Evaluation of immunomodulatory activity of two potential probiotic Lactobacillus strains by invivo tests

Anaerobe

Volumn 35, Issue PB, 2015, Pages 22-27

  Ren, Dayong ^a,b,c   Li, Chang ^b,c   Qin, Yanqing ^a,b,c   Yin, Ronglan ^d   Du, Shouwen ^b,c   Liu, Hongfeng ^b   Zhang, Yanfang ^b,c   Wang, Cuiyan ^a   Rong, Fengjun ^a   Jin, Ningyi ^b,c  

^a JILIN AGRICULTURAL UNIVERSITY   (China)

^b BEIJING INSTITUTE OF MICROBIOLOGY AND EPIDEMIOLOGY   (China)

^c Jiangsu Co innovation Center for Prevention Control of Important Animal Infectious Diseases and Zoonoses   (China)

^d Academy of Animal Science and Veterinary Medicine in Jilin Province   (China)

Author keywords

Immune response; Lactobacillus plantarum; Lactobacillus salivarius; Probiotics

Indexed keywords

PROBIOTIC AGENT; IMMUNOLOGIC FACTOR; SECRETORY IMMUNOGLOBULIN;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BACTERIAL STRAIN; CD11C+ CD80+ T LYMPHOCYTE; CONTROLLED STUDY; FEMALE; IMMUNE RESPONSE; IMMUNOCOMPETENT CELL; IMMUNOMODULATION; IMMUNOSTIMULATION; IN VIVO STUDY; LACTOBACILLUS PLANTARUM; LACTOBACILLUS SALIVARIUS; MACROPHAGE; MOUSE; NONHUMAN; PHAGOCYTOSIS; PRIORITY JOURNAL; SPLEEN LYMPHOCYTE; T LYMPHOCYTE; TH1 TH2 BALANCE; ADAPTIVE IMMUNITY; ANIMAL; BAGG ALBINO MOUSE; BLOOD; GROWTH, DEVELOPMENT AND AGING; IMMUNOLOGY; LACTOBACILLUS; LYMPHOCYTE;

LACTOBACILLUS; LACTOBACILLUS PLANTARUM; LACTOBACILLUS SALIVARIUS; MUS;

ADAPTIVE IMMUNITY; ANIMALS; FEMALE; IMMUNOGLOBULIN A, SECRETORY; IMMUNOLOGIC FACTORS; LACTOBACILLUS; LYMPHOCYTES; MACROPHAGES; MICE, INBRED BALB C; PHAGOCYTOSIS; PROBIOTICS;

EID: 84936754138     PISSN: 10759964     EISSN: 10958274     Source Type: Journal    
DOI: 10.1016/j.anaerobe.2015.06.008     Document Type: Article

References (30)

1. Wells J. Mucosal vaccination and therapy with genetically modified lactic acid bacteria. Annu Rev. Food Sci. Technol. 2011, 2:423-445.
2. van Baarlen P., Wells J.M., Kleerebezem M. Regulation of intestinal homeostasis and immunity with probiotic lactobacilli. Trends Immunol. 2013, 34(5):208-215.
3. Zhu X., Zhao Y., Sun Y., Gu Q. Purification and characterization of plantaricin ZJ008, a novel bacteriocin against Staphylococcus spp. from Lactobacillus plantarum ZJ008. Food Chem. 2014, 165(15):216-223.
4. Dongarrà M.L., Rizzello V., Muccio L., Fries W., Cascio A., Bonaccorsi I., et al. Mucosal immunology and probiotics. Curr. Allergy Asthm R. 2013, 13(1):19-26.
5. Argyri A.A., Zoumpopoulou G., Karatzas K.-A.G., Tsakalidou E., Nychas G.-J.E., Panagou E.Z., et al. Selection of potential probiotic lactic acid bacteria from fermented olives by invitro tests. Food Microbiol. 2013, 33(2):282-291.
6. Chon H., Choi B. The effects of a vegetable-derived probiotic lactic acid bacterium on the immune response. Microbiol. Immunol. 2010, 54(4):228-236.
7. Tsai Y.-T., Cheng P.-C., Pan T.-M. Immunomodulating activity of Lactobacillus paracasei subsp. paracasei NTU 101 in enterohemorrhagic Escherichia coli O157H7-infected mice. J.Agr Food Chem. 2010, 58(21):11265-11272.
8. Kotzamanidis C., Kourelis A., Litopoulou-Tzanetaki E., Tzanetakis N., Yiangou M. Evaluation of adhesion capacity, cell surface traits and immunomodulatory activity of presumptive probiotic Lactobacillus strains. Int. J. Food Microbiol. 2010, 140(2):154-163.
9. Ren D., Li C., Qin Y., Yin R., Li X., Tian M., et al. Inhibition of Staphylococcus aureus adherence to Caco-2 cells by lactobacilli and cell surface properties that influence attachment. Anaerobe 2012, 18(5):508-515.
10. Ren D., Li C., Qin Y., Yin R., Du S., Ye F., et al. Lactobacilli reduce chemokine IL-8 production in response to TNF-α and Salmonella challenge of Caco-2 Cells. BioMed Res. Int. 2013, 2013:9.
11. Ren D., Li C., Qin Y., Yin R., Du S., Ye F., et al. Invitro evaluation of the probiotic and functional potential of Lactobacillus strains isolated from fermented food and human intestine. Anaerobe 2014, 30c:1-10.
12. Yan F., Polk D.B. Probiotics and immune health. Curr. Opin. Gastroenterol. 2011, 27(6):496-501.
13. López P., Gueimonde M., Margolles A., Suárez A. Distinct Bifidobacterium strains drive different immune responses invitro. Int. J. Food Microbiol. 2010, 138(1):157-165.
14. Ku H.-K., Lee H., Choi I.D., Ra J.-H., Kim T.-Y., Jeong J.-W., et al. Immuno-stimulatory effect of Lactobacillus plantarum HY7712 via toll-like receptor 2 signaling pathway. Cytokine 2014, 70(1):52.
15. Nakamura S., Kuda T., An C., Kanno T., Takahashi H., Kimura B. Inhibitory effects of Leuconostoc mesenteroides 1RM3 isolated from narezushi, a fermented fish with rice, on Listeria monocytogenes infection to Caco-2 cells and A/J mice. Anaerobe 2012, 18(1):19-24.
16. Gan L., Hua Zhang S., Liang Yang X., Bi Xu H. Immunomodulation and antitumor activity by a polysaccharide-protein complex from Lycium barbarum. Int. Immunopharmacol. 2004, 4(4):563-569.
17. Li C.-Y., Lin H.-C., Lai C.-H., Lu J.-Y., Wu S.-F., Fang S.-H. Immunomodulatory effects of Lactobacillus and Bifidobacterium on both murine and human mitogen-activated T cells. Int. Arch. Allergy Imm 2011, 156(2):128-136.
18. Li S., Zhao X., Wang J. Synergy of Astragalus polysaccharides and probiotics (Lactobacillus and Bacillus cereus) on immunity and intestinal microbiota in chicks. Poult. Sci. 2009, 88(3):519-525.
19. Mehr M., Hassanabadi A., Moghaddam H., Kermanshahi H. Supplementation of clove essential oils and probiotic on blood components, lymphoid organs and immune response in broiler chickens. Opin. Anim. Vet. Sci. 2014, 4(4):218-223.
20. Steppe M., Van Nieuwerburgh F., Vercauteren G., Boyen F., Eeckhaut V., Deforce D., et al. Safety assessment of the butyrate-producing Butyricicoccus pullicaecorum strain 25-3T, a potential probiotic for patients with inflammatory bowel disease, based on oral toxicity tests and whole genome sequencing. Food Chem. Toxicol. 2014, 72:129-137.
21. Son E., Moon E., Rhee D., Pyo S. Stimulation of various functions in murine peritoneal macrophages by high mannuronic acid-containing alginate (HMA) exposure invivo. Int. Immunopharmacol. 2001, 1(1):147-154.
22. Ya T., Zhang Q., Chu F., Merritt J., Bilige M., Sun T., et al. Immunological evaluation of Lactobacillus casei Zhang: a newly isolated strain from koumiss in Inner Mongolia, China. BMC Immunol. 2008, 9(1):68.
23. Kimoto H., Mizumachi K., Okamoto T., Kurisaki Ji New Lactococcus strain with Immunomodulatory activity: enhancement of Th1-Type immune response. Microbiol. Immunol. 2004, 48(2):75-82.
24. Ghadimi D., de Vrese M., Heller K.J., Schrezenmeir J. Lactic acid bacteria enhance autophagic ability of mononuclear phagocytes by increasing Th1 autophagy-promoting cytokine (IFN-γ) and nitric oxide (NO) levels and reducing Th2 autophagy-restraining cytokines (IL-4 and IL-13) in response to mycobacterium tuberculosis antigen. Int. Immunopharmacol. 2010, 10(6):694-706.
25. Fukushima Y., Kawata Y., Hara H., Terada A., Mitsuoka T. Effect of a probiotic formula on intestinal immunoglobulin A production in healthy children. Int. J. Food Microbiol. 1998, 42(1):39-44.
26. Shu Q., Gill H.S. Immune protection mediated by the probiotic Lactobacillus rhamnosus HN001 (DR20™) against Escherichia coli O157: H7 infection in mice. FEMS Immunol. Med. Microbiol. 2002, 34(1):59-64.
27. Chen P., Chen R., Yang Y., Yu Y., Xie Y., Zou Y., et al. Coxsackievirus B3 infection promotes generation of myeloid dendritic cells from bone marrow and accumulation in the myocardium. Int. Immunopharmacol. 2009, 9(11):1304-1312.
28. Jiangyang L., Qian L., Xiaohong W., Yi Y., Ling L., Yi L., et al. Changes of spleen dendritic cells in the terminal stage of multiple organ dysfunction syndrome. Acta Bio-Medica Atenei Parm. 2011, 82(2):146-153.
29. Gong L., Wang Y., Zhou L., Bai X., Wu S., Zhu F., et al. Activation of toll-like receptor-7 exacerbates lupus nephritis by modulating regulatory T cells. Am. J. Nephrol. 2014, 40(4):325-344.
30. Tsai Y.-T., Cheng P.-C., Liao J.-W., Pan T.-M. Effect of the administration of Lactobacillus paracasei subsp. paracasei NTU 101 on Peyer's patch-mediated mucosal immunity. Int. Immunopharmacol. 2010, 10(7):791-798.