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...
Autores principales: | , , , , , , , , |
---|---|
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 |