Abstract

Life on this planet has been intricately associated with bacterial activity at all levels of evolution and bacteria represent the earliest form of autonomous existence. Plants such as those from the Leguminosae family that form root nodules while harboring nitrogen-fixing soil bacteria are a primordial example of symbiotic existence. Similarly, cooperative activities between bacteria and animals can also be observed in multiple domains, including the most inhospitable geographical regions of the planet such as Antarctica and the Lower Geyser Basin of Yellowstone National Park. In humans bacteria are often classified as either beneficial or pathogenic and in this regard we posit that this artificial nomenclature is overly simplistic and as such almost misinterprets the complex activities and inter-relationships that bacteria have with the environment as well as the human host and the plethora of biochemical activities that continue to be identified. We further suggest that in humans there are neither pathogenic nor beneficial bacteria, just bacteria embraced by those that tolerate the host and those that do not. The densest and most complex association exists in the human gastrointestinal tract, followed by the oral cavity, respiratory tract, and skin, where bacteria—pre- and post-birth—instruct the human cell in the fundamental language of molecular biology that normally leads to immunological tolerance over a lifetime. The overall effect of this complex output is the elaboration of a beneficial milieu, an environment that is of equal or greater importance than the bacterium in maintaining homeostasis.

Highlights

  • Bacteria that live on and within humans outnumber human cells by a factor of 10 [1]

  • It is estimated that 1014 bacteria populate the human gut and this active cohort is separated from the mucosal layer of the intestines by a single layer of intestinal epithelial cells; the bacteria, do not come into direct contact with the epithelial cells under normal physiological conditions, but rather remain in the lumen or outer mucus layer [2]

  • This review presents an overview of the research that has demonstrated that the gastrointestinal tract (GIT) microbiota provide essential metabolic and physiological functions for human survival such as the harvesting of essential food nutrients, vitamins and energy; metabolism of xenobiotics; protection from opportunistic pathobionts; influencing neurological pathways; development and maturation of the intestinal epithelium; and the development and maintenance of homeostasis of localized immune function

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Summary

Introduction

Bacteria that live on and within humans outnumber human cells by a factor of 10 [1]. It is estimated that 1014 bacteria populate the human gut and this active cohort is separated from the mucosal layer of the intestines by a single layer of intestinal epithelial cells; the bacteria, do not come into direct contact with the epithelial cells under normal physiological conditions, but rather remain in the lumen or outer mucus layer [2]. The second trend is the increasing complexity and diversity of the bacterial species that occur in the same GIT proximal to distal direction. Most of the bacterial species are GIT lumen residents, whereas fewer but well established proteobacteria including Akkermansia muciniphila reside and perpetuate within the mucus layers close to the epithelial tissue [4]. Other bacteria, such as the segmented filamentous bacteria (SFB) [5], are indigenous GIT commensal bacteria that interact directly with the intestinal epithelial cells in the terminal ileum [6]. Bacteria and the host elaborate a multitude of chemical compounds that have a fundamental role in the maintenance of homeostasis of host-microbe and microbe-microbe physiology (Figure 1)

What this Review Proposes to Add
The Gastrointestinal Tract Barrier and Chemical Transmitters
Diet-Independent Metabolites from the GIT Microbiota
Diet-Dependent Metabolites from the GIT Microbiota
The Metabolic Effects of Probiotics
Metabolites that Risk Disrupting GIT Host-Microbial Homeostasis
GIT Bacteriophages Chemical Modulators of the GIT Microbiome
Findings
Discussion
Conclusions
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