首页> 外文OA文献 >Whole genome metagenomic analysis of the gut microbiome of differently fed infants identifies differences in microbial composition and functional genes, including an absent CRISPR/Cas9 gene in the formula-fed cohort
【2h】

Whole genome metagenomic analysis of the gut microbiome of differently fed infants identifies differences in microbial composition and functional genes, including an absent CRISPR/Cas9 gene in the formula-fed cohort

机译:不同喂养婴儿的肠道微生物组的全基因组半导体分析鉴定了微生物组合物和功能基因的差异,包括式喂养队列中的不存在克拉/ Cas9基因

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Background: Advancements in sequencing capabilities have enhanced the study of the human microbiome. There are limited studies focused on the gastro-intestinal (gut) microbiome of infants, particularly the impact of diet between breast-fed (BF) versus formula-fed (FF). It is unclear what effect, if any, early feeding has on short-term or long-term composition and function of the gut microbiome. Results: Using a shotgun metagenomics approach, differences in the gut microbiome between BF (n = 10) and FF (n = 5) infants were detected. A Jaccard distance principle coordinate analysis was able to cluster BF versus FF infants based on the presence or absence of species identified in their gut microbiome. Thirty-two genera were identified as statistically different in the gut microbiome sequenced between BF and FF infants. Furthermore, the computational workflow identified 371 bacterial genes that were statistically different between the BF and FF cohorts in abundance. Only seven genes were lower in abundance (or absent) in the FF cohort compared to the BF cohort, including CRISPR/Cas9; whereas, the remaining candidates, including autotransporter adhesins, were higher in abundance in the FF cohort compared to BF cohort. Conclusions: These studies demonstrated that FF infants have, at an early age, a significantly different gut microbiome with potential implications for function of the fecal microbiota. Interactions between the fecal microbiota and host hinted at here have been linked to numerous diseases. Determining whether these non-abundant or more abundant genes have biological consequence related to infant feeding may aid in understanding the adult gut microbiome, and the pathogenesis of obesity. Keywords: Metagenomics, Next generation sequencing, Gut microbiome, Whole genome, Breast-feeding, Infants
机译:背景:测序能力的进步增强了人类微生物组的研究。有限的研究重点是婴儿的胃肠(肠道)微生物组,特别是母乳(BF)与配方喂养(FF)之间的饮食的影响。目前尚不清楚肠道短期或长期组成和肠道微生物组的长期或长期组成和功能是什么效果。结果:使用霰弹枪偏心组虫方法,检测到BF(n = 10)和FF(n = 5)婴儿之间的肠道微生物组的差异。 Jaccard距离原理坐标分析能够基于在其肠道微生物组中鉴定的物种的存在或不存在而基于FF婴儿进行聚类。在BF和FF婴儿之间测序的肠道微生物组中,将三十二属鉴定为统计不同。此外,计算工作流程鉴定了371个细菌基因,其在丰度中的BF和FF群之间的统计学上不同。与BF队列相比,在FF群组中,仅在FF群组中较少(或缺席),包括CRISPR / CAS9,只有7个基因较​​低;然而,与BF群组相比,剩余的候选者包括自耦体口粘附素,包括FF队列的丰富性较高。结论:这些研究表明,在早期,FF婴儿具有显着不同的肠道微生物组,具有粪便微生物群功能的潜在影响。粪便微生物群和宿主之间的相互作用与众多疾病有关。确定这些非丰富或更丰富的基因是否具有与婴儿饲养相关的生物后果,可能有助于了解成人肠道微生物组,以及肥胖的发病机制。关键词:偏见,下一代测序,肠道微生物组,全基因组,母乳喂养,婴儿

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号