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Changes in the gut bacterial communities in colon cancer surgery patients: an observational study
BACKGROUND: Colon surgery has been shown to modulate the intestinal microbiota. Our objective was to characterize these changes using state-of-the-art next generation sequencing techniques. METHODS: We performed a single-centre prospective observational cohort study to evaluate the changes in the gu...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8729125/ https://www.ncbi.nlm.nih.gov/pubmed/34983654 http://dx.doi.org/10.1186/s13099-021-00477-7 |
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author | Abbas, Mohamed Gaïa, Nadia Buchs, Nicolas C. Delaune, Vaihere Girard, Myriam Andrey, Diego O. Meyer, Jeremy Schrenzel, Jacques Ris, Frédéric Harbarth, Stephan Lazarevic, Vladimir |
author_facet | Abbas, Mohamed Gaïa, Nadia Buchs, Nicolas C. Delaune, Vaihere Girard, Myriam Andrey, Diego O. Meyer, Jeremy Schrenzel, Jacques Ris, Frédéric Harbarth, Stephan Lazarevic, Vladimir |
author_sort | Abbas, Mohamed |
collection | PubMed |
description | BACKGROUND: Colon surgery has been shown to modulate the intestinal microbiota. Our objective was to characterize these changes using state-of-the-art next generation sequencing techniques. METHODS: We performed a single-centre prospective observational cohort study to evaluate the changes in the gut microbiota, i.e., taxon distribution, before and after elective oncologic colon surgery in adult patients with different antimicrobial prophylaxis regimens (standard prophylaxis with cefuroxime/metronidazole versus carbapenems for extended-spectrum beta-lactamase-producing Enterobacterales [ESBL-E] carriers). We obtained rectal samples on the day of surgery, intraoperative luminal samples, and rectal or stoma samples 3 days after surgery. We performed metataxonomic analysis based on sequencing of the bacterial 16S rRNA gene marker. Similarities and differences between bacterial communities were assessed using Bray–Curtis similarity, visualised using principal coordinates analysis and statistically tested by PERMANOVA. Comparison of taxa relative abundance was performed using ANCOM. RESULTS: We included 27 patients between March 27, 2019 and September 17, 2019. The median age was 63.6 years (IQR 56.4–76.3) and 44% were females. Most (81%) patients received standard perioperative prophylaxis as they were not ESBL carriers. There was no significant association between ESBL carriage and differences in gut microbiome. We observed large and significant increases in the genus Enterococcus between the preoperative/intraoperative samples and the postoperative sample, mainly driven by Enterococcus faecalis. There were significant differences in the postoperative microbiome between patients who received standard prophylaxis and carbapenems, specifically in the family Erysipelotrichaceae. CONCLUSION: This hypothesis-generating study showed rapid changes in the rectal microbiota following colon cancer surgery. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13099-021-00477-7. |
format | Online Article Text |
id | pubmed-8729125 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-87291252022-01-07 Changes in the gut bacterial communities in colon cancer surgery patients: an observational study Abbas, Mohamed Gaïa, Nadia Buchs, Nicolas C. Delaune, Vaihere Girard, Myriam Andrey, Diego O. Meyer, Jeremy Schrenzel, Jacques Ris, Frédéric Harbarth, Stephan Lazarevic, Vladimir Gut Pathog Research BACKGROUND: Colon surgery has been shown to modulate the intestinal microbiota. Our objective was to characterize these changes using state-of-the-art next generation sequencing techniques. METHODS: We performed a single-centre prospective observational cohort study to evaluate the changes in the gut microbiota, i.e., taxon distribution, before and after elective oncologic colon surgery in adult patients with different antimicrobial prophylaxis regimens (standard prophylaxis with cefuroxime/metronidazole versus carbapenems for extended-spectrum beta-lactamase-producing Enterobacterales [ESBL-E] carriers). We obtained rectal samples on the day of surgery, intraoperative luminal samples, and rectal or stoma samples 3 days after surgery. We performed metataxonomic analysis based on sequencing of the bacterial 16S rRNA gene marker. Similarities and differences between bacterial communities were assessed using Bray–Curtis similarity, visualised using principal coordinates analysis and statistically tested by PERMANOVA. Comparison of taxa relative abundance was performed using ANCOM. RESULTS: We included 27 patients between March 27, 2019 and September 17, 2019. The median age was 63.6 years (IQR 56.4–76.3) and 44% were females. Most (81%) patients received standard perioperative prophylaxis as they were not ESBL carriers. There was no significant association between ESBL carriage and differences in gut microbiome. We observed large and significant increases in the genus Enterococcus between the preoperative/intraoperative samples and the postoperative sample, mainly driven by Enterococcus faecalis. There were significant differences in the postoperative microbiome between patients who received standard prophylaxis and carbapenems, specifically in the family Erysipelotrichaceae. CONCLUSION: This hypothesis-generating study showed rapid changes in the rectal microbiota following colon cancer surgery. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13099-021-00477-7. BioMed Central 2022-01-04 /pmc/articles/PMC8729125/ /pubmed/34983654 http://dx.doi.org/10.1186/s13099-021-00477-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Abbas, Mohamed Gaïa, Nadia Buchs, Nicolas C. Delaune, Vaihere Girard, Myriam Andrey, Diego O. Meyer, Jeremy Schrenzel, Jacques Ris, Frédéric Harbarth, Stephan Lazarevic, Vladimir Changes in the gut bacterial communities in colon cancer surgery patients: an observational study |
title | Changes in the gut bacterial communities in colon cancer surgery patients: an observational study |
title_full | Changes in the gut bacterial communities in colon cancer surgery patients: an observational study |
title_fullStr | Changes in the gut bacterial communities in colon cancer surgery patients: an observational study |
title_full_unstemmed | Changes in the gut bacterial communities in colon cancer surgery patients: an observational study |
title_short | Changes in the gut bacterial communities in colon cancer surgery patients: an observational study |
title_sort | changes in the gut bacterial communities in colon cancer surgery patients: an observational study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8729125/ https://www.ncbi.nlm.nih.gov/pubmed/34983654 http://dx.doi.org/10.1186/s13099-021-00477-7 |
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