leverage microbiome restoration to rehabilitate degraded ecosystems. In post-mining soils, strategic revegetation and organic amendments promote microbial community recovery, with bacterial diversity trajectories aligning closer to reference sites over time through enhanced nutrient cycling and aggregate formation.^[161] For marine environments, probiotic consortia of beneficial bacteria (e.g., Pseudoalteromonas and Cobetia species) inoculated into corals like Pocillopora damicornis mitigate bleaching by antagonizing pathogens and stabilizing symbioses under thermal stress, reducing color loss by up to 50% in experimental conditions.^[162] Sustainability in agriculture benefits from precision monitoring of soil microbiomes, integrating remote sensing with metagenomic analysis. Drone-based sampling, using unmanned aerial vehicles equipped with multispectral sensors, enables high-resolution assessment of soil health and microbial eDNA, facilitating targeted interventions like biofertilizer application to optimize nutrient efficiency and reduce chemical inputs.^[163] This approach, combined with metabarcoding, detects microbial shifts linked to crop stress, supporting scalable ecosystem management.^[164]

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Marine probiotics: increasing coral resistance to bleaching through ...
Here, we describe a successful manipulation of the coral microbiome through the addition of pBMCs that significantly improved coral resistance when exposed to ...
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Ocean currents shape the microbiome of Arctic marine sediments
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Biological or microbial carbon pump? The role of phytoplankton ...
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A metabolic, phylogenomic and environmental atlas of diatom ...
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The life sulfuric: microbial ecology of sulfur cycling in marine ...
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Microbiome diversity protects against pathogens by nutrient blocking
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Intestinal microbiota-derived short-chain fatty acids regulation of ...
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Germ-free mice exhibit profound gut microbiota-dependent ...
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AGA Clinical Practice Guideline on Fecal Microbiota–Based ...
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The practice of fecal microbiota transplantation in inflammatory ...
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Fecal microbiota transplantation in gastrointestinal disorders
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Microbiome at the Frontier of Personalized Medicine
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Review Regulation, risk and safety of Faecal Microbiota Transplant
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Present and future of microbiome-targeting therapeutics - JCI
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Microbiome Therapeutics - Commercialization Opportunities and ...
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Plant Growth-Promoting Rhizobacteria for Sustainable Agricultural ...
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Microbial Degradation of Petroleum Hydrocarbon Contaminants
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The effect of terpenes on the biodegradation of polychlorinated ...
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Mitigating methane emissions in grazing beef cattle with a seaweed ...
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Marine probiotics: increasing coral resistance to bleaching through ...
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Synergistic integration of remote sensing and soil metagenomics data
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Drone Imagery and Metabarcoding as Diagnostic Tools of Poor ...
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