Rumen and hindgut microbiome regulate average daily gain of preweaning Holstein heifer calves in different ways.

IF 13.8 1区 生物学 Q1 MICROBIOLOGY Microbiome Pub Date : 2024-07-19 DOI:10.1186/s40168-024-01844-7
Sheng-Yang Xu, Xiao-Ran Feng, Wei Zhao, Yan-Liang Bi, Qi-Yu Diao, Yan Tu
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Abstract

Background: The average daily gain (ADG) of preweaning calves significantly influences their adult productivity and reproductive performance. Gastrointestinal microbes are known to exert an impact on host phenotypes, including ADG. The aim of this study was to investigate the mechanisms by which gastrointestinal microbiome regulate ADG in preweaning calves and to further validate them by isolating ADG-associated rumen microbes in vitro.

Results: Sixteen Holstein heifer calves were selected from a cohort with 106 calves and divided into higher ADG (HADG; n = 8) and lower ADG (LADG; n = 8) groups. On the day of weaning, samples of rumen contents, hindgut contents, and plasma were collected for rumen metagenomics, rumen metabolomics, hindgut metagenomics, hindgut metabolomics, and plasma metabolomics analyses. Subsequently, rumen contents of preweaning Holstein heifer calves from the same dairy farm were collected to isolate ADG-associated rumen microbes. The results showed that the rumen microbes, including Pyramidobacter sp. C12-8, Pyramidobacter sp. CG50-2, Pyramidobacter porci, unclassified_g_Pyramidobacter, Pyramidobacter piscolens, and Acidaminococcus fermentans, were enriched in the rumen of HADG calves (LDA > 2, P < 0.05). Enrichment of these microbes in HADG calves' rumen promoted carbohydrate degradation and volatile fatty acid production, increasing proportion of butyrate in the rumen and ultimately contributing to higher preweaning ADG in calves (P < 0.05). The presence of active carbohydrate degradation in the rumen was further suggested by the negative correlation of the rumen microbes P. piscolens, P. sp. C12-8 and unclassified_g_Pyramidobacter with the rumen metabolites D-fructose (R <  - 0.50, P < 0.05). Widespread positive correlations were observed between rumen microbes (such as P. piscolens, P. porci, and A. fermentans) and beneficial plasma metabolites (such as 1-pyrroline-5-carboxylic acid and 4-fluoro-L-phenylalanine), which were subsequently positively associated with the growth rate of HADG calves (R > 0.50, P < 0.05). We succeeded in isolating a strain of A. fermentans from the rumen contents of preweaning calves and named it Acidaminococcus fermentans P41. The in vitro cultivation revealed its capability to produce butyrate. In vitro fermentation experiments demonstrated that the addition of A. fermentans P41 significantly increased the proportion of butyrate in the rumen fluid (P < 0.05). These results further validated our findings. The relative abundance of Bifidobacterium pseudolongum in the hindgut of HADG calves was negatively correlated with hindgut 4-hydroxyglucobrassicin levels, which were positively correlated with plasma 4-hydroxyglucobrassicin levels, and plasma 4-hydroxyglucobrassicin levels were positively correlated with ADG (P < 0.05).

Conclusions: This study's findings unveil that rumen and hindgut microbes play distinctive roles in regulating the preweaning ADG of Holstein heifer calves. Additionally, the successful isolation of A. fermentans P41 not only validated our findings but also provided a valuable strain resource for modulating rumen microbes in preweaning calves. Video Abstract.

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瘤胃和后肠微生物组以不同方式调节断奶前荷斯坦小母牛的平均日增重。
背景:断奶前犊牛的平均日增重(ADG)对其成年生产力和繁殖性能有很大影响。众所周知,胃肠道微生物会对宿主表型(包括 ADG)产生影响。本研究旨在探讨胃肠道微生物群调节断奶前犊牛ADG的机制,并通过体外分离与ADG相关的瘤胃微生物进一步验证这些机制:从106头荷斯坦小母牛中挑选出16头,分为ADG较高组(HADG,n = 8)和ADG较低组(LADG,n = 8)。断奶当天,收集瘤胃内容物、后肠内容物和血浆样本,进行瘤胃元基因组学、瘤胃代谢组学、后肠元基因组学、后肠代谢组学和血浆代谢组学分析。随后,收集了同一牧场断奶前荷斯坦小母牛的瘤胃内容物,以分离与ADG相关的瘤胃微生物。结果表明,HADG犊牛瘤胃中富含的瘤胃微生物包括C12-8金字塔菌、CG50-2金字塔菌、孔隙金字塔菌、未分类金字塔菌、piscolens金字塔菌和Acidaminococcus fermentans(LDA>2,P 0.50,P 结论):本研究的结果表明,瘤胃和后肠微生物在调节荷斯坦小母牛断奶前ADG方面发挥着不同的作用。此外,A. fermentans P41 的成功分离不仅验证了我们的发现,还为调节断奶前犊牛的瘤胃微生物提供了宝贵的菌株资源。视频摘要。
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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
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