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ISSN 2522-9028 (Print)
ISSN 2522-9036 (Online)
DOI: https://doi.org/10.15407/fz

Fiziologichnyi Zhurnal

is a scientific journal issued by the

Bogomoletz Institute of Physiology
National Academy of Sciences of Ukraine

Editor-in-chief: V.F. Sagach

The journal was founded in 1955 as
1955 – 1977 "Fiziolohichnyi zhurnal" (ISSN 0015 – 3311)
1978 – 1993 "Fiziologicheskii zhurnal" (ISSN 0201 – 8489)
1994 – 2016 "Fiziolohichnyi zhurnal" (ISSN 0201 – 8489)
2017 – "Fiziolohichnyi zhurnal" (ISSN 2522-9028)

Fiziol. Zh. 2017; 63(6): 16-24


The effect of probiotic strains of lactic acid bacteria and bifidobacteria on the Th1 and Th2 type cytokines production in intravaginal staphylococcosis in mice

L.M. Lazarenko1, L.P. Babenko1, М.Yu. Hryhorash1, V.V. Mokrozub1, O.M. Demchenko1, L.M. Sichel1,2, M.Ya. Spivak1,3

  1. D.K. Zabolotny Institute of microbiology and virology, National Academy of Sciences of Ukraine, Kyiv
  2. Pure Research Products, LLC, Colorado, USA
  3. LLC “Diaprof”, Ukraine
DOI: https://doi.org/10.15407/fz63.06.016


Abstract

The probiotic strains of Lactobacillus casei IMV B-7280, Bifidobacterium animalis VKL, B. animalis VKB (individually) or L. casei IMV B-7280 - B. animalis VKB - B. animalis VKL composition balanced the Th1/Th2 cytokines production at normal condition and in the cases of experimental intravaginal staphylococcosis in BALB/c mice in different periods of observation. L. casei IMV B-7280 and B. animalis VKB (individually) at normal condition increased the Th1 type cytokines interleukin (IL)-12 and interferon (IFN)-γ production. Instead, B. animalis VKL after injection into intact mice did not affect the IL-12 production but slightly increased the IFN-γ production. In the cases of experimental intravaginal staphylococcosis in mice the balancing of Th1/Th2 immune response under the influence of L. casei IMV B-7280 is due to increased production of IL-12 and IFN-γ, as well as decreased Th2 type cytokine IL-4 production. The IL-12 and IFN-γ production in staphylococcus-infected mice that received B. animalis VKL or B. animalis VKB (individually) was increased, but these probiotic bacteria had no significant effect on IL-4 production. Under the influence of L. casei IMV B-7280, B. animalis VKB, B. animalis VKL (individually) in the cases of experimental intravaginal staphylococcosis in mice the IL-4/IFN-γ ratio was significantly decreased. The shift from Th2 to Th1 type cytokines production was also observed in staphylococcus-infected mice that received L. casei IMV B-7280 - B. animalis VKB - B. animalis VKL composition. The IL-12 and IFN-γ production was increased, instead, IL-4 production as well as IL-4/IFN-γ ratio were decreased in mice that received this probiotic composition in different periods of observation.So, L. casei IMV B-7280, B. animalis VKB and B. animalis VKL (individually) and L. casei IMV B-7280 - B. animalis VKB - B. animalis VKL composition are promising to create highly effective immunobiotics with immunomodulatory effect that are able to balance Th1/Th2 type of immunity by shifting the cytokine profile with decreased the IL-4/IFN-γ ratio. Key words:

Keywords: Lactic acid bacteria; bifidobacteria; mice; intravaginal staphylococcosis; cytokines

References

  1. Bruce AW, Reid G. Intravaginal instillation of lactobacilli for prevention of recurrent urinary tract infections. Can J Microbiol. 1988 ; 34(3):339-43. CrossRef  
  2. Delia A, Morgante G, Rago G, Musacchio MC, Petraglia F, De Leo V. Effectiveness of oral administration of Lactobacillus paracasei subsp. paracasei F19 in association with vaginal suppositories of Lactobacillus acidofilus in the treatment of vaginosis and in the prevention of recurrent vaginitis. Minerva Ginecol. 2006; 58(3): 227-31. PubMed
  3.  
  4. Drago L, De Vecchi E, Nicola L, Zucchetti E, Gismondo MR, Vicariotto F. Activity of a Lactobacillus acidophilusbased douche for the treatment of bacterial vaginosis. J Altern Complement Med. 2007; 13 (14): 435–8. CrossRef PubMed
  5.  
  6. Falagas ME, Betsi GI, Athanasiou S. Probiotics for the treatment of women with bacterial vaginosis. Clin Microbiol Infect. 2007; 13(7): 657-64. CrossRef PubMed
  7.  
  8. Amdekar S, Singh V, Singh DD. Probiotic therapy: immunomodulating approach toward urinary tract infection. Curr Microbiol. 2011; 63(5): 484-90. CrossRef PubMed
  9.  
  10. 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. CrossRef PubMed
  11.  
  12. Iwabuchi N, Takahashi N, Xiao JZ, Miyaji K, Iwatsuki K. In vitro Th1 cytokine-independent Th2 suppressive effects of bifidobacteria. Microbiol Immunol. 2007; 51(7): 649-60. CrossRef PubMed
  13.  
  14. Gad M, Ravn P, Soborg DA, Lund-Jensen K, Ouwehand AC, Jensen SS. Regulation of the IL-10/IL-12 axis in human dendritic cells with probiotic bacteria. FEMS Immunol Med Microbiol. 2011; 63(1) :93-107. CrossRef PubMed
  15.  
  16. Shida K, Nanno M, Nagata S. Flexible cytokine production by macrophages and T-cells in response to probiotic bacteria: a possible mechanism by which probiotics exert multifunctional immune regulatory activities. Gut Microbes. 2011; 2(2) :109-14. CrossRef PubMed
  17.  
  18. Weiss G, Christensen HR, Zeuthen LH, Vogensen FK, Jakobsen M, Froki?r H. Lactobacilli and bifidobacteria induce differential interferon-? profiles in dendritic cells. Cytokine. 2011; 56(2): 520-30. CrossRef PubMed
  19.  
  20. Haruki Kitazawa, Julio Villena, Susana Avarez, editors. Probiotics: immunobiotics and immunogenic. New York: CRC Press; 2014.
  21.  
  22. de Roock S, van Elk M, van Dijk MEA, Timmerman HM, Rijkers GT, Prakken BJ, et al. Lactic acid bacteria differ in their ability to induce functional regulatory T cells in humans. Clin Exp Allergy. 2010; 40(1): 103-10 PubMed
  23.  
  24. Smelt MJ, de Haan BJ, Bron PA, van Swam I, Meijerink M, Wells JM, et al. L. plantarum, L. salivarius, and L. lactis attenuate Th2 responses and increase Treg frequencies in healthy mice in a strain dependent manner. PLoS One. 2012; 7(10): e47244. CrossRef PubMed PubMedCentral
  25.  
  26. Liu Y, Fatheree NY, Dingle BM, Tran DQ, Rhoads JM. 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. 2013; 8(2): e56547. CrossRef PubMed PubMedCentral
  27.  
  28. Yan F, Liu L, Cao H, Moore DJ, Washington MK, Wang B, et al. Neonatal colonization of mice with LGG promotes intestinal development and decreases susceptibility to colitis in adulthood. Mucosal Immunol. 2017; 10(1): 117-127. CrossRef PubMed PubMedCentral
  29.  
  30. Galdeano CM, de Moreno de LeBlanc A, Vinderola G, Bonet ME, Perdigon G. Proposed model: mechanisms of immunomodulation induced by probiotic bacteria. Clin Vaccine Immunol. 2007; 14 (15): 485-92. CrossRef PubMed PubMedCentral
  31.  
  32. Menard O, Butel MJ, Gaboriau-Routhiau V, Waligora- Dupriet AJ. Gnotobiotic mouse immune response induced by Bifidobacterium sp. strains isolated from infants. Appl Environ Microbiol. 2008; 74(3): 660-6. CrossRef PubMed PubMedCentral
  33.  
  34. Verbeek R, Bsibsi M, Plomp A, van Neerven RJ, te Biesebeke R, van Noort JM. Late rather than early responses of human dendritic cells highlight selective induction of cytokines, chemokines and growth factors by probiotic bacteria. Benef Microbes. 2010; 1(2): 109-19. CrossRef PubMed
  35.  
  36. Lee J, Yang W, Hostetler A, Schultz N, Suckow MA, Stewart KL, et al. Characterization of the anti-inflammatory Lactobacillus reuteri BM36301 and its probiotic benefits 10.1186/s12866-016-0686-7.
  37.  
  38. House Robert V, Descotes Jacques, editors. Cytokines in Human Health. Immunotoxicology, Pathology, and Therapeutic Applications Immunotoxicology, Pathology, and Therapeutic Applications. New Jersey: Humana Press Inc; 2007.
  39.  
  40. Spivak MYa, Pidgorskyi VS, Lazarenko LM, Shynkarenko LM, Rachkova LT, Olevinska ZM. Lactobacillus and Bifidobacterium influence the indices of immune response of the organism showed on experimental model. Microbiol Biotechnol. 2009; 1: 39-46.
  41.  
  42. Lazarenko L, Babenko L, Shynkarenko-Sichel L, Pidgorskyi V, Mokrozub V, Voronkova O, et al. Antagonistic action of Lactobacilli and Bifidobacteria in relation to Staphylococcus aureus and their influence on the immune response in cases of intravaginal staphylococcosis in mice. Probiotics & Antimicrob. Prot. 2012; 84: 78-89. CrossRef PubMed PubMedCentral
  43.  
  44. Pochard P, Gosset P, Grangette C, Andre C, Tonnel AB, Pestel J, et al. Lactic acid bacteria inhibit TH2 cytokine production by mononuclear cells from allergic patients. J Allergy Clin Immunol. 2002; 110(4): 617-23. CrossRef PubMed
  45.  
  46. Li AL, Ma DX, Meng XC. Effect of lactobacilli on Th1/ Th2 cells balance in primary lymphocytes. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2011; 27: 389-91. PubMed
  47.  
  48. Ren D, Li C, Qin Y, Yin R, Du S, Liu H, et al. Evaluation of immunomodulatory activity of two potential probiotic Lactobacillus strains by in vivo tests. Anaerobe. 2015; 35(Pt B): 22-7.
  49.  
  50. Xie J, Yu Q, Nie S, Fan S, Xiong T, Xie M. Effects of Lactobacillus plantarum NCU116 on Intestine Mucosal Immunity in Immunosuppressed Mice. J Agric Food Chem. 2015; 63(51): 10914-20. CrossRef PubMed
  51.  
  52. Sharma R, Kapila R, Dass G, Kapila S. Improvement in Th1/Th2 immune homeostasis, antioxidative status and resistance to pathogenic E. coli on consumption of probiotic Lactobacillus rhamnosus fermented milk in aging mice. Age (Dordr). 2014; 36(4): 9686. CrossRef PubMed PubMedCentral
  53.  
  54. Saliganti V, Kapila R, Kapila S. Consumption of probiotic Lactobacillus rhamnosus (MTCC: 5897) containing fermented milk plays a key role in development of the immune system in newborn mice during the suckling-weaning transition. Microbiol Immunol. 2016; 60(4): 261-7. CrossRef PubMed
  55.  
  56. Lopez P, GueIMVnde M, Margolles A, Suarez A. Distinct Bifidobacterium strains drive different immune responses in vitro. Int J Food Microbiol. 2010; 138(1-2): 157-65. CrossRef PubMed
  57.  
  58. Lopez P, Gonzalez-Rodriguez I, GueIMVnde M, Margolles A, Suarez A. Immune response to Bifidobacterium bifidum strains support Treg/Th17 plasticity. PLoS One. 2011; 6(9): e24776. CrossRef PubMed PubMedCentral
  59.  
  60. Martin R, Laval L, Chain F, Miquel S, Natividad J, Cherbuy C, et al. Bifidobacterium animalis ssp. lactis CNCM-I2494 Restores Gut Barrier Permeability in Chronically Low- Grade Inflamed Mice. Front Microbiol. 2016; 7:608. CrossRef PubMed PubMedCentral
  61.  

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