Faecal microbiota from patients with cirrhosis has a low capacity to ferment non‐digestible carbohydrates into short‐chain fatty acids

• Published in: Liver international Vol. 39; no. 8; pp. 1437 - 1447
• Main Authors: Jin, Mingliang, Kalainy, Sylvia, Baskota, Nami, Chiang, Diana, Deehan, Edward C., McDougall, Chelsea, Tandon, Puneeta, Martínez, Inés, Cervera, Carlos, Walter, Jens, Abraldes, Juan G.
• Format: Journal Article
• Language: English
• Published: United States Wiley Subscription Services, Inc 01.08.2019
• Subjects: Abnormalities; Antibiotics; Carbohydrates; Cirrhosis; Composition; Dysbacteriosis; Fatty acids; Gene sequencing; Intestinal microflora; Lactulose; Liver cirrhosis; Liver diseases; Males; Microbiomes; Microbiota; Pectin; Production methods; Proton pump inhibitors; rRNA 16S; short-chain fatty acids; Starch; Substrates; microbiota; short-chain fatty acids; cirrhosis
• ISSN: 1478-3223; 1478-3231
• DOI: 10.1111/liv.14106

Background and Aims Cirrhosis is associated with dysbiosis, but its functional consequences are still largely unknown. Short‐chain fatty acids (SCFAs) account for physiological interactions between the gut microbiota and host. Our aim was to assess the impact of cirrhotic dysbiosis on the production of SCFAs. Methods Seventeen patients with cirrhosis and 17 controls were selected. Microbiota composition in faecal samples was assessed by next‐generation 16S rRNA gene sequencing. SCFAs were measured with GC‐MS in faecal samples and after in vitro batch fermentations using arabinoxylan, resistant starch, pectin, and lactulose as substrates. Results Among the 17 cirrhotic patients (mean age 58, eight males), six, nine and two were, respectively, Child‐Pugh class A, B and C. Eleven patients were on oral antibiotics, 11 on lactulose and 13 on proton pump inhibitors. Cirrhotic patients showed marked differences in the composition and diversity of gut microbiome when compared to controls, that were more pronounced with increased severity. Stool samples from cirrhotic patients showed lower SCFAs content and reduced capacity to produce SCFAs in batch fermentations, with butyrate production being the most abnormal. These functional aberrancies were more pronounced with greater liver disease severity. Abundance of Ruminococcus faecis (in family Ruminococcaceae), Faecalicatena fissicatena and Fusicatenibacter saccharivorans (in family Lachnospiraceae) was positively correlated with the SCFAs production. Conclusion Cirrhotic dysbiosis is associated with a decreased capacity to ferment non‐digestible carbohydrates into SCFAs, especially into butyrate. These functional abnormalities are more pronounced as disease progresses. These results might inform the design of gut‐targeted therapies for cirrhosis.