从肠道到配子:微生物群如何影响生育能力和孕前健康。

IF 12.7 1区 生物学 Q1 MICROBIOLOGY
Sarah K Munyoki, Natalie Vukmer, Julie M Rios, Amanda Kallen, Eldin Jašarević
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引用次数: 0

摘要

尽管辅助生殖技术取得了进步,但全球生育率仍在继续下降,这凸显了我们对孕前生理学机制的理解存在重大差距。在这篇评论中,我们回顾了越来越多的工作,这些工作表明微生物组在妇女生殖健康中起着至关重要但尚未得到充分探索的作用。这项工作表明,在这一关键时期,微生物群落产生支持代谢、免疫和激素功能的底物,影响生育能力、妊娠结局和后代健康。患有生殖疾病的妇女,包括子宫内膜异位症、多囊卵巢综合征、原发性卵巢功能不全和复发性流产,都有明显的微生物特征。动物研究提供了关键的机制见解,表明微生物群的破坏加速了卵巢衰老,但将这些发现转化为人类孕前健康需要仔细考虑。虽然这些发现令人信服,但这一新兴领域目前缺乏对微生物信号如何通过代谢物、免疫反应或激素途径影响生殖组织的清晰理解。我们概述了在孕前健康中建立微生物因果关系的标准,包括充分性、必要性、特异性和时机。超越相关性包括选择合适的模型,关注关键的发育窗口,在受孕前进行纵向研究,以及调查特定的微生物代谢物如何影响生殖结果。将微生物组研究纳入孕前护理可能会导致新疗法和干预措施的发展。虽然这里概述的原则主要涉及孕前生殖健康,但它们也为微生物组研究提供了一个总体框架,强调在这个快速发展的领域中需要了解机制、及时干预和从关联到因果关系的进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
From gut to gamete: how the microbiome influences fertility and preconception health.

Global fertility rates continue to decline despite advancements in assisted reproductive technologies, highlighting a significant gap in our understanding of the mechanisms underlying preconception physiology. In this commentary, we review a growing body of work demonstrating that the microbiome plays a crucial yet underexplored role in women's reproductive health. This work has shown that microbial communities produce substrates that support metabolic, immune, and hormonal functions during this critical period, affecting fertility, pregnancy outcomes, and offspring health. Women with reproductive disorders, including endometriosis, polycystic ovarian syndrome, primary ovarian insufficiency, and recurrent pregnancy loss, harbor distinct microbial signatures. Animal studies provide key mechanistic insights, showing that disruption of microbiota accelerates ovarian aging, but translating these findings to human preconception health requires careful consideration. While these findings are compelling, this emerging field currently lacks a clear understanding of how microbial signals affect reproductive tissues through metabolites, immune responses, or hormonal pathways. We outline criteria for establishing microbial causation in preconception health, including sufficiency, necessity, specificity, and timing. Moving beyond correlations involves selecting appropriate models, focusing on key developmental windows, conducting longitudinal studies before conception, and investigating how specific microbial metabolites influence reproductive outcomes. Incorporating microbiome research into preconception care could lead to the development of new therapies and interventions. While the principles outlined here primarily address preconception reproductive health, they also offer a framework for microbiome research in general, emphasizing the need for a mechanistic understanding, timely interventions, and progress from association to causation in this rapidly evolving field.

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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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