The impact of early-life exposures on growth and adult gut microbiome composition is dependent on genetic strain and parent- of- origin.

IF 13.8 1区 生物学 Q1 MICROBIOLOGY
M Nazmul Huda, Emer Kelly, Keri Barron, Jing Xue, William Valdar, Lisa M Tarantino, Sarah Schoenrock, Folami Y Ideraabdullah, Brian J Bennett
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引用次数: 0

Abstract

Background: Early-life exposure to environmental factors can have long-lasting impacts on offspring health into adulthood and therefore is an emerging public health concern. In particular, the impact of maternal environmental exposures such as diet and antibiotic use on the establishment of the offspring gut microbiome has been recently highlighted as a potential link to disease risk. However, the long-term effects are poorly understood. Moreover, interindividual host genetic differences have also been implicated in modulating the gut microbiome, suggesting that these differences may modulate susceptibility to environmentally induced dysbiosis and exacerbate related health outcomes. Our understanding of how the developmental environment and genetics interact to modulate offspring long-term gut microbiota and health is still limited.

Methods: In this study, we investigated the effects of early exposure to known or putative dietary insults on the microbiome (antibiotic exposure, protein deficiency, and vitamin D deficiency) in a novel population of mice. Dams were maintained on purified AIN93G antibiotic-containing (AC), low-protein (LP), low-vitamin D (LVD), or mouse control (CON) diets from 5 weeks prior to pregnancy until the end of lactation. After weaning, mice were transferred to new cages and fed a standardized chow diet. The parent-of-origin (PO) effect was determined via F1 offspring from reciprocal crosses of recombinant inbred intercross (RIX) of Collaborative Cross (CC) mice, where all F1 offspring within a reciprocal pair were genetically identical except for the X- and Y-chromosomes and mitochondrial genomes. We assayed offspring bodyweight and the gut bacterial microbiota via 16S rRNA gene sequencing at 8 weeks of age.

Results: Our study revealed that early developmental exposure to antibiotics, protein deficiency, and vitamin D deficiency had long-lasting effects on offspring bodyweight and gut microbial diversity and composition, depending on the genetic background. Several bacterial genera and ASVs, including Bacteroides, Muribaculaceae, Akkermansia, and Bifidobacterium, are influenced by developmental insults. We also observed a significant effect of PO on offspring gut microbiota and growth. For example, the offspring of CC011xCC001 mice had increased bodyweight, microbial diversity indices, and several differential bacterial abundances, including those of Faecalibaculum, compared with those of the corresponding reciprocal cross CC001xCC011.

Conclusion: Our results show that maternal exposure to nutritional deficiencies and antibiotics during gestation and lactation has a lasting impact on offspring gut microbiota composition. The specific responses to a diet or antibiotic can vary among F1 strains and may be driven by maternal genetics. Video Abstract.

早期生活暴露对生长和成年肠道微生物组成的影响取决于遗传菌株和父母来源。
背景:生命早期暴露于环境因素可对后代直至成年的健康产生长期影响,因此是一个新兴的公共卫生问题。特别是,母亲的环境暴露,如饮食和抗生素的使用,对后代肠道微生物群的建立的影响,最近被强调为与疾病风险的潜在联系。然而,人们对其长期影响知之甚少。此外,宿主个体间的遗传差异也与肠道微生物组的调节有关,这表明这些差异可能调节对环境诱导的生态失调的易感性,并加剧相关的健康结果。我们对发育环境和遗传相互作用如何调节后代长期肠道微生物群和健康的理解仍然有限。方法:在这项研究中,我们研究了早期暴露于已知或假定的饮食损害(抗生素暴露、蛋白质缺乏和维生素D缺乏)对一种新型小鼠群体微生物组的影响。从妊娠前5周至哺乳期结束,饲喂含纯化AIN93G抗生素(AC)、低蛋白(LP)、低维生素D (LVD)或小鼠对照(CON)饲粮。断奶后,小鼠被转移到新的笼子里,喂食标准化的饲料。亲本起源(PO)效应是通过合作杂交(CC)小鼠重组自交系间杂交(RIX)的互惠杂交的F1后代来确定的,其中互惠对中的所有F1后代除了X染色体和y染色体以及线粒体基因组外在遗传上是相同的。我们在8周龄时通过16S rRNA基因测序测定了子代体重和肠道细菌微生物群。结果:我们的研究表明,早期发育暴露于抗生素、蛋白质缺乏和维生素D缺乏对后代体重和肠道微生物多样性和组成有长期影响,这取决于遗传背景。一些细菌属和asv,包括拟杆菌科、Muribaculaceae、Akkermansia和双歧杆菌,都受到发育损伤的影响。我们还观察到PO对后代肠道微生物群和生长的显著影响。例如,与相应的反向杂交CC001xCC011相比,CC011xCC001小鼠的后代体重、微生物多样性指数以及包括Faecalibaculum在内的几种不同细菌丰度都有所增加。结论:我们的研究结果表明,母亲在妊娠和哺乳期间暴露于营养缺乏和抗生素对后代肠道微生物群组成有持久的影响。对饮食或抗生素的特定反应可能因F1菌株而异,可能受母体遗传驱动。视频摘要。
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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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