Submitted:
15 September 2025
Posted:
16 September 2025
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Abstract
The increasing prevalence of antimicrobial resistance (AMR) among foodborne pathogens has emerged as a critical global health concern, undermining the efficacy of conventional antimicrobial agents and threatening the safety and integrity of the food supply chain. In response, probiotics, prebiotics, and their combinations as synbiotics are increasingly recognised as sustainable, health-oriented strategies to mitigate AMR across the food chain. Probiotics—live microorganisms that, when administered in adequate amounts, confer health benefits to the host—contribute to AMR mitigation through multiple mechanisms, including competitive exclusion of resistant pathogens, production of antimicrobial metabolites (e.g., bacteriocins and organic acids), modulation of host immunity, and restoration of gut microbial balance. Prebiotics, defined as non-digestible food ingredients, selectively stimulate the growth and/or metabolic activity of beneficial bacteria such as Lactobacillus and Bifidobacterium spp., thereby reinforcing colonisation resistance. When combined as synbiotics, these agents may exert synergistic effects, enhancing microbial resilience, promoting gut health, and reducing the colonisation and persistence of AMR-related pathogens. The integration of these bio-based approaches into food systems—particularly in the development of fermented and functional foods—supports broader One Health objectives by reducing the need for antibiotics and contributing to global AMR containment efforts. This review summarises current scientific insights, explores practical applications, and outlines future perspectives on the role of probiotics, prebiotics, and synbiotics in combating AMR throughout the food chain.
Keywords:
1. Introduction
2. Materials and Methods
3. Antimicrobial Resistance and the Food Chain
3.1. Historical Context of Antibiotic Discovery and AMR Emergence
3.2. Drivers of AMR in Medicine and Animal Agriculture
3.3. Global Trends and One Health Challenges
4. Probiotics, Prebiotics and Synbiotics for Combating Antimicrobial Resistance in the Food Chain
4.1. Probiotics for Combating AMR in the Food Chain
4.1.1. Definition, Diversity, and Health Effects
4.1.2. Sustainable Strategies for Combating AMR
4.2. Prebiotics for Combating AMR in the Food Chain
4.2.1. Definition, Types, and Health Effects
4.2.2. Mechanisms of Prebiotic Action in AMR Mitigation
4.3. Synbiotics for Combating AMR in the Food Chain
4.3.1. Definition and Relevance in AMR Mitigation
5. Conclusions and Future Directions
Author Contributions
Funding
Data Availability Statement
Acknowledgments
Conflicts of Interest
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| Carnobacterium divergens | Lactobacillus johnsonii | Ligilactobacillus (formerly Lactobacillus) animalis |
| Companilactobacillus (formerly Lactobacillus) alimentarius | Lactobacillus kefiranofaciens | Ligilactobacillus (formerly Lactobacillus) aviarius |
| Companilactobacillus (formerly Lactobacillus) farciminis | Lactococcus lactis | Ligilactobacillus (formerly Lactobacillus) salivarius |
| Fructilactobacillus (formerly Lactobacillus) sanfranciscensis | Lapidilactobacillus (formerly Pediococcus) dextrinicus | Limosilactobacillus (formerly Lactobacillus) fermentum |
| Lacticaseibacillus (formerly Lactobacillus) casei | Latilactobacillus (formerly Lactobacillus) curvatus | Limosilactobacillus (formerly Lactobacillus) mucosae |
| Lacticaseibacillus (formerly Lactobacillus) paracasei | Latilactobacillus (formerly Lactobacillus) sakei | Limosilactobacillus (formerly Lactobacillus) panis |
| Lacticaseibacillus (formerly Lactobacillus) rhamnosus | Lentilactobacillus (formerly Lactobacillus) buchneri | Limosilactobacillus (formerly Lactobacillus) pontis |
| Lactiplantibacillus (formerly Lactobacillus) pentosus | Lentilactobacillus (formerly Lactobacillus) diolivorans | Limosilactobacillus (formerly Lactobacillus) reuteri |
| Lactiplantibacillus (formerly Lactobacillus) plantarum | Lentilactobacillus (formerly Lactobacillus) hilgardii | Loigolactobacillus (formerly Lactobacillus) coryniformis |
| Lactobacillus acidophilus | Lentilactobacillus (formerly Lactobacillus) kefiri | Oenococcus oeni |
| Lactobacillus amylolyticus | Lentilactobacillus (formerly Lactobacillus) parafarraginis | Pediococcus acidilactici |
| Lactobacillus amylovorus | Lentilactobacillus (formerly Lactobacillus) paraplantarum | Pediococcus parvulus |
| Lactobacillus crispatus | Leuconostoc citreum | Pediococcus pentosaceus |
| Lactobacillus delbrueckii | Leuconostoc lactis | Secundilactobacillus (formerly Lactobacillus) collinoides |
| Lactobacillus gallinarum | Leuconostoc mesenteroides | Streptococcus thermophilus |
| Lactobacillus gasseri | Leuconostoc pseudomesenteroides | |
| Lactobacillus helveticus | Levilactobacillus (formerly Lactobacillus) brevis |
|
Probiotic strains |
Target foodborne pathogens |
Reported effects | Mechanisms of action | References |
| L. rhamnosus GG | C. jejuni | Reduced adhesion and invasion |
Competitive exclusion, immunomodulation | [68] |
| L. plantarum strains |
Salmonella spp., E. coli, C. jejuni |
Growth inhibition, reduced adhesion |
Organic acids, bacteriocins, competition for nutrients |
[69,70] |
| Bifidobacterium longum |
S. enterica, E. coli |
Reduced colonisation | SCFA production, epithelial barrier enhancement | [71,72] |
| Saccharomyces boulardii |
C. difficile, E. coli, Salmonella spp. |
Protection from diarhoea; modulation of inflammation | Toxin neutralisation, anti-inflammatory activity |
[73,74] |
| L. acidophilus |
L. monocytogenes, E. coli |
In vitro and in vivo pathogen reduction |
Bacteriocin production, inhibition of quorum sensing |
[50,75] |
|
Heyndrickxia coagulans (formerly B. coagulans) |
E. coli, Salmonella spp. |
Growth inhibition; gut barrier enhancement |
Spore formation, SCFA production |
[76] |
| Fermented Woodfordia fruticosa (with L. plantarum and L. rhamnosus) |
L. monocytogenes, Vibrio parahaemolyticus |
Reduced epithelial adhesion; immunostimulation | Interference with adhesion; ↑ IL-6 production (immunomodulation) |
[77] |
|
L. fermentum and L. salivarius |
S. Typhi | Reduced virulence gene expression | Quorum sensing interfeence, inhibition of biofilm formation |
[77] |
| Class | Examples | Sources | Reported effects | References |
| Carbohydrate-based (traditional) | Inulin, GOS, FOS | Chicory root, onion, garlic, banana, legumes, human milk | Selective stimulation of bifidobacteria and lactobacilli; improved gut health; enhanced mineral absorption | [13,107] |
| Human milk oligosaccharides | 2′-fucosyllactose, lacto-N-neotetraose |
Human milk | Bifidogenic effect; immune modulation; pathogen protection | [110,111] |
| Non-carbohydrate substrates | Conjugated linoleic acid, polyunsaturated fatty acids | Dairy, meat, plant oils | Anti-inflammatory activity; immunomodulation; microbiota modulation | [108] |
| Plant-derived polyphenols | Flavonoids (catechins, anthocyanins), stibenes (resveratrol) | Berries, grapes, tea, cocoa | Fermentation by gut microbiota; antioxidant and anti-inflammatory effects; modulation of microbial composition | [108,112] |
| Marine- and fungal-derived polysaccharides | Fucoidan, laminarin, alginate oligosaccharides, chitosan oligosaccharides, β-glucans | Seaweeds, shellfish, yeast, mushrooms | Immunomodulation; antioxidant activity; stimulation of beneficial bacteria | [113,114,115] |
| Proteins and peptides | Bioactive peptides (milk- and soy-derived) | Dairy, legumes, cereals | Microbiota modulation; enhanced mineral bioavailability; immune stimulation | [116] |
| Minerals as prebiotic co-factors | Calcium, magnesium, zinc | Dairy products, cereals, vegetables | Synergistic effects with fibers; support for microbiota and host health | [109,117] |
| Carbohydrate-based oligosaccharides with antiviral activity | GOS, FOS, lactosucrose | Infant formula, human milk, synthetic oligosaccharides | GOS+FOS: reduced rotavirus shedding; improved stool consistency; alleviated gastroenteritis symptoms; improved immune responses. Lactosucrose: enhanced innate immune responses; increased survival against influenza A virus infection |
[17,118,119] |
| Mechanism of Action | Effects | References |
| Enhanced probiotic survival and implantation | Improved viability and colonisation of Lactobacillus and Bifidobacterium during gastrointestinal transit | [136,137] |
| Synergistic fermentation of prebiotics by co-administered probiotics | Higher SCFA production (acetate, butyrate, propionate); reduced colonic pH; inhibition of pathogens | [19,128] |
| Immune modulation | Increased IgA secretion, enhanced antimicrobial peptide production, reduced systemic inflammation | [14,129] |
| Suppression of resistant pathogens | Reduced colonisation by Salmonella spp., E. coli, C. perfringens, Campylobacter spp. |
[126,131] |
| Antiviral protection | Attenuated rotavirus gastroenteritis and influenza A infection in vivo | [118,119] |
| Reduction of clinical infections and antimicrobial use | Decreased incidence of surgical site infections, sepsis, diarrhea, pneumonia; shortened hospital stay and reduced antibiotic therapy | [132,133,134] |
| Synbiotic composition | Target pathogens / conditions | Effects | References |
| L. fermentum CECT5716 + GOS | Rotavirus, respiratory infections | Inhibition of rotavirus; fewer gastrointestinal infections in infants | [106,130] |
| B. lactis B94 + inulin | Salmonella, Shigella, C. difficile, adenovirus, Campylobacter | Reduced duration of diarrhea; protection against multiple enteric pathogens | [138] |
| L. rhamnosus + inulin / FOS | Vancomycin-resistant Enterococcus | Significant inhibition of VRE growth | [20] |
| L. plantarum ATCC-202195 + FOS | Infant sepsis, respiratory infections | Reduced sepsis incidence and respiratory tract infections | [139] |
| Multi-strain mix (e.g., L. acidophilus, L. rhamnosus, B. bifidum + FOS) |
Surgical site infections | Reduced postoperative infections and shortened antibiotic therapy | [133,134] |
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