A metagenomic approach to unveil the association between fecal gut microbiota and short-chain fatty acids in diarrhea caused by diarrheagenic Escherichia coli in children

Gallardo, Pablo; Izquierdo, Mariana; Viver, Tomeu; Bustos-Caparros, Esteban; Piras, Dana; Vidal, Roberto M.; Harmsen, Hermie M. J.; Farfan, Mauricio J.

Abstract

Diarrheagenic Escherichia coli (DEC) is the main cause of diarrhea in children under five years old. The virulence of DEC is tightly regulated by environmental signals influenced by the gut microbiota and its metabolites. Short-chain fatty acids (SCFAs) are the main metabolic product of anaerobic fermentation in the gut, but their role in DEC diarrhea has not yet been established. In this study, we determine the levels of acetate, propionate, and butyrate in stool samples from children with diarrhea caused by DEC, and we identify bacteria from the fecal gut microbiota associated with the production of SCFAs. The microbiota and SCFAs levels in stool samples obtained from 40 children with diarrhea and 43 healthy children were determined by 16S rRNA gene sequencing and HPLC, respectively. Additionally, shotgun metagenomics was used to identify metagenomeassembled genomes (MAGs) in a subgroup of samples. The results showed significantly higher levels of all SCFAs tested in diarrheal samples than in healthy controls. The abundance of Streptococcus sp., Limosilactobacillus , Blautia , Escherichia , Bacteroides , Megamonas, and Roseburia was higher in the DEC group than in healthy individuals. Functional analysis of bacteria and their main metabolic pathways made it possible to identify species MAGs that could be responsible for the detected SCFAs levels in DEC-positive diarrhea. In conclusion, based on our results and published data, we suggest that SCFAs may be important in the crosstalk between the microbiota and DEC pathogens in the gut.

Más información

Título según WOS: ID WOS:001230175700002 Not found in local WOS DB
Título de la Revista: MICROBIAL CELL
Volumen: 11
Número: 1
Editorial: Shared Science Publishers OG
Fecha de publicación: 2024
Página de inicio: 116
Página final: 127
DOI:

10.15698/mic2024.04.820

Notas: ISI