Role of Lactobacillus reuteri in Human Health and Diseases
Open accessAbstract
Lactobacillus reuteri (L. reuteri) is a well-studied probiotic bacterium that can colonize a large number of mammals. In humans, L. reuteri is found in different body sites, including the gastrointestinal tract, urinary tract, skin and breast milk. The abundance of L. reuteri varies among different individuals. Several beneficial effects of L. reuteri have been noted. Firstly, L. reuteri can produce antimicrobial molecules, such as organic acids, ethanol and reuterin. Due to its antimicrobial activity, L. reuteri is able to inhibit the colonization of pathogenic microbes and remodel the commensal microbiota composition in the host. Secondly, L. reuteri can benefit the host immune system. For instance, some L. reuteri strains can reduce the production of pro-inflammatory cytokines while promoting regulatory T cell development and function. Thirdly, bearing the ability to strengthen the intestinal barrier, the colonization of L. reuteri may decrease the microbial translocation from the gut lumen to the tissues. Microbial translocation across the intestinal epithelium has been hypothesized as an initiator of inflammation. Therefore, inflammatory diseases, including those located in the gut as well as in remote tissues, may be ameliorated by increasing the colonization of L. reuteri. Notably, the decrease in the abundance of L. reuteri in humans in the past decades is correlated with an increase in the incidences of inflammatory diseases over the same period of time. Direct supplementation or prebiotic modulation of L. reuteri may be an attractive preventive and/or therapeutic avenue against inflammatory diseases.
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The adhesion capacity to the epithelium provides for the ability of bacterial strains to continue their antimicrobial activities over time by maintaining their presence in the host.
“Furthermore, the adhesion capacity to the epithelium provides for the ability of bacterial strains to continue their antimicrobial activities over time by maintaining their presence in the host [14, 15].”
From EVALUATION OF ADHESIVE AND AGGREGATION PROPERTIES OF LACTIC ACID BACTERIA ISOLATED FROM DIFFERENT BIOTOPES (2025) · cites this paper as [15]
The ‘Gut Colonization of L. reuteri’ section describes epithelial adhesion and its association with colonization, while ‘Production of Metabolites With Health-Promoting Effect’ describes antimicrobial substances made by some L. reuteri strains. The paper does not establish that adhesion maintains those strains’ antimicrobial activity over time, or make that claim for bacterial strains generally. The indexed passages provide section labels but no page numbers. (LLM, conf=0.82)
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Zelante, T., Iannitti, R. G., Cunha, C., De Luca, A., Giovannini, G., Pieraccini, G., Zecchi, R., D’Angelo, C., Massi-Benedetti, C., Fallarino, F., et al. (2013) · Immunity · doi:10.1016/j.immuni.2013.08.003 · Cited by 2,614 · see citing works
Role of the gut microbiota in immunity and inflammatory disease
Kamada, N., Seo, S.-U., Chen, G. Y., & Núñez, G. (2013) · Nature reviews. Immunology · doi:10.1038/nri3430 · Cited by 2,256 · see citing works
Genes and Molecules of Lactobacilli Supporting Probiotic Action
Lebeer, S., Vanderleyden, J., & De Keersmaecker, S. C. J. (2008) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00017-08 · Cited by 1,013 · see citing works
Gut microbial products regulate murine gastrointestinal motility via Toll-like receptor 4 signaling
Anitha, M., Vijay–Kumar, M., Sitaraman, S. V., Gewirtz, A. T., & Srinivasan, S. (2012) · Gastroenterology · doi:10.1053/j.gastro.2012.06.034 · Cited by 397 · see citing works
Importance of lactobacilli in food and feed biotechnology
Giraffa, G., Chanishvili, N., & Widyastuti, Y. (2010) · Research in Microbiology · doi:10.1016/j.resmic.2010.03.001 · Cited by 341 · see citing works
Bailey, M. T., Dowd, S. E., Parry, N. M. A., Galley, J. D., Schauer, D. B., & Lyte, M. (2010) · Infection and Immunity · doi:10.1128/iai.00862-09 · Cited by 335 · see citing works
Intestinal microbiota influence the early postnatal development of the enteric nervous system
Collins, J., Borojevic, R., Verdu, E. F., Huizinga, J. D., & Ratcliffe, E. M. (2014) · Neurogastroenterology & Motility · doi:10.1111/nmo.12236 · Cited by 318 · cited 1× · see citing works
“Moreover, germ-free animals show defective ENS morphology and excitability, which can be reversed by microbiota colonization (McVey Neufeld et al., 2013; Collins et al., 2014).”
BackgroundMicrobial symbionts accelerate wound healing via the neuropeptide hormone oxytocin
Poutahidis, T., Kearney, S. M., Levkovich, T., Qi, P., Varian, B. J., Lakritz, J. R., Ibrahim, Y. M., Chatzigiagkos, A., Alm, E. J., & Erdman, S. E. (2013) · PLoS ONE · doi:10.1371/journal.pone.0078898 · Cited by 310 · see citing works
Jones, M. L., Martoni, C. J., & Prakash, S. (2012) · European Journal of Clinical Nutrition · doi:10.1038/ejcn.2012.126 · Cited by 277 · see citing works
Indrio, F., Di Mauro, A., Riezzo, G., Civardi, E., Intini, C., Corvaglia, L., Ballardini, E., Bisceglia, M., Cinquetti, M., Brazzoduro, E., et al. (2014) · JAMA Pediatrics · doi:10.1001/jamapediatrics.2013.4367 · Cited by 228 · see citing works
He, B., Hoang, T. K., Wang, T., Ferris, M., Taylor, C. M., Tian, X., Luo, M., Tran, D. Q., Zhou, J., Tatevian, N., et al. (2017) · Journal of Experimental Medicine · doi:10.1084/jem.20160961 · Cited by 196 · see citing works
Microbial Reprogramming Inhibits Western Diet-Associated Obesity
Poutahidis, T., Kleinewietfeld, M., Smillie, C., Levkovich, T., Perrotta, A., Bhela, S., Varian, B. J., Ibrahim, Y. M., Lakritz, J. R., Kearney, S. M., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0068596 · Cited by 164 · see citing works
Connolly, N., Anixt, J., Manning, P., Ping‐I Lin, D., Marsolo, K. A., & Bowers, K. (2016) · Autism Research · doi:10.1002/aur.1586 · Cited by 125 · see citing works
Kšonžeková, P., Bystrický, P., Vlčková, S., Pätoprstý, V., Pulzová, L., Mudroňová, D., Kubašková, T., Csank, T., & Tkáčiková, Ľ. (2016) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2015.12.037 · Cited by 122 · cited 1× · see citing works
“In addition, EPS synthesized by L. reuteri is able to inhibit E. coli adhesion to porcine epithelial cells in vitro (Ksonzekova et al., 2016).”
BackgroundJørgensen, M. R., Kragelund, C., Jensen, P. Ø., Keller, M. K., & Twetman, S. (2017) · Journal of Oral Microbiology · doi:10.1080/20002297.2016.1274582 · Cited by 107 · cited 1× · see citing works
“Furthermore, some studies suggest that L. reuteri may have antifungal properties as well, where L. reuteri antagonizes, stops the growth of, and eventually kills various species of Candida (Jorgensen et al., 2017).”
ResultLee, J., Yang, W., Hostetler, A., Schultz, N., Suckow, M. A., Stewart, K. L., Kim, D. D., & Kim, H. S. (2016) · BMC Microbiology · doi:10.1186/s12866-016-0686-7 · Cited by 107 · see citing works
<i>Lactobacillus reuteri</i> in children with functional abdominal pain (FAP)
Romano, C., Ferrau', V., Cavataio, F., Iacono, G., Spina, M., Lionetti, E., Comisi, F., Famiani, A., & Comito, D. (2014) · Journal of Paediatrics and Child Health · doi:10.1111/j.1440-1754.2010.01797.x · Cited by 99 · see citing works
Weizman, Z., Abu-Abed, J., & Binsztok, M. (2016) · The Journal of Pediatrics · doi:10.1016/j.jpeds.2016.04.003 · Cited by 95 · see citing works
Brun, P., Gobbo, S., Caputi, V., Spagnol, L., Schirato, G., Pasqualin, M., Levorato, E., Palù, G., Giron, M. C., & Castagliuolo, I. (2015) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2015.03.018 · Cited by 92 · see citing works
Savino, F., Ceratto, S., Poggi, E., Cartosio, M. E., Cordero di Montezemolo, L., & Giannattasio, A. (2015) · Beneficial Microbes · doi:10.3920/bm2014.0090 · Cited by 62 · see citing works
Flagged first, then by citations
Research works printed but not linked: 216
- Abediankenari S. Ghasemi M. (2009). Generation of immune inhibitory dendritic cells and CD4+T regulatory cells inducing by TGF-beta. Iran. J. Allergy Asthma Immunol. 8 25– 30. 19279356
- Abhisingha M. Dumnil J. Pitaksutheepong C. (2017). Selection of potential probiotic Lactobacillus with inhibitory activity against Salmonella and fecal coliform bacteria. Probiotics Antimicrob. Proteins 10.1007/s12602-017-9304-8 [Epub ahead of print]. 28712023 · DOI
- Abrahamsson T. R. Jakobsson T. Bjorksten B. Oldaeus G. Jenmalm M. C. (2013). No effect of probiotics on respiratory allergies: a seven-year follow-up of a randomized controlled trial in infancy. Pediatr. Allergy Immunol. 24 556– 561. 10.1111/pai.12104 23902407 · DOI
- Abrahamsson T. R. Jakobsson T. Bottcher M. F. Fredrikson M. Jenmalm M. C. Bjorksten B. (2007). Probiotics in prevention of IgE-associated eczema: a double-blind, randomized, placebo-controlled trial. J. Allergys Clin. Immunol. 119 1174– 1180. 10.1016/j.jaci.2007.01.007 17349686 · DOI
- Agustina R. Kok F. J. van de Rest O. Fahmida U. Firmansyah A. Lukito W. (2012). Randomized trial of probiotics and calcium on diarrhea and respiratory tract infections in Indonesian children. Pediatrics 129 e1155– e1164. 10.1542/peds.2011-1379 22492764 · DOI
- Amara A. A. Shibl A. (2015). Role of probiotics in health improvement, infection control and disease treatment and management. Saudi Pharm. J. 23 107– 114. 10.1016/j.jsps.2013.07.001 25972729 PMC4421088 · DOI
- Ang L. Y. Too H. K. Tan E. L. Chow T. K. Shek P. C. Tham E. (2016). Antiviral activity of Lactobacillus reuteri Protectis against Coxsackievirus A and Enterovirus 71 infection in human skeletal muscle and colon cell lines. Virol. J. 13: 111. 10.1186/s12985-016-0567-6 27341804 PMC4920999 · DOI
- Armougom F. Henry M. Vialettes B. Raccah D. Raoult D. (2009). Monitoring bacterial community of human gut microbiota reveals an increase in Lactobacillus in obese patients and Methanogens in anorexic patients. PLoS One 4: e7125. 10.1371/journal.pone.0007125 19774074 PMC2742902 · DOI · Paper page
- Barrett E. Ross R. P. O’Toole P. W. Fitzgerald G. F. Stanton C. (2012). gamma-Aminobutyric acid production by culturable bacteria from the human intestine. J. Appl. Microbiol. 113 411– 417. 10.1111/j.1365-2672.2012.05344.x 22612585 · DOI · Paper page
- Bene K. Varga Z. Petrov V. O. Boyko N. Rajnavolgyi E. (2017). Gut microbiota species can provoke both inflammatory and tolerogenic immune responses in human dendritic cells mediated by retinoic acid receptor alpha ligation. Front. Immunol. 8: 427. 10.3389/fimmu.2017.00427 28458670 PMC5394128 · DOI
- Bervoets L. Van Hoorenbeeck K. Kortleven I. Van Noten C. Hens N. Vael C. (2013). Differences in gut microbiota composition between obese and lean children: a cross-sectional study. Gut Pathog. 5: 10. 10.1186/1757-4749-5-10 23631345 PMC3658928 · DOI
- Bisanz J. E. Seney S. McMillan A. Vongsa R. Koenig D. Wong L. (2014). A systems biology approach investigating the effect of probiotics on the vaginal microbiome and host responses in a double blind, placebo-controlled clinical trial of post-menopausal women. PLoS One 9: e104511. 10.1371/journal.pone.0104511 25127240 PMC4134203 · DOI
- Bottcher M. F. Abrahamsson T. R. Fredriksson M. Jakobsson T. Bjorksten B. (2008). Low breast milk TGF-beta2 is induced by Lactobacillus reuteri supplementation and associates with reduced risk of sensitization during infancy. Pediatr. Allergy Immunol. 19 497– 504. 10.1111/j.1399-3038.2007.00687.x 18221472 · DOI
- Braathen G. Ingildsen V. Twetman S. Ericson D. Jorgensen M. R. (2017). Presence of Lactobacillus reuteri in saliva coincide with higher salivary IgA in young adults after intake of probiotic lozenges. Benef. Microbes 8 17– 22. 10.3920/BM2016.0081 27873545 · DOI
- Braegger C. Chmielewska A. Decsi T. Kolacek S. Mihatsch W. Moreno L. (2011). Supplementation of infant formula with probiotics and/or prebiotics: a systematic review and comment by the ESPGHAN committee on nutrition. J. Pediatr. Gastroenterol. Nutr. 52 238– 250. 10.1097/MPG.0b013e3181fb9e80 21150647 · DOI
- Brenner T. A. Rice T. A. Anderson E. D. Percopo C. M. Rosenberg H. F. (2016). Immortalized MH-S cells lack defining features of primary alveolar macrophages and do not support mouse pneumovirus replication. Immunol. Lett. 172 106– 112. 10.1016/j.imlet.2016.02.012 26916143 PMC4846554 · DOI
- Britton R. A. Irwin R. Quach D. Schaefer L. Zhang J. Lee T. (2014). Probiotic L. reuteri treatment prevents bone loss in a menopausal ovariectomized mouse model. J. Cell. Physiol. 229 1822– 1830. 10.1002/jcp.24636 24677054 PMC4129456 · DOI · Paper page
- Brun P. Giron M. C. Qesari M. Porzionato A. Caputi V. Zoppellaro C. (2013). Toll-like receptor 2 regulates intestinal inflammation by controlling integrity of the enteric nervous system. Gastroenterology 145 1323– 1333. 10.1053/j.gastro.2013.08.047 23994200 · DOI · Paper page
- Buffington S. A. Di Prisco G. V. Auchtung T. A. Ajami N. J. Petrosino J. F. Costa-Mattioli M. (2016). Microbial reconstitution reverses maternal diet-induced social and synaptic deficits in offspring. Cell 165 1762– 1775. 10.1016/j.cell.2016.06.001 27315483 PMC5102250 · DOI · Paper page
- Burge G. Saulou-Berion C. Moussa M. Pollet B. Flourat A. Allais F. (2015). Diversity of Lactobacillus reuteri strains in converting glycerol into 3-hydroxypropionic acid. Appl. Biochem. Biotechnol. 177 923– 939. 10.1007/s12010-015-1787-8 26319567 · DOI
- Cadieux P. Wind A. Sommer P. Schaefer L. Crowley K. Britton R. A. (2008). Evaluation of reuterin production in urogenital probiotic Lactobacillus reuteri RC-14. Appl. Environ. Microbiol. 74 4645– 4649. 10.1128/AEM.00139-08 18539802 PMC2519358 · DOI
- Camilleri M. Nadeau A. Lamsam J. Nord S. L. Ryks M. Burton D. (2010). Understanding measurements of intestinal permeability in healthy humans with urine lactulose and mannitol excretion. Neurogastroenterol. Motil. 22 e15– e26. 10.1111/j.1365-2982.2009.01361.x 19614866 PMC2802677 · DOI
- Cekola P. L. Czerkies L. A. Storm H. M. Wang M. H. Roberts J. Saavedra J. M. (2015). Growth and tolerance of term infants fed formula with probiotic Lactobacillus reuteri. Clin. Pediatr. 54 1175– 1184. 10.1177/0009922815574076 25758426 · DOI
- Cervantes-Barragan L. Chai J. N. Tianero M. D. Di Luccia B. Ahern P. P. Merriman J. (2017). Lactobacillus reuteri induces gut intraepithelial CD4+CD8alphaalpha+ T cells. Science 357 806– 810. 10.1126/science.aah5825 28775213 PMC5687812 · DOI · Paper page
- Chau K. Lau E. Greenberg S. Jacobson S. Yazdani-Brojeni P. Verma N. (2015). Probiotics for infantile colic: a randomized, double-blind, placebo-controlled trial investigating Lactobacillus reuteri DSM 17938. J. Pediatr. 166 74– 78. 10.1016/j.jpeds.2014.09.020 25444531 · DOI
- Chen G. Chen J. (2013). A novel cell modification method used in biotransformation of glycerol to 3-HPA by Lactobacillus reuteri. Appl. Microbiol. Biotechnol. 97 4325– 4332. 10.1007/s00253-013-4723-2 23359000 · DOI
- Chen X. Y. Woodward A. Zijlstra R. T. Ganzle M. G. (2014). Exopolysaccharides synthesized by Lactobacillus reuteri protect against enterotoxigenic Escherichia coli in piglets. Appl. Environ. Microbiol. 80 5752– 5760. 10.1128/AEM.01782-14 25015886 PMC4178603 · DOI
- Cherian P. T. Wu X. Yang L. Scarborough J. S. Singh A. P. Alam Z. A. (2015). Gastrointestinal localization of metronidazole by a lactobacilli-inspired tetramic acid motif improves treatment outcomes in the hamster model of Clostridium difficile infection. J. Antimicrob. Chemother. 70 3061– 3069. 10.1093/jac/dkv231 26286574 PMC4677261 · DOI
- Chung H. J. Yu J. G. Lee I. A. Liu M. J. Shen Y. F. Sharma S. P. (2016). Intestinal removal of free fatty acids from hosts by Lactobacilli for the treatment of obesity. FEBS Open Bio 6 64– 76. 10.1002/2211-5463.12024 27047743 PMC4794792 · DOI
- Cleusix V. Lacroix C. Vollenweider S. Duboux M. Le Blay G. (2007). Inhibitory activity spectrum of reuterin produced by Lactobacillus reuteri against intestinal bacteria. BMC Microbiol. 7: 101. 10.1186/1471-2180-7-101 17997816 PMC2222629 · DOI
- Dahiya D. K. Renuka Puniya M. Shandilya U. K. Dhewa T. Kumar N. (2017). Gut microbiota modulation and its relationship with obesity using prebiotic fibers and probiotics: a review. Front. Microbiol. 8: 563. 10.3389/fmicb.2017.00563 28421057 PMC5378938 · DOI
- De Benedetto A. Rafaels N. M. McGirt L. Y. Ivanov A. I. Georas S. N. Cheadle C. (2011). Tight junction defects in patients with atopic dermatitis. J. Allergy Clin. Immunol. 127 771. e7– 786.e7. 10.1016/j.jaci.2010.10.018 21163515 PMC3049863 · DOI
- de Oliveira G. L. V. Leite A. Z. Higuchi B. S. Gonzaga M. I. Mariano V. S. (2017). Intestinal dysbiosis and probiotic applications in autoimmune diseases. Immunology 152 1– 12. 10.1111/imm.12765 28556916 PMC5543467 · DOI
- del Campo R. Garriga M. Perez-Aragon A. Guallarte P. Lamas A. Maiz L. (2014). Improvement of digestive health and reduction in proteobacterial populations in the gut microbiota of cystic fibrosis patients using a Lactobacillus reuteri probiotic preparation: a double blind prospective study. J. Cyst. Fibros. 13 716– 722. 10.1016/j.jcf.2014.02.007 24636808 · DOI
- Diaz M. Ladero V. del Rio B. Redruello B. Fernandez M. Martin M. C. (2016). Biofilm-forming capacity in biogenic amine-producing bacteria isolated from dairy products. Front. Microbiol. 7: 591. 10.3389/fmicb.2016.00591 27242675 PMC4864664 · DOI
- Dicksved J. Schreiber O. Willing B. Petersson J. Rang S. Phillipson M. (2012). Lactobacillus reuteri maintains a functional mucosal barrier during DSS treatment despite mucus layer dysfunction. PLoS One 7: e46399. 10.1371/journal.pone.0046399 23029509 PMC3459901 · DOI
- Dinleyici E. C. Dalgic N. Guven S. Metin O. Yasa O. Kurugol Z. (2015). Lactobacillus reuteri DSM 17938 shortens acute infectious diarrhea in a pediatric outpatient setting. J. Pediatr. 91 392– 396. 10.1016/j.jped.2014.10.009 25986615 · DOI
- Dinleyici E. C. Probage Study Group Vandenplas Y. (2014). Lactobacillus reuteri DSM 17938 effectively reduces the duration of acute diarrhoea in hospitalised children. Acta Paediatr. 103 e300– e305. 10.1111/apa.12617 24579935 · DOI
- Dore M. P. Cuccu M. Pes G. M. Manca A. Graham D. Y. (2014). Lactobacillus reuteri in the treatment of Helicobacter pylori infection. Intern. Emerg. Med. 9 649– 654. 10.1007/s11739-013-1013-z 24178436 · DOI
- Dore M. P. Soro S. Rocchi C. Loria M. F. Bibbo S. Pes G. M. (2016). Inclusion of Lactobacillus reuteri in the treatment of Helicobacter pylori in Sardinian patients: a case report series. Medicine 95: e3411. 10.1097/MD.0000000000003411 27082621 PMC4839865 · DOI
- Duar R. M. Lin X. B. Zheng J. Martino M. E. Grenier T. Perez-Munoz M. E. (2017). Lifestyles in transition: evolution and natural history of the genus Lactobacillus. FEMS Microbiol. Rev. 41(Suppl. 1) S27– S48. 10.1093/femsre/fux030 28673043 · DOI
- Edwards M. R. Dai R. Heid B. Cecere T. E. Khan D. Mu Q. (2017). Commercial rodent diets differentially regulate autoimmune glomerulonephritis, epigenetics and microbiota in MRL/lpr mice. Int. Immunol. 29 263– 276. 10.1093/intimm/dxx033 28637300 PMC5890898 · DOI
- Engels C. Schwab C. Zhang J. Stevens M. J. Bieri C. Ebert M. O. (2016). Acrolein contributes strongly to antimicrobial and heterocyclic amine transformation activities of reuterin. Sci. Rep. 6: 36246. 10.1038/srep36246 27819285 PMC5098142 · DOI
- Ericson D. Hamberg K. Bratthall G. Sinkiewicz-Enggren G. Ljunggren L. (2013). Salivary IgA response to probiotic bacteria and mutans streptococci after the use of chewing gum containing Lactobacillus reuteri. Pathog. Dis. 68 82– 87. 10.1111/2049-632X.12048 23737255 · DOI
- Esmaeili S. A. Mahmoudi M. Momtazi A. A. Sahebkar A. Doulabi H. Rastin M. (2017). Tolerogenic probiotics: potential immunoregulators in Systemic Lupus Erythematosus. J. Cell. Physiol. 232 1994– 2007. 10.1002/jcp.25748 27996081 · DOI
- Fåk F. Bäckhed F. (2012). Lactobacillus reuteri prevents diet-induced obesity, but not atherosclerosis, in a strain dependent fashion in Apoe-/- mice. PLoS One 7: e46837. 10.1371/journal.pone.0046837 23056479 PMC3467285 · DOI
- Francavilla R. Lionetti E. Castellaneta S. Ciruzzi F. Indrio F. Masciale A. (2012). Randomised clinical trial: Lactobacillus reuteri DSM 17938 vs. placebo in children with acute diarrhoea–a double-blind study. Aliment. Pharmacol. Ther. 36 363– 369. 10.1111/j.1365-2036.2012.05180.x 22680836 · DOI
- Francavilla R. Lionetti E. Castellaneta S. P. Magista A. M. Maurogiovanni G. Bucci N. (2008). Inhibition of Helicobacter pylori infection in humans by Lactobacillus reuteri ATCC 55730 and effect on eradication therapy: a pilot study. Helicobacter 13 127– 134. 10.1111/j.1523-5378.2008.00593.x 18321302 · DOI
- Francavilla R. Polimeno L. Demichina A. Maurogiovanni G. Principi B. Scaccianoce G. (2014). Lactobacillus reuteri strain combination in Helicobacter pylori infection: a randomized, double-blind, placebo-controlled study. J. Clin. Gastroenterol. 48 407– 413. 10.1097/MCG.0000000000000007 24296423 · DOI
- Franceschi F. Cazzato A. Nista E. C. Scarpellini E. Roccarina D. Gigante G. (2007). Role of probiotics in patients with Helicobacter pylori infection. Helicobacter 12(Suppl. 2) 59– 63. 10.1111/j.1523-5378.2007.00565.x 17991178 · DOI
- Frese S. A. Benson A. K. Tannock G. W. Loach D. M. Kim J. Zhang M. (2011). The evolution of host specialization in the vertebrate gut symbiont Lactobacillus reuteri. PLoS Genet. 7: e1001314. 10.1371/journal.pgen.1001314 21379339 PMC3040671 · DOI
- Frese S. A. Mackenzie D. A. Peterson D. A. Schmaltz R. Fangman T. Zhou Y. (2013). Molecular characterization of host-specific biofilm formation in a vertebrate gut symbiont. PLoS Genet. 9: e1004057. 10.1371/journal.pgen.1004057 24385934 PMC3873254 · DOI
- Galley J. D. Mackos A. R. Varaljay V. A. Bailey M. T. (2017). Stressor exposure has prolonged effects on colonic microbial community structure in Citrobacter rodentium-challenged mice. Sci. Rep. 7: 45012. 10.1038/srep45012 28344333 PMC5366811 · DOI
- Galley J. D. Nelson M. C. Yu Z. Dowd S. E. Walter J. Kumar P. S. (2014). Exposure to a social stressor disrupts the community structure of the colonic mucosa-associated microbiota. BMC Microbiol. 14: 189. 10.1186/1471-2180-14-189 25028050 PMC4105248 · DOI
- Ganzle M. G. Vogel R. F. (2003). Studies on the mode of action of reutericyclin. Appl. Environ. Microbiol. 69 1305– 1307. 10.1128/AEM.69.2.1305-1307.2003 12571063 PMC143594 · DOI
- Gao C. Major A. Rendon D. Lugo M. Jackson V. Shi Z. (2015). Histamine H2 Receptor-Mediated Suppression of Intestinal Inflammation by Probiotic Lactobacillus reuteri. mBio 6: e01358-15. 10.1128/mBio.01358-15 26670383 PMC4701830 · DOI · Paper page
- Garcia Rodenas C. L. Lepage M. Ngom-Bru C. Fotiou A. Papagaroufalis K. Berger B. (2016). Effect of formula containing Lactobacillus reuteri DSM 17938 on fecal microbiota of infants born by cesarean-section. J. Pediatr. Gastroenterol. Nutr. 63 681– 687. 10.1097/MPG.0000000000001198 27035371 · DOI
- Garofoli F. Civardi E. Indrio F. Mazzucchelli I. Angelini M. Tinelli C. (2014). The early administration of Lactobacillus reuteri DSM 17938 controls regurgitation episodes in full-term breastfed infants. Int. J. Food Sci. Nutr. 65 646– 648. 10.3109/09637486.2014.898251 24635827 · DOI
- Genis S. Sanchez-Chardi A. Bach A. Fabregas F. Aris A. (2017). A combination of lactic acid bacteria regulates Escherichia coli infection and inflammation of the bovine endometrium. J. Dairy Sci. 100 479– 492. 10.3168/jds.2016-11671 27837977 · DOI
- Gille C. Boer B. Marschal M. Urschitz M. S. Heinecke V. Hund V. (2016). Effect of probiotics on vaginal health in pregnancy. EFFPRO, a randomized controlled trial. Am. J. Obstet. Gynecol. 215 608. e1– 608.e7. 10.1016/j.ajog.2016.06.021 27342046 · DOI
- Gopi G. R. Ganesh N. Pandiaraj S. Sowmiya B. Brajesh R. G. Ramalingam S. (2015). A study on enhanced expression of 3-hydroxypropionic acid pathway genes and impact on its production in Lactobacillus reuteri. Food Technol. Biotechnol. 53 331– 336. 10.17113/ftb.53.03.15.3976 27904365 PMC5068375 · DOI
- Greifova G. Majekova H. Greif G. Body P. Greifova M. Dubnickova M. (2017). Analysis of antimicrobial and immunomodulatory substances produced by heterofermentative Lactobacillus reuteri. Folia Microbiol. 62 515– 524. 10.1007/s12223-017-0524-9 28401403 · DOI
- Grover S. Rastogi A. Singh J. Rajbongshi A. Bihari C. (2014). Spectrum of histomorphologic findings in liver in patients with SLE: a review. Hepat. Res. Treat. 2014: 562979. 10.1155/2014/562979 25136456 PMC4130189 · DOI
- Gu Q. Zhang C. Song D. Li P. Zhu X. (2015). Enhancing vitamin B12 content in soy-yogurt by Lactobacillus reuteri. Int. J. Food Microbiol. 206 56– 59. 10.1016/j.ijfoodmicro.2015.04.033 25955289 · DOI
- Gunning A. P. Kavanaugh D. Thursby E. Etzold S. MacKenzie D. A. Juge N. (2016). Use of atomic force microscopy to study the multi-modular interaction of bacterial adhesins to mucins. Int. J. Mol. Sci. 17: E1854. 10.3390/ijms17111854 27834807 PMC5133854 · DOI
- Gutierrez-Castrellon P. Lopez-Velazquez G. Diaz-Garcia L. Jimenez-Gutierrez C. Mancilla-Ramirez J. Estevez-Jimenez J. (2014). Diarrhea in preschool children and Lactobacillus reuteri: a randomized controlled trial. Pediatrics 133 e904– e909. 10.1542/peds.2013-0652 24639271 · DOI
- Harakeh S. M. Khan I. Kumosani T. Barbour E. Almasaudi S. B. Bahijri S. M. (2016). Gut microbiota: a contributing factor to obesity. Front. Cell. Infect. Microbiol. 6: 95 10.3389/fcimb.2016.00095 PMC5003832 27625997 · DOI
- Hemarajata P. Gao C. Pflughoeft K. J. Thomas C. M. Saulnier D. M. Spinler J. K. (2013). Lactobacillus reuteri-specific immunoregulatory gene rsiR modulates histamine production and immunomodulation by Lactobacillus reuteri. J. Bacteriol. 195 5567– 5576. 10.1128/JB.00261-13 24123819 PMC3889603 · DOI
- Hill C. Guarner F. Reid G. Gibson G. R. Merenstein D. J. Pot B. (2014). 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. 11 506– 514. 10.1038/nrgastro.2014.66 24912386 · DOI
- Holz C. Busjahn A. Mehling H. Arya S. Boettner M. Habibi H. (2015). Significant reduction in Helicobacter pylori load in humans with non-viable Lactobacillus reuteri DSM17648: a pilot study. Probiotics Antimicrob. Proteins 7 91– 100. 10.1007/s12602-014-9181-3 25481036 PMC4415890 · DOI
- Hou C. Wang Q. Zeng X. Yang F. Zhang J. Liu H. (2014). Complete genome sequence of Lactobacillus reuteri I5007, a probiotic strain isolated from healthy piglet. J. Biotechnol. 179 63– 64. 10.1016/j.jbiotec.2014.03.019 24685642 · DOI
- Hou C. Zeng X. Yang F. Liu H. Qiao S. (2015). Study and use of the probiotic Lactobacillus reuteri in pigs: a review. J. Anim. Sci. Biotechnol. 6: 14. 10.1186/s40104-015-0014-3 25954504 PMC4423586 · DOI
- Hoy-Schulz Y. E. Jannat K. Roberts T. Zaidi S. H. Unicomb L. Luby S. (2016). Safety and acceptability of Lactobacillus reuteri DSM 17938 and Bifidobacterium longum subspecies infantis 35624 in Bangladeshi infants: a phase I randomized clinical trial. BMC Complement. Altern. Med. 16: 44. 10.1186/s12906-016-1016-1 26832746 PMC4736167 · DOI
- Hsieh F. C. Lan C. C. Huang T. Y. Chen K. W. Chai C. Y. Chen W. T. (2016). Heat-killed and live Lactobacillus reuteri GMNL-263 exhibit similar effects on improving metabolic functions in high-fat diet-induced obese rats. Food Funct. 7 2374– 2388. 10.1039/c5fo01396h 27163114 · DOI
- Hsu T. C. Huang C. Y. Chiang S. Y. Lai W. X. Tsai C. H. Tzang B. S. (2008). Transglutaminase inhibitor cystamine alleviates the abnormality in liver from NZB/W F1 mice. Eur. J. Pharmacol. 579 382– 389. 10.1016/j.ejphar.2007.10.059 18031733 · DOI
- Hsu T. C. Huang C. Y. Liu C. H. Hsu K. C. Chen Y. H. Tzang B. S. (2017). Lactobacillus paracasei GMNL-32, Lactobacillus reuteri GMNL-89 and L. reuteri GMNL-263 ameliorate hepatic injuries in lupus-prone mice. Br. J. Nutr. 117 1066– 1074. 10.1017/S0007114517001039 28502277 · DOI
- Imase K. Tanaka A. Tokunaga K. Sugano H. Ishida H. Takahashi S. (2007). Lactobacillus reuteri tablets suppress Helicobacter pylori infection–a double-blind randomised placebo-controlled cross-over clinical study. Kansenshogaku Zasshi 81 387– 393. 10.11150/kansenshogakuzasshi1970.81.387 17695792 · DOI
- Indrio F. Riezzo G. Raimondi F. Bisceglia M. Cavallo L. Francavilla R. (2008). The effects of probiotics on feeding tolerance, bowel habits, and gastrointestinal motility in preterm newborns. J. Pediatr. 152 801– 806. 10.1016/j.jpeds.2007.11.005 18492520 · DOI
- Indrio F. Riezzo G. Raimondi F. Bisceglia M. Cavallo L. Francavilla R. (2009). Effects of probiotic and prebiotic on gastrointestinal motility in newborns. J. Physiol. Pharmacol. 60(Suppl. 6) 27– 31. 20224148
- Iniesta M. Herrera D. Montero E. Zurbriggen M. Matos A. R. Marin M. J. (2012). Probiotic effects of orally administered Lactobacillus reuteri-containing tablets on the subgingival and salivary microbiota in patients with gingivitis. A randomized clinical trial. J. Clin. Periodontol. 39 736– 744. 10.1111/j.1600-051X.2012.01914.x 22694350 · DOI
- Islam S. U. (2016). Clinical uses of probiotics. Medicine 95: e2658. 10.1097/MD.0000000000002658 26844491 PMC4748908 · DOI
- Jacobsen C. N. Rosenfeldt Nielsen V. Hayford A. E. Moller P. L. Michaelsen K. F. Paerregaard A. (1999). Screening of probiotic activities of forty-seven strains of Lactobacillus spp. by in vitro techniques and evaluation of the colonization ability of five selected strains in humans. Appl. Environ. Microbiol. 65 4949– 4956. 10543808 PMC91666
- Jensen H. Roos S. Jonsson H. Rud I. Grimmer S. van Pijkeren J. P. (2014). Role of Lactobacillus reuteri cell and mucus-binding protein A (CmbA) in adhesion to intestinal epithelial cells and mucus in vitro. Microbiology 160(Pt 4) 671– 681. 10.1099/mic.0.073551-0 24473252 PMC7336543 · DOI
- Jones M. L. Martoni C. J. Di Pietro E. Simon R. R. Prakash S. (2012a). Evaluation of clinical safety and tolerance of a Lactobacillus reuteri NCIMB 30242 supplement capsule: a randomized control trial. Regul. Toxicol. Pharmacol. 63 313– 320. 10.1016/j.yrtph.2012.04.003 22561556 · DOI · Paper page
- Jones M. L. Martoni C. J. Tamber S. Parent M. Prakash S. (2012c). Evaluation of safety and tolerance of microencapsulated Lactobacillus reuteri NCIMB 30242 in a yogurt formulation: a randomized, placebo-controlled, double-blind study. Food Chem. Toxicol. 50 2216– 2223. 10.1016/j.fct.2012.03.010 22425689 · DOI
- Jones S. E. Versalovic J. (2009). Probiotic Lactobacillus reuteri biofilms produce antimicrobial and anti-inflammatory factors. BMC Microbiol. 9: 35. 10.1186/1471-2180-9-35 19210794 PMC2653509 · DOI
- Jorgensen M. R. Keller M. K. Kragelund C. Hamberg K. Ericson D. Nielsen C. H. (2016). Lactobacillus reuteri supplements do not affect salivary IgA or cytokine levels in healthy subjects: a randomized, double-blind, placebo-controlled, cross-over trial. Acta Odontol. Scand. 74 399– 404. 10.3109/00016357.2016.1169439 27104984 · DOI
- Kamiya T. Wang L. Forsythe P. Goettsche G. Mao Y. Wang Y. (2006). Inhibitory effects of Lactobacillus reuteri on visceral pain induced by colorectal distension in Sprague-Dawley rats. Gut 55 191– 196. 10.1136/gut.2005.070987 16361309 PMC1856513 · DOI · Paper page
- Kandler O. Stetter K. O. Kohl R. (1980). Lactobacillus reuteri sp. nov., a new species of heterofermentative lactobacilli. Zentralbl. Bakteriol. Hyg. I Abt Orig. 1 264– 269. 10.1016/S0172-5564(80)80007-8 · DOI
- Karaffova V. Csank T. Mudronova D. Kiraly J. Revajova V. Gancarcikova S. (2017). Influence of Lactobacillus reuteri L26 Biocenol on immune response against porcine circovirus type 2 infection in germ-free mice. Benef. Microbes 8 367– 378. 10.3920/BM2016.0114 28504566 · DOI
- Karimi K. Inman M. D. Bienenstock J. Forsythe P. (2009). Lactobacillus reuteri-induced regulatory T cells protect against an allergic airway response in mice. Am. J. Respir. Crit. Care Med. 179 186– 193. 10.1164/rccm.200806-951OC 19029003 · DOI
- Kechagia M. Basoulis D. Konstantopoulou S. Dimitriadi D. Gyftopoulou K. Skarmoutsou N. (2013). Health benefits of probiotics: a review. ISRN Nutr. 2013: 481651. 10.5402/2013/481651 24959545 PMC4045285 · DOI
- Keller M. K. Nohr Larsen I. Karlsson I. Twetman S. (2014). Effect of tablets containing probiotic bacteria (Lactobacillus reuteri) on early caries lesions in adolescents: a pilot study. Benef. Microbes 5 403– 407. 10.3920/BM2013.0089 24889893 · DOI
- Kleerebezem M. Hols P. Bernard E. Rolain T. Zhou M. Siezen R. J. (2010). The extracellular biology of the lactobacilli. FEMS Microbiol. Rev. 34 199– 230. 10.1111/j.1574-6976.2010.00208.x 20088967 · DOI
- Koleva P. T. Bridgman S. L. Kozyrskyj A. L. (2015). The infant gut microbiome: evidence for obesity risk and dietary intervention. Nutrients 7 2237– 2260. 10.3390/nu7042237 25835047 PMC4425142 · DOI
- Krumbeck J. A. Marsteller N. L. Frese S. A. Peterson D. A. Ramer-Tait A. E. Hutkins R. W. (2016). Characterization of the ecological role of genes mediating acid resistance in Lactobacillus reuteri during colonization of the gastrointestinal tract. Environ. Microbiol. 18 2172– 2184. 10.1111/1462-2920.13108 26530032 · DOI
- Kunze W. A. Mao Y. K. Wang B. Huizinga J. D. Ma X. Forsythe P. (2009). Lactobacillus reuteri enhances excitability of colonic AH neurons by inhibiting calcium-dependent potassium channel opening. J. Cell Mol. Med. 13 2261– 2270. 10.1111/j.1582-4934.2009.00686.x 19210574 PMC6529958 · DOI · Paper page
- Lai N. Y. Mills K. Chiu I. M. (2017). Sensory neuron regulation of gastrointestinal inflammation and bacterial host defence. J. Intern. Med. 282 5– 23. 10.1111/joim.12591 28155242 PMC5474171 · DOI
- Lesbros-Pantoflickova D. Corthesy-Theulaz I. Blum A. L. (2007). Helicobacter pylori and probiotics. J. Nutr. 137(3 Suppl. 2) 812S– 818S. 10.1093/jn/137.3.812S 17311980 · DOI
- Li X. J. Yue L. Y. Guan X. F. Qiao S. Y. (2008). The adhesion of putative probiotic lactobacilli to cultured epithelial cells and porcine intestinal mucus. J. Appl. Microbiol. 104 1082– 1091. 10.1111/j.1365-2672.2007.03636.x 18081774 · DOI
- Liao P. H. Kuo W. W. Hsieh D. J. Yeh Y. L. Day C. H. Chen Y. H. (2016). Heat-killed Lactobacillus reuteri GMNL-263 prevents epididymal fat accumulation and cardiac injury in high-calorie diet-fed rats. Int. J. Med. Sci. 13 569– 577. 10.7150/ijms.15597 27499689 PMC4974905 · DOI
- Linares D. M. Gomez C. Renes E. Fresno J. M. Tornadijo M. E. Ross R. P. (2017). Lactic acid bacteria and bifidobacteria with potential to design natural biofunctional health-promoting dairy foods. Front. Microbiol. 8: 846. 10.3389/fmicb.2017.00846 28572792 PMC5435742 · DOI · Paper page
- Lionetti E. Miniello V. L. Castellaneta S. P. Magista A. M. de Canio A. Maurogiovanni G. (2006). Lactobacillus reuteri therapy to reduce side-effects during anti-Helicobacter pylori treatment in children: a randomized placebo controlled trial. Aliment. Pharmacol. Ther. 24 1461– 1468. 10.1111/j.1365-2036.2006.03145.x 17032283 · DOI
- Liu F. Wang X. Shi H. Wang Y. Xue C. Tang Q. J. (2017). Polymannuronic acid ameliorated obesity and inflammation associated with a high-fat and high-sucrose diet by modulating the gut microbiome in a murine model. Br. J. Nutr. 117 1332– 1342. 10.1017/S0007114517000964 28528593 · DOI
- Liu H. Hou C. Wang G. Jia H. Yu H. Zeng X. (2017). Lactobacillus reuteri I5007 modulates intestinal host defense peptide expression in the model of IPEC-J2 cells and neonatal piglets. Nutrients 9: E559. 10.3390/nu9060559 28561758 PMC5490538 · DOI
- Liu Y. Fatheree N. Y. Dingle B. M. Tran D. Q. Rhoads J. M. (2013). Lactobacillus reuteri DSM 17938 changes the frequency of Foxp3+ regulatory T cells in the intestine and mesenteric lymph node in experimental necrotizing enterocolitis. PLoS One 8: e56547. 10.1371/journal.pone.0056547 23437165 PMC3577854 · DOI
- Liu Y. Tran D. Q. Fatheree N. Y. Marc Rhoads J. (2014). Lactobacillus reuteri DSM 17938 differentially modulates effector memory T cells and Foxp3+ regulatory T cells in a mouse model of necrotizing enterocolitis. Am. J. Physiol. Gastrointest. Liver Physiol. 307 G177– G186. 10.1152/ajpgi.00038.2014 24852566 PMC4101683 · DOI
- Livingston M. Loach D. Wilson M. Tannock G. W. Baird M. (2010). Gut commensal Lactobacillus reuteri 100-23 stimulates an immunoregulatory response. Immunol. Cell Biol. 88 99– 102. 10.1038/icb.2009.71 19786979 · DOI
- Lorea Baroja M. Kirjavainen P. V. Hekmat S. Reid G. (2007). Anti-inflammatory effects of probiotic yogurt in inflammatory bowel disease patients. Clin. Exp. Immunol. 149 470– 479. 10.1111/j.1365-2249.2007.03434.x 17590176 PMC2219330 · DOI
- Ma X. Mao Y. K. Wang B. Huizinga J. D. Bienenstock J. Kunze W. (2009). Lactobacillus reuteri ingestion prevents hyperexcitability of colonic DRG neurons induced by noxious stimuli. Am. J. Physiol. Gastrointest. Liver Physiol. 296 G868– G875. 10.1152/ajpgi.90511.2008 19179624 · DOI
- Mackenzie D. A. Jeffers F. Parker M. L. Vibert-Vallet A. Bongaerts R. J. Roos S. (2010). Strain-specific diversity of mucus-binding proteins in the adhesion and aggregation properties of Lactobacillus reuteri. Microbiology 156(Pt 11) 3368– 3378. 10.1099/mic.0.043265-0 20847011 · DOI
- Macklaim J. M. Clemente J. C. Knight R. Gloor G. B. Reid G. (2015). Changes in vaginal microbiota following antimicrobial and probiotic therapy. Microb. Ecol. Health Dis. 26: 27799. 10.3402/mehd.v26.27799 26282697 PMC4539393 · DOI · Paper page
- Mackos A. R. Eubank T. D. Parry N. M. Bailey M. T. (2013). Probiotic Lactobacillus reuteri attenuates the stressor-enhanced severity of Citrobacter rodentium infection. Infect. Immun. 81 3253– 3263. 10.1128/IAI.00278-13 23798531 PMC3754198 · DOI · Paper page
- Mackos A. R. Galley J. D. Eubank T. D. Easterling R. S. Parry N. M. Fox J. G. (2016). Social stress-enhanced severity of Citrobacter rodentium-induced colitis is CCL2-dependent and attenuated by probiotic Lactobacillus reuteri. Mucosal Immunol. 9 515– 526. 10.1038/mi.2015.81 26422754 PMC4794400 · DOI
- Mangalat N. Liu Y. Fatheree N. Y. Ferris M. J. Van Arsdall M. R. Chen Z. (2012). Safety and tolerability of Lactobacillus reuteri DSM 17938 and effects on biomarkers in healthy adults: results from a randomized masked trial. PLoS One 7: e43910. 10.1371/journal.pone.0043910 22970150 PMC3435331 · DOI
- Markle J. G. Frank D. N. Mortin-Toth S. Robertson C. E. Feazel L. M. Rolle-Kampczyk U. (2013). Sex differences in the gut microbiome drive hormone-dependent regulation of autoimmunity. Science 339 1084– 1088. 10.1126/science.1233521 23328391 · DOI · Paper page
- Martoni C. J. Labbe A. Ganopolsky J. G. Prakash S. Jones M. L. (2015). Changes in bile acids, FGF-19 and sterol absorption in response to bile salt hydrolase active L. reuteri NCIMB 30242. Gut Microbes 6 57– 65. 10.1080/19490976.2015.1005474 25612224 PMC4615650 · DOI · Paper page
- McFall-Ngai M. (2007). Adaptive immunity: care for the community. Nature 445: 153. 10.1038/445153a 17215830 · DOI
- McMillan A. Dell M. Zellar M. P. Cribby S. Martz S. Hong E. (2011). Disruption of urogenital biofilms by lactobacilli. Colloids Surf. B Biointerfaces 86 58– 64. 10.1016/j.colsurfb.2011.03.016 21497071 · DOI
- McVey Neufeld K. A. Mao Y. K. Bienenstock J. Foster J. A. Kunze W. A. (2013). The microbiome is essential for normal gut intrinsic primary afferent neuron excitability in the mouse. Neurogastroenterol. Motil. 25 e183– e188. 10.1111/nmo.12049 23181420 · DOI · Paper page
- Mehling H. Busjahn A. (2013). Non-viable Lactobacillus reuteri DSMZ 17648 (Pylopass) as a new approach to Helicobacter pylori control in humans. Nutrients 5 3062– 3073. 10.3390/nu5083062 23917169 PMC3775242 · DOI
- Mi G. L. Zhao L. Qiao D. D. Kang W. Q. Tang M. Q. Xu J. K. (2015). Effectiveness of Lactobacillus reuteri in infantile colic and colicky induced maternal depression: a prospective single blind randomized trial. Antonie Van Leeuwenhoek 107 1547– 1553. 10.1007/s10482-015-0448-9 25876529 · DOI
- Million M. Angelakis E. Maraninchi M. Henry M. Giorgi R. Valero R. (2013a). Correlation between body mass index and gut concentrations of Lactobacillus reuteri, Bifidobacterium animalis, Methanobrevibacter smithii and Escherichia coli. Int. J. Obes. 37 1460– 1466. 10.1038/ijo.2013.20 23459324 PMC3826031 · DOI · Paper page
- Million M. Maraninchi M. Henry M. Armougom F. Richet H. Carrieri P. (2012). Obesity-associated gut microbiota is enriched in Lactobacillus reuteri and depleted in Bifidobacterium animalis and Methanobrevibacter smithii. Int. J. Obes. 36 817– 825. 10.1038/ijo.2011.153 21829158 PMC3374072 · DOI
- Million M. Thuny F. Angelakis E. Casalta J. P. Giorgi R. Habib G. (2013b). Lactobacillus reuteri and Escherichia coli in the human gut microbiota may predict weight gain associated with vancomycin treatment. Nutr. Diabetes 3: e87. 10.1038/nutd.2013.28 24018615 PMC3789131 · DOI
- Miniello V. L. Brunetti L. Tesse R. Natile M. Armenio L. Francavilla R. (2010). Lactobacillus reuteri modulates cytokines production in exhaled breath condensate of children with atopic dermatitis. J. Pediatr. Gastroenterol. Nutr. 50 573– 576. 10.1097/MPG.0b013e3181bb343f 20639717 · DOI
- Mishra S. K. Malik R. K. Manju G. Pandey N. Singroha G. Behare P. (2012). Characterization of a reuterin-producing Lactobacillus reuteri BPL-36 strain isolated from human infant fecal sample. Probiotics Antimicrob. Proteins 4 154– 161. 10.1007/s12602-012-9103-1 26782041 · DOI
- Mobini R. Tremaroli V. Stahlman M. Karlsson F. Levin M. Ljungberg M. (2017). Metabolic effects of Lactobacillus reuteri DSM 17938 in people with type 2 diabetes: a randomized controlled trial. Diabetes Obes. Metab. 19 579– 589. 10.1111/dom.12861 28009106 · DOI
- Molina V. C. Medici M. Taranto M. P. Font de Valdez G. (2009). Lactobacillus reuteri CRL 1098 prevents side effects produced by a nutritional vitamin B deficiency. J. Appl. Microbiol. 106 467– 473. 10.1111/j.1365-2672.2008.04014.x 19200314 · DOI
- Montalban-Arques A. De Schryver P. Bossier P. Gorkiewicz G. Mulero V. Gatlin D. M. (2015). Selective manipulation of the gut microbiota improves immune status in vertebrates. Front. Immunol. 6: 512. 10.3389/fimmu.2015.00512 26500650 PMC4598590 · DOI
- Morita H. Toh H. Fukuda S. Horikawa H. Oshima K. Suzuki T. (2008). Comparative genome analysis of Lactobacillus reuteri and Lactobacillus fermentum reveal a genomic island for reuterin and cobalamin production. DNA Res. 15 151– 161. 10.1093/dnares/dsn009 18487258 PMC2650639 · DOI
- Mu Q. Kirby J. Reilly C. M. Luo X. M. (2017a). Leaky gut as a danger signal for autoimmune diseases. Front. Immunol. 8: 598. 10.3389/fimmu.2017.00598 28588585 PMC5440529 · DOI
- Mu Q. Tavella V. J. Kirby J. L. Cecere T. E. Chung M. Lee J. (2017b). Antibiotics ameliorate lupus-like symptoms in mice. Sci. Rep. 7: 13675. 10.1038/s41598-017-14223-0 29057975 PMC5651817 · DOI
- Mu Q. Zhang H. Liao X. Lin K. Liu H. Edwards M. R. (2017c). Control of lupus nephritis by changes of gut microbiota. Microbiome 5: 73. 10.1186/s40168-017-0300-8 28697806 PMC5505136 · DOI
- Mu Q. Zhang H. Luo X. M. (2015). SLE: another autoimmune disorder influenced by microbes and diet? Front. Immunol. 6: 608. 10.3389/fimmu.2015.00608 26648937 PMC4663251 · DOI
- Mukai T. Asasaka T. Sato E. Mori K. Matsumoto M. Ohori H. (2002). Inhibition of binding of Helicobacter pylori to the glycolipid receptors by probiotic Lactobacillus reuteri. FEMS Immunol. Med. Microbiol. 32 105– 110. 10.1111/j.1574-695X.2002.tb00541.x 11821231 · DOI · Paper page
- Nagpal R. Tsuji H. Takahashi T. Kawashima K. Nagata S. Nomoto K. (2016). Sensitive quantitative analysis of the meconium bacterial microbiota in healthy term infants born vaginally or by cesarean section. Front. Microbiol. 7: 1997 10.3389/fmicb.2016.01997 PMC5156933 28018325 · DOI
- Navarro J. B. Mashburn-Warren L. Bakaletz L. O. Bailey M. T. Goodman S. D. (2017). Enhanced probiotic potential of Lactobacillus reuteri when delivered as a biofilm on dextranomer microspheres that contain beneficial cargo. Front. Microbiol. 8: 489. 10.3389/fmicb.2017.00489 28396655 PMC5366311 · DOI
- Nguyen N. T. Hanieh H. Nakahama T. Kishimoto T. (2013). The roles of aryl hydrocarbon receptor in immune responses. Int. Immunol. 25 335– 343. 10.1093/intimm/dxt011 23580432 · DOI
- Oh P. L. Benson A. K. Peterson D. A. Patil P. B. Moriyama E. N. Roos S. (2010). Diversification of the gut symbiont Lactobacillus reuteri as a result of host-driven evolution. ISME J. 4 377– 387. 10.1038/ismej.2009.123 19924154 · DOI
- Ojetti V. Bruno G. Ainora M. E. Gigante G. Rizzo G. Roccarina D. (2012). Impact of Lactobacillus reuteri supplementation on anti-Helicobacter pylori levofloxacin-based second-line therapy. Gastroenterol. Res. Pract. 2012: 740381. 10.1155/2012/740381 22690211 PMC3368352 · DOI
- Okeke F. Roland B. C. Mullin G. E. (2014). The role of the gut microbiome in the pathogenesis and treatment of obesity. Glob. Adv. Health Med. 3 44– 57. 10.7453/gahmj.2014.018 24891993 PMC4030605 · DOI
- Olson J. K. Rager T. M. Navarro J. B. Mashburn-Warren L. Goodman S. D. Besner G. E. (2016). Harvesting the benefits of biofilms: a novel probiotic delivery system for the prevention of necrotizing enterocolitis. J. Pediatr. Surg. 51 936– 941. 10.1016/j.jpedsurg.2016.02.062 27032609 · DOI
- Oncel M. Y. Sari F. N. Arayici S. Guzoglu N. Erdeve O. Uras N. (2014). Lactobacillus reuteri for the prevention of necrotising enterocolitis in very low birthweight infants: a randomised controlled trial. Arch. Dis. Child. Fetal Neonatal Ed. 99 F110– F115. 10.1136/archdischild-2013-304745 24309022 · DOI
- Pallin A. Agback P. Jonsson H. Roos S. (2016). Evaluation of growth, metabolism and production of potentially bioactive components during fermentation of barley with Lactobacillus reuteri. Food Microbiol. 57 159– 171. 10.1016/j.fm.2016.02.011 27052715 · DOI
- Park S. K. Park D. I. Choi J. S. Kang M. S. Park J. H. Kim H. J. (2007). The effect of probiotics on Helicobacter pylori eradication. Hepatogastroenterology 54 2032– 2036. 18251154
- Petricevic L. Unger F. M. Viernstein H. Kiss H. (2008). Randomized, double-blind, placebo-controlled study of oral lactobacilli to improve the vaginal flora of postmenopausal women. Eur. J. Obstet. Gynecol. Reprod. Biol. 141 54– 57. 10.1016/j.ejogrb.2008.06.003 18701205 · DOI
- Piyathilake C. J. Ollberding N. J. Kumar R. Macaluso M. Alvarez R. D. Morrow C. D. (2016). Cervical microbiota associated with higher grade cervical intraepithelial neoplasia in women infected with high-risk human papillomaviruses. Cancer Prev. Res. 9 357– 366. 10.1158/1940-6207.CAPR-15-0350 26935422 PMC4869983 · DOI
- Preidis G. A. Saulnier D. M. Blutt S. E. Mistretta T. A. Riehle K. P. Major A. M. (2012). Host response to probiotics determined by nutritional status of rotavirus-infected neonatal mice. J. Pediatr. Gastroenterol. Nutr. 55 299– 307. 10.1097/MPG.0b013e31824d2548 22343914 PMC4010314 · DOI
- Raynaud C. Sarcabal P. Meynial-Salles I. Croux C. Soucaille P. (2003). Molecular characterization of the 1,3-propanediol (1,3-PD) operon of Clostridium butyricum. Proc. Natl. Acad. Sci. U.S.A. 100 5010– 5015. 10.1073/pnas.0734105100 12704244 PMC154289 · DOI
- Reid G. Burton J. (2002). Use of Lactobacillus to prevent infection by pathogenic bacteria. Microbes Infect. 4 319– 324. 10.1016/S1286-4579(02)01544-7 11909742 · DOI
- Rojas M. A. Lozano J. M. Rojas M. X. Rodriguez V. A. Rondon M. A. Bastidas J. A. (2012). Prophylactic probiotics to prevent death and nosocomial infection in preterm infants. Pediatrics 130 e1113– e1120. 10.1542/peds.2011-3584 23071204 · DOI
- Romani Vestman N. Chen T. Lif Holgerson P. Ohman C. Johansson I. (2015). Oral microbiota shift after 12-week supplementation with Lactobacillus reuteri DSM 17938 and PTA 5289; a randomized control trial. PLoS One 10: e0125812. 10.1371/journal.pone.0125812 25946126 PMC4422650 · DOI · Paper page
- Roos S. Dicksved J. Tarasco V. Locatelli E. Ricceri F. Grandin U. (2013). 454 pyrosequencing analysis on faecal samples from a randomized DBPC trial of colicky infants treated with Lactobacillus reuteri DSM 17938. PLoS One 8: e56710. 10.1371/journal.pone.0056710 23468874 PMC3585302 · DOI
- Roos S. Jonsson H. (2002). A high-molecular-mass cell-surface protein from Lactobacillus reuteri 1063 adheres to mucus components. Microbiology 148(Pt 2) 433– 442. 10.1099/00221287-148-2-433 11832507 · DOI
- Rosenfeldt V. Benfeldt E. Nielsen S. D. Michaelsen K. F. Jeppesen D. L. Valerius N. H. (2003). Effect of probiotic Lactobacillus strains in children with atopic dermatitis. J. Allergy Clin. Immunol. 111 389– 395. 10.1067/mai.2003.389 12589361 · DOI
- Rosenfeldt V. Benfeldt E. Valerius N. H. Paerregaard A. Michaelsen K. F. (2004). Effect of probiotics on gastrointestinal symptoms and small intestinal permeability in children with atopic dermatitis. J. Pediatr. 145 612– 616. 10.1016/j.jpeds.2004.06.068 15520759 · DOI
- Rosenfeldt V. Michaelsen K. F. Jakobsen M. Larsen C. N. Moller P. L. Pedersen P. (2002a). Effect of probiotic Lactobacillus strains in young children hospitalized with acute diarrhea. Pediatr. Infect. Dis. J. 21 411– 416. 10.1097/00006454-200205000-00012 12150178 · DOI
- Rosenfeldt V. Michaelsen K. F. Jakobsen M. Larsen C. N. Moller P. L. Tvede M. (2002b). Effect of probiotic Lactobacillus strains on acute diarrhea in a cohort of nonhospitalized children attending day-care centers. Pediatr. Infect. Dis. J. 21 417– 419. 12150179
- Rossi F. Gardini F. Rizzotti L. La Gioia F. Tabanelli G. Torriani S. (2011). Quantitative analysis of histidine decarboxylase gene (hdcA) transcription and histamine production by Streptococcus thermophilus PRI60 under conditions relevant to cheese making. Appl. Environ. Microbiol. 77 2817– 2822. 10.1128/AEM.02531-10 21378060 PMC3126354 · DOI
- Salas-Jara M. J. Ilabaca A. Vega M. Garcia A. (2016). Biofilm forming Lactobacillus: new challenges for the development of probiotics. Microorganisms 4: E35. 10.3390/microorganisms4030035 27681929 PMC5039595 · DOI
- Santos F. Spinler J. K. Saulnier D. M. Molenaar D. Teusink B. de Vos W. M. (2011). Functional identification in Lactobacillus reuteri of a PocR-like transcription factor regulating glycerol utilization and vitamin B12 synthesis. Microb. Cell Fact. 10: 55. 10.1186/1475-2859-10-55 21777454 PMC3162504 · DOI
- Santos F. Vera J. L. van der Heijden R. Valdez G. de Vos W. M. Sesma F. (2008a). The complete coenzyme B12 biosynthesis gene cluster of Lactobacillus reuteri CRL1098. Microbiology 154(Pt 1) 81– 93. 10.1099/mic.0.2007/011569-0 18174128 · DOI
- Santos F. Wegkamp A. de Vos W. M. Smid E. J. Hugenholtz J. (2008b). High-Level folate production in fermented foods by the B12 producer Lactobacillus reuteri JCM1112. Appl. Environ. Microbiol. 74 3291– 3294. 10.1128/AEM.02719-07 18344331 PMC2394963 · DOI
- Savino F. Cordisco L. Tarasco V. Palumeri E. Calabrese R. Oggero R. (2010). Lactobacillus reuteri DSM 17938 in infantile colic: a randomized, double-blind, placebo-controlled trial. Pediatrics 126 e526– e533. 10.1542/peds.2010-0433 20713478 · DOI
- Savino F. Fornasero S. Ceratto S. De Marco A. Mandras N. Roana J. (2015b). Probiotics and gut health in infants: a preliminary case-control observational study about early treatment with Lactobacillus reuteri DSM 17938. Clin. Chim. Acta 451(Pt A) 82– 87. 10.1016/j.cca.2015.02.027 25704298 · DOI
- Savino F. Pelle E. Palumeri E. Oggero R. Miniero R. (2007). Lactobacillus reuteri (American Type Culture Collection Strain 55730) versus simethicone in the treatment of infantile colic: a prospective randomized study. Pediatrics 119 e124– e130. 10.1542/peds.2006-1222 17200238 · DOI
- Scaccianoce G. Zullo A. Hassan C. Gentili F. Cristofari F. Cardinale V. (2008). Triple therapies plus different probiotics for Helicobacter pylori eradication. Eur. Rev. Med. Pharmacol. Sci. 12 251– 256. 18727457
- Scott K. P. Antoine J. M. Midtvedt T. van Hemert S. (2015). Manipulating the gut microbiota to maintain health and treat disease. Microb. Ecol. Health Dis. 26: 25877. 10.3402/mehd.v26.25877 25651995 PMC4315778 · DOI
- Seo B. J. Mun M. R. J R. K. Kim C. J. Lee I. Chang Y. H. (2010). Bile tolerant Lactobacillus reuteri isolated from pig feces inhibits enteric bacterial pathogens and porcine rotavirus. Vet. Res. Commun. 34 323– 333. 10.1007/s11259-010-9357-6 20396947 · DOI
- Shi L. H. Balakrishnan K. Thiagarajah K. Mohd Ismail N. I. Yin O. S. (2016). Beneficial properties of probiotics. Trop. Life Sci. Res. 27 73– 90. 10.21315/tlsr2016.27.2.6 27688852 PMC5031164 · DOI
- Shornikova A. V. Casas I. A. Isolauri E. Mykkanen H. Vesikari T. (1997a). Lactobacillus reuteri as a therapeutic agent in acute diarrhea in young children. J. Pediatr. Gastroenterol. Nutr. 24 399– 404. 9144122
- Shornikova A. V. Casas I. A. Mykkanen H. Salo E. Vesikari T. (1997b). Bacteriotherapy with Lactobacillus reuteri in rotavirus gastroenteritis. Pediatr. Infect. Dis. J. 16 1103– 1107. 9427453
- Sims I. M. Frese S. A. Walter J. Loach D. Wilson M. Appleyard K. (2011). Structure and functions of exopolysaccharide produced by gut commensal Lactobacillus reuteri 100-23. ISME J. 5 1115– 1124. 10.1038/ismej.2010.201 21248858 PMC3146279 · DOI
- Sinkiewicz G. (2010). Lactobacillus reuteri in Health and Disease. Doctoral dissertation, Malmö University Malmö.
- Soto A. Martin V. Jimenez E. Mader I. Rodriguez J. M. Fernandez L. (2014). Lactobacilli and bifidobacteria in human breast milk: influence of antibiotherapy and other host and clinical factors. J. Pediatr. Gastroenterol. Nutr. 59 78– 88. 10.1097/MPG.0000000000000347 24590211 PMC4086764 · DOI
- Spinler J. K. Taweechotipatr M. Rognerud C. L. Ou C. N. Tumwasorn S. Versalovic J. (2008). Human-derived probiotic Lactobacillus reuteri demonstrate antimicrobial activities targeting diverse enteric bacterial pathogens. Anaerobe 14 166– 171. 10.1016/j.anaerobe.2008.02.001 18396068 PMC2494590 · DOI
- Sriramulu D. D. Liang M. Hernandez-Romero D. Raux-Deery E. Lunsdorf H. Parsons J. B. (2008). Lactobacillus reuteri DSM 20016 produces cobalamin-dependent diol dehydratase in metabolosomes and metabolizes 1,2-propanediol by disproportionation. J. Bacteriol. 190 4559– 4567. 10.1128/JB.01535-07 18469107 PMC2446795 · DOI · Paper page
- Stensson M. Koch G. Coric S. Abrahamsson T. R. Jenmalm M. C. Birkhed D. (2014). Oral administration of Lactobacillus reuteri during the first year of life reduces caries prevalence in the primary dentition at 9 years of age. Caries Res. 48 111– 117. 10.1159/000354412 24296746 · DOI
- Stevens J. F. Maier C. S. (2008). Acrolein: sources, metabolism, and biomolecular interactions relevant to human health and disease. Mol. Nutr. Food Res. 52 7– 25. 10.1002/mnfr.200700412 18203133 PMC2423340 · DOI
- Stevens M. J. Vollenweider S. Meile L. Lacroix C. (2011). 1,3-Propanediol dehydrogenases in Lactobacillus reuteri: impact on central metabolism and 3-hydroxypropionaldehyde production. Microb. Cell Fact. 10: 61. 10.1186/1475-2859-10-61 21812997 PMC3180264 · DOI
- Su M. S. Ganzle M. G. (2014). Novel two-component regulatory systems play a role in biofilm formation of Lactobacillus reuteri rodent isolate 100-23. Microbiology 160(Pt 4) 795– 806. 10.1099/mic.0.071399-0 24509500 · DOI
- Su M. S. Schlicht S. Ganzle M. G. (2011). Contribution of glutamate decarboxylase in Lactobacillus reuteri to acid resistance and persistence in sourdough fermentation. Microb. Cell Fact. 10(Suppl. 1): S8. 10.1186/1475-2859-10-S1-S8 21995488 PMC3231934 · DOI
- Su Y. Chen X. Liu M. Guo X. (2017). Effect of three lactobacilli with strain-specific activities on the growth performance, faecal microbiota and ileum mucosa proteomics of piglets. J. Anim. Sci. Biotechnol. 8: 52. 10.1186/s40104-017-0183-3 28616225 PMC5466754 · DOI
- Sung V. Hiscock H. Tang M. L. Mensah F. K. Nation M. L. Satzke C. (2014). Treating infant colic with the probiotic Lactobacillus reuteri: double blind, placebo controlled randomised trial. BMJ 348: g2107. 10.1136/bmj.g2107 24690625 PMC3972414 · DOI
- Szajewska H. Gyrczuk E. Horvath A. (2013). Lactobacillus reuteri DSM 17938 for the management of infantile colic in breastfed infants: a randomized, double-blind, placebo-controlled trial. J. Pediatr. 162 257– 262. 10.1016/j.jpeds.2012.08.004 22981952 · DOI
- Talarico T. L. Casas I. A. Chung T. C. Dobrogosz W. J. (1988). Production and isolation of reuterin, a growth inhibitor produced by Lactobacillus reuteri. Antimicrob. Agents Chemother. 32 1854– 1858. 10.1128/AAC.32.12.1854 3245697 PMC176032 · DOI
- Talarico T. L. Dobrogosz W. J. (1989). Chemical characterization of an antimicrobial substance produced by Lactobacillus reuteri. Antimicrob. Agents Chemother. 33 674– 679. 10.1128/AAC.33.5.674 2751282 PMC172512 · DOI
- Talarico T. L. Dobrogosz W. J. (1990). Purification and characterization of glycerol dehydratase from Lactobacillus reuteri. Appl. Environ. Microbiol. 56 1195– 1197. 16348166 PMC184372
- Taranto M. P. Vera J. L. Hugenholtz J. De Valdez G. F. Sesma F. (2003). Lactobacillus reuteri CRL1098 produces cobalamin. J. Bacteriol. 185 5643– 5647. 10.1128/JB.185.18.5643-5647.2003 12949118 PMC193752 · DOI
- Thomas C. M. Hong T. van Pijkeren J. P. Hemarajata P. Trinh D. V. Hu W. (2012). Histamine derived from probiotic Lactobacillus reuteri suppresses TNF via modulation of PKA and ERK signaling. PLoS One 7: e31951. 10.1371/journal.pone.0031951 22384111 PMC3285189 · DOI · Paper page
- Thomas C. M. Saulnier D. M. Spinler J. K. Hemarajata P. Gao C. Jones S. E. (2016). FolC2-mediated folate metabolism contributes to suppression of inflammation by probiotic Lactobacillus reuteri. Microbiologyopen 5 802– 818. 10.1002/mbo3.371 27353144 PMC5061717 · DOI
- Tsokos G. C. (2011). Systemic lupus erythematosus. N. Engl. J. Med. 365 2110– 2121. 10.1056/NEJMra1100359 22129255 · DOI
- Tubelius P. Stan V. Zachrisson A. (2005). Increasing work-place healthiness with the probiotic Lactobacillus reuteri: a randomised, double-blind placebo-controlled study. Environ. Health 4: 25. 10.1186/1476-069X-4-25 16274475 PMC1298318 · DOI
- Tzang B. S. Liu C. H. Hsu K. C. Chen Y. H. Huang C. Y. Hsu T. C. (2017). Effects of oral Lactobacillus administration on antioxidant activities and CD4+CD25+forkhead box P3 (FoxP3)+ T cells in NZB/W F1 mice. Br. J. Nutr. 118 333– 342. 10.1017/S0007114517002112 28901888 · DOI
- Valeur N. Engel P. Carbajal N. Connolly E. Ladefoged K. (2004). Colonization and immunomodulation by Lactobacillus reuteri ATCC 55730 in the human gastrointestinal tract. Appl. Environ. Microbiol. 70 1176– 1181. 10.1128/AEM.70.2.1176-1181.2004 14766603 PMC348788 · DOI
- Walter J. Britton R. A. Roos S. (2011). Host-microbial symbiosis in the vertebrate gastrointestinal tract and the Lactobacillus reuteri paradigm. Proc. Natl. Acad. Sci. U.S.A. 108(Suppl. 1) 4645– 4652. 10.1073/pnas.1000099107 20615995 PMC3063604 · DOI
- Walter J. Chagnaud P. Tannock G. W. Loach D. M. Dal Bello F. Jenkinson H. F. (2005). A high-molecular-mass surface protein (Lsp) and methionine sulfoxide reductase B (MsrB) contribute to the ecological performance of Lactobacillus reuteri in the murine gut. Appl. Environ. Microbiol. 71 979– 986. 10.1128/AEM.71.2.979-986.2005 15691956 PMC546760 · DOI
- Walter J. Loach D. M. Alqumber M. Rockel C. Hermann C. Pfitzenmaier M. (2007). D-alanyl ester depletion of teichoic acids in Lactobacillus reuteri 100-23 results in impaired colonization of the mouse gastrointestinal tract. Environ. Microbiol. 9 1750– 1760. 10.1111/j.1462-2920.2007.01292.x 17564608 · DOI
- Walter J. Schwab C. Loach D. M. Ganzle M. G. Tannock G. W. (2008). Glucosyltransferase A (GtfA) and inulosucrase (Inu) of Lactobacillus reuteri TMW1.106 contribute to cell aggregation, in vitro biofilm formation, and colonization of the mouse gastrointestinal tract. Microbiology 154(Pt 1) 72– 80. 10.1099/mic.0.2007/010637-0 18174127 · DOI
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“These effects can be achieved by the secretion of inhibitory molecules such as bacteriocins and other antimicrobial chemicals [15].”
- Authors
- Mu, Q., Tavella, V. J., & Luo, X. M.
- Affiliations
- Virginia–Maryland College of Veterinary Medicine (US)
- Corresponding author
- Luo, Xin M.
- Venue
- Frontiers in Microbiology
- Publisher
- Frontiers Media SA
- Published
- 2018-04-19
- Volume
- 9
- Pages
- 757-757
- ISSN
- 1664-302X (ISSN-L)
- PMC
- PMC5917019
- OpenAlex
- W2795389370
- Cited by
- 744
- References
- 20
- Citations by year
- 2026: 78 · 2025: 116 · 2024: 104 · 2023: 115 · 2022: 118 · 2021: 102 · 2020: 71 · 2019: 32 · 2018: 7
- FWCI
- 5.38
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Frontiers in Microbiology (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- VTechWorks (Virginia Tech) (submittedVersion, cc-by)
- Funders
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (AR067418)
- 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 › Microbiology › Reproductive tract infections research
- Keywords
- Lactobacillus reuteri, probiotics, gut microbiota, antimicrobial activity, reuterin, organic acids, immunomodulation, regulatory T cells, inflammatory cytokines, intestinal barrier, microbial translocation, inflammatory diseases, prebiotics, breast milk, urinary tract colonization, skin colonization
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