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16S核糖体RNA基因测序以及来自人类肠道微生物组的28种临床相关微生物分类群的健康参考范围。

16S rRNA gene sequencing and healthy reference ranges for 28 clinically relevant microbial taxa from the human gut microbiome.

作者信息

Almonacid Daniel E, Kraal Laurens, Ossandon Francisco J, Budovskaya Yelena V, Cardenas Juan Pablo, Bik Elisabeth M, Goddard Audrey D, Richman Jessica, Apte Zachary S

机构信息

uBiome, Inc., San Francisco, California, United States of America.

Department of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, California, United States of America.

出版信息

PLoS One. 2017 May 3;12(5):e0176555. doi: 10.1371/journal.pone.0176555. eCollection 2017.

Abstract

Changes in the relative abundances of many intestinal microorganisms, both those that naturally occur in the human gut microbiome and those that are considered pathogens, have been associated with a range of diseases. To more accurately diagnose health conditions, medical practitioners could benefit from a molecular, culture-independent assay for the quantification of these microorganisms in the context of a healthy reference range. Here we present the targeted sequencing of the microbial 16S rRNA gene of clinically relevant gut microorganisms as a method to provide a gut screening test that could assist in the clinical diagnosis of certain health conditions. We evaluated the possibility of detecting 46 clinical prokaryotic targets in the human gut, 28 of which could be identified with high precision and sensitivity by a bioinformatics pipeline that includes sequence analysis and taxonomic annotation. These targets included 20 commensal, 3 beneficial (probiotic), and 5 pathogenic intestinal microbial taxa. Using stool microbiome samples from a cohort of 897 healthy individuals, we established a reference range defining clinically relevant relative levels for each of the 28 targets. Our assay quantifies 28 targets in the context of a healthy reference range and correctly reflected 38/38 verification samples of real and synthetic stool material containing known gut pathogens. Thus, we have established a method to determine microbiome composition with a focus on clinically relevant taxa, which has the potential to contribute to patient diagnosis, treatment, and monitoring. More broadly, our method can facilitate epidemiological studies of the microbiome as it relates to overall human health and disease.

摘要

许多肠道微生物的相对丰度发生变化,包括那些自然存在于人类肠道微生物群中的微生物以及那些被认为是病原体的微生物,都与一系列疾病有关。为了更准确地诊断健康状况,医生可以从一种分子、不依赖培养的检测方法中受益,该方法可在健康参考范围内对这些微生物进行定量分析。在这里,我们提出对临床相关肠道微生物的微生物16S rRNA基因进行靶向测序,作为一种提供肠道筛查检测的方法,该检测有助于某些健康状况的临床诊断。我们评估了检测人类肠道中46个临床原核生物靶点的可能性,其中28个靶点可以通过包括序列分析和分类注释的生物信息学流程以高精度和灵敏度进行鉴定。这些靶点包括20种共生菌、3种有益菌(益生菌)和5种致病性肠道微生物分类群。我们使用来自897名健康个体队列的粪便微生物群样本,建立了一个参考范围,定义了28个靶点中每个靶点的临床相关相对水平。我们的检测方法在健康参考范围内对28个靶点进行定量,并正确反映了38/38份含有已知肠道病原体的真实和合成粪便材料的验证样本。因此,我们建立了一种以临床相关分类群为重点来确定微生物群组成的方法,这有可能有助于患者的诊断、治疗和监测。更广泛地说,我们的方法可以促进与人类整体健康和疾病相关的微生物群的流行病学研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2220/5414997/68b6a038eeb8/pone.0176555.g001.jpg

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