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茶皂素对秦川肉牛瘤胃微生物群及瘤胃功能的影响

Effect of Tea Saponins on Rumen Microbiota and Rumen Function in Qinchuan Beef Cattle.

作者信息

Qu Xiaopeng, Raza Sayed Haidar Abbas, Zhao Yanqing, Deng Jiahan, Ma Jing, Wang Juze, Alkhorayef Nada, Alkhalil Samia S, Pant Sameer D, Lei Hongtao, Zan Linsen

机构信息

College of Animal Science and Technology, Northwest A&F University, Yangling, Xianyang 712100, China.

Safety of Livestock and Poultry Products, College of Food Science, South China Agricultural University, Guangzhou 510642, China.

出版信息

Microorganisms. 2023 Feb 1;11(2):374. doi: 10.3390/microorganisms11020374.

DOI:10.3390/microorganisms11020374
PMID:36838339
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9963011/
Abstract

Antibiotics can promote livestock growth but have side effects, so the search for safe and effective alternatives to antibiotics is urgent. This study aimed to evaluate the effect of supplementing cattle feed with tea saponins on ruminal bacteria and fungi. Sixteen Qinchuan beef cattle with a live body weight of 250 ± 10 kg were divided into four groups (four animals in each group) using a completely randomized experimental design. Four different levels of tea saponins were provided to the Qinchuan cattle as treatments, including 0 g/cattle per day control, CON), 10 g/cattle per day (low-level, LT), 20 g/cattle per day (medium-level, MT) and 30 g/cattle per day (high-level, HT). The pre-feeding period was 10 days and the official period was 80 days in this experiment. After 90 days of feeding, the rumen fluid from sixteen Qinchuan beef cattle was collected using an oral stomach tube for evaluating changes in ruminal microbiota and rumen fermentation parameters. Results indicate that the total VFAs and proportions of propionate in the LT group was significantly higher than that in the CON and HT groups ( < 0.05). For ruminal bacteria, results indicate that the Chao1 index of the MT group was significantly lower than the CON and HT groups ( < 0.05). The phyla Bacteroidetes and Firmicutes were found to be the most abundant in all treatment groups, with the LT group having significantly increased relative abundances of Proteobacteria, Actinobacteria and Ascomycota at the phylum level ( < 0.05). The relative abundance of Bacteroides was found to be relatively lower in the LT, MT and HT treatment groups compared with the CON treatment group at the genus level ( < 0.05). For ruminal fungi, the LT treatment group was found to have higher relative abundances of Saccharomyces and Aspergillus, and lower relative abundances of Succiniclasticum and Bacteroides at the at the phylum level ( < 0.05). Compared with the CON treatment group, a significant increase in the relative abundance of Saccharomyces and Aspergillus were observed in the LT treatment group at the genus level ( < 0.05). PICRUSt analyses identified pathways associated with Xenobiotic biodegradation and metabolism and glycolysisIII to be significantly enriched in the LT and HT treatment groups ( < 0.05). These findings could provide insights on how tea saponins may influence ruminal bacteria and fungi, providing a theoretical basis for replacing antibiotics with tea saponins for promoting growth in cattle.

摘要

抗生素可促进家畜生长,但存在副作用,因此迫切需要寻找安全有效的抗生素替代品。本研究旨在评估在牛饲料中添加茶皂素对瘤胃细菌和真菌的影响。采用完全随机试验设计,将16头体重为250±10 kg的秦川肉牛分为四组(每组4头)。给秦川牛提供四种不同水平的茶皂素作为处理,包括每天每头牛0 g(对照组,CON)、每天每头牛10 g(低水平,LT)、每天每头牛20 g(中等水平,MT)和每天每头牛30 g(高水平,HT)。本试验预饲期为10天,正式期为80天。饲养90天后,用口腔胃管采集16头秦川肉牛的瘤胃液,以评估瘤胃微生物群和瘤胃发酵参数的变化。结果表明,LT组的总挥发性脂肪酸(VFAs)和丙酸比例显著高于CON组和HT组(P<0.05)。对于瘤胃细菌,结果表明MT组的Chao1指数显著低于CON组和HT组(P<0.05)。在所有处理组中,拟杆菌门和厚壁菌门是最丰富的门类,LT组在门水平上变形菌门、放线菌门和子囊菌门的相对丰度显著增加(P<0.05)。在属水平上,与CON处理组相比,LT、MT和HT处理组中拟杆菌属的相对丰度相对较低(P<0.05)。对于瘤胃真菌,在门水平上,LT处理组的酿酒酵母属和曲霉属相对丰度较高,琥珀酸分解菌属和拟杆菌属相对丰度较低(P<0.05)。在属水平上,与CON处理组相比,LT处理组中酿酒酵母属和曲霉属的相对丰度显著增加(P<0.05)。PICRUSt分析确定,与异生物质生物降解和代谢以及糖酵解III相关的途径在LT和HT处理组中显著富集(P<0.05)。这些发现可以为茶皂素如何影响瘤胃细菌和真菌提供见解,为用茶皂素替代抗生素促进牛生长提供理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af33/9963011/d7fbd144a0ba/microorganisms-11-00374-g007a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af33/9963011/001a8fb83b86/microorganisms-11-00374-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af33/9963011/179105979d7a/microorganisms-11-00374-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af33/9963011/4c2efa80aba6/microorganisms-11-00374-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af33/9963011/5df8deb7446f/microorganisms-11-00374-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af33/9963011/81978f9bab0a/microorganisms-11-00374-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af33/9963011/e356d99fa40b/microorganisms-11-00374-g006a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af33/9963011/d7fbd144a0ba/microorganisms-11-00374-g007a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af33/9963011/001a8fb83b86/microorganisms-11-00374-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af33/9963011/179105979d7a/microorganisms-11-00374-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af33/9963011/4c2efa80aba6/microorganisms-11-00374-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af33/9963011/5df8deb7446f/microorganisms-11-00374-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af33/9963011/81978f9bab0a/microorganisms-11-00374-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af33/9963011/e356d99fa40b/microorganisms-11-00374-g006a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af33/9963011/d7fbd144a0ba/microorganisms-11-00374-g007a.jpg

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