Cargando…

Characterization of biliary microbiota dysbiosis in extrahepatic cholangiocarcinoma

Extrahepatic cholangiocarcinoma (CCA) accounts for 3% of digestive cancers. The role of biliary microbiota as an environment-related modulator has been scarcely investigated in CCA, and the putative impact of associated diseases has not been yet assessed. We characterized the biliary microbiota in C...

Descripción completa

Detalles Bibliográficos
Autores principales: Saab, Massa, Mestivier, Denis, Sohrabi, Masoudreza, Rodriguez, Christophe, Khonsari, Mahmood Reza, Faraji, Amirhossein, Sobhani, Iradj
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943025/
https://www.ncbi.nlm.nih.gov/pubmed/33690612
http://dx.doi.org/10.1371/journal.pone.0247798
_version_ 1783662417058725888
author Saab, Massa
Mestivier, Denis
Sohrabi, Masoudreza
Rodriguez, Christophe
Khonsari, Mahmood Reza
Faraji, Amirhossein
Sobhani, Iradj
author_facet Saab, Massa
Mestivier, Denis
Sohrabi, Masoudreza
Rodriguez, Christophe
Khonsari, Mahmood Reza
Faraji, Amirhossein
Sobhani, Iradj
author_sort Saab, Massa
collection PubMed
description Extrahepatic cholangiocarcinoma (CCA) accounts for 3% of digestive cancers. The role of biliary microbiota as an environment-related modulator has been scarcely investigated in CCA, and the putative impact of associated diseases has not been yet assessed. We characterized the biliary microbiota in CCA patients in order to identify a specific CCA-related dysbiosis. The biliary effluents were collected through an endoscopic retrograde pancreatic cholangiography (ERCP) examination involving 28 CCA and 47 patients with gallstones, herein considered as controls. The biliary effluents were submitted to bacterial DNA extraction and 16S rRNA sequencing, using Illumina technology. Overall, 32% of CCA and 22% of controls displayed another associated disease, such as diabetes, pancreatitis, inflammatory bowel disease, or primary sclerosing cholangitis. Such associated diseases were considered in the comparisons that were made. Principal coordinate analysis (PCoA) detected a significant disparity of biliary microbiota composition between CCA patients and controls without an associated disease. Amongst the most abundant phyla, Proteobacteria did not significantly differ between CCA patients and controls, whereas Firmicutes levels were lower and Bacteroidetes higher in CCAs’ biliary microbiota than in the controls’ microbiota. The most abundant genera were Enterococcus, Streptococcus, Bacteroides, Klebsiella, and Pyramidobacter in CCA’s biliary microbiota. Additionally, levels of Bacteroides, Geobacillus, Meiothermus, and Anoxybacillus genera were significantly higher in CCA patients’ biliary microbiota, without an associated disease, in comparison with controls. A specific CCA-related dysbiosis was identified as compared to controls independently from associated diseases. This suggests that a microorganism community may be involved in CCA pathogenesis.
format Online
Article
Text
id pubmed-7943025
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-79430252021-03-19 Characterization of biliary microbiota dysbiosis in extrahepatic cholangiocarcinoma Saab, Massa Mestivier, Denis Sohrabi, Masoudreza Rodriguez, Christophe Khonsari, Mahmood Reza Faraji, Amirhossein Sobhani, Iradj PLoS One Research Article Extrahepatic cholangiocarcinoma (CCA) accounts for 3% of digestive cancers. The role of biliary microbiota as an environment-related modulator has been scarcely investigated in CCA, and the putative impact of associated diseases has not been yet assessed. We characterized the biliary microbiota in CCA patients in order to identify a specific CCA-related dysbiosis. The biliary effluents were collected through an endoscopic retrograde pancreatic cholangiography (ERCP) examination involving 28 CCA and 47 patients with gallstones, herein considered as controls. The biliary effluents were submitted to bacterial DNA extraction and 16S rRNA sequencing, using Illumina technology. Overall, 32% of CCA and 22% of controls displayed another associated disease, such as diabetes, pancreatitis, inflammatory bowel disease, or primary sclerosing cholangitis. Such associated diseases were considered in the comparisons that were made. Principal coordinate analysis (PCoA) detected a significant disparity of biliary microbiota composition between CCA patients and controls without an associated disease. Amongst the most abundant phyla, Proteobacteria did not significantly differ between CCA patients and controls, whereas Firmicutes levels were lower and Bacteroidetes higher in CCAs’ biliary microbiota than in the controls’ microbiota. The most abundant genera were Enterococcus, Streptococcus, Bacteroides, Klebsiella, and Pyramidobacter in CCA’s biliary microbiota. Additionally, levels of Bacteroides, Geobacillus, Meiothermus, and Anoxybacillus genera were significantly higher in CCA patients’ biliary microbiota, without an associated disease, in comparison with controls. A specific CCA-related dysbiosis was identified as compared to controls independently from associated diseases. This suggests that a microorganism community may be involved in CCA pathogenesis. Public Library of Science 2021-03-09 /pmc/articles/PMC7943025/ /pubmed/33690612 http://dx.doi.org/10.1371/journal.pone.0247798 Text en © 2021 Saab et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Saab, Massa
Mestivier, Denis
Sohrabi, Masoudreza
Rodriguez, Christophe
Khonsari, Mahmood Reza
Faraji, Amirhossein
Sobhani, Iradj
Characterization of biliary microbiota dysbiosis in extrahepatic cholangiocarcinoma
title Characterization of biliary microbiota dysbiosis in extrahepatic cholangiocarcinoma
title_full Characterization of biliary microbiota dysbiosis in extrahepatic cholangiocarcinoma
title_fullStr Characterization of biliary microbiota dysbiosis in extrahepatic cholangiocarcinoma
title_full_unstemmed Characterization of biliary microbiota dysbiosis in extrahepatic cholangiocarcinoma
title_short Characterization of biliary microbiota dysbiosis in extrahepatic cholangiocarcinoma
title_sort characterization of biliary microbiota dysbiosis in extrahepatic cholangiocarcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943025/
https://www.ncbi.nlm.nih.gov/pubmed/33690612
http://dx.doi.org/10.1371/journal.pone.0247798
work_keys_str_mv AT saabmassa characterizationofbiliarymicrobiotadysbiosisinextrahepaticcholangiocarcinoma
AT mestivierdenis characterizationofbiliarymicrobiotadysbiosisinextrahepaticcholangiocarcinoma
AT sohrabimasoudreza characterizationofbiliarymicrobiotadysbiosisinextrahepaticcholangiocarcinoma
AT rodriguezchristophe characterizationofbiliarymicrobiotadysbiosisinextrahepaticcholangiocarcinoma
AT khonsarimahmoodreza characterizationofbiliarymicrobiotadysbiosisinextrahepaticcholangiocarcinoma
AT farajiamirhossein characterizationofbiliarymicrobiotadysbiosisinextrahepaticcholangiocarcinoma
AT sobhaniiradj characterizationofbiliarymicrobiotadysbiosisinextrahepaticcholangiocarcinoma