Abstract

BackgroundA better understanding of mechanisms underlying dose-effects of probiotics in their applications as treatments of intestinal infectious or inflammatory diseases and as vaccine adjuvant is needed. In this study, we evaluated the modulatory effects of Lactobacillus rhamnosus GG (LGG) on transplanted human gut microbiota (HGM) and on small intestinal immune cell signaling pathways in gnotobiotic pigs vaccinated with an oral attenuated human rotavirus (AttHRV) vaccine.ResultsNeonatal HGM transplanted pigs were given two doses of AttHRV on 5 and 15 days of age and were divided into three groups: none-LGG (AttHRV), 9-doses LGG (AttHRV + LGG9X), and 14-doses LGG (AttHRV + LGG14X) (n = 3–4). At post-AttHRV-inoculation day 28, all pigs were euthanized and intestinal contents and ileal tissue and mononuclear cells (MNC) were collected. AttHRV + LGG14X pigs had significantly increased LGG titers in the large intestinal contents and shifted structure of the microbiota as indicated by the formation of a cluster that is separated from the cluster formed by the AttHRV and AttHRV + LGG9X pigs. The increase in LGG titers concurred with significantly increased ileal HRV-specific IFN-γ producing T cell responses to the AttHRV vaccine reported in our previous publication, suggesting pro-Th1 adjuvant effects of the LGG. Both 9- and 14-doses LGG fed pig groups had significantly higher IkBα level and p-p38/p38 ratio, while significantly lower p-ERK/ERK ratio than the AttHRV pigs, suggesting activation of regulatory signals during immune activation. However, 9-doses, but not 14-doses LGG fed pigs had enhanced IL-6, IL-10, TNF-α, TLR9 mRNA levels, and p38 MAPK and ERK expressions in ileal MNC. Increased TLR9 mRNA was in parallel with higher mRNA levels of cytokines, p-NF-kB and higher p-p38/p38 ratio in MNC of the AttHRV + LGG9X pigs.ConclusionsThe relationship between modulation of gut microbiota and regulation of host immunity by different doses of probiotics is complex. LGG exerted divergent dose-dependent effects on the intestinal immune cell signaling pathway responses, with 9-doses LGG being more effective in activating the innate immunostimulating TLR9 signaling pathway than 14-doses in the HGM pigs vaccinated with AttHRV.Electronic supplementary materialThe online version of this article (doi:10.1186/s12866-016-0727-2) contains supplementary material, which is available to authorized users.

Highlights

  • A better understanding of mechanisms underlying dose-effects of probiotics in their applications as treatments of intestinal infectious or inflammatory diseases and as vaccine adjuvant is needed

  • The Lactobacillus rhamnosus GG (LGG) titers increased over time from the beginning of LGG feeding for both dosage groups

  • Bacterial communities in feces of human gut microbiota (HGM) transplanted pigs The Denaturing gradient gel electrophoresis (DGGE) profile of the HGM transplanted Gn pigs at PPD 33 are showed in Figs. 2 and 3

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Summary

Introduction

A better understanding of mechanisms underlying dose-effects of probiotics in their applications as treatments of intestinal infectious or inflammatory diseases and as vaccine adjuvant is needed. Human gastrointestinal tract (GI) can be colonized at birth by facultative anaerobes including enterobacter, lactobacillus and streptococcus in genus level, forming a reducing environment during the first week of life enabling colonization by strict anaerobes such as bacteroides, clostridium, bifidobacterium in genus level [4]. This microbial colonization contributes to recruitment of immune cells to the gastrointestinal tract and is a major contributor to the development of the mucosal and systemic immune systems in neonates [5]. Colonization in early infancy is crucial in relation to the final composition of the permanent microbiota in adults and in inducing immunological maturation in the intestine and shaping future immune responses of the host [6]

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