INVESTIGADORES
SERRADELL Maria De Los Angeles
artículos
Título:
Administration of kefir-fermented milk protects mice against Giardia intestinalis infection
Autor/es:
CORREA FRANCO, M; GOLOWCZYC, M; DE ANTONI, GL; PÉREZ, PF; HUMEN, MA; SERRADELL, MA
Revista:
JOURNAL OF MEDICAL MICROBIOLOGY
Editorial:
SOC GENERAL MICROBIOLOGY
Referencias:
Lugar: London; Año: 2013 vol. 62 p. 1815 - 1822
ISSN:
0022-2615
Resumen:
Giardiasis, caused by the protozoan Giardia intestinalis, is one of the most common intestinal diseases worldwide and constitutes an important problem for public health systems of different countries. Kefir is a probiotic beverage obtained through fermentation of milk with ?kefir grains?, which consisting mainly of bacteria and yeasts that coexist in a complex symbiotic association. In this work, we studied the ability of kefir to protect mice from a G. intestinalis infection, and characterized the host immune response to this probiotic in the context of the intestinal infection. Six to eight weeks old C75BL/6 mice were separated into 4 groups: C (control mice), K (mice receiving 1/100 dilution of kefir in drinking water for 14 days), G (mice infected orally with 4x107 trophozoites of G. intestinalis at day 7), and GK (kefir-treated G. intestinalis-infected mice), and were sacrificed at 2 and 7 days post-infection (pi). Kefir administration was able to significantly reduce the intensity of Giardia infection at 7 days pi. An increase in CD4+ T cells percentage at 2 days pi was observed in Peyer´s patches (PP) of mice belonging to G group compared with C and K groups, meanwhile in GK group, the percentage of CD4+ T cells in PP was similar to controls. At 2 days pi, a reduction in the percentage of B220+ MHC-II medium in PP was observed in infected mice compared with the other groups. At 7 days pi, Giardia-infected mice showed a reduction in RcF+ cells compared with C group, suggesting a downregulation of inflammatory response. However, in K and GK groups, the percentages of RcF+ cells did not differ from controls. An increment in IgA+ cells was observed in the lamina propria of K group compared with to control at 2 days pi. Interestingly, the diminished number of IgA+ cells registered in G group at 7 days pi, was restored by kefir feeding although the increase of IgA+ cells was no longer observed in K group at that time. No significant differences in CXCL10 expression were registered between groups, in concordance with the absence of inflammation in small intestinal tissue. Interestingly, a slight reduction on CCL20 expression was observed in G group suggesting that G. intestinalis might downregulate its expression as a way to evade inflammatory immune response. On the other hand, a trend to an increase in TNF- expression was observed in K group, meanwhile GK group showed a significant increment in its expression. Moreover, kefir receiving-mice (K and GK groups) showed an increment in the expression of IFN-, the most relevant Th1-cytokine, at 2 days pi. Our results demonstrated that feeding with kefir reduces G. intestinalis infection and promotes the activation of different mechanisms of humoral and cellular immunity down-regulated by parasitic infection, which contributes to protection.