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International Journal of Microbiology logoLink to International Journal of Microbiology
. 2026 Aug 24;2026:1721210. doi: 10.1155/ijm/1721210

Probiotics in Human Health: Current Evidence, Mechanism of Action, and Future Perspectives

Guesh Mulaw 1,✉, Gebrekidan Kidanemariam 1, Mouslim Bara 2, Teklemichael Tesfay 1
Editor: Todd R Callaway
PMCID: PMC13501397  PMID: 42639367

Abstract

Probiotics are widely recognized for their potential to promote human health through diverse mechanisms that influence host physiology and microbial ecology. This review synthesizes current evidence on the biological functions, mechanisms of action, and therapeutic applications of probiotics. A comprehensive narrative literature review was conducted, with 143 records identified, screened, and assessed for eligibility before inclusion in the final analysis. The available evidence indicates that probiotics exert their beneficial effects through modulation of gut microbiota composition, enhancement of intestinal barrier integrity, competitive exclusion of pathogens, production of antimicrobial metabolites, and regulation of innate and adaptive immune responses. Clinical and experimental studies further suggest potential benefits in the prevention or management of antibiotic‐associated diarrhea, lactose intolerance, allergic diseases, hypercholesterolemia, colorectal cancer, neurological disorders, and heavy metal toxicity. Despite promising findings, probiotic efficacy remains strain‐specific and influenced by host characteristics, dosage, and treatment duration. Challenges related to strain selection, safety assessment, and standardization continue to limit broader clinical application. Overall, this narrative review provides an integrated overview of current knowledge on probiotic functionality, highlights emerging therapeutic opportunities, and identifies key research gaps that should be addressed to support evidence‐based probiotic use.

Keywords: functionality, human health, physiology, probiotics, therapeutic applications

1. Introduction

The history of probiotics began with the history of man [1]. The health‐promoting properties of yogurt were first widely recognized through the work of the Russian scientist Elie Metchnikoff at the Pasteur Institute in Paris. He proposed that lactic acid bacteria (LAB) present in yogurt help counteract harmful putrefactive bacteria in the intestine, thereby contributing to improved gut health [2]. At the same time, Henry Tissier isolated Bifidobacterium species from the feces of breastfed infants and observed that these bacteria constituted a dominant component of the normal human intestinal microbiota [3]. Tissier advised giving Bifidobacteria to infants who had diarrhea because he thought the bacteria would replace the putrefactive bacteria that cause stomach troubles and reassume their position as the pre‐eminent intestinal microorganisms [4].

Probiotics are live bacteria that promote health by supporting the digestive and immune system, and they are used to refer to microbes that have positive effects on both humans and animals [5]. Probiotics are reported as the representative group of microorganisms associated with traditional fermented foods [6]. Prebiotics are nondigestible dietary carbohydrates that selectively stimulate the growth and activity of beneficial gut microorganisms. Synbiotics combine probiotics and prebiotics to synergistically enhance intestinal health and immune function. In addition, postbiotics, which consist of bioactive compounds produced during probiotic fermentation, have been recognized for their diverse health‐promoting properties [7]. Besides, consuming both prebiotics and probiotics (synbiotics) simultaneously may increase the survival of advantageous bacteria during their transit through the upper gastrointestinal system, as a result, they have a bigger positive effect on germs that have already colonized the intestines [8, 9].

Early‐life probiotic interventions that enhance gut resilience in infants represent a promising approach to reducing the emergence and dissemination of antibiotic resistance. Probiotic‐driven Bifidobacterium colonization can modulate the infant gut microbiota, resulting in a reduced abundance of antibiotic resistance genes and a lower antibiotic resistance burden [10]. The effects of prebiotic, probiotic, or synbiotic supplementations on parameters feed and water intake, weight gain, feed conversion ratio, performance index, digestibility, small intestine morphometry, and carcass traits were significantly affected on synbiotic supplementation compared with prebiotic, probiotic, and control [11]. The definition of probiotics has changed in tandem with the development of our understanding of the mechanisms underlying the usage of supplements containing live bacteria. Then, in 1974, Parker made the following claim: “Organisms and substances which help to gut microbial equilibrium are probiotics” [12]. Today, the universal definition of probiotic was established by the World Health Organization (WHO) and the Food and Agriculture Organization of the United States (FAO). These two organizations defined probiotics as “live microorganisms,” which when administered in adequate amounts, have a beneficial effect on the health of the host organism [13].

The most common types of microorganisms used as probiotics are LAB and Bifidobacteria, although other bacteria and certain yeasts are also used [14]. LAB are associated with habitats that are rich in nutrients, such as various food products and plant materials. They can be found in soil, water, manure, sewage, and silage and can ferment or spoil food. Particular LAB inhabit the human oral cavity, intestinal tract, and vagina, where they exert beneficial effects on the human microbiota and contribute to maintaining the health of these ecosystems. They may therefore also be candidates for application as probiotics [15]. The main probiotic microorganisms used belong to the Bifidobacterium and Lactobacillus genera [16]. They occupy different ecological positions in the human gastrointestinal tract (GIT). Lactobacilli are normal inhabitants of the small intestine, whereas Bifidobacteria reside in the colon [17, 18]. These bacteria are “generally regarded as safe” (GRAS) because they can reside in the human body causing no harm. Some of the common probiotic microorganisms are shown in Table 1.

Table 1.

Microorganisms used as probiotics culture.

Number Lactobacillus spp. Bifidobacterium spp. Other probiotic microorganisms
1. L. acidophilus B. adolescentis Bacillus subtilis
2. Lacticaseibacillus casei B. bifidum Aspergillus oryzae
3. Lacticaseibacillus paracasei B. breve Saccharomyces cerevisiae var. boulardii
4. L. delbrueckii B. longum S. cerevisiae
5. L. helveticus B. infantis Escherichia coli Nissle
6. Lactiplantibacillus plantarum B. lactis Lactococcus lactis
7. Ligilactobacillus gasseri B. animalis Propionibacterium freudenreichii
8. Lacticaseibacillus rhamnosus B. essensis Leuconostoc mesenteroides
9. Ligilactobacillus johnsonii B. laterosporus Pediococcus acidilactici
10. Limosilactobacillus reuteri Enterococcus faecium
11. Limosilactobacillus fermentum Streptococcus thermophilus

Note: Source: [14].

Early‐life microbial exposures are essential for the normal growth of human physiology [19]. The ability of probiotics to modify the immunological response of the host, antagonize pathogenic microbes, or compete for adhesion sites with pathogenic microorganisms is related to the action of probiotics against microorganisms [20]. Gut microorganisms are essential for the proper development of the host immune system. Probiotics may improve intestinal immune responses by altering the composition and functional activity of the gut microbiota, thereby promoting immune homeostasis [21]. Besides, probiotics are the good microbes naturally found in the human stomach that keep our digestive health balanced. Probiotics are significant because they have both an application in industrial product development and a favorable influence on human health [22]. Besides, LAB population in gut microbiota of broilers affected nondetectable population of C. perfringens [23].

Given the expanding interest in microbiome‐based therapies, a comprehensive synthesis of current knowledge on probiotics is needed. Therefore, this narrative review is aimed at critically examining the current evidence on the mechanisms of action and health‐promoting effects of probiotics. Particular attention is given to their roles in modulating gut microbiota composition, strengthening intestinal barrier function, inhibiting pathogenic microorganisms, and regulating immune responses. The review further explores the potential applications of probiotics in the prevention and management of human diseases, discusses current limitations, and identifies future research directions to support their effective and evidence‐based use in healthcare.

2. Material and Methods

2.1. Search Strategy

A comprehensive narrative literature review was conducted to synthesize current evidence regarding the mechanisms of action, therapeutic applications, and future perspectives of probiotics in human health. Relevant studies were retrieved from the Scopus, Web of Science, and Elsevier databases using combinations of keywords linked by Boolean operators (AND and OR). The search strategy included terms such as “probiotics,” “probiotic strains,” “fermented foods,” “gut microbiota,” “16S rRNA gene metagenomics,” “intestinal barrier,” “immune modulation,” “host–microbe interactions,” “pathogen inhibition,” “animal models,” and “human health.”

2.2. Study Selection

A representative search string was applied during our analysis; we used keywords to extract data. All records identified through database searches were imported into a reference management system and screened for duplicates. Titles and abstracts were evaluated for relevance, followed by a full‐text assessment of potentially eligible studies. The Boolean operator used:

(“probiotics” OR “probiotic strains” OR “beneficial microorganisms”)

AND

(“human health” OR “gut microbiota” OR “intestinal health” OR “immune modulation” OR “host–microbe interactions” OR “pathogen inhibition”).

No restrictions were applied regarding publication year to ensure broad coverage of both foundational and contemporary studies. Peer‐reviewed research articles, clinical trials, experimental studies, reviews, and meta‐analyses were considered for inclusion. Publications were selected based on their scientific relevance, methodological quality, and contribution to understanding probiotic functionality and health outcomes.

Following screening and evaluation, a total of 143 references were retained for detailed analysis. Information concerning probiotic strains, mechanisms of action, microbiota modulation, antimicrobial activity, immunological effects, and clinical applications was extracted and synthesized narratively. The collected evidence was subsequently organized into thematic sections addressing probiotic biology, mechanisms of action, health benefits, safety considerations, and future research directions.

3. Results and Discussion

3.1. General Overview

The selection of probiotic strains is guided by recommendations from the WHO, FAO, and the European Food Safety Authority (EFSA), which emphasize three fundamental criteria: safety, functionality, and technological suitability [24, 25] (Figure 1). Functional properties include the ability to survive passage through the GIT, adhere to intestinal surfaces, and exert immunomodulatory effects [27]. Technological requirements involve maintaining viability and functional properties during production, storage, and distribution [28]. From a safety perspective, probiotic strains should preferably originate from the healthy human gastrointestinal microbiota, possess a documented history of safe use, lack pathogenic characteristics, and transmissible antibiotic resistance genes, and should not exhibit undesirable bile salt deconjugation activity [29] (Figure 1).

Figure 1.

Figure 1

Selection criteria of potential probiotic LAB strains [26].

To standardize probiotic evaluation, the FAO and WHO established guidelines requiring strain identification through phenotypic and genotypic characterization, comprehensive safety assessments, and validation of efficacy through well‐designed human clinical trials, preferably randomized, double‐blind, and placebo‐controlled studies [30]. In addition, probiotic candidates must withstand harsh gastrointestinal conditions, including acidic gastric environments and bile exposure, adhere to intestinal epithelial cells, and inhibit pathogen colonization through competitive exclusion, immune modulation, or antimicrobial production [31, 32].

Acid tolerance is among the primary criteria for probiotic selection because microorganisms must survive gastric transit before reaching the intestine [33]. Although gastric pH can fall below 2.0, food consumption may increase it to approximately 3.0, improving bacterial survival [34]. Numerous studies have demonstrated that LAB can tolerate acidic conditions during the relatively short gastric transit period [35–37]. Similarly, probiotic yeast isolates from traditional fermented foods showed survival rates up to 100% at pH 2.0–2.5 [38], whereas Bacillus spp. isolated from fermented products also exhibited high survival under acidic conditions [39].

Resistance to bile salts is another essential probiotic characteristic, as bile can disrupt bacterial membranes and reduce microbial viability [40, 41]. Physiological bile concentrations in the human intestine generally range between 0.1% and 0.5%, and concentrations of 0.15%–0.3% are commonly used for probiotic screening [32, 42] and 0.5% [43]. Several probiotic isolates, including Lactobacillus spp., have demonstrated strong tolerance to bile exposure, maintaining high survival rates under these conditions [44].

A key functional property of probiotics is their antimicrobial activity against pathogenic microorganisms [45]. LAB produce a variety of antimicrobial compounds, including organic acids, hydrogen peroxide, carbon dioxide, diacetyl, ethanol, and bacteriocins [46, 47]. Organic acids inhibit pathogens by lowering intracellular pH, disrupting membrane potential, and interfering with essential metabolic processes, thereby exerting broad‐spectrum antimicrobial effects against bacteria, yeasts, and molds [47, 48]. Other metabolites, such as hydrogen peroxide and diacetyl, further contribute to microbial inhibition through oxidative and metabolic mechanisms [49].

Among antimicrobial compounds, bacteriocins are particularly important due to their targeted inhibitory activity against closely related and pathogenic bacteria [50]. Nisin, produced by Lactococcus lactis subsp. lactis, is the most extensively studied bacteriocin and is approved for use in foods intended for human consumption [51]. Additional bacteriocins, including lactococcin, salivaricin, acidocin, plantaricin, and lacticin, are produced by various probiotic species and have demonstrated potential for controlling spoilage and pathogenic microorganisms in food systems [52, 53]. Consequently, bacteriocin‐producing strains have been successfully employed as starter cultures and natural preservatives to improve food safety and quality [54, 55].

The safety assessment of probiotics also includes evaluation of antibiotic resistance profiles because the global rise of antimicrobial resistance represents a significant public health concern [56, 57]. Antibiotic resistance may be intrinsic, reflecting a natural species characteristic, or acquired through mutation or horizontal gene transfer [58, 59]. Many Lactobacillus species exhibit intrinsic resistance to certain antibiotics, including vancomycin, due to structural differences in their cell wall peptidoglycan precursors [60–62]. Importantly, these resistance traits are generally nontransmissible and have not been associated with the transfer of resistance genes to other microorganisms, supporting the long history of safe probiotic use of strains such as Lactobacillus rhamnosus GG [63].

Similarly, Bifidobacterium species often display intrinsic resistance to several antibiotics, including nalidixic acid, aminoglycosides, and metronidazole [60, 64]. Although studies have reported variable susceptibility to vancomycin, these differences may largely reflect methodological variations in antimicrobial susceptibility testing. Therefore, careful characterization of antibiotic resistance remains an essential component of probiotic safety evaluation.

3.2. Mechanism of Action

Probiotics exert their beneficial effects through multiple mechanisms involving metabolic activity, enhancement of intestinal barrier function, modulation of the gut microbiota, and regulation of host immune responses (Figure 2). One important characteristic of LAB is their ability to produce extracellular proteinases that initiate the hydrolysis of dietary proteins, particularly milk proteins, thereby releasing amino acids essential for bacterial growth. These enzymatic activities enhance protein and fat bioavailability and increase the production of free amino acids, which may improve the nutritional status of the host, especially in individuals with reduced endogenous protease activity. Moreover, microbial proteolysis can release a variety of bioactive peptides that contribute to host health benefits [66].

Figure 2.

Figure 2

Mechanisms of action of probiotics [65].

Many probiotic microorganisms, including LAB and certain Bifidobacterium strains, produce exopolysaccharides (EPS), either as capsular polysaccharides attached to the cell surface or as extracellular polymers released into the surrounding environment [67]. Besides their industrial importance as natural biopolymers [68], EPS contribute significantly to the quality of fermented foods by acting as stabilizers, emulsifiers, viscosifiers, and gelling agents, thereby improving texture, viscosity, and reducing syneresis [69]. EPS‐producing strains belonging to the genera Lactococcus, Streptococcus, Lactobacillus, Leuconostoc, and Pediococcus have traditionally been used in fermented dairy products to enhance desirable rheological properties [70].

Adhesion to the intestinal mucosa is considered an important probiotic trait because it facilitates temporary colonization, prolongs persistence within the GIT, and promotes interactions with the mucosal immune system. Through adhesion, probiotics can influence gut‐associated lymphoid tissues, strengthen the intestinal barrier, and exert local and systemic immunomodulatory effects [71]. Furthermore, adhesion may contribute to competitive exclusion, a process in which probiotics inhibit pathogen attachment to intestinal epithelial cells by competing for binding sites and nutrients [72]. In vitro studies have demonstrated the ability of several probiotic strains, including Lactobacillus acidophilus, Leuconostoc mesenteroides, and Enterococcus faecium, to adhere to epithelial or abiotic surfaces and interfere with pathogen colonization [73–76]. However, despite extensive research, the exact role of adhesion in probiotic efficacy remains uncertain, as some poorly adhering strains still confer health benefits, and in vitro adhesion assays often show limited reproducibility [24].

The concept of competitive exclusion, also known as colonization resistance, is one of the most widely recognized mechanisms of probiotic action. It refers to the ability of the resident intestinal microbiota to restrict the growth and colonization of potentially pathogenic microorganisms, thereby maintaining microbial balance within the GIT. This concept was first demonstrated in the 1970s when administration of adult intestinal microorganisms protected newly hatched chicks against Salmonella infection [77]. Research has demonstrated that incorporating dry fermented feed fermented with Saccharomyces sp. into broiler diets can promote growth, improve feed conversion efficiency, increase intestinal villus height and beneficial LAB, and suppress pathogenic microorganisms in the intestine [78]. In addition to this, functional nutrition involves the regular consumption of natural or artificially derived products that regulate physiological functions and biochemical processes by maintaining or restoring the body′s microecological balance [79]. Besides, bacteria that compose the intestinal flora are influenced by the feeding habits of host animals [80].

The biological effects of probiotics are generally classified into three major modes of action [81]. First, probiotics modulate both innate and adaptive immune responses, contributing to the prevention and treatment of infectious diseases, chronic intestinal inflammation, and potentially supporting the elimination of neoplastic cells. Second, they exert direct antagonistic effects against pathogenic microorganisms while helping to maintain the balance of beneficial gut microbiota. Third, probiotics can influence microbial metabolites and host‐derived compounds, including toxins, bile salts, and dietary components, resulting in detoxification and reduced toxicity within the intestinal environment [82, 83].

At the cellular level, probiotics influence numerous components of the host immune system and intestinal barrier. They interact with epithelial cells and immune cells such as dendritic cells, macrophages, monocytes, B lymphocytes, T lymphocytes, regulatory T cells, and natural killer (NK) cells, thereby affecting both innate and adaptive immune responses. Through these interactions, probiotics contribute to maintaining intestinal homeostasis, strengthening mucosal defenses, and regulating inflammatory processes [84].

The safety of probiotic strains is increasingly assessed through whole‐genome sequencing, which complements traditional safety evaluations by identifying genes associated with virulence, antimicrobial resistance, and other potential risk factors. For example, genomic analysis of Lactobacillus plantarum JDM1 identified several genes associated with virulence‐related functions; however, most were classified as defensive or nonclassical factors and were not considered harmful to the host [85].

The evaluation of probiotic viability and quality traditionally relies on plate count methods, which measure the ability of bacterial cells to grow and form colonies [86]. However, these methods cannot accurately detect damaged or viable but nonculturable cells, potentially leading to underestimation of probiotic populations [87]. To overcome these limitations, culture‐independent techniques such as quantitative PCR (qPCR) and flow cytometry have been developed to assess bacterial viability more accurately and provide rapid characterization of cellular physiological states [88, 89].

More recently, postbiotics—bioactive compounds produced by probiotic microorganisms—have attracted considerable interest because they may provide health benefits similar to those of live probiotics while avoiding risks associated with viable microorganisms, such as bacteremia, transfer of virulence genes, or dissemination of antibiotic resistance determinants. In addition, postbiotics offer greater stability during storage and can remain effective at room temperature for extended periods [84].

3.3. Benefits of Probiotics

Probiotics contribute to human health by maintaining intestinal microbial balance and suppressing pathogenic microorganisms as well as noncommunicable disease [90, 91]. Extensive evidence indicates that probiotics enhance immune function, improve gastrointestinal health, reduce metabolic and inflammatory disorders, support neurological health, and protect against environmental toxicants [92, 93]. They are also important in alleviating the symptoms of lactose intolerance and in enhancing growth [94]. Probiotics are useful in food biodetoxification and effectively reduce food contamination [95].

3.3.1. Immunomodulatory and Antimicrobial Effects

Studies conducted in vitro, animal models, and human clinical trials have demonstrated that probiotics can modulate host immune responses [96]. Consumption of B. lactis HN019 and L. rhamnosus HN001 has been associated with enhanced immune parameters and increased NK cell activity in elderly individuals [97–99]. These effects are mediated through stimulation of mucus production, macrophage activation, increased immunoglobulin A (IgA) secretion, neutrophil activity, and regulation of cytokine production [98].

In addition, probiotics exert antimicrobial activity through the production of short‐chain fatty acids (SCFAs), bacteriocins, organic acids, hydrogen peroxide, and other bioactive compounds that inhibit pathogen growth and survival [100]. They also enhance host antimicrobial defenses and compete with pathogens for nutrients and epithelial binding sites [100].

3.3.2. Gastrointestinal and Metabolic Benefits

Probiotics have demonstrated significant benefits in gastrointestinal health, particularly in alleviating lactose intolerance and reducing antibiotic‐associated diarrhea (AAD) [101, 102]. The presence of β‐galactosidase–producing bacteria improves lactose digestion and reduces symptoms such as bloating, abdominal pain, and diarrhea [103]. Likewise, probiotic supplementation helps restore intestinal microbiota disrupted by antibiotic treatment, thereby reducing the incidence and severity of AAD [104].

Probiotics may also contribute to improved lipid metabolism. Several studies suggest that certain Lactobacillus and Bifidobacterium strains reduce serum cholesterol by deconjugating bile acids, promoting cholesterol excretion, and inhibiting cholesterol synthesis [104, 105]. These mechanisms may help lower cardiovascular disease risk in hypercholesterolemic individuals [105]. Our intestinal microbiota serve many roles vital to the normal daily function of the human GIT. Many probiotics are derived from our intestinal bacteria and have been shown to provide clinical benefit in a variety of gastrointestinal conditions [106, 107] (Table 2). It also possesses mechanisms to eliminate harmful agents that penetrate this barrier [109]. These physiological functions are strongly influenced by the gut microbiota, which regulate the expression of epithelial genes associated with nutrient transport and metabolism, maintenance of mucosal integrity, xenobiotic metabolism, enteric nervous system function, intestinal motility, hormonal and developmental responses, angiogenesis, and the organization of the cytoskeleton and extracellular matrix [110]. The gut microbiome plays a pivotal role in digestion, immunity, and disease resistance [111].

Table 2.

Potential beneficial effects of probiotic supplementation against metabolic disorders.

S/no Probiotic action Mechanism Physiological outcome
1. Energy metabolism Short‐chain fatty acids (SCFA) production, vitamin synthesis, bile acid metabolism Improved glucose homeostasis, lipid metabolism
2. Barrier function Strengthened tight junctions, increased mucus secretion Reduced intestinal permeability
3. Immune modulation Increased IgA, macrophage activation, anti‐inflammatory cytokines Reduced inflammation
4. Gut microbiota Increased beneficial bacteria, bacteriocins, pathogen inhibition Improved microbial diversity and colonization resistance

Note: Source: [108].

3.3.3. Prevention of Chronic and Allergic Diseases

Growing evidence suggests that probiotics may reduce the risk of colorectal cancer by modulating gut microbiota composition, suppressing carcinogenic bacterial enzymes, regulating immune responses, and reducing intestinal inflammation [112, 113]. Probiotics have demonstrated anti‐inflammatory and antitumor effects in preclinical and clinical studies [114]. Moreover, probiotic supplementation significantly decreases the occurrence of diarrhea and the frequency of daily bowel movements [115]. Dysbiosis, an imbalance in gut microorganisms, can promote cancer. Conversely, probiotics have the potential to enhance gut health and restore immunological equilibrium [116]. It is characterized by the depletion or overrepresentation of specific bacterial taxa and alterations in their metabolic activities. Therapeutic supplementation with conventional probiotics, either alone or in combination with prebiotics, as well as next‐generation probiotics (NGPs) or postbiotics, has emerged as a promising adjunctive approach to cancer treatment by restoring microbial homeostasis and modulating host physiological and immune responses [117]. The therapeutic potential of probiotics in the management of depression is supported by the mechanisms of the microbiota–gut–brain axis (MGBA), which is known to contribute to the pathophysiology of depressive disorders. Consequently, probiotics may serve as effective adjuncts to conventional therapy for major depressive disorder (MDD) and could also be considered as a stand‐alone intervention for mild MDD, offering a promising avenue for improving the treatment of depression [118]. Researchers also reported that psychobiotics are efficacious in improving neurodegenerative and neurodevelopmental disorders, including autism spectrum disorder (ASD), Parkinson′s disease (PD), and Alzheimer′s disease (AD) [119] (Figure 3). Probiotics represent a novel and promising strategy for managing neurodegeneration particularly AD and PD [121]. Certain probiotic strains have also been associated with increased microbial diversity and reduced tumor‐promoting factors in colorectal cancer patients [122, 123].

Figure 3.

Figure 3

Mechanisms of probiotic action on the gut–brain axis [120].

Probiotics may additionally play a role in preventing allergic disorders, particularly eczema in children [124]. Their beneficial effects are attributed to enhanced mucosal barrier function, immune regulation, reduced inflammatory responses, and improved degradation of dietary antigens. Clinical studies have reported a lower incidence of eczema among infants receiving probiotic supplementation, particularly L. rhamnosus GG [125]. Other studies indicate that addition of probiotics to the diet for weeks improved the immune response without the release of inflammatory cytokines, thereby reducing the onset of systemic inflammatory induced diabetes [126].

3.3.4. Neuroprotective Effects and Protection Against Heavy Metal Toxicity

The gut–brain axis has emerged as an important pathway through which probiotics influence neurological health [127, 128]. Clinical studies suggest that specific probiotic strains may improve behavioral outcomes in children with ASDs and reduce symptoms of anxiety, stress, and depression [129, 130]. These effects may be mediated through modulation of gut microbiota composition and production of neuroactive compounds such as γ‐aminobutyric acid (GABA) [131]. The MGBA is a complex bidirectional communication system linking the GIT and the brain through neural, endocrine, and immunological signaling pathways. Perturbations within this network can have reciprocal effects on both systems, whereas dysregulation of the axis may contribute to functional abnormalities in the enteric and central nervous systems [132].

Probiotics also show promise in mitigating heavy metal toxicity. Several Lactobacillus and Bifidobacterium strains can bind cadmium and lead, reduce intestinal absorption, alleviate oxidative stress, and limit tissue accumulation of toxic metals [133, 134]. Experimental and human studies indicate that probiotic supplementation may protect against heavy metal‐induced toxicity, highlighting its potential as a dietary strategy for populations exposed to environmental contaminants [135, 136].

4. Future Perspectives

The increasing prevalence of microbiota that exhibit resistance and tolerance to traditional drugs and antibiotics has reduced the effectiveness of many therapeutic agents. In response, several probiotic strains have demonstrated promising health benefits, particularly through their strong anti‐inflammatory and antiallergic activities. Probiotics offer a promising preventive and therapeutic advancement [137]. Increasing evidence indicates that regular consumption of these products may contribute to the prevention and management of several health disorders, such as irritable bowel syndrome, lactose intolerance, gastroenteritis, obesity, chronic diarrhea, allergic diseases, atopic dermatitis, and infectious diseases [138]. The field of probiotics is rapidly evolving, with the development of novel microbiome‐modulating strategies, including prebiotics, synbiotics, postbiotics, microbial consortia, live biotherapeutic products, and genetically engineered microorganisms. Concurrently, increasing attention is being directed toward polyphenols, dietary fibers, and fermented foods because of their potential to promote human health [139]. However, most NGP candidates have complex nutritional requirements and are highly sensitive to oxygen, creating significant technological challenges for their large‐scale production [140]. The next generation of probiotics has become a major topic in scientific research [141].

Recent advances in high‐throughput sequencing technologies have enabled the identification of gut microorganisms with substantial health‐promoting properties, facilitating the development of NGPs allowing for more precise and customized treatment approaches [142]. By integrating synthetic biology and bioinformatics approaches, these NGPs are designed to target specific disease conditions while exhibiting improved stability and viability [143]. Improvements in metabolomic and genetic technologies have increased our understanding of how probiotics work, allowing for more precise and customized treatment approaches.

5. Conclusion

Probiotics have emerged as future biological elements able to promote human health through multiple mechanisms, including modulation of gut microbiota composition, enhancement of intestinal barrier function, competitive exclusion of pathogens, production of antimicrobial metabolites, and regulation of immune responses. The most extensively studied probiotic microorganisms are species belonging to the genera Lactobacillus and Bifidobacterium, although a growing number of other beneficial microorganisms are being investigated for their therapeutic potential.

This narrative review highlights the potential role of probiotics in the prevention and management of a wide range of health conditions, including gastrointestinal disorders, metabolic diseases, allergic conditions, neurological disorders, and infections. Furthermore, advances in microbiome research and molecular technologies have improved our understanding of host–microbe interactions and the mechanisms underlying probiotic functionality.

Despite these, probiotic efficacy remains highly strain‐specific and is influenced by factors such as dosage, treatment duration, formulation, and host characteristics. Future well‐designed, randomized, double‐blind, placebo‐controlled clinical trials are needed to establish standardized guidelines for probiotic use and to validate their long‐term safety and effectiveness. Overall, probiotics represent a rapidly evolving field with considerable potential to contribute to the prevention of human diseases.

Funding

No funding was received for this manuscript.

Conflicts of Interest

The authors declare no conflicts of interest.

Acknowledgments

The College of Natural and Computational Sciences of Aksum University is acknowledged by the authors for providing access to journals demanding subscription.

Mulaw, Guesh , Kidanemariam, Gebrekidan , Bara, Mouslim , Tesfay, Teklemichael , Probiotics in Human Health: Current Evidence, Mechanism of Action, and Future Perspectives, International Journal of Microbiology, 2026, 1721210, 13 pages, 2026. 10.1155/ijm/1721210

Academic Editor: Todd R. Callaway

Contributor Information

Guesh Mulaw, Email: guesh2001@gmail.com.

Todd R. Callaway, Email: todd.callaway@uga.edu

Data Availability Statement

As this is a review paper, no additional data are available. Rather, the findings came from reviewing original research articles.

References

  • 1. Soccol C. R., Vandenberghe L. D., Spier M. R., Medeiros A. B., Yamaguishi C. T., Lindner J. D., Ashok Pandey A. P., and Thomaz-Soccol V., The Potential of Probiotics: A Review, Food Technology and Biotechnology. (2010) 48, no. 4, 413–434. [Google Scholar]
  • 2. Hughes D. B. and Hoover D. G., Bifidobacteria: Their Potential for Use in American Dairy Products, Food Technology. (1991) 45, no. 4, 74–83. [Google Scholar]
  • 3. Ishibashi N. and Shimamura S., Bifidobacteria: Research and Development in Japan, Food Technology. (1993) 47, no. 6, 126–136. [Google Scholar]
  • 4. O′sullivan M., Thornton G., O′sullivan G. C., and Collins J. K., Probiotic Bacteria: Myth or Reality?, Trends in Food Science & Technology. (1992) 3, 309–314, 10.1016/S0924-2244(10)80018-4. [DOI] [Google Scholar]
  • 5. Suvarna V. C. and Boby V. U., Probiotics in Human Health: A Current Assessment, Current Science. (2005) 88, no. 11, 1744–1748. [Google Scholar]
  • 6. Ho P. H., Pham T. A., Truong Q. P., Nguyen L. H., Nguyen T. T., Dam H. T., Nguyen C. N., Nguyen H. A., Phi Q. T., Nguyen H. A., and Chu-Ky S., Isolation, Identification and Characterization of Beneficial Microorganisms From Traditional Fermented Foods, Probiotics, Prebiotics and Synbiotics, 2022, John Wiley & Sons, Ltd, 14–56, 10.1002/9781119702160.ch2. [DOI] [Google Scholar]
  • 7. Al-Habsi N., Al-Khalili M., Haque S. A., Elias M., Olqi N. A., and Al Uraimi T., Health Benefits of Prebiotics, Probiotics, Synbiotics, and Postbiotics, Nutrients. (2024) 16, no. 22, 10.3390/nu16223955, 39599742. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. Singh K., Mariki A. F., Singh P. A., Arora S., and Bajwa N., Dua K., Introduction to Synbiotics, Synbiotics in Human Health: Biology to Drug Delivery, 2024, Springer Nature Singapore, 3–23, 10.1007/978-981-99-5575-6_1. [DOI] [Google Scholar]
  • 9. Rehman M. A. U., Azeem M., Saeed K., and Javed S., The Role of Probiotics and Prebiotics in Modulating Human Gut Health and Immunity, Nutritional Foundations of Holistic Health, 2025, CABI International & Unique Scientific Publisher, 185–191, 10.47278/book.HH/2025.292. [DOI] [Google Scholar]
  • 10. Bargheet A., Bø G. H., Hetland M. A. K., Justine M., Moyo S. J., Löhr I. H., Blomberg B., Langeland N., Klingenberg C., and Pettersen V. K., Metabolic Reprogramming of the Infant Gut by Bifidobacteria-Based Probiotics Drives Exclusion of Antibiotic-Resistant Pathobionts, Cell Reports Medicine. (2026) 7, no. 5, 102752, 10.1016/j.xcrm.2026.102752, 42013844. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11. Awaluddin D. P., Rahardja D. P., and Mujnisa A., The Effects of Prebiotic, Probiotic and Synbiotic Supplementation on the Performance, Small Intestinal Morphometry, and Carcass Traits of Broiler Chicken, Journal of Global Innovations in Agricultural and Social Sciences. (2025) 13, no. 2, 485–493, 10.22194/JGIAS/25.1553. [DOI] [Google Scholar]
  • 12. Fioramonti J., Theodorou V., and Bueno L., Probiotics: What Are They? What are Their Effects on Gut Physiology?, Best Practice & Research Clinical Gastroenterology. (2003) 17, no. 5, 711–724, 10.1016/S1521-6918(03)00075-1. [DOI] [PubMed] [Google Scholar]
  • 13. Corcionivoschi N., Stef L., Ioan P., Julean C., Drinceanu D., Popa M., Sarafis G., Pham K. G., Gundogdu O., Dorrell N., and Wren B., Probiotics-Identification and Ways of Action, Innovative Romanian Food Biotechnology. (2010) 6, 1–11. [Google Scholar]
  • 14. Didari T., Solki S., Mozaffari S., Nikfar S., and Abdollahi M., A Systematic Review of the Safety of Probiotics, Expert Opinion on Drug Safety. (2014) 13, no. 2, 227–239, 10.1517/14740338.2014.872627. [DOI] [PubMed] [Google Scholar]
  • 15. Reuter G. J. Z. B. H. I. O., Das Vorkommen von Laktobazillen in Lebensmitteln und ihr Verhalten im menschlichen Intestinaltrakt, Zentralblatt fur Bakteriologie, Parasitenkunde, Infektionskrankheiten und Hygiene. Erste Abteilung Originale. (1965) 197, no. 4, 468–487. [Google Scholar]
  • 16. Goyal M., Bansal M., Yadav S., and Malhotra K., Probiotics: The Friendly Microbes, Indian Journal of Clinical Practice. (2012) 23, no. 3, 126–130. [Google Scholar]
  • 17. Wang J., Tang H., Zhang C., Zhao Y., Derrien M., Rocher E., van-Hylckama Vlieg J. E. T., Strissel K., Zhao L., Obin M., and Shen J., Modulation of Gut Microbiota During Probiotic-Mediated Attenuation of Metabolic Syndrome in High Fat Diet-Fed Mice, ISME Journal. (2015) 9, no. 1, 1–15, 10.1038/ismej.2014.99. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18. Pedretti S. J. N., Probiotic Market: Up or Down, Food Technology. (2013) 12, no. 1. [Google Scholar]
  • 19. Pettersen V. K., Ponsero A. J., Jian C., Riumin A., Kurilshikov A., Moyo S. J., Justine M., Klingenberg C., Debelius J., Valles-Colomer M., Noordzij H. T., Zhernakova A., Korpela K., Esteban-Torres M., and Brusselaers N., Off to a Good Start: Current Gaps and Priorities in Early-Life Microbiome Research, FEMS Microbiology Reviews. (2026) 50, no. 2, 1–19, 10.1093/femsre/fuag010, 41802201. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20. Bodke H. and Jogdand S., Role of Probiotics in Human Health, Cureus. (2022) 14, no. 11, e31313, 10.7759/cureus.31313, 36514580. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21. Ding S., Yan W., Ma Y., and Fang J., The Impact of Probiotics on Gut Health via Alternation of Immune Status of Monogastric Animals, Animal Nutrition. (2021) 7, no. 1, 24–30, 10.1016/j.aninu.2020.11.004, 33997328. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22. Thakur A., Sharma P., Sharma A. J., Sharma N., Singh S., Chamoli N., and Kumar R., Probiotics: Microbes for Human Health and Beyond, Food Materials Research. (2025) 5, no. 1, 1–11, 10.48130/fmr-0024-0029. [DOI] [Google Scholar]
  • 23. Alonzo N. A. N., Badua A. T., and Martin E. A., Combined Use of Alpha Monolaurin and Probiotics an Alternative to Antibiotic Growth Promoter in Broilers, Journal of Global Innovations in Agricultural Sciences. (2025) 13, no. 4, 11–16, 10.22194/JGIAS/26.1855. [DOI] [Google Scholar]
  • 24. Saarela M., Mogensen G., Fondén R., Mättö J., and Mattila-Sandholm T., Probiotic Bacteria: Safety, Functional and Technological Properties, Functional and Technological Properties. (2000) 84, no. 3, 197–215, 10.1016/S0168-1656(00)00375-8. [DOI] [PubMed] [Google Scholar]
  • 25. Mattila-Sandholm T., Myllärinen P., Crittenden R., Mogensen G., Fondén R., and Saarela M., Technological Challenges for Future Probiotic Foods, International Dairy Journal. (2002) 12, no. 2-3, 173–182, 10.1016/S0958-6946(01)00099-1. [DOI] [Google Scholar]
  • 26. Millette M., Luquet F. M., Ruiz M. T., and Lacroix M., Characterization of Probiotic Properties of Lactobacillus Strains, Dairy Science & Technology. (2008) 88, no. 6, 695–705, 10.1051/dst:2008018. [DOI] [Google Scholar]
  • 27. Lee Y.-K., Lee Y.-K. and Salminen S., Selection and Maintenance of Probiotic Microorganisms, Handbook of Probiotics and Prebiotics, 2008, 2nd edition, John Wiley & Sons, Inc, 177–187, 10.1002/9780470432624.ch2. [DOI] [Google Scholar]
  • 28. Marteau P., Gerhardt M. F., Myara A., Bouvier E., Trivin F., and Rambaud J. C., Metabolism of Bile Salts by Alimentary Bacteria During Transit in the Human Small Intestine, Microbial Ecology in Health and Disease. (1995) 8, no. 4, 151–157, 10.3109/08910609509140093. [DOI] [Google Scholar]
  • 29. Markowiak P. and Śliżewska K. J. N., Effects of Probiotics, Prebiotics, and Synbiotics on Human Health, Nutrients. (2017) 9, no. 9, 10.3390/nu9091021. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30. Joint FAO/WHO Working Group, Guidelines for the Evaluation of Probiotics in Food: Report of a Joint FAO/WHO Working Group on Drafting Guidelines for the Evaluation of Probiotics in Food, 2002, Food and Agriculture Organization of the United Nations & World Health Organization. [Google Scholar]
  • 31. Guarner F. and Schaafsma G. J., Probiotics, International Journal of Food Microbiology. (1998) 39, no. 3, 237–238, 10.1016/S0168-1605(97)00136-0. [DOI] [PubMed] [Google Scholar]
  • 32. Dunne C., O’Mahony L., Murphy L., Thornton G., Morrissey D., O’Halloran S., Feeney M., Flynn S., Fitzgerald G., Daly C., Kiely B., O’Sullivan G. C., Shanahan F., and Collins J. K., In Vitro Selection Criteria for Probiotic Bacteria of Human Origin: Correlation With In Vivo Findings, American Journal of Clinical Nutrition. (2001) 73, no. 2, 386s–392s, 10.1093/ajcn/73.2.386s. [DOI] [PubMed] [Google Scholar]
  • 33. Hyronimus B., le Marrec C., Hadj Sassi A., and Deschamps A., Acid and Bile Tolerance of Spore-Forming Lactic Acid Bacteria, International Journal of Food Microbiology. (2000) 61, no. 2-3, 193–197, 10.1016/S0168-1605(00)00366-4. [DOI] [PubMed] [Google Scholar]
  • 34. Casula G. and Cutting S. M., BacillusProbiotics: Spore Germination in the Gastrointestinal Tract, Applied and Environmental Microbiology. (2002) 68, no. 5, 2344–2352, 10.1128/AEM.68.5.2344-2352.2002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35. Conway P., Gorbach S., and Goldin B., Survival of Lactic Acid Bacteria in the Human Stomach and Adhesion to Intestinal Cells, Journal of Dairy Science. (1987) 70, no. 1, 1–12, 10.3168/jds.S0022-0302(87)79974-3. [DOI] [PubMed] [Google Scholar]
  • 36. Erkkilä S. and Petäjä E., Screening of Commercial Meat Starter Cultures at Low pH and in the Presence of Bile Salts for Potential Probiotic Use, Meat Science. (2000) 55, no. 3, 297–300, 10.1016/S0309-1740(99)00156-4. [DOI] [PubMed] [Google Scholar]
  • 37. Gotcheva V., Hristozova E., Hristozova T., Guo M., Roshkova Z., and Angelov A., Assessment of Potential Probiotic Properties of Lactic Acid Bacteria and Yeast Strains, Food Biotechnology. (2002) 16, no. 3, 211–225, 10.1081/FBT-120016668. [DOI] [Google Scholar]
  • 38. Syal P. and Vohra A., Probiotic Potential of Yeasts Isolated From Traditional Indian Fermented Foods, International Journal of Microbiology Research. (2013) 5, no. 2, 390–398, 10.9735/0975-5276.5.2.390-398. [DOI] [Google Scholar]
  • 39. Compaoré C. S., Nielsen D. S., Sawadogo-Lingani H., Berner T. S., Nielsen K. F., Diawara B., and Jakobsen M., Resistance to Antimicrobials and Acid and Bile Tolerance of Bacillus spp Isolated From Bikalga, fermented seeds of Hibiscus sabdariffa, African Journal of Food Science. (2013) 7, no. 11, 408–414, 10.5897/AJFS2013.1018. [DOI] [Google Scholar]
  • 40. Hoseinifar S. H., Ringø E., Masoumi M., and Harikrishnan R., Ringø E. and Sarkar S. K., Feed Additives, Gut Microbiota, and Health in Finfish Aquaculture, Gut Microbiota and Health in Aquaculture, 2019, Springer, Cham, 121–142, 10.1007/978-3-030-16190-3_5. [DOI] [Google Scholar]
  • 41. Succi M., Tremonte P., Reale A., Sorrentino E., Grazia L., Pacifico S., and Coppola R., Bile Salt and Acid Tolerance of Lactobacillus rhamnosus Strains Isolated From Parmigiano Reggiano Cheese, FEMS Microbiology Letters. (2005) 244, no. 1, 129–137, 10.1016/j.femsle.2005.01.037. [DOI] [PubMed] [Google Scholar]
  • 42. Gibson G. R. and Roberfroid M. B., Dietary Modulation of the Human Colonic Microbiota: Introducing the Concept of Prebiotics, Journal of Nutrition. (1995) 125, no. 6, 1401–1412, 10.1093/jn/125.6.1401. [DOI] [PubMed] [Google Scholar]
  • 43. Mathara J. M., Schillinger U., Guigas C., Franz C., Kutima P. M., Mbugua S. K., Shin H. K., and Holzapfel W. H., Functional Characteristics of Lactobacillus spp. From Traditional Maasai Fermented Milk Products in Kenya, International Journal of Food Microbiology. (2008) 126, no. 1-2, 57–64, 10.1016/j.ijfoodmicro.2008.04.027. [DOI] [PubMed] [Google Scholar]
  • 44. Victor S. D., Zambou N. F., Kaktcham P. M., Cresci A., and Fonteh F., Probiotic Properties of Lactobacilli Strains Isolated From Raw Cow Milk in the Western Highlands of Cameroon, Innovative Romanian Food Biotechnology. (2011) no. 9, 12–28, http://www.gup.ugal.ro/ugaljournals/index.php/IFRB/article/view/3374. [Google Scholar]
  • 45. Jampaphaeng K., Passorn S., and Keeratipibul S., Bacterial Population Diversity in Sataw-Dong, a Traditional Fermented Stink Bean, Songklanakarin Journal of Science and Technology. (2019) 41, no. 2, 285–291. [Google Scholar]
  • 46. Leite A. M., Miguel M. A. L., Peixoto R. S., Ruas-Madiedo P., Paschoalin V. M. F., Mayo B., and Delgado S., Probiotic Potential of Selected Lactic Acid Bacteria Strains Isolated From Brazilian Kefir Grains, Journal of Dairy Science. (2015) 98, no. 6, 3622–3632, 10.3168/jds.2014-9265. [DOI] [PubMed] [Google Scholar]
  • 47. Chelule P., Mokoena M. P., and Gqaleni N., Mendez-Vilas A., Advantages of Traditional Lactic Acid Bacteria Fermentation of Food in Africa, Current Research, Technology and Education Topics in Applied Microbiology and Microbial Biotechnology, 2010, 2, Formatex Research Center, 1160–1167. [Google Scholar]
  • 48. Ouwehand A. C. J. L. A. B., Salminen S. and Wright A., Antimicrobial Components From Lactic Acid Bacteria, Lactic Acid Bacteria: Microbiology and Functional Aspects, 1998, 2nd edition, Marcel Dekker, 139–159. [Google Scholar]
  • 49. Yang J.-M. and Moon G. S., Isolation of a Lactococcus lactis Strain Producing Anti-Staphylococcal Bacteriocin, Korean Journal for Food Science of Animal Resources. (2018) 38, no. 6, 1315–1321, 10.5851/kosfa.2018.e67. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50. Gänzle M. G. and Salovaara H. J., Salminen S., Ouwehand A., Lahtinen S., and Wright A., Lactic Acid Bacteria in Rye Sourdough Fermentation, Lactic Acid Bacteria: Microbiological and Functional Aspects, 2019, 5th edition, CRC Press, 199–214. [Google Scholar]
  • 51. Cleveland J., Montville T. J., Nes I. F., and Chikindas M. L., Bacteriocins: Safe, Natural Antimicrobials for Food Preservation, International Journal of Food Microbiology. (2001) 71, no. 1, 1–20, 10.1016/S0168-1605(01)00560-8. [DOI] [PubMed] [Google Scholar]
  • 52. Dash S. J. I. J. S. B., Selection Criteria for Probiotics, International Journal of Systematic Bacteriology. (1980) 30, 225–420. [Google Scholar]
  • 53. Mishra V. and Prasad D. J. I. D., Probiotics and Their Potential Health Benefits, Indian Dairyman. (2000) 52, no. 4, 7–14. [Google Scholar]
  • 54. Wouters J. T., Ayad E. H. E., Hugenholtz J., and Smit G., Microbes From Raw Milk for Fermented Dairy Products, International Dairy Journal. (2002) 12, no. 2-3, 91–109, 10.1016/S0958-6946(01)00151-0. [DOI] [Google Scholar]
  • 55. Delves-Broughton J., Nisin and Its Application as a Food Preservative, Journal of the Society of Dairy Technology. (1990) 43, no. 3, 73–76, 10.1111/j.1471-0307.1990.tb02449.x. [DOI] [Google Scholar]
  • 56. Austin D. J., Kristinsson K. G., and Anderson R. M., The Relationship Between the Volume of Antimicrobial Consumption in Human Communities and the Frequency of Resistance, Proceedings of the National Academy of Sciences. (1999) 96, no. 3, 1152–1156, 10.1073/pnas.96.3.1152, 9927709. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57. Robredo B., Singh K. V., Baquero F., Murray B. E., and Torres C., Vancomycin-Resistant Enterococci Isolated From Animals and Food, International Journal of Food Microbiology. (2000) 54, no. 3, 197–204, 10.1016/S0168-1605(99)00195-6. [DOI] [PubMed] [Google Scholar]
  • 58. EFSA Panel on Additives and Products or Substances used in Animal Feed (FEEDAP, Guidance on the Assessment of Bacterial Susceptibility to Antimicrobials of Human and Veterinary Importance, EFSA Journal. (2012) 10, no. 6, 10.2903/j.efsa.2012.2740. [DOI] [Google Scholar]
  • 59. Abriouel H., Knapp C. W., Gálvez A., and Benomar N., Antibiotic Resistance Profile of Microbes From Traditional Fermented Foods, Fermented Foods in Health and Disease Prevention, 2017, Elsevier, 675–704, 10.1016/B978-0-12-802309-9.00029-7. [DOI] [Google Scholar]
  • 60. Charteris, Morelli, and Collins, Antibiotic Susceptibility of Potentially Probiotic Bifidobacterium Isolates From the Human Gastrointestinal Tract, Letters in Applied Microbiology. (1998) 26, no. 5, 333–337, 10.1046/j.1472-765X.1998.00342.x. [DOI] [PubMed] [Google Scholar]
  • 61. Nicas T., Cole C. T., Preston D. A., Schabel A. A., and Nagarajan R., Activity of Glycopeptides Against Vancomycin-Resistant Gram-Positive Bacteria, Antimicrobial Agents and Chemotherapy. (1989) 33, no. 9, 1477–1481, 10.1128/AAC.33.9.1477. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62. Swenson J., Facklam R. R., and Thornsberry C., Antimicrobial Susceptibility of Vancomycin-Resistant Leuconostoc, Pediococcus, and Lactobacillus species, Antimicrobial Agents and Chemotherapy. (1990) 34, no. 4, 543–549, 10.1128/AAC.34.4.543. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 63. Tynkkynen S., Singh K. V., and Varmanen P., Vancomycin Resistance Factor of Lactobacillus rhamnosus GG in Relation to Enterococcal Vancomycin Resistance (van) Genes, International journal of food microbiology. (1998) 41, no. 3, 195–204, 10.1016/S0168-1605(98)00051-8. [DOI] [PubMed] [Google Scholar]
  • 64. Miller L. G. and Finegold S. M., Antibacterial Sensitivity of Bifidobacterium (Lactobacillus bifidus) , Journal of Bacteriology. (1967) 93, no. 1, 125–130, 10.1128/jb.93.1.125-130.1967, 6020399. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 65. Friend B. A. and Shahani K. M., Antitumor Properties of Lactobacilli and Dairy Products Fermented by Lactobacilli, Journal of Food Protection. (1984) 47, no. 9, 717–723, 10.4315/0362-028X-47.9.717. [DOI] [PubMed] [Google Scholar]
  • 66. Ng S., Hart A. L., Kamm M. A., Stagg A. J., and Knight S. C., Mechanisms of Action of Probiotics: Recent Advances, Inflammatory Bowel Diseases. (2009) 15, no. 2, 300–310, 10.1002/ibd.20602. [DOI] [PubMed] [Google Scholar]
  • 67. Sanni A. I., Onilude A., Ogunbanwo S., Fadahunsi I., and Afolabi R., Production of Exopolysaccharides by Lactic Acid Bacteria Isolated From Traditional Fermented Foods in Nigeria, European Food Research and Technology. (2002) 214, no. 5, 405–407, 10.1007/s00217-002-0499-9. [DOI] [Google Scholar]
  • 68. Gassem M., Schmidt K., and Frank J. F., Exopolysaccharide Production From Whey Lactose by Fermentation With Lactobacillus delbrueckii ssp. bulgaricus , Journal of Food Science. (1997) 62, no. 1, 171–173, 10.1111/j.1365-2621.1997.tb04393.x. [DOI] [Google Scholar]
  • 69. Ruas-Madiedo P. and De Los Reyes-Gavilán C. G., Invited Review: Methods for the Screening, Isolation, and Characterization of Exopolysaccharides Produced by Lactic Acid Bacteria, Journal of Dairy Science. (2005) 88, no. 3, 843–856, 10.3168/jds.S0022-0302(05)72750-8. [DOI] [PubMed] [Google Scholar]
  • 70. Behare P. V., Mohanty B., Pal P. K., and Mandal S., Exopolysaccharides of Lactic Acid Bacteria: A Review, Journal of Food Science and Technology. (2009) 46, no. 1, 1–11. [Google Scholar]
  • 71. Tuomola E. M. and Salminen S. J., Adhesion of Some Probiotic and Dairy Lactobacillus Strains to Caco-2 Cell Cultures, International Journal of Food Microbiology. (1998) 41, no. 1, 45–51, 10.1016/S0168-1605(98)00033-6. [DOI] [PubMed] [Google Scholar]
  • 72. Bernet M.-F., Brassart D., Neeser J. R., and Servin A. L., Adhesion of Human Bifidobacterial Strains to Cultured Human Intestinal Epithelial Cells and Inhibition of Enteropathogen-Cell Interactions, Applied and Environmental Microbiology. (1993) 59, no. 12, 4121–4128, 10.1128/aem.59.12.4121-4128.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 73. Coconnier M. H., Bernet M. F., Chauviere G., and Servin A., Adhering Heat-Killed Human Lactobacillus Acidophilus, Strain LB, Inhibits the Process of Pathogenicity of Diarrhoeagenic Bacteria in Cultured Human Intestinal Cells, Journal of Diarrhoeal Diseases Research. (1993) 11, no. 4, 235–242, 8188996. [PubMed] [Google Scholar]
  • 74. El-Jeni R., El Bour M., Calo-Mata P., Böhme K., Fernández-No I. C., Barros-Velázquez J., and Bouhaouala-Zahar B., In Vitro Probiotic Profiling of Novel Enterococcus faecium and Leuconostoc mesenteroides From Tunisian Freshwater Fishes, Canadian Journal of Microbiology. (2016) 62, no. 1, 60–71, 10.1139/cjm-2015-0481. [DOI] [PubMed] [Google Scholar]
  • 75. Paramithiotis S., Melissari I., and Drosinos E. H., In Vitro Assessment of Properties Associated With the Survival Through the Gastro-Intestinal Tract of Staphylococci Isolated from Traditional Sausage Fermentation, Food Microbiology. (2006) 23, no. 7, 663–671, 10.1016/j.fm.2005.11.003. [DOI] [PubMed] [Google Scholar]
  • 76. Giaouris E., Chorianopoulos N., and Nychas G. J., Effect of Temperature, pH, and Water Activity on Biofilm Formation by Salmonella enterica Enteritidis PT4 on Stainless Steel Surfaces as Indicated by the Bead Vortexing Method and Conductance Measurements, Journal of Food Protection. (2005) 68, no. 10, 2149–2154, 10.4315/0362-028X-68.10.2149. [DOI] [PubMed] [Google Scholar]
  • 77. Nurmi E., Nuotio L., and Schneitz C., The Competitive Exclusion Concept: Development and Future, International Journal of Food Microbiology. (1992) 15, no. 3-4, 237–240, 10.1016/0168-1605(92)90054-7. [DOI] [PubMed] [Google Scholar]
  • 78. Bidura I. G. N. G., Wibawa A. A., Bulkaini S. N. W., and Puspani E., The Impact of Inclusion of Fermented Feed With Probiotic Yeast on Performance, Intestinal Histology and Intestinal Microbiota of Broilers, Journal of Poultry Science. (2026) 63, no. 2, 112–121. [Google Scholar]
  • 79. Ospanov A., Velyamov S., Tlevlessova D., Schetinina E., Kairbayeva A., Makeeva R., and Tastanova R., Survival of Lactic Acid Bacteria When Using the Developed Yogurt From the Milk of Small Cattle Under In-Vitro Conditions, Food Science and Technology. (2023) 43, e117722, 10.1590/fst.117722. [DOI] [Google Scholar]
  • 80. Horie M., Ohno T., Iwahashi H., Umemura M., and Murotomi K., Associations Between Intestinal Lactic Acid Bacteria Species and Feeding Habits of Zoo Animals, Microbiome Research Reports. (2024) 3, no. 3, 10.20517/mrr.2024.08, 39421257. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 81. Oelschlaeger T. A., Mechanisms of Probiotic actions – A Review, International Journal of Medical Microbiology. (2010) 300, no. 1, 57–62, 10.1016/j.ijmm.2009.08.005. [DOI] [PubMed] [Google Scholar]
  • 82. Chen X., Li Q., Xie J., and Nie S., Immunomodulatory Effects of Probiotic-Derived Extracellular Vesicles: Opportunities and Challenges, Journal of Agricultural and Food Chemistry. (2024) 72, no. 35, 19259–19273, 10.1021/acs.jafc.4c04223, 39177683. [DOI] [PubMed] [Google Scholar]
  • 83. Zhao Y., Liu S., Tang Y., You T., and Xu H., Lactobacillus rhamnosusGG Ameliorated Long-Term Exposure to TiO2Nanoparticles Induced Microbiota-Mediated Liver and Colon Inflammation and Fructose-Caused Metabolic Abnormality in Metabolism Syndrome Mice, Journal of Agricultural and Food Chemistry. (2021) 69, no. 34, 9788–9799, 10.1021/acs.jafc.1c03301, 34382390. [DOI] [PubMed] [Google Scholar]
  • 84. Zhang T., Zhang W., Feng C., Kwok L. Y., He Q., and Sun Z., Stronger Gut Microbiome Modulatory Effects by Postbiotics Than Probiotics in a Mouse Colitis Model, NPJ Science of Food. (2022) 6, no. 1, 10.1038/s41538-022-00169-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 85. Zhang Z.-Y., Liu C., Zhu Y. Z., Wei Y. X., Tian F., Zhao G. P., and Guo X. K., Safety Assessment of Lactobacillus plantarum JDM1 Based on the Complete Genome, Journal of Food Microbiology. (2012) 153, no. 1-2, 166–170, 10.1016/j.ijfoodmicro.2011.11.003. [DOI] [PubMed] [Google Scholar]
  • 86. Chiron C., Tompkins T. A., and Burguière P., Flow Cytometry: A Versatile Technology for Specific Quantification and Viability Assessment of Micro-Organisms in Multistrain Probiotic Products, Journal of Applied Microbiology. (2018) 124, no. 2, 572–584, 10.1111/jam.13666. [DOI] [PubMed] [Google Scholar]
  • 87. Lahtinen S., Ahokoski H., Reinikainen J. P., Gueimonde M., Nurmi J., Ouwehand A. C., and Salminen S. J., Degradation of 16S rRNA and Attributes of Viability of Viable but Nonculturable Probiotic Bacteria, Letters in Applied Microbiology. (2008) 46, no. 6, 693–698, 10.1111/j.1472-765X.2008.02374.x. [DOI] [PubMed] [Google Scholar]
  • 88. Kramer M., Obermajer N., Bogovič Matijašić B., Rogelj I., and Kmetec V., Quantification of Live and Dead Probiotic Bacteria in Lyophilised Product by Real-Time PCR and by Flow Cytometry, Applied Microbiology and Biotechnology. (2009) 84, no. 6, 1137–1147, 10.1007/s00253-009-2068-7. [DOI] [PubMed] [Google Scholar]
  • 89. Nocker A., Cheung C.-Y., and Camper A. K., Comparison of Propidium Monoazide With Ethidium Monoazide for Differentiation of Live vs. Dead Bacteria by Selective Removal of DNA From Dead Cells, Journal of Microbiological Methods. (2006) 67, no. 2, 310–320, 10.1016/j.mimet.2006.04.015. [DOI] [PubMed] [Google Scholar]
  • 90. Hussain T., Probiotics and Controversies, Journal of Microbiology and Antimicrobials. (2013) 5, no. 9, 96–105, 10.5897/JMA2013.0279. [DOI] [Google Scholar]
  • 91. Endex E., Health-Benefits-of-Probiotics, Journal of Bacteriology and Infectious Diseases. (2018) 2, no. 1, 1–15. [Google Scholar]
  • 92. Jankovic I., Sybesma W., Phothirath P., Ananta E., and Mercenier A., Application of Probiotics in Food Products—Challenges and New Approaches, Current Opinion in Biotechnology. (2010) 21, no. 2, 175–181, 10.1016/j.copbio.2010.03.009. [DOI] [PubMed] [Google Scholar]
  • 93. Rijkers G. T., Bengmark S., Enck P., Haller D., Herz U., Kalliomaki M., Kudo S., Lenoir-Wijnkoop I., Mercenier A., Myllyluoma E., Rabot S., Rafter J., Szajewska H., Watzl B., Wells J., Wolvers D., and Antoine J. M., Guidance for Substantiating the Evidence for Beneficial Effects of Probiotics: Current Status and Recommendations for Future Research, Journal of Nutrition. (2010) 140, no. 3, 671S–676S, 10.3945/jn.109.113779. [DOI] [PubMed] [Google Scholar]
  • 94. Goldin B. R., Health Benefits of Probiotics, British Journal of Nutrition. (1998) 80, no. S2, S203–S207, 10.1017/S0007114500006036. [DOI] [PubMed] [Google Scholar]
  • 95. Sionek B., Szydłowska A., Jaworska D., and Kołożyn-Krajewska D., Benefits of Probiotics—Biodetoxification, Applied Sciences. (2025) 15, no. 10, 10.3390/app15105297. [DOI] [Google Scholar]
  • 96. Gill H. S., Rutherfurd K. J., Prasad J., and Gopal P. K., Enhancement of Natural and Acquired Immunity by Lactobacillus rhamnosus (HN001), Lactobacillus acidophilus (HN017) and Bifidobacterium lactis (HN019), British Journal of Nutrition. (2000) 83, no. 2, 167–176, 10.1017/S0007114500000210, 10743496. [DOI] [PubMed] [Google Scholar]
  • 97. Arunachalam K., Gill H., and Chandra R., Enhancement of Natural Immunity Function by Dietary Consumption of Bifidobacterium lactis HN019, European Journal of Clinical Nutrition. (2000) 54, no. 3, 263–267. [DOI] [PubMed] [Google Scholar]
  • 98. Gill H., Rutherfurd K., and Cross M., Dietary Probiotic Supplementation Enhances Natural Killer Cell Activity in the Elderly: An Investigation of Age-Related Immunological Changes, Journal of Clinical Immunology. (2001) 21, 264–271. [DOI] [PubMed] [Google Scholar]
  • 99. Sheih Y.-H., Chiang B. L., Wang L. H., Liao C. K., and Gill H. S., Systemic Immunity-Enhancing Effects in Healthy Subjects Following Dietary Consumption of the Lactic Acid Bacterium Lactobacillus rhamnosus HN001, Journal of the American College of Nutrition. (2001) 20, no. 2, 149–156, 10.1080/07315724.2001.10719027. [DOI] [PubMed] [Google Scholar]
  • 100. O′toole P. W., Marchesi J. R., and Hill C., Next-Generation Probiotics: The Spectrum From Probiotics to Live Biotherapeutics, Nature Microbiology. (2017) 2, no. 5, 17057, 10.1038/nmicrobiol.2017.57. [DOI] [PubMed] [Google Scholar]
  • 101. Hill C., Guarner F., Reid G., Gibson G. R., Merenstein D. J., Pot B., Morelli L., Canani R. B., Flint H. J., Salminen S., Calder P. C., and Sanders M. E., The International Scientific Association for Probiotics and Prebiotics Consensus Statement on the Scope and Appropriate Use of the Term Probiotic, Nature Reviews Gastroenterology & Hepatology. (2014) 11, no. 8, 506–514, 10.1038/nrgastro.2014.66, 24912386. [DOI] [PubMed] [Google Scholar]
  • 102. McFarland L. V., Probiotics for the Primary and Secondary Prevention of C. difficile Infections: A Meta-Analysis and Systematic Review, Antibiotics. (2015) 4, no. 2, 160–178, 10.3390/antibiotics4020160, 27025619. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 103. Ahmed M., Henson D. A., Sanderson M. C., Nieman D. C., Zubeldia J. M., and Shanely R. A., Rhodiola rosea Exerts Antiviral Activity in Athletes Following a Competitive Marathon Race, Frontiers in Nutrition. (2015) 2, 10.3389/fnut.2015.00024. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 104. Goldenberg J. Z., Lytvyn L., Steurich J., Parkin P., Mahant S., Johnston B. C., and Cochrane IBD Group, Probiotics for the Prevention of Pediatric Antibiotic-Associated Diarrhea, Cochrane Database of Systematic Reviews. (2015) no. 12, CD004827, 10.1002/14651858.CD004827.pub4. [DOI] [PubMed] [Google Scholar]
  • 105. Mo R., Zhang X., and Yang Y., Effect of Probiotics on Lipid Profiles in Hypercholesterolaemic Adults: A Meta-Analysis of Randomized Controlled Trials, Medicina Clínica (English Edition). (2019) 152, no. 12, 473–481, 10.1016/j.medcle.2018.09.013. [DOI] [PubMed] [Google Scholar]
  • 106. Petrof E. O., Probiotics and Gastrointestinal Disease: Clinical Evidence and Basic Science, Anti-Inflammatory & Anti-Allergy Agents in Medicinal Chemistryrrent Medicinal Chemistry-Anti-Inflammatory and Anti-Allergy. (2009) 8, no. 3, 260–269, 10.2174/187152309789151977, 20890386. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 107. Ohland C. L. and Mac Naughton W. K., Probiotic bacteria and intestinal Epithelial Barrier Function, American Journal of Physiology-Gastrointestinal and Liver Physiology. (2010) 298, no. 6, G807–G819, 10.1152/ajpgi.00243.2009. [DOI] [PubMed] [Google Scholar]
  • 108. Hooper L. V., Littman D. R., and Macpherson A. J., Interactions Between the Microbiota and the Immune System, Science. (2012) 336, no. 6086, 1268–1273, 10.1126/science.1223490, 22674334. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 109. Leser T. D. and Mølbak L., Better Living Through Microbial Action: The Benefits of the Mammalian Gastrointestinal Microbiota on the Host, Environmental Microbiology. (2009) 11, no. 9, 2194–2206, 10.1111/j.1462-2920.2009.01941.x, 19737302. [DOI] [PubMed] [Google Scholar]
  • 110. Cai D., Hao-Yu L., Dong H., and Ahmed A. A., Editorial: Integrated Role of Nutrition and Digestive Physiology for Animal Health, Volume II, Frontiers in Veterinary Science. (2022) 9, 1109703, 10.3389/fvets.2022.1109703. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 111. Le Barz M., Probiotics as Complementary Treatment for Metabolic Disorders, Diabetes & Metabolism Journal. (2015) 39, no. 4, 291–303, 10.4093/dmj.2015.39.4.291, 26301190. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 112. Gayathri D. and Rashmi B., Anti-Cancer Properties of Probiotics: A Natural Strategy for Cancer Prevention, EC Nutrition. (2016) 5, no. 4, 1191–1202. [Google Scholar]
  • 113. Kuugbee E. D., Shang X., Gamallat Y., Bamba D., Awadasseid A., Suliman M. A., Zang S., Ma Y., Chiwala G., Xin Y., and Shang D., Structural Change in Microbiota by a Probiotic Cocktail Enhances the Gut Barrier and Reduces Cancer via TLR2 Signaling in a Rat Model of Colon Cancer, Digestive Diseases and Sciences. (2016) 61, no. 10, 2908–2920, 10.1007/s10620-016-4238-7, 27384052. [DOI] [PubMed] [Google Scholar]
  • 114. Morsli D. S., Tbahriti H. F., Rahli F., Mahammi F. Z., Nagdalian A., Hemeg H. A., Imran M., Rauf A., and Shariati M. A., Probiotics in Colorectal Cancer Prevention and Therapy: Mechanisms, Benefits, and Challenges, Discover Oncology. (2025) 16, no. 1, 10.1007/s12672-025-01996-4, 40140210. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 115. Drago L., Probiotics and Colon Cancer, Microorganisms. (2019) 7, no. 3, 10.3390/microorganisms7030066. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 116. Saebi M., Barjasteh A. H., Mahmoudi M., Kheder R. K., Ramazanpour S., Ebadpour N., Fadaee A., and Esmaeili S. A., Probiotics Cancer Interaction, Prevention, and Therapy, Immunity, Inflammation and Disease. (2026) 14, no. 5, e70435, 10.1002/iid3.70435, 42136123. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 117. Kvakova M., Kamlarova A., Stofilova J., Benetinova V., and Bertkova I., Probiotics and Postbiotics in Colorectal Cancer: Prevention and Complementary Therapy, World Journal of Gastroenterology. (2022) 28, no. 27, 3370–3382, 10.3748/wjg.v28.i27.3370, 36158273. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 118. Johnson D., Letchumanan V., Thum C. C., Thurairajasingam S., and Lee L. H., A Microbial-Based Approach to Mental Health: The Potential of Probiotics in the Treatment of Depression, Nutrients. (2023) 15, no. 6, 10.3390/nu15061382, 36986112. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 119. Cheng L. H., Liu Y. W., Wu C. C., Wang S., and Tsai Y. C., Psychobiotics in Mental Health, Neurodegenerative and Neurodevelopmental Disorders, Journal of Food and Drug Analysis. (2019) 27, no. 3, 632–648, 10.1016/j.jfda.2019.01.002, 31324280. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 120. Chambilo B., Dhiver T., Sahu K., and Parashar R., Gut Microbiota Modulation With Probiotics: Potential Therapeutic Avenues for Alzheimer′s and Parkinson′s Diseases, Neurological Sciences and Neurophysiology. (2025) 42, no. 3, 75–83, 10.4103/nsn.nsn_39_25. [DOI] [Google Scholar]
  • 121. Fan X., Wang X., Chao Y., and Xu E., Probiotic and Prebiotic Mechanisms in IBD-Associated Colorectal Carcinogenesis: Recent Advances, Frontiers in Nutrition. (2026) 12, 1693875, 10.3389/fnut.2025.1693875, 41635904. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 122. Song D., Wang X., Ma Y., Liu N. N., and Wang H., Beneficial Insights Into Postbiotics Against Colorectal Cancer, Frontiers in Nutrition. (2023) 10, 1111872, 10.3389/fnut.2023.1111872, 36969804. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 123. Jafari M., Alipour M., Zamani S., Mohtasham Amiri A., Pourabbas P., and Hasannejad-Bibalan M., Probiotics as a Complementary Medicine in Neurologic Disorders, Health Science Reports. (2025) 8, no. 11, e71422, 10.1002/hsr2.71422, 41163934. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 124. Matijašić B. B., Probiotics in Pregnancy and Lactation, Probiotics and Child Gastrointestinal Health, 2022, Elsevier, 239–260, 10.1016/B978-0-323-89908-600012-1. [DOI] [Google Scholar]
  • 125. Vadala B. S., Kumar P., and Dwivedi M. K., Probiotics in Mitigation of Food Allergies and Lactose Intolerance, Probiotics in the Prevention and Management of Human Diseases, 2022, Elsevier, 213–221, 10.1016/B978-0-12-823733-5.00022-2. [DOI] [Google Scholar]
  • 126. Aggarwal J., Swami G., and Kumar M., Probiotics and Their Effects on Metabolic Diseases: An Update, Journal of Clinical and Diagnostic Research. (2013) 7, no. 1, 173–177, 10.7860/JCDR/2012/5004.2701, 23449881. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 127. Sundaram S., Ponnambath D. K., and Nair S. S., Microbiota-Gut-Brain Axis in Neurological Disorders, Human Microbiome: Clinical Implications and Therapeutic Interventions, 2022, Springer, 147–167, 10.1007/978-981-16-7672-7_7. [DOI] [Google Scholar]
  • 128. Sun X., Xue L., Wang Z., and Xie A., Update to the Treatment of Parkinson′s Disease Based on the Gut-Brain Axis Mechanism, Frontiers in Neuroscience. (2022) 16, 878239, 10.3389/fnins.2022.878239, 35873830. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 129. Dahiya D. and Nigam P. S., Clinical Potential of Microbial Strains, Used in Fermentation for Probiotic Food, Beverages and in Synbiotic Supplements, as Psychobiotics for Cognitive Treatment Through Gut–Brain Signaling, Microorganisms. (2022) 10, no. 9, 10.3390/microorganisms10091687, 36144289. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 130. Bleibel L., Dziomba S., Waleron K. F., Kowalczyk E., and Karbownik M. S., Deciphering Psychobiotics′ Mechanism of Action: Bacterial Extracellular Vesicles in the Spotlight, Frontiers in Microbiology. (2023) 14, 1211447, 10.3389/fmicb.2023.1211447, 37396391. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 131. Ahmed H., Leyrolle Q., Koistinen V., Kärkkäinen O., Layé S., Delzenne N., and Hanhineva K., Microbiota-Derived Metabolites as Drivers of Gut–Brain Communication, Gut Microbes. (2022) 14, no. 1, 2102878, 10.1080/19490976.2022.2102878, 35903003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 132. Sowmiya S., Dhivya L. S., Harikrishnan N., and Ankul Singh S., Exploring the Potential of Probiotics in Alzheimer′s Disease and Gut Dysbiosis, IBRO Neuroscience Reports. (2024) 17, 441–455, 10.1016/j.ibneur.2024.11.004, 39629018. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 133. Bist P. and Choudhary S., Impact of Heavy Metal Toxicity on the Gut Microbiota and Its Relationship With Metabolites and Future Probiotics Strategy: A Review, Biological Trace Element Research. (2022) 200, no. 12, 5328–5350, 10.1007/s12011-021-03092-4, 34994948. [DOI] [PubMed] [Google Scholar]
  • 134. Pop O. L., Suharoschi R., and Gabbianelli R., Biodetoxification and Protective Properties of Probiotics, Microorganisms. (2022) 10, no. 7, 10.3390/microorganisms10071278, 35888997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 135. Kieliszek M., Waśko A., Michalak K., Kot A. M., Piwowarek K., and Winiarczyk S., Effect of Selenium and Methods of Protein Extraction on the Proteomic Profile of Saccharomyces Yeast, Open Life Sciences. (2022) 17, no. 1, 1117–1128, 10.1515/biol-2022-0496, 36133425. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 136. Conway E., An Investigation Into the Potential of Beta Glucans and Other Bioactives to Enhance Gastrointestinal Health, Performance and Product Quality in Pigs, 2022, University College Dublin, School of Agriculture and Food Science. [Google Scholar]
  • 137. Jan T., Negi R., Sharma B., Singh S., Kumar S., Rustagi S., Shreaz S., Rai A. K., Rai P. K., Sheikh M. A., and Kumar K., Probiotic Formulations for Human Health: Current Research and Future Perspective, Journal of Applied Biology and Biotechnology. (2024) 12, no. 4, 14–29, 10.7324/JABB.2024.167380. [DOI] [Google Scholar]
  • 138. El-Saadony M. T., Saad A. M., Sitohy M., Alkafaas S. S., Dladla M., Ghosh S., Mohammed D. M., Ibrahim E. H., Fahmy M. A., Elkelish A., and AbuQamar S. F., Probiotics and Human Health: Biological Activities, Nutritional Aspects, Immunomodulatory Properties, Applications, and Future Perspectives - A Comprehensive Review, Frontiers in Immunology. (2025) 16, 1713426, 10.3389/fimmu.2025.1713426. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 139. Maftei N.-M., Raileanu C. R., Balta A. A., Ambrose L., Boev M., Marin D. B., and Lisa E. L., The Potential Impact of Probiotics on Human Health: An Update on Their Health-Promoting Properties, Microorganisms. (2024) 12, no. 2, 10.3390/microorganisms12020234, 38399637. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 140. Jan T., Negi R., Sharma B., Kumar S., Singh S., Rai A. K., Shreaz S., Rustagi S., Chaudhary N., Kaur T., Kour D., Sheikh M. A., Kumar K., Yadav A. N., and Ahmed N., Next Generation Probiotics for Human Health: An Emerging Perspective, Heliyon. (2024) 10, no. 16, e35980, 10.1016/j.heliyon.2024.e35980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 141. Fakruddin M., Shishir M. A., Yousuf Z., and Khan M. S., Next-Generation Probiotics-The Future of Biotherapeutics, Microbial Bioactive. (2022) 5, 156–163. [Google Scholar]
  • 142. Amin M. R., Biswas A. P., Tasnim M., Islam M. N., and Azam M. S., Probiotics and Their Applications in Functional Foods: A Health Perspective, Applied Food Research. (2025) 5, no. 2, 101193, 10.1016/j.afres.2025.101193. [DOI] [Google Scholar]
  • 143. Tiwari A., Ika Krisnawati D., Susilowati E., Mutalik C., and Kuo T. R., Next-Generation Probiotics and Chronic Diseases: A Review of Current Research and Future Directions, Journal of Agricultural and Food Chemistry. (2024) 72, no. 50, 27679–27700, 10.1021/acs.jafc.4c08702, 39588716. [DOI] [PMC free article] [PubMed] [Google Scholar]

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Data Availability Statement

As this is a review paper, no additional data are available. Rather, the findings came from reviewing original research articles.


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