Mucosal Microbiome Profiles Polygenic Irritable Bowel Syndrome in Mestizo Individuals


Por: Arredondo-Hernandez, Rene, Schmulson, Max, Orduna, Patricia, Lopez-Leal, Gamaliel, Zarate, Angel-Mario, Alanis-Funes, Gerardo, David Alcaraz, Luis, Santiago-Cruz, Rubi, Cevallos, Miguel A., Villa, Antonio R., Ponce-de-Leon Rosales, Samuel, Lopez-Vidal, Yolanda, Consorcio Mexicano Estudio Microbi

Publicada: 20 mar 2020
Resumen:
Irritable bowel syndrome (IBS) is the most frequent functional gastrointestinal disorder, worldwide, with a high prevalence among Mestizo Latin Americans. Because several inflammatory disorders appear to affect this population, a further understanding of host genomic background variants, in conjunction with colonic mucosa dysbiosis, is necessary to determine IBS physiopathology and the effects of environmental pressures. Using a simple polygenic model, host single nucleotide polymorphisms (SNPs) and the taxonomic compositions of microbiota were compared between IBS patients and healthy subjects. As proof of concept, five IBS-Rome III patients and five healthy controls (HCs) were systematically studied. The human and bacterial intestinal metagenome of each subject was taxonomically annotated and screened for previously annotated IBS, ulcerative colitis, and Crohn's disease-associated SNPs or taxon abundance. Dietary data and fecal markers were collected and associated with the intestinal microbiome. However, more than 1,000 variants were found, and at least 76 SNPs differentiated IBS patients from HCs, as did associations with 4 phyla and 10 bacterial genera. In this study, we found elements supporting a polygenic background, with frequent variants, among the Mestizo population, and the colonic mucosal enrichment of Bacteroides, Alteromonas, Neisseria, Streptococcus, and Microbacterium, may serve as a hallmark for IBS.

Filiaciones:
Arredondo-Hernandez, Rene:
 Univ Nacl Autonoma Mexico, Fac Med, Lab Microbioma, Div Estudios Posgrad, Mexico City, DF, Mexico

 Univ Nacl Autonoma Mexico, Fac Med, Div Invest, Mexico City, DF, Mexico

Schmulson, Max:
 Univ Nacl Autonoma Mexico, Fac Med, Lab Higado Pancreas & Motilidad HIPAM, Unidad Invest Med Expt, Mexico City, DF, Mexico

Orduna, Patricia:
 Univ Nacl Autonoma Mexico, Fac Med, Lab Microbioma, Div Estudios Posgrad, Mexico City, DF, Mexico

 Univ Nacl Autonoma Mexico, Fac Med, Div Invest, Mexico City, DF, Mexico

Lopez-Leal, Gamaliel:
 Univ Nacl Autonoma Mexico, Fac Med, Dept Microbiol & Parasitol, Programa Inmunol Mol Microbiana, Mexico City, DF, Mexico

Zarate, Angel-Mario:
 Hosp Gen Mexico City, Mexico City, DF, Mexico

Alanis-Funes, Gerardo:
 Tecnol Monterrey, Sch Med & Hlth Sci, Monterrey, Mexico

David Alcaraz, Luis:
 Univ Nacl Autonoma Mexico, Fac Ciencias, Dept Biol Celular, Mexico City, DF, Mexico

Santiago-Cruz, Rubi:
 Univ Nacl Autonoma Mexico, Fac Med, Dept Microbiol & Parasitol, Programa Inmunol Mol Microbiana, Mexico City, DF, Mexico

Cevallos, Miguel A.:
 Univ Nacl Autonoma Mexico, Programa Genom Evolut, Ctr Ciencias Genom, Cuernavaca, Morelos, Mexico

Villa, Antonio R.:
 Univ Nacl Autonoma Mexico, Fac Med, Lab Microbioma, Div Estudios Posgrad, Mexico City, DF, Mexico

 Univ Nacl Autonoma Mexico, Fac Med, Div Invest, Mexico City, DF, Mexico

Ponce-de-Leon Rosales, Samuel:
 Univ Nacl Autonoma Mexico, Fac Med, Lab Microbioma, Div Estudios Posgrad, Mexico City, DF, Mexico

 Univ Nacl Autonoma Mexico, Fac Med, Div Invest, Mexico City, DF, Mexico

Lopez-Vidal, Yolanda:
 Univ Nacl Autonoma Mexico, Fac Med, Dept Microbiol & Parasitol, Programa Inmunol Mol Microbiana, Mexico City, DF, Mexico
ISSN: 22352988
Editorial
FRONTIERS RESEARCH FOUNDATION, PO BOX 110, LAUSANNE, 1015, SWITZERLAND, Suiza
Tipo de documento: Article
Volumen: 10 Número:
Páginas:
WOS Id: 000525509100001
ID de PubMed: 32266159