Greifová G, Májeková H, Greif G, Body P, Greifová M, Dubničková M. Analysis of antimicrobial and immunomodulatory substances produced by heterofermentative Lactobacillus reuteri. Folia Microbiol (Praha). 2017 Nov;62(6):515-524. doi: 10.1007/s12223-017-0524-9
Citations in Web of Science database:
- Li W, He H, Li S, Jiang B, Liu C, Huang Y. Effects of dietary Lactobacillus reuteri on antimicrobial activity, antioxidant capacity, non-specific immune response, and resistance to Streptococcus agalactiae infection of the Nile tilapia (Oreochromis niloticus). Aquaculture Reports. 2024;35:N°101976. 10.1016/j.aqrep.2024.101976
- Mbaye B, Wasfy RM, Alou MT, Borentain P, Gerolami R, Dufour JC, Million M. A catalog of ethanol-producing microbes in humans. Future Microbiol. 2024;19(8):697-714. doi: 10.2217/fmb-2023-0250.
- Shaposhnikov LA, Tishkov VI, Pometun AA. Lactobacilli and Klebsiella: Two Opposites in the Fight for Human Health. Biochemistry (Mosc). 2024;89(Suppl 1):S71-S89. doi: 10.1134/S0006297924140050.
- Abdel Ghany Elrahmany HM, Ali A, El-Batawy OI, Khedr M, Hassan MA. Genetic engineering of UV-mutated Bifidobacterium longum and Lactobacillus acidophilus in relation to folic acid and Anti-inflammatory productivity. Egyptian Journal of Chemistry. 2023;66(13), 983-992. doi: 10.21608/ejchem.2023.199128.7711
- [o1]El-Aidie SAM, Mabrouk AM, Abd-Elgawad AR, El- Garhi HM. Physicochemical, textural and organoleptic properties of functional processed cheese manufactured from ultrafiltered milk. Biocatalysis and Agricultural Biotechnology,. 2023;51:102798, doi: 10.1016/j.bcab.2023.102798
- [o1]Wu Y, Cao X, Du H, Guo X, Han Y, McClements DJ, Decker E, Xing B, Xiao H. Adverse effects of titanium dioxide nanoparticles on beneficial gut bacteria and host health based on untargeted metabolomics analysis. Environmental Research. 2023 Jul 1;228:115921. doi: 10.1016/j.envres.2023.115921
- [o1]Rodrigues FJ, Cedran MF, Bicas JL, Sato HH.Inhibitory effect of reuterin-producing Limosilactobacillus reuteri and edible alginate-konjac gum film against foodborne pathogens and spoilage microorganisms. Food Bioscience. 2023;52:102443. doi: 10.1016/j.fbio.2023.102443.
- [o1]Jiang J, Li K, Xiao Y, Zhong A, Tang J, Duan Y, Li Z. Limosilactobacillus reuteri Regulating Intestinal Function: A Review. Fermentation. 2023; 9(1):19. https://doi.org/10.3390/fermentation9010019
- [o1]Lee HL, Kim JM, Moon JH, Kim MJ, Jeong HR, Go MJ, Kim HJ, Eo HJ, Lee U, Heo HJ. Anti-Amnesic Effect of Synbiotic Supplementation Containing Corni fructus and Limosilactobacillus reuteri in DSS-Induced Colitis Mice. International Journal of Molecular Sciences. 2022 Dec 21;24(1):90. doi: 10.3390/ijms24010090.
- [o1]Ali MS, Lee EB, Quah Y, Birhanu BT, Suk K, Lim SK, Park SC. Heat-killed Limosilactobacillus reuteri PSC102 Ameliorates Impaired Immunity in Cyclophosphamide-induced Immunosuppressed Mice. Frontiers in Microbiology. 2022;13:820838. doi: 10.3389/fmicb.2022.820838.
- [o1]Wang X, Ji Y, Qiu C, Zhang H, Bi L, Xi H, Lei L, Liu B, Han W, Gu J. A phage cocktail combined with the enteric probiotic Lactobacillus reuteri ameliorated mouse colitis caused by S. typhimurium. Food and Function. 2022;13 (16):8509-8523. doi: 10.1039/D2FO00699E
- [o1]Zhang S, Zhu J. Untargeted Metabolomics Sensitively Differentiates Gut Bacterial Species in Single Culture and Co-Culture Systems. ACS Omega. 2022;7(17):14643-14652. doi: 10.1021/acsomega.1c07114.
- [o1]Yang Z, Zhu X, Wen A, Qin L. Development of probiotics beverage using cereal enzymatic hydrolysate fermented with Limosilactobacillus reuteri. Food Science and Nutrition. 2022;10(9):3143-3153. doi: 10.1002/fsn3.2913.
- [o1]Meruvu H, Harsa ST. Lactic acid bacteria: isolation-characterization approaches and industrial applications. Critical Reviews in Food Science and Nutrition. 2022 Mar 29:1-20. doi: 10.1080/10408398.2022.2054936.
- [o1]Abuqwider J, Altamimi M, Mauriello G. Limosilactobacillus reuteri in Health and Disease. Microorganisms. 2022;28;10(3):522. doi: 10.3390/microorganisms10030522.
- [o1]Jang AY, Rod-In W, Monmai C, Sohn M, Kim TR, Jeon MG, Park WJ. Anti-inflammatory potential of Lactobacillus reuteri LM1071 via eicosanoid regulation in LPS-stimulated RAW264.7 cells. Journal of Applied Microbiology. 2022;133(1):67-75. doi: 10.1111/jam.15331.
- [o1] Zhu T, Mao J, Zhong Y, Huang C, Deng Z, Cui Y, Liu J, Wang H. L. reuteri ZJ617 inhibits inflammatory and autophagy signaling pathways in gut-liver axis in piglet induced by lipopolysaccharide. Journal of Animal Science and Biotechnology. 2021;12(1):110. doi: 10.1186/s40104-021-00624-9.
- [o1]Shazadi K, Ahmad SZ, Ahmad SS, Arshad N. In vivo prophylactic efficacy of Lactobacillus reuteri MT180537 against aerobic vaginitis. Microbial Pathogenesis. 2021;160:105197. doi: 10.1016/j.micpath.2021.105197
- [o1]Zhang C, Xia S, Zhang Y, Zhu S, Li H, Liu X. Identification of soybean peptides and their effect on the growth and metabolism of Limosilactobacillus reuteri LR08. Food Chemistry. 2022;369:130923. doi: 10.1016/j.foodchem.2021.130923.
- [o1]Luo H, Li P, Wang H, Roos S, Ji B, Nielsen J. Genome-scale insights into the metabolic versatility of Limosilactobacillus reuteri. BMC Biotechnology. 2021;21(1):46. doi: 10.1186/s12896-021-00702-w.
- [o1]Rajanikar RV, Nataraj BH, Naithani H, Ali SA, Panjagari NR, Behare PV. Phenyllactic acid: A green compound for food biopreservation. Food Control. 2021;128:108184. doi: 10.1016/j.foodcont.2021.108184.
- [o1]Popovic M, Stojanovic M, Veličkovic Z, Kovačevic A, Miljkovic R, Mirkovic N, Marinkovic A. Characterization of potential probiotic strain, L. reuteri B2, and its microencapsulation using alginate-based biopolymers. International Journal of Biological Macromolecules. 2021;183:423-434. doi: 10.1016/j.ijbiomac.2021.04.177.
- [o1]Johari B, Maghsood F, Madanchi H, Moradi M, Kadivar M. Investigating the anti-inflammatory effects of high molecular weight secretions from Limosilactobacillus reuteri PTCC 1655 on LPS-stimulated PMA-differentiated THP-1 cells. Journal of Applied Microbiology. 2021;131(2):938-948. doi: 10.1111/jam.14984.
- [o1]Soltani S, Couture F, Boutin Y, Ben Said L, Cashman-Kadri S, Subirade M, Biron E, Fliss I. In vitro investigation of gastrointestinal stability and toxicity of 3-hyrdoxypropionaldehyde (reuterin) produced by Lactobacillus reuteri. Toxicology Reports. 2021;8:740-746. doi: 10.1016/j.toxrep.2021.03.025.
- [o1]Zheng TX, Pu SL, Tan P, Du YC, Qian BL, Chen H, Fu WG, Huang MZ. Liver Metabolomics Reveals the Effect of Lactobacillus reuteri on Alcoholic Liver Disease. Frontiers in Physiology. 2020;11:595382. doi: 10.3389/fphys.2020.595382.
- [o1]Maccelli A, Carradori S, Puca V, Sisto F, Lanuti P, Crestoni ME, Lasalvia A, Muraro R, Bysell H, Di Sotto A, Roos S, Grande R. Correlation between the Antimicrobial Activity and Metabolic Profiles of Cell Free Supernatants and Membrane Vesicles Produced by Lactobacillus reuteri DSM 17938. Microorganisms. 2020;8(11):1653. doi: 10.3390/microorganisms8111653.
- [o1]Al-Balawi M, Morsy FM. Enterococcus faecalis Is a Better Competitor Than Other Lactic Acid Bacteria in the Initial Colonization of Colon of Healthy Newborn Babies at First Week of Their Life. Frontiers in Microbiology. 2020;11:2017. doi: 10.3389/fmicb.2020.02017.
- [o1]Knysh OV, Martynov AV. Lactobacillus reuteri cell-free extracts against antibiotic-resistant bacteria. Zaporozhye Medical Journal. 2020;22(4):547-553. doi: 10.14739/2310-1210.2020.4.208397
- [o1]Rama GR, Führ AJ, da Silva JABS, Gennari A, Giroldi M, Goettert MI, Volken de Souza CF. Encapsulation of Lactobacillus spp. using bovine and buffalo cheese whey and their application in orange juice. 3 Biotech. 2020;10(6):263. doi: 10.1007/s13205-020-02255-9.
- [o1]Dudík B, Kiňová Sepová H, Bilka F, Pašková Ľ, Bilková A. Mucin pre-cultivated Lactobacillus reuteri E shows enhanced adhesion and increases mucin expression in HT-29 cells. Antonie Van Leeuwenhoek. 2020;113(8):1191-1200. doi: 10.1007/s10482-020-01426-1.
- [o1]Wang H, Zhou C, Huang J, Kuai X, Shao X. The potential therapeutic role of Lactobacillus reuteri for treatment of inflammatory bowel disease. Am J Transl Res. 2020;12(5):1569-1583.
- [o1]Knysh OV, Martynov AV. Potentiation of the Antimicrobial Effect of Lactobacillus Reuteri DSM 17938 Cell-free Extracts by Ascorbic Acid." Medicni Perspektivi. 2020;25(1):17-24. doi:10.26641/2307-0404.2020.1.200393.
- [o1]Geraldo BMC, Batalha MN, Milhan NVM, Rossoni RD, Scorzoni L, Anbinder AL. Heat-killed Lactobacillus reuteri and cell-free culture supernatant have similar effects to viable probiotics during interaction with Porphyromonas gingivalis. J Periodontal Res. 2020;55(2):215-220. doi: 10.1111/jre.12704.
- [o1]Rama GR, Fuhr AJ, da Silva JABS, Gennari A, Giroldi M, Goettert MI, Volken de Souza CF. Potential applications of dairy whey for the production of lactic acid bacteria cultures. 3 Biotech. 2020;10(6):25-37. doi:10.1016/j.idairyj.2019.06.012
- [o1]Jiang P, Yang W, Jin Y, Huang H, Shi C, Jiang Y, Wang J, Kang Y, Wang C, Yang G. Lactobacillus reuteri protects mice against Salmonella typhimurium challenge by activating macrophages to produce nitric oxide. Microb Pathog. 2019;137:103754. doi: 10.1016/j.micpath.2019.103754.
- [o1]Esposito F, Montuori P, Schettino M, Velotto S, Stasi T, Romano R, Cirillo T. Level of Biogenic Amines in Red and White Wines, Dietary Exposure, and Histamine-Mediated Symptoms upon Wine Ingestion. Molecules. 2019;24(19):3629. doi: 10.3390/molecules24193629.
- [o1]Khmaladze I, Butler É, Fabre S, Gillbro JM. Lactobacillus reuteri DSM 17938-A comparative study on the effect of probiotics and lysates on human skin. Exp Dermatol. 2019;28(7):822-828. doi: 10.1111/exd.13950.
- [o3]Knysh OV, Isayenko OY, Voyda YV, Kizimenko OO, Babych YM. Influence of cell-free extracts of Bifidobacterium bifidum and Lactobacillus reuteri on proliferation and biofilm formation by Escherichia coli and Pseudomonas aeruginosa. Regulatory Mechanisms in Biosystems. 2019;10(2):251-256. doi: 10.15421/021938
- [o1]Mu Q, Tavella VJ, Luo XM. Role of Lactobacillus reuteri in Human Health and Diseases. Front Microbiol. 2018;9:757. doi: 10.3389/fmicb.2018.00757.
Citations in Scopus database:
- Tian W, Du T, He G, Tan T, Meng Y, Wei H. Intranasal administration of Lactobacillus reuteri TR02 attenuates Mycoplasma pneumoniae-induced lung inflammatory response in mice [鼻内滴入罗伊氏乳杆菌 TR02 减轻肺炎支原体诱导的小鼠肺部炎症损伤]. Chinese Journal of Microbiology and Immunology. 2024;44(4):323 – 32930. 10.3760/cma.j.cn112309-20230417-00099
- [o1]Zhu MZ, Xu HM, Liang YJ, Xu J, Yue NN, Zhang Y, Tian CM, Yao J, Wang LS, Nie YQ, Li DF. Edible exosome-like nanoparticles from portulaca oleracea L mitigate DSS-induced colitis via facilitating double-positive CD4+CD8+T cells expansion. J Nanobiotechnology. 2023;21(1):309. doi: 10.1186/s12951-023-02065
- [o1]Wang X, Wu M, Yu Q, Ma L, Yao D, Zhang L. Isolation and Identification of Lactiplantibacillus plantarum ST3.5 and Its Inhibitory Effect on Mold. Science and Technology of Food Industry. 2023;44(13):141−149. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2022080334
- [o1]Contaldo M. Use of Probiotics for Oral Candidiasis: State of the Art and Perspective. A Further Step Toward Personalized Medicine? Front Biosci (Elite Ed). 2023;15(1):6. doi: 10.31083/j.fbe1501006.
- [o1]Shelby RD, Mar P, Janzow GE, Mashburn-Warren L, Tengberg N, Navarro JB, Allen JM, Wickham J, Wang Y, Bailey MT, Goodman SD, Besner GE. Antibacterial and anti-inflammatory effects of Lactobacillus reuteri in its biofilm state contribute to its beneficial effects in a rat model of experimental necrotizing enterocolitis. Journal of Pediatric Surgery. 2022;57(7):1382-1390. doi: 10.1016/j.jpedsurg.2021.09.001
- [o1]Jiang L, Zheng Z, Zhu S,,et al.Antibacterial effect of Lactobacillus plantarum, Lactobacillus rhamnosus and Lactobacillus reuteri on common pathogenic bacteria in hospital. Journal of Xinxiang Medical University,2022;39(6):501-506.doi:10.7683/xxyxyxb.2022.06.001
- [o1]CEN Q, PANG R, HU X, et al. New Developments in the Role of Lactobacillus Reuteri in Regulating Intestinal Barrier Function. Chinese General Practice, 2022;25(15): 1918-1922. DOI: 10.12114/j.issn.1007-9572.2021.02.123.
- [o1]Ledesma SC, Rubio MC, Aredes-Fernández P. Identification of histidine and tyrosine decarboxylating bacteria from Tucumán red wine, Journal of Wine Research, 2022;33:4, 235-245, DOI: 10.1080/09571264.2022.2143338
- [o3]Widyarman, A.S. - Pranoto, S. - Theodorea, C.F. - Bachtiar, E.W. - Bachtiar, B.M. - In: Scientific Dental Journal, Vol. 2, No. 2, 2018 ; s. 77
- [o1]Qian, G. - Ho, J.W.K. - In: Biophysical Reviews, Vol. 12, No. 4, 2020 ; s. 863 ; SCOPUS
- Yaseen, A.A. - Khashan, B.A. - Hasan, A.N. - Abedalhammed, H.S. - In: IOP Conference Series: Earth and Environmental
- [o3]Seijo, A. - María, M. - Ramón, S. - In: Investigation Clinica, Vol. 61, No. 3, 2020 ; s. 1168
- [o2]Karaffová, V. - Revajová, V. - Nemcová, R. - Ševčíková, Z. - Levkutová, M. - Levkut, M. - In: Folia Veterinaria, Vol. 64, No. 1, 2020 ; s. 47
- Ukraintsev, S.E. - Kornienko, E.A. - Kafarskaya, L.I. - Dubrovskaya, M.I. - In: Pediatriya - Zhurnal im G.N. Speranskogo, Vol. 99, No. 6, 2020 ; s. 171 ; SCOPUS