Metagenomic and metatranscriptomic analysis reveals the enzymatic mechanism of plant polysaccharide degradation through gut microbiome in plateau model animal (Ochotona curzoniae).

IF 2.2 4区 生物学 Q3 MICROBIOLOGY
Xueying Gan, Qiaoling Yu, Xueqian Hu, Yuan Qian, Xianxian Mu, Huan Li
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引用次数: 0

Abstract

Herbivorous animals can obtain energy by decomposing plant polysaccharides through gut microbiota, but the mechanism of gut microbiota decomposing plant polysaccharides in high-altitude model animals is still unclear. Plateau pika (Ochotona curzoniae) is a key model animal native to the Qinghai-Tibet Plateau with a high intake of grass. Thus, Plateau pika is an excellent animal model for studying how herbivorous animals digest and metabolize grass polysaccharides. Here, we used 16S rDNA, 16S rRNA, metagenomic and metatranscriptomic sequencing to characterize gut microbial composition, gene potential and expressed function in pikas from different altitudes. Unlike total bacteria, Oscillospira and Ruminococcus were main active bacterial genera in pika's gut. The metabolic pathways of cellulose and hemicellulose were up-regulated in the middle and high-altitude groups, those genes encoding polysaccharide enzymes were enriched. Notably, the proportion of lignin metabolic genes expressed in pika's gut was the highest, followed by cellulase and hemicellulase genes. According to comparative metagenomics of different animals, the number and relative abundance of cellulase and hemicellulase genes in pika's gut were at higher level compared with steer, etc. These results indicated that plateau pika obtained sufficient energy from grass-based diet by increasing the expression of related metabolic enzymes.

宏基因组和超转录组学分析揭示了高原模型动物(Ochotona curzoniae)肠道菌群降解植物多糖的酶促机制。
草食性动物可以通过肠道菌群分解植物多糖来获取能量,但高原模式动物肠道菌群分解植物多糖的机制尚不清楚。高原鼠兔(Ochotona curzoniae)是青藏高原的一种重要模式动物,以草为食。高原鼠兔是研究草食性动物消化和代谢草多糖的良好动物模型。本研究利用16S rDNA、16S rRNA、宏基因组和亚转录组测序技术,对不同海拔地区鼠兔的肠道微生物组成、基因潜能和表达功能进行了研究。与总细菌不同,鼠兔肠道的主要活性细菌属为示波器螺旋体和瘤胃球菌。中、高海拔组纤维素和半纤维素代谢途径上调,多糖酶编码基因富集。木质素代谢基因在鼠兔肠道中的表达比例最高,其次是纤维素酶和半纤维素酶基因。根据不同动物的比较宏基因组学,鼠兔肠道中纤维素酶和半纤维素酶基因的数量和相对丰度均高于阉牛等。上述结果表明,高原鼠兔通过增加相关代谢酶的表达,从草基饲粮中获得足够的能量。
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来源期刊
Fems Microbiology Letters
Fems Microbiology Letters 生物-微生物学
CiteScore
4.30
自引率
0.00%
发文量
112
审稿时长
1.9 months
期刊介绍: FEMS Microbiology Letters gives priority to concise papers that merit rapid publication by virtue of their originality, general interest and contribution to new developments in microbiology. All aspects of microbiology, including virology, are covered. 2019 Impact Factor: 1.987, Journal Citation Reports (Source Clarivate, 2020) Ranking: 98/135 (Microbiology) The journal is divided into eight Sections: Physiology and Biochemistry (including genetics, molecular biology and ‘omic’ studies) Food Microbiology (from food production and biotechnology to spoilage and food borne pathogens) Biotechnology and Synthetic Biology Pathogens and Pathogenicity (including medical, veterinary, plant and insect pathogens – particularly those relating to food security – with the exception of viruses) Environmental Microbiology (including ecophysiology, ecogenomics and meta-omic studies) Virology (viruses infecting any organism, including Bacteria and Archaea) Taxonomy and Systematics (for publication of novel taxa, taxonomic reclassifications and reviews of a taxonomic nature) Professional Development (including education, training, CPD, research assessment frameworks, research and publication metrics, best-practice, careers and history of microbiology) If you are unsure which Section is most appropriate for your manuscript, for example in the case of transdisciplinary studies, we recommend that you contact the Editor-In-Chief by email prior to submission. Our scope includes any type of microorganism - all members of the Bacteria and the Archaea and microbial members of the Eukarya (yeasts, filamentous fungi, microbial algae, protozoa, oomycetes, myxomycetes, etc.) as well as all viruses.
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