Skip to content
naulon

No retraction, correction or concern found when last checked on Oct 18, 2026.

Effects of Probiotics on Gut Microbiota: An Overview

Preethi Chandrasekaran, Sabine Weiskirchen, Ralf Weiskirchen

International Journal of Molecular Sciences · 2024 · Review · CC BY

doi:10.3390/ijms25116022

Abstract

The role of probiotics in regulating intestinal flora to enhance host immunity has recently received widespread attention. Altering the human gut microbiota may increase the predisposition to several disease phenotypes such as gut inflammation and metabolic disorders. The intestinal microbiota converts dietary nutrients into metabolites that serve as biologically active molecules in modulating regulatory functions in the host. Probiotics, which are active microorganisms, play a versatile role in restoring the composition of the gut microbiota, helping to improve host immunity and prevent intestinal disease phenotypes. This comprehensive review provides firsthand information on the gut microbiota and their influence on human health, the dietary effects of diet on the gut microbiota, and how probiotics alter the composition and function of the human gut microbiota, along with their corresponding effects on host immunity in building a healthy intestine. We also discuss the implications of probiotics in some of the most important human diseases. In summary, probiotics play a significant role in regulating the gut microbiota, boosting overall immunity, increasing the abundance of beneficial bacteria, and helping ameliorate the symptoms of multiple diseases.

References 138

  1. 1.

    Kumar R., Sood U., Gupta V., Singh M., Scaria J., Lal R. Recent advancements in the development of modern probiotics for restoring human gut microbiome dysbiosis. Indian J. Microbiol. 2020;60:12-25.

    Not in our library10.1007/s12088-019-00808-y

  2. 2.

    Kerry R.G., Patra J.K., Gouda S., Park Y., Shin H.S., Das G. Benefaction of probiotics for human health: A review. J. Food Drug Anal. 2018;26:927-939.

    Not in our library10.1016/j.jfda.2018.01.002

  3. 3.

    Health and Nutritional Properties of Probiotics in Food Including Powder Milk with Live Lactic Acid Bacteria—Report of a Joint FAO/WHO Expert Consultation on Evaluation of Health and Nutritional Properties of Probiotics in Food Including Power Milk with Liver Lactic Acid Bacteria. 2001.

    Not in our library

  4. 4.

    Hill C., Guarner F., Reid G., Gibson G.R., Merenstein D.J., Pot B., Morelli L., Canani R.B., Flint H.J., Salminen S., et al. Expert consensus document. The International Scientific Association for Probiotics and Prebiotics consensus statement on the scope and appropriate use of the term probiotic. Nat. Rev. Gastroenterol. Hepatol. 2014;11:506-514.

    Not in our library10.1038/nrgastro.2014.66

  5. 5.

    Rooks M.G., Garrett W.S. Gut microbiota, metabolites and host immunity. Nat. Rev. Immunol. 2016;16:341-352.

    Not in our library10.1038/nri.2016.42

  6. 6.

    Cullender T.C., Chassaing B., Janzon A., Kumar K., Muller C.E., Werner J.J., Angenent L.T., Bell M.E., Hay A.G., Peterson D.A., et al. Innate and adaptive immunity interact to quench microbiome flagellar motility in the gut. Cell Host Microbe. 2013;14:571-581.

    Not in our library10.1016/j.chom.2013.10.009

  7. 7.

    Sakandar H.A., Zhang H. Trends in probiotic(s)-fermented milks and their in vivo functionality: A review. Trends Food Sci. Technol. 2021;110:55-65.

    Not in our library10.1016/j.tifs.2021.01.054

  8. 8.
  9. 9.
  10. 10.
  11. 11.

    Hollins S.L., Hodgson D.M. Stress, microbiota, and immunity. Curr. Opin. Behav. Sci. 2019;28:66-71.

    Not in our library10.1016/j.cobeha.2019.01.015

  12. 12.

    Agus A., Clément K., Sokol H. Gut microbiota-derived metabolites as central regulators in metabolic disorders. Gut. 2021;70:1174-1182.

    Not in our library10.1136/gutjnl-2020-323071

  13. 13.

    Cresci G.A., Bawden E. Gut microbiome: What we do and don’t know. Nutr. Clin. Pract. 2015;30:734-746.

    Not in our library10.1177/0884533615609899

  14. 14.
  15. 15.

    Fassarella M., Blaak E.E., Penders J., Nauta A., Smidt H., Zoetendal E.G. Gut microbiome stability and resilience: Elucidating the response to perturbations in order to modulate gut health. Gut. 2021;70:595-605.

    Not in our library10.1136/gutjnl-2020-321747

  16. 16.
  17. 17.

    Valeriano V.D., Bagon B.B., Balolong M.P., Kang D.K. Carbohydrate-binding specificities of potential probiotic Lactobacillus strains in porcine jejunal (IPEC-J2) cells and porcine mucin. J. Microbiol. 2016;54:510-519.

    Not in our library10.1007/s12275-016-6168-7

  18. 18.
  19. 19.
  20. 20.
  21. 21.

    Litvak Y., Mon K.K.Z., Nguyen H., Chanthavixay G., Liou M., Velazquez E.M., Kutter L., Alcantara M.A., Byndloss M.X., Tiffany C.R., et al. Commensal Enterobacteriaceae protect against Salmonella colonization through oxygen competition. Cell Host Microbe. 2019;25:128-139.e5.

    Not in our library10.1016/j.chom.2018.12.003

  22. 22.

    Shao Y., Evers S.S., Shin J.H., Ramakrishnan S.K., Bozadjieva-Kramer N., Yao Q., Shah Y.M., Sandoval D.A., Seeley R.J. Vertical sleeve gastrectomy increases duodenal Lactobacillus spp. richness associated with the activation of intestinal HIF2α signaling and metabolic benefits. Mol. Metab. 2022;57:101432.

    Not in our library10.1016/j.molmet.2022.101432

  23. 23.

    Mao N., Cubillos-Ruiz A., Cameron D.E., Collins J.J. Probiotic strains detect and suppress cholera in mice. Sci. Transl. Med. 2018;10:eaao2586.

    Not in our library10.1126/scitranslmed.aao2586

  24. 24.
  25. 25.

    Aljohani A.M., El-Chami C., Alhubail M., Ledder R.G., O’Neill C.A., McBain A.J. Escherichia coli Nissle 1917 inhibits biofilm formation and mitigates virulence in Pseudomonas aeruginosa. Front. Microbiol. 2023;14:1108273.

    Not in our library10.3389/fmicb.2023.1108273

  26. 26.

    Mousavi Khaneghah A., Abhari K., Eş I., Soares M.B., Oliveira R.B.A., Hosseini H., Rezaei M., Balthazar C.F., Silva R., Cruz A.G., et al. Interactions between probiotics and pathogenic microorganisms in hosts and foods: A review. Trends Food Sci. Technol. 2020;95:205-218.

    Not in our library10.1016/j.tifs.2019.11.022

  27. 27.

    Cho Y.E., Kim D.K., Seo W., Gao B., Yoo S.H., Song B.J. Fructose promotes leaky gut, endotoxemia, and liver fibrosis through ethanol-inducible cytochrome P450-2E1-mediated oxidative and nitrative stress. Hepatology. 2021;73:2180-2195.

    Not in our library10.1002/hep.30652

  28. 28.

    Ahluwalia B., Magnusson M.K., Öhman L. Mucosal immune system of the gastrointestinal tract: Maintaining balance between the good and the bad. Scand. J. Gastroenterol. 2017;52:1185-1193.

    Not in our library10.1080/00365521.2017.1349173

  29. 29.

    Krndija D., El Marjou F., Guirao B., Richon S., Leroy O., Bellaiche Y., Hannezo E., Matic Vignjevic D. Active cell migration is critical for steady-state epithelial turnover in the gut. Science. 2019;365:705-710.

    Not in our library10.1126/science.aau3429

  30. 30.
  31. 31.

    Hou Q., Ye L., Liu H., Huang L., Yang Q., Turner J.R., Yu Q. Lactobacillus accelerates ISCs regeneration to protect the integrity of intestinal mucosa through activation of STAT3 signaling pathway induced by LPLs secretion of IL-22. Cell Death Differ. 2018;25:1657-1670.

    Not in our library10.1038/s41418-018-0070-2

  32. 32.
  33. 33.
  34. 34.
  35. 35.

    Citi S. Intestinal barriers protect against disease. Science. 2018;359:1097-1098.

    Not in our library10.1126/science.aat0835

  36. 36.

    Liu Q., Tian H., Kang Y., Tian Y., Li L., Kang X., Yang H., Wang Y., Tian J., Zhang F., et al. Probiotics alleviate autoimmune hepatitis in mice through modulation of gut microbiota and intestinal permeability. J. Nutr. Biochem. 2021;98:108863.

    Not in our library10.1016/j.jnutbio.2021.108863

  37. 37.
  38. 38.

    White R., Atherly T., Guard B., Rossi G., Wang C., Mosher C., Webb C., Hill S., Ackermann M., Sciabarra P., et al. Randomized, controlled trial evaluating the effect of multi-strain probiotic on the mucosal microbiota in canine idiopathic inflammatory bowel disease. Gut Microbes. 2017;8:451-466.

    Not in our library10.1080/19490976.2017.1334754

  39. 39.

    Martin-Gallausiaux C., Garcia-Weber D., Lashermes A., Larraufie P., Marinelli L., Teixeira V., Rolland A., Béguet-Crespel F., Brochard V., Quatremare T., et al. Akkermansia muciniphila upregulates genes involved in maintaining the intestinal barrier function via ADP-heptose-dependent activation of the ALPK1/TIFA pathway. Gut Microbes. 2022;14:2110639.

    Not in our library10.1080/19490976.2022.2110639

  40. 40.

    Sangineto M., Grander C., Grabherr F., Mayr L., Enrich B., Schwärzler J., Dallio M., Bukke V.N., Moola A., Moschetta A., et al. Recovery of Bacteroides thetaiotaomicron ameliorates hepatic steatosis in experimental alcohol-related liver disease. Gut Microbes. 2022;14:2089006.

    Not in our library10.1080/19490976.2022.2089006

All 138 references

Reads

Read by people on this page

None yet.

Checked or read by AI through naulon

None yet.

A person counts once a day per paper. We keep no cookie and no address: a reader is a hash that changes every day. Any month under five reads shows no number.

Are you an author?

Is this your paper?

Claim it to add your note and be paid when agents cite it. Free.