Cargando…

Microbial metabolite deoxycholic acid shapes microbiota against Campylobacter jejuni chicken colonization

Despite reducing the prevalent foodborne pathogen Campylobacter jejuni in chickens decreases campylobacteriosis, few effective approaches are available. The aim of this study was to use microbial metabolic product bile acids to reduce C. jejuni chicken colonization. Broiler chicks were fed with deox...

Descripción completa

Detalles Bibliográficos
Autores principales: Alrubaye, Bilal, Abraha, Mussie, Almansour, Ayidh, Bansal, Mohit, Wang, Hong, Kwon, Young Min, Huang, Yan, Hargis, Billy, Sun, Xiaolun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6611565/
https://www.ncbi.nlm.nih.gov/pubmed/31276498
http://dx.doi.org/10.1371/journal.pone.0214705
_version_ 1783432717765967872
author Alrubaye, Bilal
Abraha, Mussie
Almansour, Ayidh
Bansal, Mohit
Wang, Hong
Kwon, Young Min
Huang, Yan
Hargis, Billy
Sun, Xiaolun
author_facet Alrubaye, Bilal
Abraha, Mussie
Almansour, Ayidh
Bansal, Mohit
Wang, Hong
Kwon, Young Min
Huang, Yan
Hargis, Billy
Sun, Xiaolun
author_sort Alrubaye, Bilal
collection PubMed
description Despite reducing the prevalent foodborne pathogen Campylobacter jejuni in chickens decreases campylobacteriosis, few effective approaches are available. The aim of this study was to use microbial metabolic product bile acids to reduce C. jejuni chicken colonization. Broiler chicks were fed with deoxycholic acid (DCA), lithocholic acid (LCA), or ursodeoxycholic acid (UDCA). The birds were also transplanted with DCA modulated anaerobes (DCA-Anaero) or aerobes (DCA-Aero). The birds were infected with human clinical isolate C. jejuni 81–176 or chicken isolate C. jejuni AR101. Notably, C. jejuni 81–176 was readily colonized intestinal tract at d16 and reached an almost plateau at d21. Remarkably, DCA excluded C. jejuni cecal colonization below the limit of detection at 16 and 28 days of age. Neither chicken ages of infection nor LCA or UDCA altered C. jejuni AR101 chicken colonization level, while DCA reduced 91% of the bacterium in chickens at d28. Notably, DCA diet reduced phylum Firmicutes but increased Bacteroidetes compared to infected control birds. Importantly, DCA-Anaero attenuated 93% of C. jejuni colonization at d28 compared to control infected birds. In conclusion, DCA shapes microbiota composition against C. jejuni colonization in chickens, suggesting a bidirectional interaction between microbiota and microbial metabolites.
format Online
Article
Text
id pubmed-6611565
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-66115652019-07-12 Microbial metabolite deoxycholic acid shapes microbiota against Campylobacter jejuni chicken colonization Alrubaye, Bilal Abraha, Mussie Almansour, Ayidh Bansal, Mohit Wang, Hong Kwon, Young Min Huang, Yan Hargis, Billy Sun, Xiaolun PLoS One Research Article Despite reducing the prevalent foodborne pathogen Campylobacter jejuni in chickens decreases campylobacteriosis, few effective approaches are available. The aim of this study was to use microbial metabolic product bile acids to reduce C. jejuni chicken colonization. Broiler chicks were fed with deoxycholic acid (DCA), lithocholic acid (LCA), or ursodeoxycholic acid (UDCA). The birds were also transplanted with DCA modulated anaerobes (DCA-Anaero) or aerobes (DCA-Aero). The birds were infected with human clinical isolate C. jejuni 81–176 or chicken isolate C. jejuni AR101. Notably, C. jejuni 81–176 was readily colonized intestinal tract at d16 and reached an almost plateau at d21. Remarkably, DCA excluded C. jejuni cecal colonization below the limit of detection at 16 and 28 days of age. Neither chicken ages of infection nor LCA or UDCA altered C. jejuni AR101 chicken colonization level, while DCA reduced 91% of the bacterium in chickens at d28. Notably, DCA diet reduced phylum Firmicutes but increased Bacteroidetes compared to infected control birds. Importantly, DCA-Anaero attenuated 93% of C. jejuni colonization at d28 compared to control infected birds. In conclusion, DCA shapes microbiota composition against C. jejuni colonization in chickens, suggesting a bidirectional interaction between microbiota and microbial metabolites. Public Library of Science 2019-07-05 /pmc/articles/PMC6611565/ /pubmed/31276498 http://dx.doi.org/10.1371/journal.pone.0214705 Text en © 2019 Alrubaye 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
Alrubaye, Bilal
Abraha, Mussie
Almansour, Ayidh
Bansal, Mohit
Wang, Hong
Kwon, Young Min
Huang, Yan
Hargis, Billy
Sun, Xiaolun
Microbial metabolite deoxycholic acid shapes microbiota against Campylobacter jejuni chicken colonization
title Microbial metabolite deoxycholic acid shapes microbiota against Campylobacter jejuni chicken colonization
title_full Microbial metabolite deoxycholic acid shapes microbiota against Campylobacter jejuni chicken colonization
title_fullStr Microbial metabolite deoxycholic acid shapes microbiota against Campylobacter jejuni chicken colonization
title_full_unstemmed Microbial metabolite deoxycholic acid shapes microbiota against Campylobacter jejuni chicken colonization
title_short Microbial metabolite deoxycholic acid shapes microbiota against Campylobacter jejuni chicken colonization
title_sort microbial metabolite deoxycholic acid shapes microbiota against campylobacter jejuni chicken colonization
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6611565/
https://www.ncbi.nlm.nih.gov/pubmed/31276498
http://dx.doi.org/10.1371/journal.pone.0214705
work_keys_str_mv AT alrubayebilal microbialmetabolitedeoxycholicacidshapesmicrobiotaagainstcampylobacterjejunichickencolonization
AT abrahamussie microbialmetabolitedeoxycholicacidshapesmicrobiotaagainstcampylobacterjejunichickencolonization
AT almansourayidh microbialmetabolitedeoxycholicacidshapesmicrobiotaagainstcampylobacterjejunichickencolonization
AT bansalmohit microbialmetabolitedeoxycholicacidshapesmicrobiotaagainstcampylobacterjejunichickencolonization
AT wanghong microbialmetabolitedeoxycholicacidshapesmicrobiotaagainstcampylobacterjejunichickencolonization
AT kwonyoungmin microbialmetabolitedeoxycholicacidshapesmicrobiotaagainstcampylobacterjejunichickencolonization
AT huangyan microbialmetabolitedeoxycholicacidshapesmicrobiotaagainstcampylobacterjejunichickencolonization
AT hargisbilly microbialmetabolitedeoxycholicacidshapesmicrobiotaagainstcampylobacterjejunichickencolonization
AT sunxiaolun microbialmetabolitedeoxycholicacidshapesmicrobiotaagainstcampylobacterjejunichickencolonization