Abstract

Many essential functions of the human body are dependent on the symbiotic microbiota, which is present at especially high numbers and diversity in the gut. This intricate host–microbe relationship is a result of the long-term coevolution between the two. While the inheritance of mutational changes in the host evolution is almost exclusively vertical, the main mechanism of bacterial evolution is horizontal gene exchange. The gut conditions, with stable temperature, continuous food supply, constant physicochemical conditions, extremely high concentration of microbial cells and phages, and plenty of opportunities for conjugation on the surfaces of food particles and host tissues, represent one of the most favorable ecological niches for horizontal gene exchange. Thus, the gut microbial system genetically is very dynamic and capable of rapid response, at the genetic level, to selection, for example, by antibiotics. There are many other factors to which the microbiota may dynamically respond including lifestyle, therapy, diet, refined food, food additives, consumption of pre- and probiotics, and many others. The impact of the changing selective pressures on gut microbiota, however, is poorly understood. Presumably, the gut microbiome responds to these changes by genetic restructuring of gut populations, driven mainly via horizontal gene exchange. Thus, our main goal is to reveal the role played by horizontal gene exchange in the changing landscape of the gastrointestinal microbiome and potential effect of these changes on human health in general and autoimmune diseases in particular.

Highlights

  • Single-celled microorganisms have shaped our planet for several billions of years before the arrival of multicellular organisms

  • In our recent work involving mice mono-associated with a human gut symbiont Roseburia hominis, we have discovered that a number of genes involved in horizontal gene transfer (HGT) are upregulated in the bacterium in response to the intestinal environment [68]

  • Probiotics can potentially respond in a similar way, with the increased expression of genes involved in HGT, upon exposure to the gut environment

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Summary

Introduction

Single-celled microorganisms have shaped our planet for several billions of years before the arrival of multicellular organisms. The role of bacteriophages, plasmids, conjugative transposons, and integrons in transfer of genes by pathogenic human enteric pathobionts and subsequent acquisition of pathogenicity pointed to HGT as an important step in the expansion of virulence traits and antibiotic resistance [52,53,54]. The transfer of a tetracycline resistance gene from probiotic L. reuteri to bacteria in the human gut has been reported [94].

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