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Probiotics and virulent human rotavirus modulate the transplanted human gut microbiota in gnotobiotic pigs
We generated a neonatal pig model with human infant gut microbiota (HGM) to study the effect of a probiotic on the composition of the transplanted microbiota following rotavirus vaccination and challenge. All the HGM-transplanted pigs received two doses of an oral attenuated rotavirus vaccine. The g...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4209515/ https://www.ncbi.nlm.nih.gov/pubmed/25349634 http://dx.doi.org/10.1186/s13099-014-0039-8 |
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author | Zhang, Husen Wang, Haifeng Shepherd, Megan Wen, Ke Li, Guohua Yang, Xingdong Kocher, Jacob Giri-Rachman, Ernawati Dickerman, Allan Settlage, Robert Yuan, Lijuan |
author_facet | Zhang, Husen Wang, Haifeng Shepherd, Megan Wen, Ke Li, Guohua Yang, Xingdong Kocher, Jacob Giri-Rachman, Ernawati Dickerman, Allan Settlage, Robert Yuan, Lijuan |
author_sort | Zhang, Husen |
collection | PubMed |
description | We generated a neonatal pig model with human infant gut microbiota (HGM) to study the effect of a probiotic on the composition of the transplanted microbiota following rotavirus vaccination and challenge. All the HGM-transplanted pigs received two doses of an oral attenuated rotavirus vaccine. The gut microbiota of vaccinated pigs were investigated for effects of Lactobacillus rhamnosus GG (LGG) supplement and homotypic virulent human rotavirus (HRV) challenge. High-throughput sequencing of V4 region of 16S rRNA genes demonstrated that HGM-transplanted pigs carried microbiota similar to that of the C-section delivered baby. Firmicutes and Proteobacteria represented over 98% of total bacteria in the human donor and the recipient pigs. HRV challenge caused a phylum-level shift from Firmicutes to Proteobacteria. LGG supplement prevented the changes in microbial communities caused by HRV challenge. In particular, members of Enterococcus in LGG-supplemented pigs were kept at the baseline level, while they were enriched in HRV challenged pigs. Taken together, our results suggested that HGM pigs are valuable for testing the microbiota’s response to probiotic interventions for treating infantile HRV infection. |
format | Online Article Text |
id | pubmed-4209515 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42095152014-10-28 Probiotics and virulent human rotavirus modulate the transplanted human gut microbiota in gnotobiotic pigs Zhang, Husen Wang, Haifeng Shepherd, Megan Wen, Ke Li, Guohua Yang, Xingdong Kocher, Jacob Giri-Rachman, Ernawati Dickerman, Allan Settlage, Robert Yuan, Lijuan Gut Pathog Research We generated a neonatal pig model with human infant gut microbiota (HGM) to study the effect of a probiotic on the composition of the transplanted microbiota following rotavirus vaccination and challenge. All the HGM-transplanted pigs received two doses of an oral attenuated rotavirus vaccine. The gut microbiota of vaccinated pigs were investigated for effects of Lactobacillus rhamnosus GG (LGG) supplement and homotypic virulent human rotavirus (HRV) challenge. High-throughput sequencing of V4 region of 16S rRNA genes demonstrated that HGM-transplanted pigs carried microbiota similar to that of the C-section delivered baby. Firmicutes and Proteobacteria represented over 98% of total bacteria in the human donor and the recipient pigs. HRV challenge caused a phylum-level shift from Firmicutes to Proteobacteria. LGG supplement prevented the changes in microbial communities caused by HRV challenge. In particular, members of Enterococcus in LGG-supplemented pigs were kept at the baseline level, while they were enriched in HRV challenged pigs. Taken together, our results suggested that HGM pigs are valuable for testing the microbiota’s response to probiotic interventions for treating infantile HRV infection. BioMed Central 2014-09-09 /pmc/articles/PMC4209515/ /pubmed/25349634 http://dx.doi.org/10.1186/s13099-014-0039-8 Text en Copyright © 2014 Zhang et al.; licensee BioMed Central Ltd. 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 work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Zhang, Husen Wang, Haifeng Shepherd, Megan Wen, Ke Li, Guohua Yang, Xingdong Kocher, Jacob Giri-Rachman, Ernawati Dickerman, Allan Settlage, Robert Yuan, Lijuan Probiotics and virulent human rotavirus modulate the transplanted human gut microbiota in gnotobiotic pigs |
title | Probiotics and virulent human rotavirus modulate the transplanted human gut microbiota in gnotobiotic pigs |
title_full | Probiotics and virulent human rotavirus modulate the transplanted human gut microbiota in gnotobiotic pigs |
title_fullStr | Probiotics and virulent human rotavirus modulate the transplanted human gut microbiota in gnotobiotic pigs |
title_full_unstemmed | Probiotics and virulent human rotavirus modulate the transplanted human gut microbiota in gnotobiotic pigs |
title_short | Probiotics and virulent human rotavirus modulate the transplanted human gut microbiota in gnotobiotic pigs |
title_sort | probiotics and virulent human rotavirus modulate the transplanted human gut microbiota in gnotobiotic pigs |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4209515/ https://www.ncbi.nlm.nih.gov/pubmed/25349634 http://dx.doi.org/10.1186/s13099-014-0039-8 |
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