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本文引用的文献

1
Exact sequence variants should replace operational taxonomic units in marker-gene data analysis.在标记基因数据分析中,精确序列变体应取代操作分类单元。
ISME J. 2017 Dec;11(12):2639-2643. doi: 10.1038/ismej.2017.119. Epub 2017 Jul 21.
2
Candidatus Mycoplasma girerdii replicates, diversifies, and co-occurs with Trichomonas vaginalis in the oral cavity of a premature infant.早产婴儿口腔中的支原体古菌与阴道毛滴虫共同复制、变异和共存。
Sci Rep. 2017 Jun 19;7(1):3764. doi: 10.1038/s41598-017-03821-7.
3
Early pregnancy vaginal microbiome trends and preterm birth.早期妊娠阴道微生物群趋势与早产
Am J Obstet Gynecol. 2017 Sep;217(3):356.e1-356.e18. doi: 10.1016/j.ajog.2017.05.030. Epub 2017 May 23.
4
The interaction between vaginal microbiota, cervical length, and vaginal progesterone treatment for preterm birth risk.阴道微生物群、宫颈长度与阴道孕酮治疗在早产风险中的相互作用。
Microbiome. 2017 Jan 19;5(1):6. doi: 10.1186/s40168-016-0223-9.
5
Lactobacillus iners: Friend or Foe?无乳链球菌:朋友还是敌人?
Trends Microbiol. 2017 Mar;25(3):182-191. doi: 10.1016/j.tim.2016.11.007. Epub 2016 Dec 1.
6
Evaluation of Lysis Methods for the Extraction of Bacterial DNA for Analysis of the Vaginal Microbiota.用于提取细菌DNA以分析阴道微生物群的裂解方法评估
PLoS One. 2016 Sep 19;11(9):e0163148. doi: 10.1371/journal.pone.0163148. eCollection 2016.
7
Systematic improvement of amplicon marker gene methods for increased accuracy in microbiome studies.系统改进扩增子标记基因方法以提高微生物组研究的准确性。
Nat Biotechnol. 2016 Sep;34(9):942-9. doi: 10.1038/nbt.3601. Epub 2016 Jul 25.
8
DADA2: High-resolution sample inference from Illumina amplicon data.DADA2:从Illumina扩增子数据进行高分辨率样本推断。
Nat Methods. 2016 Jul;13(7):581-3. doi: 10.1038/nmeth.3869. Epub 2016 May 23.
9
The Gestational Vaginal Microbiome and Spontaneous Preterm Birth among Nulliparous African American Women.未生育非裔美国女性的妊娠期阴道微生物群与自发性早产
Am J Perinatol. 2016 Jul;33(9):887-93. doi: 10.1055/s-0036-1581057. Epub 2016 Apr 8.
10
Temporal and spatial variation of the human microbiota during pregnancy.孕期人类微生物群的时空变化
Proc Natl Acad Sci U S A. 2015 Sep 1;112(35):11060-5. doi: 10.1073/pnas.1502875112. Epub 2015 Aug 17.

在美国两个不同种族的女性队列中复制和完善早产的阴道微生物特征。

Replication and refinement of a vaginal microbial signature of preterm birth in two racially distinct cohorts of US women.

机构信息

Department of Population Health and Pathobiology, College of Veterinary Medicine, North Carolina State University, Raleigh, NC 27607.

Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305.

出版信息

Proc Natl Acad Sci U S A. 2017 Sep 12;114(37):9966-9971. doi: 10.1073/pnas.1705899114. Epub 2017 Aug 28.

DOI:10.1073/pnas.1705899114
PMID:28847941
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5604014/
Abstract

Preterm birth (PTB) is the leading cause of neonatal morbidity and mortality. Previous studies have suggested that the maternal vaginal microbiota contributes to the pathophysiology of PTB, but conflicting results in recent years have raised doubts. We conducted a study of PTB compared with term birth in two cohorts of pregnant women: one predominantly Caucasian ( = 39) at low risk for PTB, the second predominantly African American and at high-risk ( = 96). We profiled the taxonomic composition of 2,179 vaginal swabs collected prospectively and weekly during gestation using 16S rRNA gene sequencing. Previously proposed associations between PTB and lower and higher abundances replicated in the low-risk cohort, but not in the high-risk cohort. High-resolution bioinformatics enabled taxonomic assignment to the species and subspecies levels, revealing that was associated with low risk of PTB in both cohorts, while was not, and that a subspecies clade of explained the genus association with PTB. Patterns of cooccurrence between and were highly exclusive, while and often coexisted at high frequencies. We argue that the vaginal microbiota is better represented by the quantitative frequencies of these key taxa than by classifying communities into five community state types. Our findings extend and corroborate the association between the vaginal microbiota and PTB, demonstrate the benefits of high-resolution statistical bioinformatics in clinical microbiome studies, and suggest that previous conflicting results may reflect the different risk profile of women of black race.

摘要

早产(PTB)是新生儿发病率和死亡率的主要原因。先前的研究表明,母体阴道微生物群有助于 PTB 的病理生理学,但近年来相互矛盾的结果引起了人们的怀疑。我们对两个孕妇队列中的 PTB 与足月分娩进行了研究:一个主要是白种人(= 39),PTB 风险低,第二个主要是非洲裔美国人,风险高(= 96)。我们使用 16S rRNA 基因测序对前瞻性收集的 2179 个阴道拭子的分类组成进行了分析,并在妊娠期间每周进行一次分析。先前提出的 PTB 与低丰度和高丰度之间的关联在低风险队列中得到了复制,但在高风险队列中没有得到复制。高分辨率生物信息学能够将分类分配到种和亚种水平,结果表明在两个队列中都与 PTB 风险低有关,而 则没有,并且 解释了与 PTB 相关的属关联的一个亚种分支。与 之间的共现模式高度排他,而 与 经常以高频率共存。我们认为,这些关键分类群的定量频率比将群落分类为五种群落状态类型更能代表阴道微生物群。我们的研究结果扩展和证实了阴道微生物群与 PTB 之间的关联,证明了高分辨率统计生物信息学在临床微生物组研究中的优势,并表明先前相互矛盾的结果可能反映了黑人女性的不同风险状况。