阴道微生物群的定量分析提高了微生物群免疫轴的分辨率。

IF 13.8 1区 生物学 Q1 MICROBIOLOGY
Eric Armstrong, Rachel Liu, James Pollock, Sanja Huibner, Suji Udayakumar, Erastus Irungu, Pauline Ngurukiri, Peter Muthoga, Wendy Adhiambo, Sergey Yegorov, Joshua Kimani, Tara Beattie, Bryan Coburn, Rupert Kaul
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引用次数: 0

摘要

背景:阴道微生物群的组成与不良的性健康和生殖健康结果密切相关,部分原因是对生殖器免疫的影响。宏基因组测序等组成方法提供了样品中所有细菌的快照,并已成为表征阴道微生物群的标准,但仅提供微生物的相对丰度。我们假设,添加绝对丰度数据将提供一个更完整的画面宿主-微生物相互作用在女性生殖道。结果:我们分析了肯尼亚196名女性性工作者的宫颈阴道分泌物,发现细菌负荷在多种细菌性阴道病(BV)型微生物群的妇女中升高,而在乳酸菌优势的妇女中较低。细菌负荷还与促炎细胞因子如IL-1α呈正相关,与趋化因子如IP-10负相关。细菌负荷与免疫因子之间的关系因细菌群落状态而异,但crispatus优势菌群是唯一细菌负荷较高与促炎细胞因子升高无关的微生物群落。在肯尼亚队列和乌干达验证队列中,阴道总细菌负荷比目前的临床标准纽金特评分(Nugent score)更能预测生殖器免疫环境。结论:我们的研究结果表明,阴道总细菌负荷至少与目前的细菌性阴道炎临床诊断工具一样,是生殖器免疫环境的一个强有力的预测因素,支持阴道细菌负荷作为不良生殖和性健康结果的预测因素的探索。视频摘要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quantitative profiling of the vaginal microbiota improves resolution of the microbiota-immune axis.

Background: The composition of the vaginal microbiota is closely linked to adverse sexual and reproductive health outcomes, due in part to effects on genital immunology. Compositional approaches such as metagenomic sequencing provide a snapshot of all bacteria in a sample and have become the standard for characterizing the vaginal microbiota, but only provide microbial relative abundances. We hypothesized that the addition of absolute abundance data would provide a more complete picture of host-microbe interactions in the female genital tract.

Results: We analyzed cervicovaginal secretions from 196 female sex workers in Kenya and found that bacterial load was elevated among women with diverse, bacterial vaginosis (BV)-type microbiota and lower among women with Lactobacillus predominance. Bacterial load was also positively associated with proinflammatory cytokines, such as IL-1α, and negatively associated with chemokines, such as IP-10. The associations between bacterial load and immune factors differed across bacterial community states, but L. crispatus predominance was the only microbial community where higher bacterial load was not associated with higher proinflammatory cytokines. Total vaginal bacterial load was also a stronger predictor of the genital immune environment than BV by Nugent score, the current clinical standard, in the Kenya-based cohort and in a Uganda-based confirmatory cohort.

Conclusions: Our results suggest that total vaginal bacterial load is at least as strong a predictor of the genital immune milieu as current BV clinical diagnostic tools, supporting exploration of the vaginal bacterial load as a predictor of adverse reproductive and sexual health outcomes. Video Abstract.

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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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