婴儿口腔和胃肠系统中厌氧微生物群和古菌群的第一年动态。

IF 5 2区 生物学 Q1 MICROBIOLOGY
mSystems Pub Date : 2025-01-21 Epub Date: 2024-12-23 DOI:10.1128/msystems.01071-24
Charlotte J Neumann, Rokhsareh Mohammadzadeh, Pei Yee Woh, Tanja Kobal, Manuela-Raluca Pausan, Tejus Shinde, Victoria Haid, Polona Mertelj, Eva-Christine Weiss, Vassiliki Kolovetsiou-Kreiner, Alexander Mahnert, Christina Kumpitsch, Evelyn Jantscher-Krenn, Christine Moissl-Eichinger
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引用次数: 0

摘要

最近的研究为婴儿肠道微生物群的早期建立提供了新的见解,强调了母乳喂养对胃肠道微生物群发育的影响。在我们的研究中,我们纵向检查了健康婴儿(n = 30)一岁时口腔和胃肠道(GIT)微生物群的分类和功能动态,重点关注了经常被忽视的方面,古菌和厌氧微生物群的发展。与非母乳喂养的婴儿相比,母乳喂养的婴儿在口腔微生物群中表现出更明确的过渡阶段,其特征是链球菌的减少和厌氧菌(如颗粒菌)的出现。这一阶段以α -多样性增加和β -多样性显著变化为特征,在非BF婴儿(1-3个月)中比在BF婴儿(4-6个月)中发生得更早,这表明母乳喂养支持更晚、更明确的微生物群成熟。我们证实了婴儿口腔中存在古细菌和婴儿期早期的胃肠道微生物群,其中甲烷杆菌是优势属。然而,瞬时模式表明没有形成稳定的古菌群。胃肠道微生物群逐渐发育,BF婴儿在第3 - 8个月间表现出多样性和复杂性的增加,以厌氧微生物网络为标志。NBF婴儿从一开始就表现出复杂的微生物共生模式。在功能水平上,BF和NBF婴儿GIT微生物组之间的这些强烈差异不如在分类水平上明显。总体而言,婴儿微生物组在第一年分化和稳定,母乳喂养在形成厌氧微生物网络和整体微生物组成熟中起着至关重要的作用。重要性:生命的第一年是建立健康人体微生物群的关键时期。我们的研究分析了古细菌和专性厌氧菌在人类口腔和肠道微生物群发育中的作用,并特别关注母乳喂养对这一过程的影响。我们的研究结果表明,母乳喂养的婴儿的口腔和肠道微生物组在生命的第一年经历了不同的动态增加阶段。相比之下,非母乳喂养婴儿的微生物组从第一个月开始就更加成熟,导致第一年的发育更加稳定,没有明显的过渡阶段。此外,我们发现在1岁以下的婴儿中存在古菌特征,但它们不能形成稳定的古菌群。与此相反,我们可以追踪特定的细菌菌株从口腔过渡到肠道,或者随着时间的推移在肠道中持续存在。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
First-year dynamics of the anaerobic microbiome and archaeome in infants' oral and gastrointestinal systems.

Recent research provides new insights into the early establishment of the infant gut microbiome, emphasizing the influence of breastfeeding on the development of gastrointestinal microbiomes. In our study, we longitudinally examined the taxonomic and functional dynamics of the oral and gastrointestinal tract (GIT) microbiomes of healthy infants (n = 30) in their first year, focusing on the often-over-looked aspects, the development of archaeal and anaerobic microbiomes. Breastfed (BF) infants exhibit a more defined transitional phase in their oral microbiome compared to non-breastfed (NBF) infants, marked by a decrease in Streptococcus and the emergence of anaerobic genera such as Granulicatella. This phase, characterized by increased alpha-diversity and significant changes in beta-diversity, occurs earlier in NBF infants (months 1-3) than in BF infants (months 4-6), suggesting that breastfeeding supports later, more defined microbiome maturation. We demonstrated the presence of archaea in the infant oral cavity and GIT microbiome from early infancy, with Methanobrevibacter being the predominant genus. Still, transient patterns show that no stable archaeome is formed. The GIT microbiome exhibited gradual development, with BF infants showing increased diversity and complexity between the third and eighth months, marked by anaerobic microbial networks. NBF infants showed complex microbial co-occurrence patterns from the start. These strong differences between BF and NBF infants' GIT microbiomes are less pronounced on functional levels than on taxonomic levels. Overall, the infant microbiome differentiates and stabilizes over the first year, with breastfeeding playing a crucial role in shaping anaerobic microbial networks and overall microbiome maturation.

Importance: The first year of life is a crucial period for establishing a healthy human microbiome. Our study analyses the role of archaea and obligate anaerobes in the development of the human oral and gut microbiome, with a specific focus on the impact of breastfeeding in this process. Our findings demonstrated that the oral and gut microbiomes of breastfed infants undergo distinct phases of increased dynamics within the first year of life. In contrast, the microbiomes of non-breastfed infants are more mature from the first month, leading to a steadier development without distinct transitional phases in the first year. Additionally, we found that archaeal signatures are present in infants under 1 year of age, but they do not form a stable archaeome. In contrast to this, we could track specific bacterial strains transitioning from oral to gut or persisting in the gut over time.

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来源期刊
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
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