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Probiotic

Authors :
Chun-wei Shi
Ming-yang Cheng
Xin Yang
Yi-yuan Lu
Hong-duo Yin
Yan Zeng
Ru-yu Wang
Yan-long Jiang
Wen-tao Yang
Jian-zhong Wang
Dan-dan Zhao
Hai-bin Huang
Li-ping Ye
Xin Cao
Gui-lian Yang
Chun-feng Wang
Source :
Frontiers in Microbiology, Frontiers in Microbiology, Vol 11 (2020)
Publication Year :
2020

Abstract

Lactic acid bacteria (LAB) are the primary genera of the intestinal flora and have many probiotic functions. In the present study, Lactobacillus rhamnosus GG (LGG) ATCC 53103 was used to treat BALB/c mice. After LGG intervention, both low and high LGG doses were shown to improve the observed OTU, Chao1, ACE, and Shannon indices, while the Simpson index decreased, demonstrating that LGG can promote intestinal microbiota abundance and diversity. Furthermore, LGG treatment increased the abundances of intestinal Firmicutes, Bacteroides and Actinomycetes while reducing that of Proteobacteria. In addition to its effect on gut the microbiota, LGG could also regulate the host immune system. In the present study, we showed that LGG could affect the percentage of CD3+ T lymphocytes in the spleens (SPLs), mesenteric lymph nodes (MLNs), Peyer’s patches (PPs) and lamina propria lymphocytes (LPLs) of mice, including total CD3+ T, CD3+CD4+ T, and CD3+CD8+ T lymphocytes. Furthermore, LGG could effectively increase the expression of Th1-type cytokines (IFN-γ) and Th2 cytokines (IL-4) in CD4+ T cells, indicating that the proportion of Th1 and Th2 cells in mice with LGG treatment was in a high equilibrium state compared to the control group. In addition, the IFN-γ/IL-4 ratio was greater than 1 in mice with LGG intervention, suggesting that LGG tends to mediate the Th1 immune response. The results of the present study also showed that LGG upregulated the expression of IL-17 in CD4+ T cells and regulated the percentage of CD4+CD25+Foxp3+ Treg cells in various secondary immunological organs, indicating that LGG may promote the balance of Th-17 and Treg cells.

Details

ISSN :
1664302X
Volume :
11
Database :
OpenAIRE
Journal :
Frontiers in microbiology
Accession number :
edsair.doi.dedup.....5bd3b1dd5336ecf13cf592621b59133e