Cargando…

Microbiota from Specific Pathogen-Free Mice Reduces Campylobacter jejuni Chicken Colonization

Campylobacter jejuni, a prevalent foodborne bacterial pathogen, is mainly transmitted from poultry with few effective prevention approaches. In this study, we aimed to investigate the role of microbiota on C. jejuni chicken colonization. Microbiota from specific pathogen-free (SPF) mouse stools were...

Descripción completa

Detalles Bibliográficos
Autores principales: Almansour, Ayidh, Fu, Ying, Alenezi, Tahrir, Bansal, Mohit, Alrubaye, Bilal, Wang, Hong, Sun, Xiaolun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8621964/
https://www.ncbi.nlm.nih.gov/pubmed/34832543
http://dx.doi.org/10.3390/pathogens10111387
_version_ 1784605582169210880
author Almansour, Ayidh
Fu, Ying
Alenezi, Tahrir
Bansal, Mohit
Alrubaye, Bilal
Wang, Hong
Sun, Xiaolun
author_facet Almansour, Ayidh
Fu, Ying
Alenezi, Tahrir
Bansal, Mohit
Alrubaye, Bilal
Wang, Hong
Sun, Xiaolun
author_sort Almansour, Ayidh
collection PubMed
description Campylobacter jejuni, a prevalent foodborne bacterial pathogen, is mainly transmitted from poultry with few effective prevention approaches. In this study, we aimed to investigate the role of microbiota on C. jejuni chicken colonization. Microbiota from specific pathogen-free (SPF) mouse stools were collected as SPF-Aerobe and SPF-Anaerobe. Birds were colonized with SPF-Aerobe or SPF-Anaerobe at day 0 and infected with C. jejuni AR101 at day 12. Notably, C. jejuni AR101 colonized at 5.3 and 5.6 log(10) C. jejuni CFU/g chicken cecal digesta at days 21 and 28, respectively, while both SPF-Aerobe and SPF-Anaerobe microbiota reduced pathogen colonization. Notably, SPF-Aerobe and SPF-Anaerobe increased cecal phylum Bacteroidetes and reduced phylum Firmicutes compared to those in the nontransplanted birds. Interestingly, microbiota from noninfected chickens, SPF-Aerobe, or SPF-Anaerobe inhibited AR101 in vitro growth, whereas microbiota from infected birds alone failed to reduce pathogen growth. The bacterium Enterobacter102 isolated from infected birds transplanted with SPF-Aerobe inhibited AR101 in vitro growth and reduced pathogen gut colonization in chickens. Together, SPF mouse microbiota was able to colonize chicken gut and reduce C. jejuni chicken colonization. The findings may help the development of effective strategies to reduce C. jejuni chicken contamination and campylobacteriosis.
format Online
Article
Text
id pubmed-8621964
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-86219642021-11-27 Microbiota from Specific Pathogen-Free Mice Reduces Campylobacter jejuni Chicken Colonization Almansour, Ayidh Fu, Ying Alenezi, Tahrir Bansal, Mohit Alrubaye, Bilal Wang, Hong Sun, Xiaolun Pathogens Article Campylobacter jejuni, a prevalent foodborne bacterial pathogen, is mainly transmitted from poultry with few effective prevention approaches. In this study, we aimed to investigate the role of microbiota on C. jejuni chicken colonization. Microbiota from specific pathogen-free (SPF) mouse stools were collected as SPF-Aerobe and SPF-Anaerobe. Birds were colonized with SPF-Aerobe or SPF-Anaerobe at day 0 and infected with C. jejuni AR101 at day 12. Notably, C. jejuni AR101 colonized at 5.3 and 5.6 log(10) C. jejuni CFU/g chicken cecal digesta at days 21 and 28, respectively, while both SPF-Aerobe and SPF-Anaerobe microbiota reduced pathogen colonization. Notably, SPF-Aerobe and SPF-Anaerobe increased cecal phylum Bacteroidetes and reduced phylum Firmicutes compared to those in the nontransplanted birds. Interestingly, microbiota from noninfected chickens, SPF-Aerobe, or SPF-Anaerobe inhibited AR101 in vitro growth, whereas microbiota from infected birds alone failed to reduce pathogen growth. The bacterium Enterobacter102 isolated from infected birds transplanted with SPF-Aerobe inhibited AR101 in vitro growth and reduced pathogen gut colonization in chickens. Together, SPF mouse microbiota was able to colonize chicken gut and reduce C. jejuni chicken colonization. The findings may help the development of effective strategies to reduce C. jejuni chicken contamination and campylobacteriosis. MDPI 2021-10-27 /pmc/articles/PMC8621964/ /pubmed/34832543 http://dx.doi.org/10.3390/pathogens10111387 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Almansour, Ayidh
Fu, Ying
Alenezi, Tahrir
Bansal, Mohit
Alrubaye, Bilal
Wang, Hong
Sun, Xiaolun
Microbiota from Specific Pathogen-Free Mice Reduces Campylobacter jejuni Chicken Colonization
title Microbiota from Specific Pathogen-Free Mice Reduces Campylobacter jejuni Chicken Colonization
title_full Microbiota from Specific Pathogen-Free Mice Reduces Campylobacter jejuni Chicken Colonization
title_fullStr Microbiota from Specific Pathogen-Free Mice Reduces Campylobacter jejuni Chicken Colonization
title_full_unstemmed Microbiota from Specific Pathogen-Free Mice Reduces Campylobacter jejuni Chicken Colonization
title_short Microbiota from Specific Pathogen-Free Mice Reduces Campylobacter jejuni Chicken Colonization
title_sort microbiota from specific pathogen-free mice reduces campylobacter jejuni chicken colonization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8621964/
https://www.ncbi.nlm.nih.gov/pubmed/34832543
http://dx.doi.org/10.3390/pathogens10111387
work_keys_str_mv AT almansourayidh microbiotafromspecificpathogenfreemicereducescampylobacterjejunichickencolonization
AT fuying microbiotafromspecificpathogenfreemicereducescampylobacterjejunichickencolonization
AT alenezitahrir microbiotafromspecificpathogenfreemicereducescampylobacterjejunichickencolonization
AT bansalmohit microbiotafromspecificpathogenfreemicereducescampylobacterjejunichickencolonization
AT alrubayebilal microbiotafromspecificpathogenfreemicereducescampylobacterjejunichickencolonization
AT wanghong microbiotafromspecificpathogenfreemicereducescampylobacterjejunichickencolonization
AT sunxiaolun microbiotafromspecificpathogenfreemicereducescampylobacterjejunichickencolonization