Cited by 44Probiotics and Fermented FoodsGut microbiota and healthAquaculture disease management and microbiota

Accounting for the health risk of probiotics

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Liu, Xiangyi, Zhao, Haiyi, Wong, Aloysius·2024·Heliyon

Abstract

Probiotics have long been associated with a myriad of health benefits, so much so that their adverse effects whether mild or severe, are often neglected or overshadowed by the enormous volume of articles describing their beneficial effects in the current literature. Recent evidence has demonstrated several health risks of probiotics that warrant serious reconsideration of their applications and further investigations. This review aims to highlight studies that report on how probiotics might cause opportunistic systemic and local infections, detrimental immunological effects, metabolic disturbance, allergic reactions, and facilitating the spread of antimicrobial resistance. To offer a recent account of the literature, articles within the last five years were prioritized. The narration of these evidence was based on the nature of the studies in the following order of preference: clinical studies or human samples, in vivo or animal models, in situ, in vitro and/or in silico. We hope that this review will inform consumers, food scientists, and medical practitioners, on the health risks, while also encouraging research that will focus on and clarify the adverse effects of probiotics.

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  • Probiotic supplementation can prevent or cure autoimmune diseases or reduce cytokine levels.

    “However, probiotic supplementation can prevent or cure autoimmune diseases or reduce cytokine levels [87].”

    From Current Concepts in Probiotic Safety and Efficacy (2026) · cites this paper as [87]

    In “Detrimental immunological effects,” the paper says probiotic supplementation has not been conclusively shown to prevent or treat autoimmune diseases or lower cytokine levels. It also reports studies finding no benefit or elevated cytokines, rather than establishing the claimed benefits. (LLM, conf=0.91)

    Checked by a reasoning model — may be wrong.

    Experimental — accuracy not yet measured
  • Results regarding probiotic use in the scientific literature are irregular and vary significantly due to differences in probiotic types, doses, and treatment regimens across studies.

    “The bottom line is that the results regarding probiotic use described in the scientific literature are irregular and vary significantly due to differences in probiotic types, their doses, and treatment regimens across studies [87].”

    From Current Concepts in Probiotic Safety and Efficacy (2026) · cites this paper as [87]

    The Conclusion and outlook says outcomes vary because probiotic types, amounts, and administration frequency differ across studies. But “these effects” refers specifically to reductions in complications and infections among surgical patients; the citing sentence generalizes that finding to results on probiotic use overall. (LLM, conf=0.84)

    Experimental — accuracy not yet measured
  • Research results on probiotics and prebiotics for prevention and treatment of allergic diseases remain inconclusive or contradictory.

    “Despite the increasing interest in probiotics and prebiotics the prevention and treatment of allergic diseases, including atopic dermatitis, asthma, rhinitis, and food allergy, research results remain inconclusive or contradictory [87].”

    From Current Concepts in Probiotic Safety and Efficacy (2026) · cites this paper as [87]

  • Vulnerable populations including newborns, immunocompromised individuals, and critically ill individuals are at greater risk from probiotics.

    “Vulnerable populations (newborns, immunocompromised individuals, and critically ill individuals) are at greater risk; therefore, assessing regulatory compliance requires a combination of biochemical and metabolomic studies, whole genome sequencing for virulence, antibiotic resistance genes and motility mapping [63,66,87].”

    From Current Concepts in Probiotic Safety and Efficacy (2026) · cites this paper as [87]

  • Conclusions on probiotics for metabolic disorders were not universally positive, and some studies reported unexpected side effects.

    “Conclusions were not universally positive, and some studies even reported unexpected side effects [87,108].”

    From Current Concepts in Probiotic Safety and Efficacy (2026) · cites this paper as [87]

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  1. [1]Ejtahed H.S. Mohtadi-Nia J. Homayouni-Rad A. Niafar M. Asghari-Jafarabadi M. Mofid V. Effect of probiotic yogurt containing Lactobacillus acidophilus and Bifidobacterium lactis on lipid profile in individuals with type 2 diabetes mellitus J. Dairy Sci. 94 7 2011 3288 3294 10.3168/jds.2010-4128 21700013 · DOI
  2. [2]Sun J. Buys N. Effects of probiotics consumption on lowering lipids and CVD risk factors: a systematic review and meta-analysis of randomized controlled trials Ann. Med. 47 6 2015 430 440 10.3109/07853890.2015.1071872 26340330 · DOI
  3. [3]Wang G. Huang W. Xia Y. Xiong Z. Ai L. Cholesterol-lowering potentials of Lactobacillus strain overexpression of bile salt hydrolase on high cholesterol diet-induced hypercholesterolemic mice Food Funct. 10 3 2019 1684 1695 10.1039/c8fo02181c 30839966 · DOI
  4. [4]Nikbakht E. Khalesi S. Singh I. Williams L.T. West N.P. Colson N. Effect of probiotics and synbiotics on blood glucose: a systematic review and meta-analysis of controlled trials Eur. J. Nutr. 57 1 2018 95 106 10.1007/s00394-016-1300-3 27590729 · DOI · Paper page
  5. [5]Sakandar H.A. Zhang H. Trends in Probiotic(s)-Fermented milks and their in vivo functionality: a review Trends Food Sci. Technol. 110 2021 55 65 10.1016/j.tifs.2021.01.054 · DOI
  6. [6]Wu H. Chiou J. Potential benefits of probiotics and prebiotics for coronary heart disease and stroke Nutrients 13 2021 2878 10.3390/nu13082878 34445037 PMC8401746 · DOI
  7. [7]Alshareef A. Attia A. Almalki M. Alsharif F. Melibari A. Mirdad B. Effectiveness of probiotic lozenges in periodontal management of chronic periodontitis patients: clinical and immunological study Eur. J. Dermatol. 14 2 2020 281 287 10.1055/s-0040-1709924 PMC7274828 32438428 · DOI
  8. [8]Bustamante M. Oomah B.D. Mosi-Roa Y. Rubilar M. Burgos-Díaz C. Probiotics as an adjunct therapy for the treatment of halitosis, dental caries and periodontitis Probiotics Antimicrob. Proteins 12 2 2020 325 334 10.1007/s12602-019-9521-4 30729452 · DOI · Paper page
  9. [9]Silva D.R. Sardi J.D. Pitangui N.D. Roque S.M. Silva A.C. Rosalen P.L. Probiotics as an alternative antimicrobial therapy: current reality and future directions J. Funct.Foods 73 2020 104080 10.1016/j.jff.2020.104080 · DOI
  10. [10]Milner E. Stevens B. An M. Lam V. Ainsworth M. Dihle P. Utilizing probiotics for the prevention and treatment of gastrointestinal diseases Front. Microbiol. 12 2021 689958 10.3389/fmicb.2021.689958 PMC8381467 34434175 · DOI
  11. [11]Goodman C. Keating G. Georgousopoulou E. Hespe C. Levett K. Probiotics for the prevention of antibiotic-associated diarrhoea: a systematic review and meta-analysis BMJ Open 11 8 2021 e043054 10.1136/bmjopen-2020-043054 PMC8362734 34385227 · DOI · Paper page
  12. [12]Lukasik J. Dierikx T. Besseling-van der Vaart I. de Meij T. Szajewska H. Multispecies probiotic in aad study group. Multispecies probiotic for the prevention of antibiotic-associated diarrhea in children: a randomized clinical trial JAMA Pediatr. 2022 10.1001/jamapediatrics.2022.1973 PMC9214631 35727573 · DOI
  13. [13]Klaenhammer T.R. Kleerebezem M. Kopp M.V. Rescigno M. The impact of probiotics and prebiotics on the immune system Nat. Rev. Immunol. 12 10 2021 728 734 10.1038/nri3312 23007572 · DOI
  14. [14]Ashraf R. Shah N.P. Immune system stimulation by probiotic microorganisms Crit. Rev. Food Sci. Nutr. 54 7 2014 938 956 10.1080/10408398.2011.619671 24499072 · DOI
  15. [15]Yan F. Polk D.B. Probiotics and immune health Curr. Opin. Gastroenterol. 27 6 2011 496 501 10.1097/MOG.0b013e32834baa4d 21897224 PMC4006993 · DOI · Paper page
  16. [16]Eastwood J. Walton G. Van Hemert S. Williams C. Lamport D. The effect of probiotics on cognitive function across the human lifespan: a systematic review Neurosci. Biobehav. Rev. 128 2021 311 327 10.1016/j.neubiorev.2021.06.032 34171323 · DOI
  17. [17]Kim C.S. Cha L. Sim M. Jung S. Chun W.Y. Baik H.W. Probiotic supplementation improves cognitive function and mood with changes in gut microbiota in community-dwelling older adults: a randomized, double-blind, placebo-controlled, multicenter trial J. Gerontol. A Biol. Sci. Med. Sci. 76 1 2021 32 40 10.1093/gerona/glaa090 32300799 PMC7861012 · DOI
  18. [18]Scholz-Ahrens K.E. Ade P. Marten B. Weber P. Timm W. Açil Y. Prebiotics, probiotics, and synbiotics affect mineral absorption, bone mineral content, and bone structure J. Nutr. 137 3 Suppl 2 2007 838S 8346S 10.1093/jn/137.3.838S 17311984 · DOI · Paper page
  19. [20]Crook N. Ferreiro A. Gasparrini A.J. Pesesky M.W. Gibson M.K. Wang B. Adaptive strategies of the candidate probiotic E. coli nissle in the mammalian gut Cell Host Microbe 25 4 2019 499 512.e8 10.1016/j.chom.2019.02.005 30926240 PMC6487504 · DOI
  20. [21]Mikołaj K. Igor Ł. Wojciech M. Global internet data on the interest in antibiotics and probiotics generated by google trends Antibiotics 8 3 2019 147 10.3390/antibiotics8030147 31547273 PMC6784173 · DOI
  21. [22]Kamiński M. Kręgielska-Narożna M. Bogdański P. Determination of the popularity of dietary supplements using Google search rankings Nutrients 12 4 2020 908 10.3390/nu12040908 32224928 PMC7231191 · DOI
  22. [23]Stanton C. Gardiner G. Meehan H. Collins K. Fitzgerald G. Lynch P.B. Market potential for probiotics Am. J. Clin. Nutr. 73 2 2001 476s 483s 10.1093/ajcn/73.2.476s 11157361 · DOI
  23. [25]de Simone C. The unregulated probiotic market Clin. Gastroenterol. Hepatol. 17 5 2019 809 817 10.1016/j.cgh.2018.01.018 29378309 · DOI · Paper page
  24. [26]Yoha K.S. Nida S. Dutta S. Moses J.A. Anandharamakrishnan C. Targeted delivery of probiotics: perspectives on research and commercialization. Probiotics antimicrob Proteins 14 1 2022 15 48 10.1007/s12602-021-09791-7 PMC8075719 33904011 · DOI
  25. [27]Somashekaraiah R. Shruthi B. Deepthi B.V. Sreenivasa M.Y. Probiotic properties of lactic acid bacteria isolated from neera: a naturally fermenting coconut palm nectar Front. Microbiol. 10 2019 1382 10.3389/fmicb.2019.01382 31316477 PMC6611078 · DOI
  26. [28]Zhang W. Wang J. Zhang D. Liu H. Wang S. Wang Y. Complete genome sequencing and comparative genome characterization of lactobacillus johnsonii ZLJ010, a potential probiotic with health-promoting properties Front. Genet. 10 2019 812 10.3389/fgene.2019.00812 31552103 PMC6746964 · DOI · Paper page
  27. [29]Tarrah A. da Silva Duarte V. Pakroo S. Corich V. Giacomini A. Genomic and phenotypic assessments of safety and probiotic properties of Streptococcus macedonicus strains of dairy origin Food Res. Int. 130 2020 108931 10.1016/j.foodres.2019.108931 32156379 · DOI
  28. [30]Zheng J. Du M. Jiang W. Zhang J. Shen W. Ma X. In vitro probiotic characteristics and whole genome sequence analysis of lactobacillus strains isolated from cattle-yak milk Biology 11 1 2021 44 10.3390/biology11010044 35053042 PMC8772927 · DOI
  29. [31]Sun Y. Li H. Zheng L. Li J. Hong Y. Liang P. iProbiotics: a machine learning platform for rapid identification of probiotic properties from whole-genome primary sequences Briefings Bioinf. 23 1 2022 bbab477 10.1093/bib/bbab477 34849572 · DOI
  30. [32]Doron S. Snydman D.R. Risk and safety of probiotics Suppl 2 Clin. Infect. Dis. 60 Suppl 2 2015 S129 S134 10.1093/cid/civ085 25922398 PMC4490230 · DOI · Paper page
  31. [33]Kothari D. Patel S. Kim S.K. Probiotic supplements might not be universally-effective and safe: a review Biomed. Pharmacother. 111 2019 537 547 10.1016/j.biopha.2018.12.104 30597307 · DOI · Paper page
  32. [35]Zucko J. Starcevic A. Diminic J. Oros D. Mortazavian A.M. Putnik P. Probiotic – friend or foe? Curr. Opin. Food Sci. 32 2020 45 49 10.1016/j.cofs.2020.01.007 · DOI
  33. [36]Žuntar I. Petric Z. Bursać Kovačević D. Putnik P. Safety of probiotics: functional fruit beverages and nutraceuticals Foods 9 7 2020 947 10.3390/foods9070947 32708933 PMC7404568 · DOI
  34. [37]Senok A.C. Ismaeel A.Y. Botta G.A. Probiotics: facts and myths Clin. Microbiol. Infect. 11 12 2005 958 966 10.1111/j.1469-0691.2005.01228.x 16307549 · DOI
  35. [38]Vouloumanou E.K. Karageorgopoulos D.E. Kazantzi M.S. Kapaskelis A.M. Falagas M.E. Antibiotics versus placebo or watchful waiting for acute otitis media: a meta-analysis of randomized controlled trials J. Antimicrob. Chemother. 64 1 2009 16 24 10.1093/jac/dkp166 19454521 · DOI
  36. [39]Chakravarty S. Parashar A. Acharyya S. Saccharomyces cerevisiae sepsis following probiotic therapy in an infant Indian Pediatr. 56 2019 971 972 10.1007/s13312-019-1655-7 31729330 · DOI
  37. [40]Chiang M.C. Chen C.L. Feng Y. Chen C.C. Lien R. Chiu C.H. Lactobacillus rhamnosus sepsis associated with probiotic therapy in an extremely preterm infant: pathogenesis and a review for clinicians J. Microbiol. Immunol. Infect. 54 4 2021 575 580 10.1016/j.jmii.2020.03.029 32307246 · DOI · Paper page
  38. [41]Aydoğan S. Dilli D. Özyazici A. Aydin N. Şimşek H. Orun U.A. Aksoy Ö.N. Lactobacillus rhamnosus sepsis associated with probiotic therapy in a term infant with congenital heart disease Fetal Pediatr. Pathol. 41 5 2022 823 827 10.1080/15513815.2021.1966144 34414856 · DOI
  39. [42]Atıcı S. Soysal A. Karadeniz Cerit K. Yılmaz Ş. Aksu B. Kıyan G. Bakır M. Catheter-related Saccharomyces cerevisiae Fungemia Following Saccharomyces boulardii Probiotic Treatment: in a child in intensive care unit and review of the literature Med. Mycol. Case Rep. 15 January 2017 33 35 10.1016/j.mmcr.2017.02.002 28280685 PMC5333505 · DOI
  40. [43]Appel-da-Silva M.C. Narvaez G.A. Perez L.R.R. Drehmer L. Lewgoy J. Saccharomyces cerevisiae var. boulardii fungemia following probiotic treatment Med. Mycol. Case Rep. 18 July 2017 15 17 10.1016/j.mmcr.2017.07.007 28794958 PMC5537395 · DOI
  41. [44]Kara I. Yıldırım F. Özgen Ö. Erganiş S. Aydoğdu M. Dizbay M. Gürsel G. Kalkanci A. Saccharomyces cerevisiae fungemia after probiotic treatment in an intensive care unit patient J. Mycol. Med. 28 1 2018 218 221 10.1016/j.mycmed.2017.09.003 29132794 · DOI
  42. [45]Fadhel M. Patel S. Liu E. Levitt M. Asif A. Saccharomyces cerevisiae fungemia in a critically ill patient with acute cholangitis and long term probiotic use Med. Mycol. Case Rep. 23 November 2018 2019 23 25 10.1016/j.mmcr.2018.11.003 30505677 PMC6251791 · DOI
  43. [46]Rannikko J. Holmberg V. Karppelin M. Arvola P. Huttunen R. Mattila E. Fungemia and other fungal infections associated with use of Saccharomyces boulardii probiotic supplements Emerg. Infect. Dis. 27 8 2021 2090 2096 10.3201/eid2708.210018 34287140 PMC8314839 · DOI
  44. [47]Latifi A.N. Saeyeldin A. Simms M. Lactobacillus acidophilus bacteremia in a diabetic patient J. Case Rep. Images Infect. Dis. 2 Figure 1 2019 100005 100021 10.5348/100005Z16AL2019CR · DOI
  45. [48]Haziri D. Prechter F. Stallmach A. Yoghurt-induced Lactobacillus bacteremia in a patient with Crohn's disease on therapy with ustekinumab and concomitant HIV-Infection Z. Gastroenterol. 59 4 2021 317 320 10.1055/a-1168-7577 32572871 · DOI
  46. [49]Lnu K. Abdelsalam A. Bambach W. Lactobacillus bacteremia: a tell-tale sign for diabetes? J. Community Hosp. Intern. Med. Perspect. 12 3 2022 86 88 10.55729/2000-9666.1061 35711388 PMC9195087 · DOI
  47. [50]Yelin I. Flett K.B. Merakou C. Mehrotra P. Stam J. Snesrud E. Genomic and epidemiological evidence of bacterial transmission from probiotic capsule to blood in ICU patients Nat. Med. 25 11 2019 1728 1732 10.1038/s41591-019-0626-9 31700189 PMC6980696 · DOI · Paper page
  48. [51]Pruccoli G. Silvestro E. Pace Napoleone C. Aidala E. Garazzino S. Scolfaro C. Are probiotics safe? Bifidobacterium bacteremia in a child with severe heart failure Infez. med. 27 2 2019 175 178 31205041
  49. [52]Sakurai Y. Watanabe T. Miura Y. Uchida T. Suda N. Yoshida M. Nawa T. Clinical and bacteriologic characteristics of six cases of Bifidobacterium breve bacteremia due to probiotic administration in the neonatal intensive care unit Pediatr. Infect. Dis. J. 41 1 2022 62 65 10.1097/INF.0000000000003232 34889871 · DOI
  50. [53]Pillai A. Tan J. Paquette V. Panczuk J. Does probiotic bacteremia in premature infants impact clinically relevant outcomes? A case report and updated review of literature Clin. Nutr. ESPEN 39 2020 255 259 10.1016/j.clnesp.2020.05.020 32859326 · DOI
  51. [54]Dajani A.S. Taubert K.A. Wilson W. Bolger A.F. Bayer A. Ferrieri P. Prevention of bacterial endocarditis. Recommendations by the American heart association JAMA 277 22 1997 1794 1801 9178793
  52. [55]Pasala S. Singer L. Arshad T. Roach K. Lactobacillus endocarditis in a healthy patient with probiotic use IDCases 22 2020 e00915 10.1016/j.idcr.2020.e00915 PMC7558031 33088710 · DOI
  53. [56]Boumis E. Capone A. Galati V. Venditti C. Petrosillo N. Probiotics and infective endocarditis in patients with hereditary hemorrhagic telangiectasia: a clinical case and a review of the literature BMC Infect. Dis. 18 1 2018 65 10.1186/s12879-018-2956-5 29390976 PMC5796351 · DOI · Paper page
  54. [57]Antoun M. Hattab Y. Akhrass F.A. Hamilton L.D. Uncommon pathogen, lactobacillus, causing infective endocarditis: case report and review Case Rep. Infect. Dis. 2020 2020 8833948 10.1155/2020/8833948 PMC7661116 33204548 · DOI
  55. [58]Khalil M.H. Lactobacillus endocarditis, a sinister consequence of an innocuous bacterium Cardiovasc. Dis. 160 4Supplement 2021 A240 10.1016/j.chest.2021.07.248 · DOI
  56. [59]Singh S. Qureshi F. Nadeau A. Singh S. Implications of infective endocarditis by probiotic microorganisms: a systematic review of case reports Curr. Dev. Nutr. 5 Supplement_2 2021 1182 10.1093/cdn/nzab054_037 · DOI
  57. [60]Bae H. Hwang T.S. Lee H.C. Jung D.I. Kim S.H. Yu D.H. Successful treatment of canine infective endocarditis caused by Bacillus amyloliquefaciens Vet. Q. 42 1 2022 41 47 10.1080/01652176.2022.2033879 35068361 PMC8843097 · DOI
  58. [61]Miwa T. Tanaka H. Shiojiri T. Infected pancreatic necrosis and retroperitoneal abscess associated with Lactobacillus paracasei BMJ Case Rep. 14 8 2021 e243936 10.1136/bcr-2021-243936 PMC8351486 34362752 · DOI
  59. [62]Vyas V. Mian S. Paolino K. Siddique Z. Lactobacillus masticator abscess after probiotics consumption SAVE Proc. 34 1 2020 93 94 10.1080/08998280.2020 PMC7785180 33456157 · DOI
  60. [63]Pararajasingam A. Uwagwu J. Lactobacillus: the not so friendly bacteria 2017 BMJ Case Rep. 2017 bcr2016218423 10.1136/bcr-2016-218423 PMC5612357 28903972 · DOI
  61. [64]Milee P.M. Zara M. Jared S. Sreeram P. Joshua P. Gunvir G. S2818 when the good goes bad: pyogenic liver abscess due to lactobacillus Am. J. Gastroenterol. 116 2021 S1171 S1172 10.14309/01.ajg.0000784804.40899.65 · DOI
  62. [65]Ramos-Coria D. Canto-Losa J. Carrillo-Vázquez D. Carbajal-Morelos L. Estrada-León R. Corona-Rodarte E. Lactobacillus gasseri liver abscess and bacteremia: a case report BMC Infect. Dis. 21 1 2021 518 10.1186/s12879-021-06181-w 34078320 PMC8173985 · DOI
  63. [66]Håkansson Å. Andrén Aronsson C. Brundin C. Oscarsson E. Molin G. Agardh D. Effects of lactobacillus plantarum and lactobacillus paracasei on the peripheral immune response in children with celiac disease autoimmunity: a randomized, double-blind, placebo-controlled clinical trial Nutrients 11 8 2019 1925 10.3390/nu11081925 31426299 PMC6723580 · DOI
  64. [67]Meyer A.L. Elmadfa I. Herbacek I. Micksche M. Probiotic, as well as conventional yogurt, can enhance the stimulated production of proinflammatory cytokines J. Hum. Nutr. Diet. 20 6 2007 590 598 10.1111/j.1365-277X.2007.00807.x 18001380 · DOI
  65. [68]Ashraf R. Vasiljevic T. Day S.L. Smith S.C. Donkor O.N. Lactic acid bacteria and probiotic organisms induce different cytokine profile and regulatory T cells mechanisms J. Funct.Foods 6 2014 395 409 10.1016/j.jff.2013.11.006 · DOI · Paper page
  66. [70]Groele L. Szajewska H. Szalecki M. Świderska J. Wysocka-Mincewicz M. Ochocińska A. Lack of effect of Lactobacillus rhamnosus GG and Bifidobacterium lactis Bb12 on beta-cell function in children with newly diagnosed type 1 diabetes: a randomised controlled trial BMJ Open Diabetes Res Care 9 1 2021 e001523 10.1136/bmjdrc-2020-001523 PMC8006832 33771763 · DOI
  67. [71]Saputro I.D. Putra O.N. Pebrianton H. Suharjono Effects of probiotic administration on IGA and IL-6 level in severe burn patients: a randomized trial Ann. Burns Fire Disasters 32 1 2019 70 76 31285738 PMC6588324
  68. [72]Blackwell T.S. Christman J.W. Sepsis and cytokines: current status Br. J. Anaesth. 77 1 1996 110 117 10.1093/bja/77.1.110 8703620 · DOI
  69. [73]Schwacha M.G. Macrophages and post-burn immune dysfunction Burns 29 1 2003 1 14 10.1016/s0305-4179(02)00187-0 12543039 · DOI
  70. [74]Koesnoe S. Masjkuri N. Adisasmita A. Djauzi S. Kartasasmita C. Sundoro J. A randomized controlled trial to evaluate the effect of influenza vaccination and probiotic supplementation on immune response and incidence of influenza-like illness in an elderly population in Indonesia PLoS One 16 12 2021 e0250234 10.1371/journal.pone.0250234 PMC8675694 34914726 · DOI
  71. [75]Sollid L.M. Molecular basis of celiac disease Annu. Rev. Immunol. 18 2000 53 81 10.1146/annurev.immunol.18.1.53 10837052 · DOI
  72. [76]Uusitalo U. Andren Aronsson C. Liu X. Kurppa K. Yang J. Liu E. TEDDY study group. Early probiotic supplementation and the risk of celiac disease in children at genetic risk Nutrients 11 8 2019 1790 10.3390/nu11081790 31382440 PMC6722940 · DOI
  73. [77]Zegarra-Ruiz D.F. El Beidaq A. Iñiguez A.J. Lubrano Di Ricco M. Manfredo Vieira S. Ruff W.E. A diet-sensitive commensal lactobacillus strain mediates TLR7-dependent systemic autoimmunity Cell Host Microbe 25 1 2019 113 127.e6 10.1016/j.chom.2018.11.009 30581114 PMC6377154 · DOI · Paper page
  74. [78]Dehner C. Fine R. Kriegel M.A. The microbiome in systemic autoimmune disease: mechanistic insights from recent studies Curr. Opin. Rheumatol. 31 2 2019 201 207 10.1097/BOR.0000000000000574 30624285 PMC6408954 · DOI
  75. [79]Manfredo Vieira S. Hiltensperger M. Kumar V. Zegarra-Ruiz D. Dehner C. Khan N. Translocation of a gut pathobiont drives autoimmunity in mice and humans Science 359 6380 2018 1156 1161 10.1126/science.aar7201 29590047 PMC5959731 · DOI
  76. [80]Crow M.K. Type I interferon in the pathogenesis of lupus J. Immunol. 192 12 2014 5459 5468 10.4049/jimmunol.1002795 24907379 PMC4083591 · DOI
  77. [81]Furuta Y. Tsai S.H. Kinoshita M. Fujimoto K. Okumura R. Umemoto E. E-NPP3 controls plasmacytoid dendritic cell numbers in the small intestine PLoS One 12 2 2017 e0172509 10.1371/journal.pone.0172509 PMC5321438 28225814 · DOI
  78. [82]Baudino L. Yoshinobu K. Morito N. Santiago-Raber M.L. Izui S. Role of endogenous retroviruses in murine SLE Autoimmun. Rev. 10 1 2010 27 34 10.1016/j.autrev.2010.07.012 20659589 · DOI · Paper page
  79. [83]Kang S.J. Yang J. Lee N.Y. Lee C.H. Park I.B. Park S.W. Monitoring cellular immune responses after consumption of selected probiotics in immunocompromised mice Food Sci. Anim. Resour. 42 5 2022 903 914 10.5851/kosfa.2022.e44 36133633 PMC9478974 · DOI
  80. [84]Jia L. Jia Q. Yang J. Jia R. Zhang H. Efficacy of probiotics supplementation on chronic kidney disease: a systematic review and meta-analysis Res 43 2018 Kidney Blood Press 1623 1635 10.1159/000494677 30380555 · DOI
  81. [85]Askari G. Ghavami A. Shahdadian F. Moravejolahkami A.R. Effect of synbiotics and probiotics supplementation on autoimmune diseases: a systematic review and meta-analysis of clinical trials Clin. Nutr. 40 5 2021 3221 3234 10.1016/j.clnu.2021.02.015 33642142 · DOI
  82. [86]Chiu C.J. Huang M.T. Asthma in the precision medicine era: biologics and probiotics Int. J. Mol. Sci. 22 9 2021 4528 10.3390/ijms22094528 33926084 PMC8123613 · DOI · Paper page
  83. [87]D'Auria E. Salvatore S. Pozzi E. Mantegazza C. Sartorio M.U.A. Pensabene L. Cow's milk allergy: immunomodulation by dietary intervention Nutrients 11 6 2019 1399 10.3390/nu11061399 31234330 PMC6627562 · DOI · Paper page
  84. [88]Tan‐Lim C.S.C. Esteban‐Ipac N.A.R. Recto M.S.T. Castor M.A.R. Casis‐Hao R.J. Nano A.L.M. Comparative effectiveness of probiotic strains on the prevention of pediatric atopic dermatitis: a systematic review and network meta‐analysis Pediatr. Allergy Immunol. 32 2021 1255 1270 10.1111/pai.13514 33811784 · DOI · Paper page
  85. [90]Peldan P.S. Kukkonen A.K. Savilahti E. Kuitunen M. Perinatal probiotic mixture and development of allergic sensitization up to 13 years of age Int. Arch. Allergy Immunol. 181 4 2020 270 277 10.1159/000504915 32018252 · DOI · Paper page
  86. [91]Taylor A.L. Dunstan J.A. Prescott S.L. Probiotic supplementation for the first 6 months of life fails to reduce the risk of atopic dermatitis and increases the risk of allergen sensitization in high-risk children: a randomized controlled trial J. Allergy Clin. Immunol. 119 1 2007 184 191 10.1016/j.jaci.2006.08.036 17208600 · DOI
  87. [92]Sestito S. D'Auria E. Baldassarre M.E. Salvatore S. Tallarico V. Stefanelli E. Tarsitano F. Concolino D. Pensabene L. The role of prebiotics and probiotics in prevention of allergic diseases in infants Front. Pediatr. 8 2020 583946 10.3389/fped.2020.583946 PMC7783417 33415087 · DOI
  88. [93]Sivamaruthi B.S. Kesika P. Chaiyasut C. Probiotic based therapy for atopic dermatitis: outcomes of clinical studies Asian Pac. J. Trop. Biomed. 8 6 2018 328 332 10.4103/2221-1691.235328 · DOI · Paper page
  89. [94]Kalliomäki M. Salminen S. Arvilommi H. Kero P. Koskinen P. Isolauri E. Probiotics in primary prevention of atopic disease: a randomised placebo-controlled trial Lancet 357 9262 2001 1076 1079 10.1016/S0140-6736(00)04259-8 11297958 · DOI
  90. [95]Iemoli E. Trabattoni D. Parisotto S. Borgonovo L. Toscano M. Rizzardini G. Probiotics reduce gut microbial translocation and improve adult atopic dermatitis J. Clin. Gastroenterol. 46 Suppl 2012 S33 S40 10.1097/MCG.0b013e31826a8468 22955355 · DOI
  91. [96]Casaro M.B. Thomas A.M. Mendes E. Fukumori C. Ribeiro W.R. Oliveira F.A. A probiotic has differential effects on allergic airway inflammation in A/J and C57BL/6 mice and is correlated with the gut microbiome Microbiome 9 1 2021 1 16 10.1186/s40168-021-01081-2 34112246 PMC8194189 · DOI · Paper page
  92. [97]Shafiei A. Moin M. Pourpak Z. Gharagozlou M. Aghamohamadi A. Sajedi V. Synbiotics could not reduce the scoring of childhood atopic dermatitis (SCORAD): a randomized double blind placebo-controlled trial. Iran J. Allergy Asthma Immunol. 10 1 2011 21 28 21358011
  93. [98]Fölster-Holst R. Müller F. Schnopp N. Abeck D. Kreiselmaier I. Lenz T. Prospective, randomized controlled trial on Lactobacillus rhamnosus in infants with moderate to severe atopic dermatitis Br. J. Dermatol. 155 6 2006 1256 1261 10.1111/j.1365-2133.2006.07558.x 17107398 · DOI
  94. [99]Grüber C. Wendt M. Sulser C. Lau S. Kulig M. Wahn U. Randomized, placebo‐controlled trial of Lactobacillus rhamnosus GG as treatment of atopic dermatitis in infancy Allergy 62 11 2007 1270 1276 10.1111/j.1398-9995.2007.01543.x 17919141 · DOI
  95. [100]D'Elios S. Trambusti I. Verduci E. Ferrante G. Rosati S. Marseglia G.L. Probiotics in the prevention and treatment of atopic dermatitis Pediatr. Allergy Immunol. 31 Suppl 26 2020 43 45 10.1111/pai.13364 33236423 · DOI
  96. [101]Wickens K. Barthow C. Mitchell E.A. Stanley T.V. Purdie G. Rowden J. Maternal supplementation alone with Lactobacillus rhamnosus HN001 during pregnancy and breastfeeding does not reduce infant eczema Pediatr. Allergy Immunol. 29 3 2018 296 302 10.1111/pai.12874 29415330 · DOI
  97. [102]Meirlaen L. Levy E.I. Vandenplas Y. Prevention and management with pro-, pre and synbiotics in children with asthma and allergic rhinitis: a narrative review Nutrients 13 3 2021 934 10.3390/nu13030934 33799367 PMC7999316 · DOI
  98. [104]Meirlaen L. Levy E.I. Vandenplas Y. Probiotics in the prevention and management of allergic diseases (asthma and allergic rhinitis) In Probiotics in the Prevention and Management of Human Diseases 2022 Academic Press 139 146 10.1016/B978-0-12-823733-5.00027-1 · DOI
  99. [105]Peldan P. Kukkonen A.K. Savilahti E. Kuitunen M. Perinatal probiotics decreased eczema up to 10 years of age, but at 5-10 years, allergic rhino-conjunctivitis was increased Clin. Exp. Allergy 47 7 2017 975 979 10.1111/cea.12924 28316095 · DOI
  100. [107]Butel M.J. Waligora-Dupriet A.J. Wydau-Dematteis S. The developing gut microbiota and its consequences for health J. Dev. Orig. Health Dis. 9 6 2018 590 597 10.1017/S2040174418000119 29562949 · DOI · Paper page
  101. [108]Peters R.L. Koplin J.J. Dharmage S.C. Tang M.L. McWilliam V.L. Gurrin L.C. Early exposure to cow's milk protein is associated with a reduced risk of cow's milk allergic outcomes J. Allergy Clin. Immunol. Pract. 7 2 2019 462 470.e1 10.1016/j.jaip.2018.08.038 30267891 · DOI
  102. [109]Katz Y. Rajuan N. Goldberg M.R. Eisenberg E. Heyman E. Cohen A. Leshno M. Early exposure to cow's milk protein is protective against IgE-mediated cow's milk protein allergy J. Allergy Clin. Immunol. 126 1 2010 77 82.e1 10.1016/j.jaci.2010.04.020 20541249 · DOI
  103. [110]Mastrorilli C. Santoro A. Caffarelli C. Primary prevention of allergic diseases: the role of early exposure to cow's milk formula Front. Pediatr. 8 2020 420 10.3389/fped.2020.00420 32850536 PMC7399633 · DOI
  104. [111]Grüber C. Van Stuijvenberg M. Mosca F. Moro G. Chirico G. Braegger C.P. Reduced occurrence of early atopic dermatitis because of immunoactive prebiotics among low-atopy-risk infants J. Allergy Clin. Immunol. 126 4 2010 791 797 10.1016/j.jaci.2010.07.022 20832848 · DOI
  105. [112]Osborn D.A. Sinn J.K. Prebiotics in infants for prevention of allergy Cochrane Database Syst. Rev. 3 2013 CD006474 10.1002/14651858.CD006474.pub3 PMC13655411 23543544 · DOI
  106. [113]Doherty A.M. Lodge C.J. Dharmage S.C. Dai X. Bode L. Lowe A.J. Human milk oligosaccharides and associations with immune-mediated disease and infection in childhood: a systematic review Front. Pediatr. 6 2018 91 10.3389/fped.2018.00091 29732363 PMC5920034 · DOI
  107. [114]Kleinjans L. Veening-Griffioen D.H. Wehkamp T. van Bergenhenegouwen J. Knol J. Garssen J. Mice co-administrated with partially hydrolysed whey proteins and prebiotic fibre mixtures show allergen-specific tolerance and a modulated gut microbiota Benef. Microbes 10 2 2019 165 178 10.3920/BM2018.0001 30525954 · DOI
  108. [115]Braegger C. Chmielewska A. Decsi T. Kolacek S. Mihatsch W. Moreno L. Supplementation of infant formula with probiotics and/or prebiotics: a systematic review and comment by the ESPGHAN committee on nutrition J. Pediatr. Gastroenterol. Nutr. 52 2 2011 238 250 10.1097/MPG.0b013e3181fb9e80 21150647 · DOI
  109. [116]Tan-Lim C.S.C. Esteban-Ipac N.A.R. Probiotics as treatment for food allergies among pediatric patients: a meta-analysis World Allergy Organ. J. 11 1 2018 25 10.1186/s40413-018-0204-5 30425779 PMC6218986 · DOI
  110. [118]Rochlani Y. Pothineni N.V. Kovelamudi S. Mehta J.L. Metabolic syndrome: pathophysiology, management, and modulation by natural compounds Ther. Adv. Cardiovasc. Dis. 11 8 2017 215 225 10.1177/1753944717711379 28639538 PMC5933580 · DOI
  111. [119]Alberti K.G. Eckel R.H. Grundy S.M. Zimmet P.Z. Cleeman J.I. Donato K.A. Fruchart J.C. James W.P. Loria C.M. Smith S.C. Jr. International diabetes federation task force on epidemiology and prevention; national heart, lung, and blood institute; American heart association; world heart federation; international atherosclerosis society; international association for the study of obesity Harmonizing the metabolic syndrome: a joint interim statement of the International Diabetes Federation Task Force on Epidemiology and Prevention; National Heart, Lung, and Blood Institute; American Heart Association; World Heart Federation; International Atherosclerosis Society; and International Association for the Study of Obesity. Circulation 120 2009 1640 1645 10.1161/CIRCULATIONAHA.109.192644 19805654 · DOI · Paper page
  112. [120]Bäckhed F. Ding H. Wang T. Hooper L.V. Koh G.Y. Nagy A. The gut microbiota as an environmental factor that regulates fat storage Proc. Natl. Acad. Sci. U.S.A. 101 44 2004 15718 15723 10.1073/pnas.0407076101 15505215 PMC524219 · DOI · Paper page
  113. [121]Turnbaugh P.J. Ley R.E. Mahowald M.A. Magrini V. Mardis E.R. Gordon J.I. An obesity-associated gut microbiome with increased capacity for energy harvest Nature 444 7122 2006 1027 1031 10.1038/nature05414 17183312 · DOI · Paper page
  114. [122]Bäckhed F. Manchester J.K. Semenkovich C.F. Gordon J.I. Mechanisms underlying the resistance to diet-induced obesity in germ-free mice Proc. Natl. Acad. Sci. U.S.A. 104 3 2007 979 984 10.1073/pnas.0605374104 17210919 PMC1764762 · DOI · Paper page
  115. [123]Shan B. Ai Z. Zeng S. Song Y. Song J. Zeng Q. Gut microbiome-derived lactate promotes to anxiety-like behaviors through GPR81 receptor-mediated lipid metabolism pathway Psychoneuroendocrinology 117 2020 104699 10.1016/j.psyneuen.2020 32402927 · DOI
  116. [124]Rao S.S. Rehman A. Yu S. De Andino N.M. Brain fogginess, gas and bloating: a link between SIBO, probiotics and metabolic acidosis Clin. Transl. Gastroenterol. 9 6 2018 162 10.1038/s41424-018-0030-7 29915215 PMC6006167 · DOI
  117. [125]Wallis A. Jackson M.L. Ball M. Lewis D.P. Bruck D. Sleep, cognitive and mood symptoms in myalgic encephalomyelitis/chronic fatigue syndrome: examining the role of the gut-brain axis Cooper C.L. Quick J.C. The Handbook of Stress and Health: A Guide to Research and Practice 2017 Wiley Blackwell 501 522 10.1002/9781118993811.ch31 · DOI
  118. [126]Zhu Y. Liu Y. Wu C. Li H. Du H. Yu H. Enterococcus faecalis contributes to hypertension and renal injury in Sprague-Dawley rats by disturbing lipid metabolism J. Hypertens. 39 6 2021 1112 1124 10.1097/HJH.0000000000002767 33967216 · DOI
  119. [127]Zhong G.C. Huang S.Q. Peng Y. Wan L. Wu Y.Q. Hu T.Y. HDL-C is associated with mortality from all causes, cardiovascular disease and cancer in a J-shaped dose-response fashion: a pooled analysis of 37 prospective cohort studies Eur. J. Prev. Cardiol. 27 11 2020 1187 1203 10.1177/2047487320914756 32283957 · DOI
  120. [128]Siripun P. Chaiyasut C. Lailerd N. Makhamrueang N. Kaewarsar E. Sirilun S. A pilot study of whether or not vegetable and fruit juice containing lactobacillus paracasei lowers blood lipid levels and oxidative stress markers in Thai patients with dyslipidemia: a randomized controlled clinical trial Appl. Sci. 12 10 2022 4913 10.3390/app12104913 · DOI
  121. [129]Sun Y. Tang Y. Hou X. Wang H. Huang L. Wen J. Novel lactobacillus reuteri HI120 affects lipid metabolism in C57bl/6 obese mice Front. Vet. Sci. 7 2020 560241 10.3389/fvets.2020.560241 PMC7592399 33195535 · DOI
  122. [132]Mack L.R. Tomich P.G. Gestational diabetes: diagnosis, classification, and clinical care Obstet. Gynecol. Clin. N. Am. 44 2 2017 207 217 10.1016/j.ogc.2017.02.002 28499531 · DOI
  123. [133]Feng Y. Jiang C.D. Chang A.M. Shi Y. Gao J. Zhu L. Zhang Z. Interactions among insulin resistance, inflammation factors, obesity-related gene polymorphisms, environmental risk factors, and diet in the development of gestational diabetes mellitus J. Matern. Fetal Neonatal Med. 32 2 2019 339 347 10.1080/14767058.2018.1446207 29519182 · DOI
  124. [134]Kassaian N. Feizi A. Aminorroaya A. Jafari P. Ebrahimi M.T. Amini M. The effects of probiotics and synbiotic supplementation on glucose and insulin metabolism in adults with prediabetes: a double-blind randomized clinical trial Acta Diabetol. 55 10 2018 1019 1028 10.1007/s00592-018-1175-2 29931423 · DOI
  125. [135]Yao K. Zeng L. He Q. Wang W. Lei J. Zou X. Effect of probiotics on glucose and lipid metabolism in type 2 diabetes mellitus: a meta-analysis of 12 randomized controlled trials Med. Sci. Monit. 23 2017 3044 3053 10.12659/msm.902600 28638006 PMC5491138 · DOI · Paper page
  126. [136]Gomez-Arango L.F. Barrett H.L. McIntyre H.D. Callaway L.K. Morrison M. Dekker Nitert M. Connections between the gut microbiome and metabolic hormones in early pregnancy in overweight and obese women SPRING Trial Group Diabetes 65 8 2016 2214 2223 10.2337/db16-0278 27217482 · DOI · Paper page
  127. [137]Kijmanawat A. Panburana P. Reutrakul S. Tangshewinsirikul C. Effects of probiotic supplements on insulin resistance in gestational diabetes mellitus: a double‐blind randomized controlled trial J. Diabetes Investig. 10 1 2019 163 170 10.1111/jdi.12863 PMC6319478 29781243 · DOI
  128. [138]Farrokhian A. Raygan F. Soltani A. Tajabadi-Ebrahimi M. Sharifi Esfahani M. Karami A.A. Asemi Z. The effects of synbiotic supplementation on carotid intima-media thickness, biomarkers of inflammation, and oxidative stress in people with overweight, diabetes, and coronary heart disease: a randomized, double-blind, placebo-controlled trial Probiotics Antimicrob. Proteins 11 1 2019 133 142 10.1007/s12602-017-9343-1 29079990 · DOI
  129. [140]Horvath A. Leber B. Feldbacher N. Tripolt N. Rainer F. Blesl A. Effects of a multispecies synbiotic on glucose metabolism, lipid marker, gut microbiome composition, gut permeability, and quality of life in diabesity: a randomized, double-blind, placebo-controlled pilot study Eur. J. Nutr. 59 7 2020 2969 2983 10.1007/s00394-019-02135-w 31729622 PMC7501130 · DOI
  130. [142]Barengolts E. Smith E.D. Reutrakul S. Tonucci L. Anothaisintawee T. The effect of probiotic yogurt on glycemic control in type 2 diabetes or obesity: a meta-analysis of nine randomized controlled trials Nutrients 11 3 2019 671 10.3390/nu11030671 30897796 PMC6471569 · DOI
  131. [144]Shoaei T. Heidari-Beni M. Tehrani H.G. Esmaillzadeh A. Askari G. Effects of probiotic supplementation on pancreatic β-cell function and c-reactive protein in women with polycystic ovary syndrome: a randomized double-blind placebo-controlled clinical trial Int. J. Prev. Med. 6 2015 27 10.4103/2008-7802.153866 25949777 PMC4387688 · DOI
  132. [145]Tamtaji O.R. Taghizadeh M. Daneshvar Kakhaki R. Kouchaki E. Bahmani F. Borzabadi S. Oryan S. Mafi A. Asemi Z. Clinical and metabolic response to probiotic administration in people with Parkinson's disease: a randomized, double-blind, placebo-controlled trial Clin. Nutr. 38 3 2019 1031 1035 10.1016/j.clnu.2018.05.018 29891223 · DOI · Paper page
  133. [146]Sharma P. Tomar S.K. Goswami P. Sangwan V. Singh R. Antibiotic resistance among commercially available probiotics Food Res. Int. 57 2014 176 195 10.1016/j.foodres.2014.01.025 · DOI
  134. [147]Jose N.M. Bunt C.R. Hussain M.A. Implications of antibiotic resistance in probiotics 2015 Food Rev. Int. 31 1 2015 52 62 10.1080/87559129.2014.961075 · DOI · Paper page
  135. [149]Broaders E. Gahan C.G. Marchesi J.R. Mobile genetic elements of the human gastrointestinal tract: potential for spread of antibiotic resistance genes Gut Microb. 4 4 2013 271 280 10.4161/gmic.24627 PMC3744512 23651955 · DOI
  136. [150]Penders J. Stobberingh E. Savelkoul P. Wolffs P. The human microbiome as a reservoir of antimicrobial resistance Front. Microbiol. 4 2013 87 10.3389/fmicb.2013.00087 23616784 PMC3627978 · DOI
  137. [151]Rolain J.M. Food and human gut as reservoirs of transferable antibiotic resistance encoding genes Front. Microbiol. 4 2013 173 10.3389/fmicb.2013.00173 23805136 PMC3690338 · DOI
  138. [152]van Schaik W. The human gut resistome Philos. Trans. R. Soc. Lond. B Biol. Sci. 370 2015 20140087 10.1098/rstb.2014.0087 PMC4424436 25918444 · DOI
  139. [153]Imperial I.C. Ibana J.A. Addressing the antibiotic resistance problem with probiotics: reducing the risk of its double-edged sword effect Front. Microbiol. 7 2016 1983 10.3389/fmicb.2016.01983 28018315 PMC5156686 · DOI
  140. [155]Chon J.W. Seo K.H. Bae D. Dongkwan J. Kwang-Young S. Status and prospect of lactic acid bacteria with antibiotic resistance J. Dairy Sci. Biotechnol. 38 2 2020 70 88 10.22424/jdsb.2020.38.2.70 · DOI
  141. [156]Das D.J. Shankar A. Johnson J.B. Thomas S. Critical insights into antibiotic resistance transferability in probiotic Lactobacillus Nutrition 69 2020 110567 10.1016/j.nut.2019.110567 31733594 · DOI
  142. [157]Turjeman S. Koren O. ARGuing the case for (or against) probiotics Trends Microbiol. 29 11 2021 959 960 10.1016/j.tim.2021.09.004 34563432 · DOI
  143. [159]Abriouel H. Casado Muñoz M.D.C. Lavilla Lerma L. Pérez Montoro B. Bockelmann W. Pichner R. New insights in antibiotic resistance of Lactobacillus species from fermented foods Food Res. Int. 78 2015 465 481 10.1016/j.foodres.2015.09.016 28433315 · DOI
  144. [160]Wong A. Ngu D.Y. Dan L.A. Ooi A. Lim R.L. Detection of antibiotic resistance in probiotics of dietary supplements Nutr. J. 14 1 2015 95 10.1186/s12937-015-0084-2 26370532 PMC4568587 · DOI
  145. [161]Campedelli I. Mathur H. Salvetti E. Clarke S. Rea M.C. Torriani S. Genus-Wide assessment of antibiotic resistance in lactobacillus spp Appl. Environ. Microbiol. 85 1 2018 e01738 10.1128/AEM.01738-18 18 PMC6293106 30366997 · DOI · Paper page
  146. [162]Sirichoat A. Flórez A.B. Vázquez L. Buppasiri P. Panya M. Lulitanond V. Mayo B. Antibiotic susceptibility profiles of lactic acid bacteria from the human vagina and genetic basis of acquired resistances Int. J. Mol. Sci. 21 7 2020 2594 10.3390/ijms21072594 32276519 PMC7178285 · DOI
  147. [163]Tóth A.G. Csabai I. Maróti G. Jerzsele Á. Dubecz A. Patai Á.V. A glimpse of antimicrobial resistance gene diversity in kefir and yoghurt Sci. Rep. 10 1 2020 22458 10.1038/s41598-020-80444-5 PMC7775456 33384459 · DOI
  148. [164]Wang Y. Dong J. Wang J. Chi W. Zhou W. Tian Q. Assessing the drug resistance profiles of oral probiotic lozenges J. Oral Microbiol. 14 1 2022 2019992 10.1080/20002297.2021.2019992 PMC8745366 35024089 · DOI
  149. [165]Wang Y. Jiang Y. Deng Y. Yi C. Wang Y. Ding M. Probiotic supplements: hope or hype? Front. Microbiol. 11 2020 160 10.3389/fmicb.2020.00160 32184760 PMC7058552 · DOI
  150. [166]Jacobsen L. Wilcks A. Hammer K. Huys G. Gevers D. Andersen S.R. Horizontal transfer of tet(M) and erm(B) resistance plasmids from food strains of Lactobacillus plantarum to Enterococcus faecalis JH2-2 in the gastrointestinal tract of gnotobiotic rats FEMS Microbiol. Ecol. 59 1 2007 158 166 10.1111/j.1574-6941.2006.00212.x 17014680 · DOI
  151. [167]Mater D.D. Langella P. Corthier G. Flores M.J. A probiotic Lactobacillus strain can acquire vancomycin resistance during digestive transit in mice J. Mol. Microbiol. Biotechnol. 14 1–3 2008 123 127 10.1159/000106091 17957119 · DOI
  152. [168]Feld L. Schjørring S. Hammer K. Licht T.R. Danielsen M. Krogfelt K. Wilcks A. Selective pressure affects transfer and establishment of a Lactobacillus plantarum resistance plasmid in the gastrointestinal environment J. Antimicrob. Chemother. 61 4 2008 845 852 10.1093/jac/dkn033 18238887 · DOI
  153. [169]Montassier E. Valdés-Mas R. Batard E. Zmora N. Dori-Bachash M. Suez J. Elinav E. Probiotics impact the antibiotic resistance gene reservoir along the human GI tract in a person-specific and antibiotic-dependent manner Nat. Microbiol. 6 8 2021 1043 1054 10.1038/s41564-021-00920-0 34226711 PMC8318886 · DOI · Paper page
  154. [170]Maier L. Pruteanu M. Kuhn M. Zeller G. Telzerow A. Anderson E.E. Extensive impact of non-antibiotic drugs on human gut bacteria Nature 555 7698 2018 623 628 10.1038/nature25979 29555994 PMC6108420 · DOI · Paper page
  155. [171]Li N. Yu H. Liu H. Wang Y. Zhou J. Ma X. Wang Z. Sun C. Qiao S. Horizontal transfer of vanA between probiotic Enterococcus faecium and Enterococcus faecalis in fermented soybean meal and in digestive tract of growing pigs J. Anim. Sci. Biotechnol. 10 2019 36 10.1186/s40104-019-0341-x 31044075 PMC6460829 · DOI
  156. [172]Thumu S.C.R. Halami P.M. Conjugal transfer of erm(B) and multiple tet genes from Lactobacillus spp. to bacterial pathogens in animal gut, in vitro and during food fermentation Food Res. Int. 116 2019 1066 1075 10.1016/j.foodres.2018.09.046 30716890 · DOI
  157. [173]Preethi C. Thumu S.C.R. Halami P.M. Occurrence and distribution of multiple antibiotic-resistant Enterococcus and Lactobacillus spp. from Indian poultry: in vivo transferability of their erythromycin, tetracycline and vancomycin resistance Ann. Microbiol. 67 2017 395 404 10.1007/s13213-017-1270-6 · DOI
  158. [174]Zarzecka U. Chajęcka-Wierzchowska W. Zadernowska A. Microorganisms from starter and protective cultures-Occurrence of antibiotic resistance and conjugal transfer of tet genes in vitro and during food fermentation Lebensm. Wiss. Technol. 153 2022 112490 10.1016/j.lwt.2021.112490 · DOI
  159. [175]Zhang P. Mao D. Gao H. Zheng L. Chen Z. Gao Y. Colonization of gut microbiota by plasmid-carrying bacteria is facilitated by evolutionary adaptation to antibiotic treatment ISME J. 16 5 2022 1284 1293 10.1038/s41396-021-01171-x 34903849 PMC9038720 · DOI
  160. [176]Lambrecht E. Van Coillie E. Van Meervenne E. Boon N. Heyndrickx M. Van de Wiele T. Commensal E. coli rapidly transfer antibiotic resistance genes to human intestinal microbiota in the Mucosal Simulator of the Human Intestinal Microbial Ecosystem (M-SHIME) Int. J. Food Microbiol. 311 2019 108357 10.1016/j.ijfoodmicro.2019.108357 31536878 · DOI
  161. [177]Heo S. Bae T. Lee J.H. Jeong D.W. Transfer of a lincomycin-resistant plasmid between coagulase-negative staphylococci during soybean fermentation and mouse intestine passage FEMS Microbiol. Lett. 366 10 2019 fnz113 10.1093/femsle/fnz113 31132119 · DOI
  162. [178]Hu Y. Yang X. Qin J. Lu N. Cheng G. Wu N. Metagenome-wide analysis of antibiotic resistance genes in a large cohort of human gut microbiota Nat. Commun. 4 2013 2151 10.1038/ncomms3151 23877117 · DOI
  163. [180]Smillie C.S. Smith M.B. Friedman J. Cordero O.X. David L.A. Alm E.J. Ecology drives a global network of gene exchange connecting the human microbiome Nature 480 2011 241 244 10.1038/nature10571 22037308 · DOI
  164. [182]Wong A. Matijasic B.B. Ibana J.A. Lim R.L.H. Editorial: antimicrobial resistance along the food chain: are we what we eat? Front. Microbiol. 13 2022 881882 10.3389/fmicb.2022.881882 PMC8971745 35369504 · DOI
  165. [183]Anisimova E.A. Yarullina D.R. Antibiotic resistance and the mobility of its genetic determinants in lactobacillus fermentum Mol. Genet. Microbiol. Virol. 35 2020 202 209 10.3103/S0891416820040035 · DOI
  166. [184]Ashwini M. Ray M. Halami P.M. Sumana K. Conjugal transfer of macrolide-lincosamide-streptogramin resistance from lactic acid bacteria isolated from food materials Mater. Today: Proc. 51 1 2021 707 714 10.1016/j.matpr.2021.06.213 · DOI
  167. [185]Li B. Chen D. Lin F. Wu C. Cao L. Chen H. Genomic island-mediated horizontal transfer of the erythromycin resistance gene erm(X) among bifidobacteria Appl. Environ. Microbiol. 88 10 2022 e0041022 10.1128/aem.00410-22 PMC9128502 35477272 · DOI
  168. [186]Kostenko V.V. Mouzykantov A.A. Baranova N.B. Boulygina E.A. Markelova M.I. Khusnutdinova D.R. Development of resistance to clarithromycin and amoxicillin-clavulanic acid in Lactiplantibacillus plantarum in vitro is followed by genomic rearrangements and evolution of virulence Microbiol. Spectr. 10 3 2022 e0236021 10.1128/spectrum.02360-21 PMC9241834 35579444 · DOI
  169. [187]Fatahi-Bafghi M. Naseri S. Alizehi A. Genome analysis of probiotic bacteria for antibiotic resistance genes Antonie Leeuwenhoek 115 3 2022 375 389 10.1007/s10482-021-01703-7 34989942 · DOI
  170. [189]Cao L. Chen H. Wang Q. Li B. Hu Y. Zhao C. Literature-based phenotype survey and in silico genotype investigation of antibiotic resistance in the genus Bifidobacterium Curr. Microbiol. 77 12 2020 4104 4113 10.1007/s00284-020-02230-w 33057753 · DOI
  171. [191]Naseri A. Seyedi-Sahebari S. Mahmoodpoor A. Sanaie S. Probiotics in critically ill patients: an umbrella review Indian J. Crit. Care Med. 26 3 2022 339 360 10.5005/jp-journals-10071-24129 35519905 PMC9015916 · DOI · Paper page
  172. [192]Lee Z.Y. Lew C.C.H. Ortiz-Reyes A. Patel J.J. Wong Y.J. Loh C.T.I. Martindale R.G. Heyland D.K. Benefits and harm of probiotics and synbiotics in adult critically ill patients. A systematic review and meta-analysis of randomized controlled trials with trial sequential analysis Clin. Nutr. 42 4 2023 519 531 10.1016/j.clnu.2023.01.019 36857961 · DOI
  173. [193]Yazdankhah S. Midtvedt T. Narvhus J. Berstad A. Lassen J. Halvorsen R. The use of probiotics for critically ill patients in hospitals Microb. Ecol. Health Dis. 21 3–4 2009 114 121 10.3109/08910600903495046 · DOI
  174. [194]Liu P.C. Yan Y.K. Ma Y.J. Wang X.W. Geng J. Wang M.C. Wei F.X. Zhang Y.W. Xu X.D. Zhang Y.C. Probiotics reduce postoperative infections in patients undergoing colorectal surgery: a systematic review and meta-analysis Gastroenterol. Res. Pract. 2017 2017 6029075 10.1155/2017/6029075 PMC5397731 28484489 · DOI · Paper page
  175. [195]Kotzampassi K. Why give my surgical patients probiotics Nutrients 14 20 2022 4389 10.3390/nu14204389 36297073 PMC9606978 · DOI
  176. [196]Purdel C. Ungurianu A. Adam-Dima I. Margină D. Exploring the potential impact of probiotic use on drug metabolism and efficacy Biomed. Pharmacother. 161 2023 114468 10.1016/j.biopha.2023.114468 36868015 · DOI
  177. [197]Greenblatt D.J. von Moltke L.L. Interaction of warfarin with drugs, natural substances, and foods J. Clin. Pharmacol. 45 2 2005 127 132 10.1177/0091270004271404 15647404 · DOI
  178. [198]Rannikko J. Holmberg V. Karppelin M. Arvola P. Huttunen R. Mattila E. Kerttula N. Puhto T. Tamm Ü. Koivula I. Vuento R. Syrjänen J. Hohenthal U. Fungemia and other fungal infections associated with use of Saccharomyces boulardii probiotic supplements Emerg. Infect. Dis. 27 8 2021 2090 2096 10.3201/eid2708.210018 34287140 PMC8314839 · DOI
  179. [199]Cerk K. Aguilera-Gómez M. Microbiota analysis for risk assessment: evaluation of hazardous dietary substances and its potential role on the gut microbiome variability and dysbiosis EFSA J. 20 Suppl 1 2022 e200404 10.2903/j.efsa.2022.e200404 PMC9131584 35634548 · DOI
  180. [200]Aggarwal N. Breedon A.M.E. Davis C.M. Hwang I.Y. Chang M.W. Engineering probiotics for therapeutic applications: recent examples and translational outlook Curr. Opin. Biotechnol. 65 2020 171 179 10.1016/j.copbio.2020.02.016 32304955 · DOI
  181. [201]Neil K. Allard N. Roy P. Grenier F. Menendez A. Burrus V. High-efficiency delivery of CRISPR-Cas9 by engineered probiotics enables precise microbiome editing Mol. Syst. Biol. 17 10 2021 e10335 10.15252/msb.202110335 PMC8527022 34665940 · DOI
  182. [202]Daeffler K.N. Galley J.D. Sheth R.U. Ortiz-Velez L.C. Bibb C.O. Shroyer N.F. Engineering bacterial thiosulfate and tetrathionate sensors for detecting gut inflammation Mol. Syst. Biol. 13 4 2017 923 10.15252/msb.20167416 28373240 PMC5408782 · DOI
  183. [204]Ho C.L. Tan H.Q. Chua K.J. Kang A. Lim K.H. Ling K.L. Engineered commensal microbes for diet-mediated colorectal-cancer chemoprevention Nat. Biomed. Eng. 2 1 2018 27 37 10.1038/s41551-017-0181-y 31015663 · DOI · Paper page
  184. [206]Peng M. Tabashsum Z. Patel P. Bernhardt C. Biswas D. Linoleic acids overproducing lactobacillus casei limits growth, survival, and virulence of Salmonella typhimurium and enterohaemorrhagic Escherichia coli Front. Microbiol. 9 2018 2663 10.3389/fmicb.2018.02663 30443248 PMC6223203 · DOI
  185. [207]Chowdhury S. Castro S. Coker C. Hinchliffe T.E. Arpaia N. Danino T. Programmable bacteria induce durable tumor regression and systemic antitumor immunity Nat. Med. 25 7 2019 1057 1063 10.1038/s41591-019-0498-z 31270504 PMC6688650 · DOI · Paper page
  186. [208]He L. Yang H. Tang J. Liu Z. Chen Y. Lu B. Intestinal probiotics E. coli Nissle 1917 as a targeted vehicle for delivery of p53 and Tum-5 to solid tumors for cancer therapy J. Biol. Eng. 13 2019 58 10.1186/s13036-019-0189-9 31297149 PMC6599283 · DOI
  187. [209]Hendrikx T. Duan Y. Wang Y. Oh J.H. Alexander L.M. Huang W. Bacteria engineered to produce IL-22 in intestine induce expression of REG3G to reduce ethanol-induced liver disease in mice Gut 68 8 2019 1504 1515 10.1136/gutjnl-2018-317232 30448775 PMC6387784 · DOI
  188. [210]Rosander A. Connolly E. Roos S. Removal of antibiotic resistance gene-carrying plasmids from Lactobacillus reuteri ATCC 55730 and characterization of the resulting daughter strain, L. reuteri DSM 17938 Appl. Environ. Microbiol. 74 19 2008 6032 6040 10.1128/AEM.00991-08 18689509 PMC2565949 · DOI
  189. [211]Buckner M.M.C. Ciusa M.L. Piddock L.J.V. Strategies to combat antimicrobial resistance: anti-plasmid and plasmid curing FEMS Microbiol. Rev. 42 6 2018 781 804 10.1093/femsre/fuy031 30085063 PMC6199537 · DOI
  190. [212]Hidalgo-Cantabrana C. O'Flaherty S. Barrangou R. CRISPR-based engineering of next-generation lactic acid bacteria Curr. Opin. Microbiol. 37 2017 79 87 10.1016/j.mib.2017.05.015 28622636 · DOI

Cited by

Sorted by citations

Authors
Liu, X., Zhao, H., & Wong, A.
Affiliations
Wenzhou-Kean University (CN)
Corresponding author
Wong, Aloysius
Venue
Heliyon
Publisher
Elsevier BV
Published
2024-03
Volume
10
Issue
6
Pages
e27908
ISSN
2405-8440 (ISSN-L)
OpenAlex
W4392764930
Cited by
44
References
24
Citations by year
2026: 20 · 2025: 19 · 2024: 5
FWCI
1.64
Type
journal article
Language
en
Open access
Locations
  • Heliyon (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
  • Wenzhou-Kean University
  • Southern Partners Fund (SpF2021002)
Topics
  • Life Sciences › Agricultural and Biological Sciences › Food Science › Probiotics and Fermented Foods
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
  • Life Sciences › Immunology and Microbiology › Immunology › Aquaculture disease management and microbiota
Keywords
probiotics, health risks, adverse effects, opportunistic infections, immunological effects, metabolic disorders, allergic reactions, antimicrobial resistance, systemic infection, local infection

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