O-6 ENHANCED METABOLISM OF AROMATIC AMINO ACIDS AND LOW-DIVERSITY GUT MICROBIOTA: SIGNATURES OF HEPATIC ENCEPHALOPATHY IN DECOMPENSATED CIRRHOTIC PATIENTS FROM WESTERN MEXICO

Introduction and Objectives

Alterations in the intestinal microbiota in decompensated cirrhosis are recognized as being critical in clinical evolution. The onset of hepatic encephalopathy (HE) worsens the prognosis. Metabolic functions related to intestinal microbiota, such as ammonia production and imbalance of amino acid biosynthesis, are believed to play a key role on the pathophysiology of HE. This study aimed to evaluate the composition and functions of the intestinal microbiota in patients with decompensated cirrhosis and HE.

Materials and Methods

Fecal samples from 31 decompensated cirrhotic patients (20 with HE, 11 without HE) and 18 age-balanced healthy controls (HC) were included. Microbial composition was characterized by 16S rRNA sequencing and analyzed using QIIME2. Metabolic pathways were inferred by PICRUSt2. SCFAs quantification was performed by gas chromatography (GC).

Results

Intestinal microbiota in HE group was characterized by a decreased α-diversity, compared to no-HE group (p<0.01) and HC (p<0.001); β-diversity was also different between HE vs. no-HE group (p<0.05) and HE vs. HC (p<0.001). Intestinal microbiota from HE was defined by the presence of taxa such as Escherichia/Shigella, Burkholderiales and Lactobacillales. Furthermore, no-HE was characterized by the presence of Veilonella and Bacteroides. Both groups were depleted of potential beneficial taxa, such as Ruminococcus or Faecalibacterium, which correlates with diminished levels of fecal SCFAs in these groups. Inferred metabolic pathways showed that HE group was characterized by an enhanced chorismate metabolism, which is a key precursor of aromatic amino acids, along with antibiotic resistance and ammonia-producing pathways. HE and no-HE group showed a significant increase in the metabolism of lipopolysaccharides.

Conclusions

The intestinal microbiota of HE patients exhibit a lower diversity compared with no-HE and HC. It is dominated by Escherichia/Shigella and characterized by an enhanced metabolism of aromatic amino acids precursors and ammonia-producing pathways, which suggests its participation in the pathophysiology of HE. These results are described for the first time in western Mexico.