Probiotic and anti-inflammatory attributes of an isolate Lactobacillus helveticus NS8 from Mongolian fermented koumiss Microbe-host interactions and microbial pathogenicity

BMC Microbiology

Volumn 15, Issue 1, 2015, Pages

  Rong, Jingjing ^a   Zheng, Houfeng ^a   Liu, Ming ^c,d   Hu, Xu ^b   Wang, Tao ^b   Zhang, Xingwei ^a   Jin, Feng ^b   Wang, Li ^a  

^a HANGZHOU NORMAL UNIVERSITY   (China)

^b INSTITUTE OF PSYCHOLOGY   (China)

^c INSTITUTE OF GENETICS AND DEVELOPMENTAL BIOLOGY   (China)

^d UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

Author keywords

Anti inflammatory effect; Koumiss; L. helveticus; S layer protein

Indexed keywords

BACTERIAL PROTEIN; INTERLEUKIN 10; LIPOPOLYSACCHARIDE; PROBIOTIC AGENT; S LAYER PROTEIN; UNCLASSIFIED DRUG; ANTIINFLAMMATORY AGENT; MEMBRANE PROTEIN; S-LAYER PROTEINS; TRINITROBENZENESULFONIC ACID;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ANTIINFLAMMATORY ACTIVITY; ARTICLE; BACTERIAL STRAIN; BACTERIAL SURVIVAL; BACTERIUM ISOLATE; CACO 2 CELL LINE; CELL ADHESION; CELL SURFACE; CHINA; COLITIS; CONTROLLED STUDY; CYTOKINE PRODUCTION; ENZYME LINKED IMMUNOSORBENT ASSAY; EX VIVO STUDY; FEMALE; GASTROINTESTINAL TRACT; HUMAN; HUMAN CELL; HYDROPHOBICITY; IMMUNE RESPONSE; IMMUNOMODULATION; IN VITRO STUDY; IN VIVO STUDY; INTESTINE EPITHELIUM CELL; KOUMISS; LACTOBACILLUS HELVETICUS; MACROPHAGE; MILK; MOLECULAR TYPING; MOUSE; NONHUMAN; PERIPHERAL BLOOD MONONUCLEAR CELL; RAW264.7 CELL LINE; SCANNING ELECTRON MICROSCOPY; ANIMAL; BACTERIUM ADHERENCE; CACO-2 CELL LINE; CELL CULTURE; CHEMICALLY INDUCED; DISEASE MODEL; FERMENTED MILK PRODUCT; GENETICS; IMMUNOLOGY; ISOLATION AND PURIFICATION; METABOLISM; MICROBIOLOGY; MONGOLIA; MONONUCLEAR CELL; RAW 264.7 CELL LINE;

ANIMALS; ANTI-INFLAMMATORY AGENTS; BACTERIAL ADHESION; CACO-2 CELLS; CELLS, CULTURED; COLITIS; CULTURED MILK PRODUCTS; DISEASE MODELS, ANIMAL; GASTROINTESTINAL TRACT; HUMANS; INTERLEUKIN-10; LACTOBACILLUS HELVETICUS; LEUKOCYTES, MONONUCLEAR; MEMBRANE GLYCOPROTEINS; MICE; MOLECULAR TYPING; MONGOLIA; PROBIOTICS; RAW 264.7 CELLS; TRINITROBENZENESULFONIC ACID;

EID: 84942929912     PISSN: None     EISSN: 14712180     Source Type: Journal    
DOI: 10.1186/s12866-015-0525-2     Document Type: Article

References (41)

1. Bergonzelli GE, Blum S, Brussow H, Corthesy-Theulaz I. Probiotics as a treatment strategy for gastrointestinal diseases? Digestion. 2005;72(1):57-68.
2. Kumar M, Nagpal R, Kumar R, Hemalatha R, Verma V, Kumar A, et al. Cholesterol-lowering probiotics as potential biotherapeutics for metabolic diseases. Exp Diabesity Res. 2012;2012:902917.
3. Ringel-Kulka T, Palsson OS, Maier D, Carroll I, Galanko JA, Leyer G, et al. Probiotic bacteria Lactobacillus acidophilus NCFM and Bifidobacterium lactis Bi-07 versus placebo for the symptoms of bloating in patients with functional bowel disorders: a double-blind study. J Clin Gastroenterol. 2011;45(6):518-25.
4. Szajewska H, Wanke M, Patro B. Meta-analysis: the effects of Lactobacillus rhamnosus GG supplementation for the prevention of healthcare-associated diarrhoea in children. Aliment Pharmacol Ther. 2011;34(9):1079-87.
5. Heller KJ. Probiotic bacteria in fermented foods: product characteristics and starter organisms. Am J Clin Nutr. 2001;73(2 Suppl):374S-9S.
6. Fortina MG, Nicastro G, Carminati D, Neviani E, Manachini PL. Lactobacillus helveticus heterogeneity in natural cheese starters: the diversity in phenotypic characteristics. J Appl Microbiol. 1998;84(1):72-80.
7. Callanan M, Kaleta P, O'Callaghan J, O'Sullivan O, Jordan K, McAuliffe O, et al. Genome sequence of Lactobacillus helveticus, an organism distinguished by selective gene loss and insertion sequence element expansion. J Bacteriol. 2008;190(2):727-35.
8. Rachid M, Matar C, Duarte J, Perdigon G. Effect of milk fermented with a Lactobacillus helveticus R389(+) proteolytic strain on the immune system and on the growth of 4 T1 breast cancer cells in mice. FEMS Immunol Med Microbiol. 2006;47(2):242-53.
9. Slattery L, O'Callaghan J, Fitzgerald GF, Beresford T, Ross RP. Invited review: Lactobacillus helveticus - a thermophilic dairy starter related to gut bacteria. J Dairy Sci. 2010;93(10):4435-54.
10. Taverniti V, Stuknyte M, Minuzzo M, Arioli S, De Noni I, Scabiosi C, et al. S-layer protein mediates the stimulatory effect of Lactobacillus helveticus MIMLh5 on innate immunity. Appl Environ Microbiol. 2013;79(4):1221-31.
11. Mu Z, Yang X, Yuan H. Detection and identification of wild yeast in Koumiss. Food Microbiol. 2012;31(2):301-8.
12. Jagielski VA. On the Various Preparations of Koumiss, and their Use in Medicine. Br Med J. 1874;1(688):299-301.
13. Tsenina VS, Frolov VM. Use of koumiss made from cow's milk in liver diseases. Meditsinskaia sestra. 1980;39(8):29-30.
14. Christensen HR, Frokiaer H, Pestka JJ. Lactobacilli differentially modulate expression of cytokines and maturation surface markers in murine dendritic cells. J Immunol. 2002;168(1):171-8.
15. Vitini E, Alvarez S, Medina M, Medici M, de Budeguer MV, Perdigon G. Gut mucosal immunostimulation by lactic acid bacteria. Biocell: Off J Sociedades Latinoamericanas de Microscopia Electronica et al. 2000;24(3):223-32.
16. Foligne B, Nutten S, Grangette C, Dennin V, Goudercourt D, Poiret S, et al. Correlation between in vitro and in vivo immunomodulatory properties of lactic acid bacteria. WJG. 2007;13(2):236-43.
17. Fortina MG, Ricci G, Mora D, Parini C, Manachini PL. Specific identification of Lactobacillus helveticus by PCR with pepC, pepN and htrA targeted primers. FEMS Microbiol Lett. 2001;198(1):85-9.
18. Chen K, Liang N, Luo X, Zhang TC. Lactobacillus acidophilus strain suppresses the transcription of proinflammatory-related factors in human HT-29 cells. J Microbiol Biotechnol. 2013;23(1):64-8.
19. Gu XC, Luo XG, Wang CX, Ma DY, Wang Y, He YY, et al. Cloning and analysis of bile salt hydrolase genes from Lactobacillus plantarum CGMCC No. 8198. Biotechnol Lett. 2013. doi: 10.1007/s10529-013-1434-9.
20. Wasko A, Polak-Berecka M, Kuzdralinski A, Skrzypek T. Variability of S-layer proteins in Lactobacillus helveticus strains. Anaerobe. 2014;25:53-60.
21. Zhang J, Zheng Y, Guo Z, Qiao J, Gesudu Q, Sun Z, et al. The diversity of intestinal microbiota of Mongolians living in Inner Mongolia, China. Benefic Microbes. 2013;4(4):319-28.
22. Tuomola EM, Salminen SJ. Adhesion of some probiotic and dairy Lactobacillus strains to Caco-2 cell cultures. Int J Food Microbiol. 1998;41(1):45-51.
23. Collado M, Meriluoto J, Salminen S. Adhesion and aggregation properties of probiotic and pathogen strains. Eur Food Res Technol. 2008;226(5):1065-73.
24. Velez MP, De Keersmaecker SC, Vanderleyden J. Adherence factors of Lactobacillus in the human gastrointestinal tract. FEMS Microbiol Lett. 2007;276(2):140-8.
25. Foligne B, Nutten S, Steidler L, Dennin V, Goudercourt D, Mercenier A, et al. Recommendations for improved use of the murine TNBS-induced colitis model in evaluating anti-inflammatory properties of lactic acid bacteria: technical and microbiological aspects. Dig Dis Sci. 2006;51(2):390-400.
26. Sheil B, McCarthy J, O'Mahony L, Bennett MW, Ryan P, Fitzgibbon JJ, et al. Is the mucosal route of administration essential for probiotic function? Subcutaneous administration is associated with attenuation of murine colitis and arthritis. Gut. 2004;53(5):694-700.
27. Lu Y-C, Yeh W-C, Ohashi PS. LPS/TLR4 signal transduction pathway. Cytokine. 2008;42(2):145-51.
28. Mohamadzadeh M, Olson S, Kalina WV, Ruthel G, Demmin GL, Warfield KL, et al. Lactobacilli activate human dendritic cells that skew T cells toward T helper 1 polarization. Proc Natl Acad Sci U S A. 2005;102(8):2880-5.
29. Jeon SG, Kayama H, Ueda Y, Takahashi T, Asahara T, Tsuji H, et al. Probiotic Bifidobacterium breve induces IL-10-producing Tr1 cells in the colon. PLoS Pathog. 2012;8(5), e1002714.
30. Rachmilewitz D, Katakura K, Karmeli F, Hayashi T, Reinus C, Rudensky B, et al. Toll-like receptor 9 signaling mediates the anti-inflammatory effects of probiotics in murine experimental colitis. Gastroenterology. 2004;126(2):520-8.
31. Lebeer S, Vanderleyden J, De Keersmaecker SC. Genes and molecules of lactobacilli supporting probiotic action. MMBR. 2008;72(4):728-64.
32. Konstantinov SR, Smidt H, de Vos WM, Bruijns SC, Singh SK, Valence F, et al. S layer protein A of Lactobacillus acidophilus NCFM regulates immature dendritic cell and T cell functions. Proc Natl Acad Sci U S A. 2008;105(49):19474-9.
33. Johnson-Henry KC, Hagen KE, Gordonpour M, Tompkins TA, Sherman PM. Surface-layer protein extracts from Lactobacillus helveticus inhibit enterohaemorrhagic Escherichia coli O157:H7 adhesion to epithelial cells. Cell Microbiol. 2007;9(2):356-67.
34. Chen X, Xu J, Shuai J, Chen J, Zhang Z, Fang W. The S-layer proteins of Lactobacillus crispatus strain ZJ001 is responsible for competitive exclusion against Escherichia coli O157:H7 and Salmonella typhimurium. Int J Food Microbiol. 2007;115(3):307-12.
35. Ludwig W. Nucleic acid techniques in bacterial systematics and identification. Int J Food Microbiol. 2007;120(3):225-36.
36. Conway PL, Gorbach SL, Goldin BR. Survival of lactic acid bacteria in the human stomach and adhesion to intestinal cells. J Dairy Sci. 1987;70(1):1-12.
37. Jacobsen CN, Rosenfeldt Nielsen V, Hayford AE, Moller PL, Michaelsen KF, Paerregaard A, et al. 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. 1999;65(11):4949-56.
38. Del Re B, Sgorbati B, Miglioli M, Palenzona D. Adhesion, autoaggregation and hydrophobicity of 13 strains of Bifidobacterium longum. Lett Appl Microbiol. 2000;31(6):438-42.
39. Rosenberg M, Gutnick D, Rosenberg E. Adherence of bacteria to hydrocarbons: A simple method for measuring cell-surface hydrophobicity. FEMS Microbiol Lett. 1980;9(1):29-33.
40. Lortal S, Van Heijenoort J, Gruber K, Sleytr UB. S-layer of Lactobacillus helveticus ATCC 12046: isolation, chemical characterization and re-formation after extraction with lithium chloride. J Gen Microbiol. 1992;138(3):611-8.
41. Grangette C, Nutten S, Palumbo E, Morath S, Hermann C, Dewulf J, et al. Enhanced antiinflammatory capacity of a Lactobacillus plantarum mutant synthesizing modified teichoic acids. Proc Natl Acad Sci U S A. 2005;102(29):10321-6.