Cargando…

Postinfective bowel dysfunction following Campylobacter enteritis is characterised by reduced microbiota diversity and impaired microbiota recovery

OBJECTIVES: Persistent bowel dysfunction following gastroenteritis (postinfectious (PI)-BD) is well recognised, but the associated changes in microbiota remain unclear. Our aim was to define these changes after gastroenteritis caused by a single organism, Campylobacter jejuni, examining the dynamic...

Descripción completa

Detalles Bibliográficos
Autores principales: Jalanka, Jonna, Gunn, David, Singh, Gulzar, Krishnasamy, Shanthi, Lingaya, Melanie, Crispie, Fiona, Finnegan, Laura, Cotter, Paul, James, Louise, Nowak, Adam, Major, Giles, Spiller, Robin C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933158/
https://www.ncbi.nlm.nih.gov/pubmed/36171082
http://dx.doi.org/10.1136/gutjnl-2021-326828
_version_ 1784889612246712320
author Jalanka, Jonna
Gunn, David
Singh, Gulzar
Krishnasamy, Shanthi
Lingaya, Melanie
Crispie, Fiona
Finnegan, Laura
Cotter, Paul
James, Louise
Nowak, Adam
Major, Giles
Spiller, Robin C
author_facet Jalanka, Jonna
Gunn, David
Singh, Gulzar
Krishnasamy, Shanthi
Lingaya, Melanie
Crispie, Fiona
Finnegan, Laura
Cotter, Paul
James, Louise
Nowak, Adam
Major, Giles
Spiller, Robin C
author_sort Jalanka, Jonna
collection PubMed
description OBJECTIVES: Persistent bowel dysfunction following gastroenteritis (postinfectious (PI)-BD) is well recognised, but the associated changes in microbiota remain unclear. Our aim was to define these changes after gastroenteritis caused by a single organism, Campylobacter jejuni, examining the dynamic changes in the microbiota and the impact of antibiotics. DESIGN: A single-centre cohort study of 155 patients infected with Campylobacter jejuni. Features of the initial illness as well as current bowel symptoms and the intestinal microbiota composition were recorded soon after infection (visit 1, <40 days) as well as 40–60 days and >80 days later (visits 2 and 3). Microbiota were assessed using 16S rRNA sequencing. RESULTS: PI-BD was found in 22 of the 99 patients who completed the trial. The cases reported significantly looser stools, with more somatic and gastrointestinal symptoms. Microbiota were assessed in 22 cases who had significantly lower diversity and altered microbiota composition compared with the 44 age-matched and sex-matched controls. Moreover 60 days after infection, cases showed a significantly lower abundance of 23 taxa including phylum Firmicutes, particularly in the order Clostridiales and the family Ruminoccocaceae, increased Proteobacteria abundance and increased levels of Fusobacteria and Gammaproteobacteria. The microbiota changes were linked with diet; higher fibre consumption being associated with lower levels of Gammaproteobacteria. CONCLUSION: The microbiota of PI-BD patients appeared more disturbed by the initial infection compared with the microbiota of those who recovered. The prebiotic effect of high fibre diets may inhibit some of the disturbances seen in PI-BD. TRIAL REGISTRATION NUMBER: NCT02040922.
format Online
Article
Text
id pubmed-9933158
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher BMJ Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-99331582023-02-17 Postinfective bowel dysfunction following Campylobacter enteritis is characterised by reduced microbiota diversity and impaired microbiota recovery Jalanka, Jonna Gunn, David Singh, Gulzar Krishnasamy, Shanthi Lingaya, Melanie Crispie, Fiona Finnegan, Laura Cotter, Paul James, Louise Nowak, Adam Major, Giles Spiller, Robin C Gut Gut Microbiota OBJECTIVES: Persistent bowel dysfunction following gastroenteritis (postinfectious (PI)-BD) is well recognised, but the associated changes in microbiota remain unclear. Our aim was to define these changes after gastroenteritis caused by a single organism, Campylobacter jejuni, examining the dynamic changes in the microbiota and the impact of antibiotics. DESIGN: A single-centre cohort study of 155 patients infected with Campylobacter jejuni. Features of the initial illness as well as current bowel symptoms and the intestinal microbiota composition were recorded soon after infection (visit 1, <40 days) as well as 40–60 days and >80 days later (visits 2 and 3). Microbiota were assessed using 16S rRNA sequencing. RESULTS: PI-BD was found in 22 of the 99 patients who completed the trial. The cases reported significantly looser stools, with more somatic and gastrointestinal symptoms. Microbiota were assessed in 22 cases who had significantly lower diversity and altered microbiota composition compared with the 44 age-matched and sex-matched controls. Moreover 60 days after infection, cases showed a significantly lower abundance of 23 taxa including phylum Firmicutes, particularly in the order Clostridiales and the family Ruminoccocaceae, increased Proteobacteria abundance and increased levels of Fusobacteria and Gammaproteobacteria. The microbiota changes were linked with diet; higher fibre consumption being associated with lower levels of Gammaproteobacteria. CONCLUSION: The microbiota of PI-BD patients appeared more disturbed by the initial infection compared with the microbiota of those who recovered. The prebiotic effect of high fibre diets may inhibit some of the disturbances seen in PI-BD. TRIAL REGISTRATION NUMBER: NCT02040922. BMJ Publishing Group 2023-03 2022-09-28 /pmc/articles/PMC9933158/ /pubmed/36171082 http://dx.doi.org/10.1136/gutjnl-2021-326828 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Gut Microbiota
Jalanka, Jonna
Gunn, David
Singh, Gulzar
Krishnasamy, Shanthi
Lingaya, Melanie
Crispie, Fiona
Finnegan, Laura
Cotter, Paul
James, Louise
Nowak, Adam
Major, Giles
Spiller, Robin C
Postinfective bowel dysfunction following Campylobacter enteritis is characterised by reduced microbiota diversity and impaired microbiota recovery
title Postinfective bowel dysfunction following Campylobacter enteritis is characterised by reduced microbiota diversity and impaired microbiota recovery
title_full Postinfective bowel dysfunction following Campylobacter enteritis is characterised by reduced microbiota diversity and impaired microbiota recovery
title_fullStr Postinfective bowel dysfunction following Campylobacter enteritis is characterised by reduced microbiota diversity and impaired microbiota recovery
title_full_unstemmed Postinfective bowel dysfunction following Campylobacter enteritis is characterised by reduced microbiota diversity and impaired microbiota recovery
title_short Postinfective bowel dysfunction following Campylobacter enteritis is characterised by reduced microbiota diversity and impaired microbiota recovery
title_sort postinfective bowel dysfunction following campylobacter enteritis is characterised by reduced microbiota diversity and impaired microbiota recovery
topic Gut Microbiota
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933158/
https://www.ncbi.nlm.nih.gov/pubmed/36171082
http://dx.doi.org/10.1136/gutjnl-2021-326828
work_keys_str_mv AT jalankajonna postinfectiveboweldysfunctionfollowingcampylobacterenteritisischaracterisedbyreducedmicrobiotadiversityandimpairedmicrobiotarecovery
AT gunndavid postinfectiveboweldysfunctionfollowingcampylobacterenteritisischaracterisedbyreducedmicrobiotadiversityandimpairedmicrobiotarecovery
AT singhgulzar postinfectiveboweldysfunctionfollowingcampylobacterenteritisischaracterisedbyreducedmicrobiotadiversityandimpairedmicrobiotarecovery
AT krishnasamyshanthi postinfectiveboweldysfunctionfollowingcampylobacterenteritisischaracterisedbyreducedmicrobiotadiversityandimpairedmicrobiotarecovery
AT lingayamelanie postinfectiveboweldysfunctionfollowingcampylobacterenteritisischaracterisedbyreducedmicrobiotadiversityandimpairedmicrobiotarecovery
AT crispiefiona postinfectiveboweldysfunctionfollowingcampylobacterenteritisischaracterisedbyreducedmicrobiotadiversityandimpairedmicrobiotarecovery
AT finneganlaura postinfectiveboweldysfunctionfollowingcampylobacterenteritisischaracterisedbyreducedmicrobiotadiversityandimpairedmicrobiotarecovery
AT cotterpaul postinfectiveboweldysfunctionfollowingcampylobacterenteritisischaracterisedbyreducedmicrobiotadiversityandimpairedmicrobiotarecovery
AT jameslouise postinfectiveboweldysfunctionfollowingcampylobacterenteritisischaracterisedbyreducedmicrobiotadiversityandimpairedmicrobiotarecovery
AT nowakadam postinfectiveboweldysfunctionfollowingcampylobacterenteritisischaracterisedbyreducedmicrobiotadiversityandimpairedmicrobiotarecovery
AT majorgiles postinfectiveboweldysfunctionfollowingcampylobacterenteritisischaracterisedbyreducedmicrobiotadiversityandimpairedmicrobiotarecovery
AT spillerrobinc postinfectiveboweldysfunctionfollowingcampylobacterenteritisischaracterisedbyreducedmicrobiotadiversityandimpairedmicrobiotarecovery