Characterizing the endometrial microbiome by analyzing the ultra-low bacteria from embryo transfer catheter tips in IVF cycles: Next generation sequencing (NGS) analysis of the 16S ribosomal gene

Q1 Medicine
Xin Tao , Jason M. Franasiak , Yiping Zhan , Richard T. Scott III , Jessica Rajchel , Jenna Bedard , Robert Newby Jr. , Richard T. Scott , Nathan R. Treff , Tinchun Chu
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引用次数: 54

Abstract

There is growing interest in the microbiome of the reproductive tract. The vaginal and placental microbiome has been partially characterized and shown to be related to obstetric outcomes. In this study, we developed a sensitive method to analyze 16S ribosomal RNA profiling from ultra-low bacteria counts, then studied the endometrial microbial environment by analyzing catheter tips after embryo transfers during in vitro fertilization (IVF). An extensive validation was performed on extracted DNA and culture lysates without DNA isolation from the single- or poly-microbial samples of Escherichia coli, Proteus vulgaris, Staphylococcus epidermidis, and Bacillus cereus by Illumina 16S V4 metagenomics workflows. The direct lysis method can reliably detect the genus or species taxonomic level for both single- and poly-microbial samples when there were more than 60 bacterial cells in the culture lysates. Over 99% total operational taxonomic units (OTUs) were assigned to correct genus or species. The endometrial microbiome at the time of embryo transfer was characterized by analyzing catheter tips with Illumina V4 metagenomics for 70 patients who underwent IVF cycles. Lactobacillus spp. were detected in all 70 samples. Other vaginal bacteria (Corynebacterium, Bifidobacterium, Staphylococcus, and Streptococcus) were also detected. The Illumina V4 metagenomics workflow with preamplification provided a rapid and sensitive method for the identification of bacterial genus or species in single- or poly-microbial samples and clinical embryo transfer specimens. Ongoing work will illuminate the relationship between endometrial microbiome and reproductive success.

通过分析IVF周期中胚胎移植导管尖端的超低细菌来表征子宫内膜微生物组:16S核糖体基因的下一代测序(NGS)分析
人们对生殖道的微生物群越来越感兴趣。阴道和胎盘微生物组已被部分表征,并显示与产科结局有关。在这项研究中,我们建立了一种敏感的方法来分析超低细菌计数的16S核糖体RNA谱,然后通过分析试管婴儿(IVF)胚胎移植后的导管尖端来研究子宫内膜微生物环境。利用Illumina 16S V4宏基因组学工作流程对大肠杆菌、普通变形杆菌、表皮葡萄球菌和蜡样芽孢杆菌的单菌或多菌样品的提取DNA和培养物进行广泛的验证。当培养物中细菌细胞数在60个以上时,直接裂解法可以可靠地检测出单个或多个微生物样品的属或种分类水平。超过99%的操作分类单位(OTUs)被正确地划分为属或种。应用Illumina V4宏基因组学对70例IVF周期患者的导管尖端进行分析,分析胚胎移植时子宫内膜微生物组的特征。70份样品均检出乳杆菌。其他阴道细菌(棒状杆菌、双歧杆菌、葡萄球菌和链球菌)也被检测到。前置扩增的Illumina V4宏基因组工作流程为单微生物或多微生物样品及临床胚胎移植标本的细菌属或种鉴定提供了一种快速、灵敏的方法。正在进行的工作将阐明子宫内膜微生物组与生殖成功之间的关系。
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来源期刊
Human Microbiome Journal
Human Microbiome Journal Medicine-Infectious Diseases
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期刊介绍: The innumerable microbes living in and on our bodies are known to affect human wellbeing, but our knowledge of their role is still at the very early stages of understanding. Human Microbiome is a new open access journal dedicated to research on the impact of the microbiome on human health and disease. The journal will publish original research, reviews, comments, human microbe descriptions and genome, and letters. Topics covered will include: the repertoire of human-associated microbes, therapeutic intervention, pathophysiology, experimental models, physiological, geographical, and pathological changes, and technical reports; genomic, metabolomic, transcriptomic, and culturomic approaches are welcome.
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