Cargando…

Rumen-protected glucose supplementation in transition dairy cows shifts fermentation patterns and enhances mucosal immunity

Manipulation of perinatal diets, such as supplementing feed with rumen-protected glucose (RPG), has been positively regarded as a strategy to improve milking performance. This study was conducted to assess the effects of RPG on the fermentation profiles, resident microbiota and mucosal immunity in t...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Xiaoli, Li, Xiaopeng, Wu, Jian, Jiao, Jinzhen, He, Zhixiong, Tan, Zhiliang, Han, Xuefeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8556486/
https://www.ncbi.nlm.nih.gov/pubmed/34754960
http://dx.doi.org/10.1016/j.aninu.2021.08.002
_version_ 1784592176499392512
author Zhang, Xiaoli
Li, Xiaopeng
Wu, Jian
Jiao, Jinzhen
He, Zhixiong
Tan, Zhiliang
Han, Xuefeng
author_facet Zhang, Xiaoli
Li, Xiaopeng
Wu, Jian
Jiao, Jinzhen
He, Zhixiong
Tan, Zhiliang
Han, Xuefeng
author_sort Zhang, Xiaoli
collection PubMed
description Manipulation of perinatal diets, such as supplementing feed with rumen-protected glucose (RPG), has been positively regarded as a strategy to improve milking performance. This study was conducted to assess the effects of RPG on the fermentation profiles, resident microbiota and mucosal immunity in the cecum. Ten Holstein dairy cows were randomly assigned to either a 25 g/kg RPG diet (DM basis) or a 11 g/kg coating fat diet (control, CON). Compared with the CON group, the acetate-to-propionate ratio was lower in the RPG group. Gene expression analysis indicated that RPG supplementation tended to upregulate the expression of Na(+)/H(+) hydrogen exchanger 3 (NHE3) (P = 0.076). RPG supplementation downregulated the expression of genes involved in self-rehabilitation such as matrix metalloproteinase 1 (MMP1), MMP3, MMP9 and MMP13. Additionally, the mRNA expression of genes involved in immunity including Toll-like receptors (TLR4, TLR6 and TLR7) and proinflammatory cytokines (immune interferon gamma [IFNG] and interleukins interleukin 17A [IL17F], IL17A, IL22), was downregulated by RPG supplementation. Nonetheless, no differences existed in the bacterial copy number and beta diversity between the 2 groups. Overall, supplementation with RPG would probably cause a shift towards propionate production in the cecal digesta, and promote the immune homeostasis of the cecal mucosa in transition dairy cows. Our results extended the basic understanding of RPG supplementation and utilization in transition dairy cows in terms of host microbe interplay in the cecum.
format Online
Article
Text
id pubmed-8556486
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher KeAi Publishing
record_format MEDLINE/PubMed
spelling pubmed-85564862021-11-08 Rumen-protected glucose supplementation in transition dairy cows shifts fermentation patterns and enhances mucosal immunity Zhang, Xiaoli Li, Xiaopeng Wu, Jian Jiao, Jinzhen He, Zhixiong Tan, Zhiliang Han, Xuefeng Anim Nutr Short Communication Manipulation of perinatal diets, such as supplementing feed with rumen-protected glucose (RPG), has been positively regarded as a strategy to improve milking performance. This study was conducted to assess the effects of RPG on the fermentation profiles, resident microbiota and mucosal immunity in the cecum. Ten Holstein dairy cows were randomly assigned to either a 25 g/kg RPG diet (DM basis) or a 11 g/kg coating fat diet (control, CON). Compared with the CON group, the acetate-to-propionate ratio was lower in the RPG group. Gene expression analysis indicated that RPG supplementation tended to upregulate the expression of Na(+)/H(+) hydrogen exchanger 3 (NHE3) (P = 0.076). RPG supplementation downregulated the expression of genes involved in self-rehabilitation such as matrix metalloproteinase 1 (MMP1), MMP3, MMP9 and MMP13. Additionally, the mRNA expression of genes involved in immunity including Toll-like receptors (TLR4, TLR6 and TLR7) and proinflammatory cytokines (immune interferon gamma [IFNG] and interleukins interleukin 17A [IL17F], IL17A, IL22), was downregulated by RPG supplementation. Nonetheless, no differences existed in the bacterial copy number and beta diversity between the 2 groups. Overall, supplementation with RPG would probably cause a shift towards propionate production in the cecal digesta, and promote the immune homeostasis of the cecal mucosa in transition dairy cows. Our results extended the basic understanding of RPG supplementation and utilization in transition dairy cows in terms of host microbe interplay in the cecum. KeAi Publishing 2021-12 2021-10-02 /pmc/articles/PMC8556486/ /pubmed/34754960 http://dx.doi.org/10.1016/j.aninu.2021.08.002 Text en © 2021 Chinese Association of Animal Science and Veterinary Medicine. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co. Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Short Communication
Zhang, Xiaoli
Li, Xiaopeng
Wu, Jian
Jiao, Jinzhen
He, Zhixiong
Tan, Zhiliang
Han, Xuefeng
Rumen-protected glucose supplementation in transition dairy cows shifts fermentation patterns and enhances mucosal immunity
title Rumen-protected glucose supplementation in transition dairy cows shifts fermentation patterns and enhances mucosal immunity
title_full Rumen-protected glucose supplementation in transition dairy cows shifts fermentation patterns and enhances mucosal immunity
title_fullStr Rumen-protected glucose supplementation in transition dairy cows shifts fermentation patterns and enhances mucosal immunity
title_full_unstemmed Rumen-protected glucose supplementation in transition dairy cows shifts fermentation patterns and enhances mucosal immunity
title_short Rumen-protected glucose supplementation in transition dairy cows shifts fermentation patterns and enhances mucosal immunity
title_sort rumen-protected glucose supplementation in transition dairy cows shifts fermentation patterns and enhances mucosal immunity
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8556486/
https://www.ncbi.nlm.nih.gov/pubmed/34754960
http://dx.doi.org/10.1016/j.aninu.2021.08.002
work_keys_str_mv AT zhangxiaoli rumenprotectedglucosesupplementationintransitiondairycowsshiftsfermentationpatternsandenhancesmucosalimmunity
AT lixiaopeng rumenprotectedglucosesupplementationintransitiondairycowsshiftsfermentationpatternsandenhancesmucosalimmunity
AT wujian rumenprotectedglucosesupplementationintransitiondairycowsshiftsfermentationpatternsandenhancesmucosalimmunity
AT jiaojinzhen rumenprotectedglucosesupplementationintransitiondairycowsshiftsfermentationpatternsandenhancesmucosalimmunity
AT hezhixiong rumenprotectedglucosesupplementationintransitiondairycowsshiftsfermentationpatternsandenhancesmucosalimmunity
AT tanzhiliang rumenprotectedglucosesupplementationintransitiondairycowsshiftsfermentationpatternsandenhancesmucosalimmunity
AT hanxuefeng rumenprotectedglucosesupplementationintransitiondairycowsshiftsfermentationpatternsandenhancesmucosalimmunity