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发酵产生的后生元可稳定瘤胃固体微生物群,并在泌乳奶牛基于谷物的亚急性瘤胃酸中毒(SARA)挑战期间促进微生物网络相互作用和核心分类群的多样性。

Postbiotics from fermentation stabilize rumen solids microbiota and promote microbial network interactions and diversity of hub taxa during grain-based subacute ruminal acidosis (SARA) challenges in lactating dairy cows.

作者信息

Guo Junfei, Zhang Zhengxiao, Guan Le Luo, Zhou Mi, Yoon Ilkyu, Khafipour Ehsan, Plaizier Jan C

机构信息

Department of Animal Science, University of Manitoba, Winnipeg, MB, Canada.

Department of Agriculture, Food and Nutrition, University of Alberta, Edmonton, AB, Canada.

出版信息

Front Microbiol. 2024 Aug 16;15:1409659. doi: 10.3389/fmicb.2024.1409659. eCollection 2024.

Abstract

BACKGROUND

High-yielding dairy cows are commonly fed high-grain rations. However, this can cause subacute ruminal acidosis (SARA), a metabolic disorder in dairy cows that is usually accompanied by dysbiosis of the rumen microbiome. Postbiotics that contain functional metabolites provide a competitive niche for influential members of the rumen microbiome, may stabilize and promote their populations, and, therefore, may attenuate the adverse effects of SARA.

METHODS

This study used a total of 32 rumen-cannulated lactating dairy cows, which were randomly assigned into four treatments: no SCFP (control), 14 g/d Original XPC (SCFPa), 19 g/d NutriTek (SCFPb-1X), and 38 g/d NutriTek (SCFPb-2X) (Diamond V, Cedar Rapids, IA) from 4 weeks before until 12 weeks after parturition. Grain-based SARA challenges were conducted during week 5 (SARA1) and week 8 (SARA2) after parturition by replacing 20% dry matter of the base total mixed ration (TMR) with pellets containing 50% ground barley and 50% ground wheat. The DNA of rumen solids digesta was extracted and subjected to V3-V4 16S rRNA gene sequencing. The characteristics of rumen solids microbiota were compared between non-SARA (Pre-SARA1, week 4; Post-SARA1, week 7; and Post-SARA2, weeks 10 and 12) and SARA stages (SARA1/1, SARA1/2, SARA2/1, SARA2/2), as well as among treatments.

RESULTS

Both SARA challenges reduced the richness and diversity of the microbiota and the relative abundances of the phylum Fibrobacteres. Supplementation with SCFP promoted the growth of several fibrolytic bacteria, including Lachnospiraceae UCG-009, , unclassified Lachnospiraceae, and unclassified Ruminococcaceae during the SARA challenges. These challenges also reduced the positive interactions and the numbers of hub taxa in the microbiota. The SCFPb treatment increased positive interactions among microbial members of the solids digesta and the number of hub taxa during the SARA and non-SARA stages. The SCFPb-2X treatment prevented changes in the network characteristics, including the number of components, clustering coefficient, modularity, positive edge percentage, and edge density of the microbiota during SARA challenges. These challenges reduced predicted carbohydrate and nitrogen metabolism in microbiota, whereas SCFP supplementation attenuated those reductions.

CONCLUSIONS

Supplementation with SCFP, especially the SCFPb-2X attenuated the adverse effects of grain-based SARA on the diversity and predicted functionality of rumen solids microbiota.

摘要

背景

高产奶牛通常饲喂高谷物日粮。然而,这可能会导致亚急性瘤胃酸中毒(SARA),这是奶牛的一种代谢紊乱,通常伴有瘤胃微生物群的失调。含有功能性代谢产物的后生元为瘤胃微生物群中有影响力的成员提供了一个竞争生态位,可能会稳定并促进它们的种群数量,因此,可能会减轻SARA的不利影响。

方法

本研究共使用了32头装有瘤胃瘘管的泌乳奶牛,将它们随机分为四种处理:不添加SCFP(对照)、分娩前4周直至分娩后12周每天添加14克原始XPC(SCFPa)、19克NutriTek(SCFPb-1X)和38克NutriTek(SCFPb-2X)(钻石V公司,爱荷华州锡达拉皮兹)。在分娩后第5周(SARA1)和第8周(SARA2)进行基于谷物的SARA挑战,方法是用含有50%大麦粉和50%小麦粉的颗粒替代基础全混合日粮(TMR)20%的干物质。提取瘤胃固体消化物的DNA,并进行V3-V4 16S rRNA基因测序。比较了非SARA阶段(SARA前1,第4周;SARA后1,第7周;以及SARA后2,第10周和第12周)和SARA阶段(SARA1/1、SARA1/2、SARA2/1、SARA2/2)以及各处理之间瘤胃固体微生物群的特征。

结果

两次SARA挑战均降低了微生物群的丰富度和多样性以及纤维杆菌门的相对丰度。在SARA挑战期间,添加SCFP促进了几种纤维分解菌的生长,包括毛螺菌科UCG-009、未分类的毛螺菌科和未分类的瘤胃球菌科。这些挑战还减少了微生物群中的正向相互作用和核心分类群的数量。SCFPb处理增加了固体消化物微生物成员之间的正向相互作用以及SARA和非SARA阶段核心分类群的数量。SCFPb-2X处理在SARA挑战期间防止了微生物群网络特征的变化,包括组分数量、聚类系数、模块性、正向边百分比和边密度。这些挑战降低了微生物群中预测的碳水化合物和氮代谢,而添加SCFP减弱了这些降低。

结论

添加SCFP,尤其是SCFPb-2X,减轻了基于谷物的SARA对瘤胃固体微生物群多样性和预测功能的不利影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d201/11362103/ae51fb7f4cba/fmicb-15-1409659-g0001.jpg

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