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Article Abstract

Understanding gut bacterial composition and proteome changes in patients with early-stage chronic kidney disease (CKD) could lead to better methods of controlling the disease progression. Here, we investigated the gut microbiome and microbial functions in patients with infection (strongyloidiasis) and early-stage CKD. Thirty-five patients with early stages (1-3) of CKD were placed in two groups matched for population characteristics and biochemical parameters, 12 patients with strongyloidiasis in one group and 23 uninfected patients in the other. From every individual, a sample of their feces was obtained and processed for 16S rRNA sequencing and metaproteomic analysis using tandem liquid chromatography-mass spectrometry (LC-MS/MS). infection per se did not significantly alter gut microbial diversity. However, certain genera (, , , , and ) were significantly more abundant in infection-free CKD patients than in infected individuals. The genera and were enriched in infected patients. Among the significantly altered genera, and were the most correlated with renal parameters. The relative abundance of members of the genus was moderately positively correlated with estimated glomerular filtration rate (eGFR) (r = 0.335, p = 0.049) and negatively with serum creatinine (r = -0.35, p = 0.039). , on the other hand, showed a near-significant positive correlation with eGFR (r = 0.296, p = 0.084). Individuals with infection had higher levels of bacterial proteins involved in amino-acid metabolism. Analysis using STITCH predicted that bacterial amino-acid metabolism may also be involved in the production of colon-derived uremic toxin (indole), a toxic substance known to promote CKD. infection is, therefore, associated with reduced abundance of and (two genera possibly beneficial for kidney function) and with increased bacterial amino-acid metabolism in the early-stages of CKD, potentially producing uremic toxin. This study provides useful information for prevention of progression of CKD beyond the early stages.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10559256PMC
http://dx.doi.org/10.1016/j.heliyon.2023.e19859DOI Listing

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