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Alterations in the jejunal microbiota and fecal metabolite profiles of rabbits infected with Eimeria intestinalis
BACKGROUND: Rabbit coccidiosis is a major disease caused by various Eimeria species and causes enormous economic losses to the rabbit industry. Coccidia infection has a wide impact on the gut microbiota and intestinal biochemical equilibrium. In the present study, we established a model of Eimeria i...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9233780/ https://www.ncbi.nlm.nih.gov/pubmed/35754027 http://dx.doi.org/10.1186/s13071-022-05340-5 |
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author | Yuan, Xu Liu, Jin Hu, Xiaofen Yang, Shanshan Zhong, Shengwei Yang, Tingyu Zhou, Yunxiao Zhao, Guotong Jiang, Yijie Li, Yong |
author_facet | Yuan, Xu Liu, Jin Hu, Xiaofen Yang, Shanshan Zhong, Shengwei Yang, Tingyu Zhou, Yunxiao Zhao, Guotong Jiang, Yijie Li, Yong |
author_sort | Yuan, Xu |
collection | PubMed |
description | BACKGROUND: Rabbit coccidiosis is a major disease caused by various Eimeria species and causes enormous economic losses to the rabbit industry. Coccidia infection has a wide impact on the gut microbiota and intestinal biochemical equilibrium. In the present study, we established a model of Eimeria intestinalis infection in rabbits to evaluate the jejunal microbiota and fecal metabolite profiles. METHODS: Rabbits in the infected group were orally inoculated with 3 × 10(3) E. intestinalis oocysts. On the eighth day of infection, jejunal contents and feces were collected for 16S rRNA gene sequencing and liquid chromatography–tandem mass spectrometry (LC–MS/MS) analysis, respectively. Jejunum tissues were harvested for hematoxylin and eosin (H&E), periodic acid-Schiff (PAS), and immunohistochemistry (IHC) staining. RESULTS: Histopathological analysis showed that the whole jejunum was parasitized by E. intestinalis in a range of life cycle stages, and PAS staining showed that E. intestinalis infection caused extensive loss of goblet cells. IHC staining revealed that TNF-α expression was higher in the E. intestinalis infection group. Moreover, both the jejunal microbiota and metabolites significantly altered after E. intestinalis infection. At the genus level, the abundances of Escherichia and Enterococcus significantly increased in the infected group compared with the control group, while those of Oscillospira, Ruminococcus, Bacteroides, Akkermansia, Coprococcus, and Sarcina significantly decreased. In addition, 20 metabolites and two metabolic pathways were altered after E. intestinalis infection, and the major disrupted metabolic pathway was lipid metabolism. CONCLUSIONS: Eimeria intestinalis infection induced intestinal inflammation and destroyed the intestinal homeostasis at the parasitized sites, leading to significant changes in the gut microbiota and subsequent corresponding changes in metabolites. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-9233780 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-92337802022-06-27 Alterations in the jejunal microbiota and fecal metabolite profiles of rabbits infected with Eimeria intestinalis Yuan, Xu Liu, Jin Hu, Xiaofen Yang, Shanshan Zhong, Shengwei Yang, Tingyu Zhou, Yunxiao Zhao, Guotong Jiang, Yijie Li, Yong Parasit Vectors Research BACKGROUND: Rabbit coccidiosis is a major disease caused by various Eimeria species and causes enormous economic losses to the rabbit industry. Coccidia infection has a wide impact on the gut microbiota and intestinal biochemical equilibrium. In the present study, we established a model of Eimeria intestinalis infection in rabbits to evaluate the jejunal microbiota and fecal metabolite profiles. METHODS: Rabbits in the infected group were orally inoculated with 3 × 10(3) E. intestinalis oocysts. On the eighth day of infection, jejunal contents and feces were collected for 16S rRNA gene sequencing and liquid chromatography–tandem mass spectrometry (LC–MS/MS) analysis, respectively. Jejunum tissues were harvested for hematoxylin and eosin (H&E), periodic acid-Schiff (PAS), and immunohistochemistry (IHC) staining. RESULTS: Histopathological analysis showed that the whole jejunum was parasitized by E. intestinalis in a range of life cycle stages, and PAS staining showed that E. intestinalis infection caused extensive loss of goblet cells. IHC staining revealed that TNF-α expression was higher in the E. intestinalis infection group. Moreover, both the jejunal microbiota and metabolites significantly altered after E. intestinalis infection. At the genus level, the abundances of Escherichia and Enterococcus significantly increased in the infected group compared with the control group, while those of Oscillospira, Ruminococcus, Bacteroides, Akkermansia, Coprococcus, and Sarcina significantly decreased. In addition, 20 metabolites and two metabolic pathways were altered after E. intestinalis infection, and the major disrupted metabolic pathway was lipid metabolism. CONCLUSIONS: Eimeria intestinalis infection induced intestinal inflammation and destroyed the intestinal homeostasis at the parasitized sites, leading to significant changes in the gut microbiota and subsequent corresponding changes in metabolites. GRAPHICAL ABSTRACT: [Image: see text] BioMed Central 2022-06-26 /pmc/articles/PMC9233780/ /pubmed/35754027 http://dx.doi.org/10.1186/s13071-022-05340-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Yuan, Xu Liu, Jin Hu, Xiaofen Yang, Shanshan Zhong, Shengwei Yang, Tingyu Zhou, Yunxiao Zhao, Guotong Jiang, Yijie Li, Yong Alterations in the jejunal microbiota and fecal metabolite profiles of rabbits infected with Eimeria intestinalis |
title | Alterations in the jejunal microbiota and fecal metabolite profiles of rabbits infected with Eimeria intestinalis |
title_full | Alterations in the jejunal microbiota and fecal metabolite profiles of rabbits infected with Eimeria intestinalis |
title_fullStr | Alterations in the jejunal microbiota and fecal metabolite profiles of rabbits infected with Eimeria intestinalis |
title_full_unstemmed | Alterations in the jejunal microbiota and fecal metabolite profiles of rabbits infected with Eimeria intestinalis |
title_short | Alterations in the jejunal microbiota and fecal metabolite profiles of rabbits infected with Eimeria intestinalis |
title_sort | alterations in the jejunal microbiota and fecal metabolite profiles of rabbits infected with eimeria intestinalis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9233780/ https://www.ncbi.nlm.nih.gov/pubmed/35754027 http://dx.doi.org/10.1186/s13071-022-05340-5 |
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