牛奶唾液寡糖介导仔猪肠道共生微生物的早期定植。

IF 13.8 1区 生物学 Q1 MICROBIOLOGY
Ryoga Hashimoto, Keita Nishiyama, Fu Namai, Kasumi Suzuki, Taiga Sakuma, Itsuko Fukuda, Yuta Sugiyama, Kenji Okano, Takafumi Shanoh, Eita Toyoshi, Ryusuke Ohgi, Sudeb Saha, Sae Tsuchida, Eri Nishiyama, Takao Mukai, Mutsumi Furukawa, Tomonori Nochi, Julio Villena, Wakako Ikeda-Ohtsubo, Gou Yoshioka, Eri Nakazaki, Yoshihito Suda, Haruki Kitazawa
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引用次数: 0

摘要

背景:猪的哺乳期是形成肠道微生物群的关键阶段,这对于维持新生儿的生物稳态至关重要。在母猪乳喂养的仔猪中,肠道微生物群主要由乳酸菌组成,表明宿主-肠道微生物群的共生关系受母猪乳成分的影响。在这项研究中,我们试图阐明哺乳仔猪肠道微生物群建立和维持的机制,特别关注乳酸菌对唾液寡糖的代谢。结果:基于液相色谱-质谱分析,我们鉴定出3'-唾液乳酸(3sl)是乳汁中的主要低聚糖,微生物组分析显示乳汁期唾液脂乳杆菌(Limosilactobacillus salivarius)占优势,断奶后转入罗伊氏脂乳杆菌(Limosilactobacillus reuteri)。值得注意的是,唾液酸代谢被确定为完全归因于L. salivarius,从而突出了3sl在确定物种特异性细菌分离中的关键作用。当与拟杆菌(Bacteroides thetaiotaomicron)共培养时,发现唾液乳杆菌(L. salivarius)代谢3sl,导致主要的短链脂肪酸从乳酸转变为醋酸。这种代谢转变反过来又抑制产肠毒素大肠杆菌的生长。此外,哺乳仔猪与低3sl配方奶仔猪肠道菌群的比较显示出明显的多样性特征。因此,我们推测,配方饲料仔猪中唾液寡糖的缺乏可能限制了唾液酸利用细菌(如唾液乳杆菌)的生长,从而导致肠杆菌科细菌的丰度更高。结论:我们的研究结果揭示了唾液酸寡糖在促进微生物多样性和肠道稳态方面的影响,从而强调了唾液酸在仔猪发育早期形成牛奶驱动微生物定植的关键因素的重要性。视频摘要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Milk sialyl-oligosaccharides mediate the early colonization of gut commensal microbes in piglets.

Background: The suckling period in pigs is a key phase in development for shaping the gut microbiota, which is essential for maintaining biological homeostasis in neonates. In piglets fed sow milk, the gut microbiota comprises predominantly lactobacilli, indicating a host-gut microbiota symbiosis that is influenced by sow milk components. In this study, we sought to elucidate the mechanisms underlying the establishment and maintenance of the gut microbiome in suckling piglets, with a specific focus on the metabolism of sialyl-oligosaccharides by lactobacilli.

Results: Based on liquid chromatography-mass spectrometry analysis, we identified 3'-sialyl-lactose (3'SL) as the major oligosaccharide in porcine milk, and microbiome profiling revealed the predominance of Ligilactobacillus salivarius during the suckling period, with a subsequent transition to Limosilactobacillus reuteri dominance post-weaning. Notably, sialic acid metabolism was established to be exclusively attributable to L. salivarius, thereby highlighting the pivotal role of 3'SL in determining species-specific bacterial segregation. L. salivarius was found to metabolize 3'SL when co-cultured with Bacteroides thetaiotaomicron, resulting in a shift in the predominant short-chain fatty acid produced, from lactate to acetate. This metabolic shift, in turn, inhibits the growth of enterotoxigenic Escherichia coli. Furthermore, the comparison of the gut microbiota between suckling piglets and those fed a low-3'SL formula revealed distinct diversity profiles. We accordingly speculate that an absence of sialyl-oligosaccharides in the formula-fed piglets may have restricted the growth of sialic acid-utilizing bacteria such as L. salivarius, thereby leading to a higher abundance of Enterobacteriaceae.

Conclusions: Our findings reveal the influence of sialyl-oligosaccharides in promoting microbial diversity and gut homeostasis, thereby highlighting the importance of sialic acid as a key factor in shaping milk-driven microbial colonization during the early stages of piglet development. Video Abstract.

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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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