Abstract

The complexity of microbiota inhabiting the intestine is increasingly apparent. Delicate balance of numerous bacterial species can affect development of the immune system, how susceptible a host is to pathogenic organisms, and the auto-inflammatory state of the host. In the last decade, with the increased use of germ-free mice, gnotobiotic mice, and animal models in which a germ-free animal has been colonized with a foreign microbiota such as humanized mice, it has been possible to delineate relationships that specific bacteria have with the host immune system and to show what role they may play in overall host health. These models have not only allowed us to tease out the roles of individual species, but have also allowed the discovery and characterization of functionally unknown organisms. For example, segmented filamentous bacteria (SFB) have been shown to play a vital role in expansion of IL-17 producing cells. Prior to linking their key role in immune system development, little was known about these organisms. Bacteroides fragilis can rescue some of the immune defects of gnotobiotic mice after mono-colonization and have anti-inflammatory properties that can alleviate colitis and experimental allergic encephalitis in murine models. Additionally, Clostridium species have most recently been shown to expand regulatory T-cell populations leading to anti-inflammatory conditions. This review will highlight and summarize some of the major findings within the last decade concerning the role of select groups of bacteria including SFB, Clostridium, Bacteroides, Bifidobacterium, and Lactobacillus, and their impact on host mucosal immune systems.

Highlights

  • Humans play host to 500–1000 different species of bacteria in the intestine and 100 times more bacterial cells than eukaryotic cells (Whitman et al, 1998)

  • Bifidobacterium and Lactobacillus are both important in the natural balance of the intestinal community and in cases of inflammatory bowel disease (IBD), both groups of bacteria are seen at decreased levels in fecal samples as opposed to Enterococcus and Bacteroides, which are seen elevated in the mucosa of patients (Frank et al, 2007)

  • We have described several different instances in which intestinal bacteria prime responses that mirror and enhance this vital balance by either promoting inflammatory (SFB and Th17 cells) or anti-inflammatory conditions (Clostridium, Bacteroides fragilis, Bifidobacterium, and Lactobacillus)

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Summary

INTRODUCTION

Humans play host to 500–1000 different species of bacteria in the intestine and 100 times more bacterial cells than eukaryotic cells (Whitman et al, 1998). Increased appreciation for the crucial role that the intestinal microbiota plays in host health and immunity is continually surfacing. The importance of commensal bacteria in host development and health is most clearly demonstrated by germ-free mice, raised in the absence of any bacteria. These mice exhibit numerous developmental defects, which can be compensated for by microbial colonization (Macpherson and Harris, 2004). Developmental problems and defects faced by germ-free mice are, in part, centered around immune system development and function (Smith et al, 2007). The number of CD8+ intestinal epithelial cells (IELs) and αβ T-cell receptor (TCR) IELs is reduced as well as Thy expression and cytolytic activity. The Peyer’s patches are small compared to conventional animals, and the spleens and MLNs have depletion of lymphocyte zones

Microbial players in intestinal health
DISCUSSION
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