Abstract

Uremic retention solutes are the compounds that accumulate in the blood when kidney excretory function is impaired. Some of these compounds are toxic at high concentrations and are usually known as “uremic toxins”. The cumulative detrimental effect of uremic toxins results in numerous health problems and eventually mortality during acute or chronic uremia, especially in end-stage renal disease. More than 100 different solutes increase during uremia; however, the exact origin for most of them is still debatable. There are three main sources for such compounds: exogenous ones are consumed with food, whereas endogenous ones are produced by the host metabolism or by symbiotic microbiota metabolism. In this article, we identify uremic retention solutes presumably of gut microbiota origin. We used database analysis to obtain data on the enzymatic reactions in bacteria and human organisms that potentially yield uremic retention solutes and hence to determine what toxins could be synthesized in bacteria residing in the human gut. We selected biochemical pathways resulting in uremic retention solutes synthesis related to specific bacterial strains and revealed links between toxin concentration in uremia and the proportion of different bacteria species which can synthesize the toxin. The detected bacterial species essential for the synthesis of uremic retention solutes were then verified using the Human Microbiome Project database. Moreover, we defined the relative abundance of human toxin-generating enzymes as well as the possibility of the synthesis of a particular toxin by the human metabolism. Our study presents a novel bioinformatics approach for the elucidation of the origin of both uremic retention solutes and uremic toxins and for searching for the most likely human microbiome producers of toxins that can be targeted and used for the therapy of adverse consequences of uremia.

Highlights

  • Chronic kidney disease (CKD) is a common health problem in adults defined as a gradual loss in kidney function

  • Compounds were found in the Kyoto Encyclopedia of Genes and Genomes (KEGG) database as products of, or participants in, some biochemical reactions, and these uremic retention solutes were included in further analysis

  • Based on the KEGG database, we showed that only eight uremic retention solutes had no attributed pathways in human metabolism but had ascribed enzymes in bacteria (Table 1, and extended version in Supplementary Table S2)

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Summary

Introduction

Chronic kidney disease (CKD) is a common health problem in adults defined as a gradual loss in kidney function. CKD is characterized by reduced glomerular filtration rate, enhanced urinary albumin excretion [2], and accumulation of many metabolic waste products in the organism that are normally excreted, predominantly by the kidneys These metabolites are called uremic retention solutes or uremic toxins in the case of toxicity at uremic concentrations [3]. The complications of uremia include multi-organ dysfunctions such as bone diseases, serositis, insulin resistance, renal fibrosis, podocyte dysfunction, decreased mental acuity, and various cardiovascular problems [4,5]. Some of these ailments are present in the World Health Organization list of widespread causes of death. The substances belong to different chemical classes and participate in a great diversity of biochemical pathways, making further classification difficult

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