Diverse vaginal microbiome was associated with pro-inflammatory vaginal milieu among pregnant women in Uganda

Q1 Medicine
Lois Bayigga , Rose Nabatanzi , Alfred Ssekagiri , David P. Kateete , Musa Sekikubo , Deborah J. Anderson , Jiawu Xu , Douglas S. Kwon , Damalie Nakanjako
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引用次数: 5

Abstract

Vaginal microbiota has been postulated as a key contributor to the disproportionately higher HIV acquisition risk in women. The commensal bacterial communities in the vaginal tract have been implicated in HIV pathogenesis, with strict anaerobes such as Gardnerella and Prevotella causing inflammation and increased frequency of HIV target cells. Young African women are up to six times more likely to be infected with HIV than their male counterparts. The underlying biological mechanisms for increased susceptibility to HIV infection are not fully known, particularly among pregnant women who are also at risk of transmitting the infection to their unborn babies.

We characterized the vaginal microbiome of pregnant women receiving antenatal care. Using 16S rRNA sequencing, we analyzed the richness and abundances of the commensal bacterial communities within the female genital tract. Data was analyzed using qiime2 version 2018, Dada2 plugin, and Naive-Bayes classifier for Taxonomic assignment.

We report that 19% (35/179) of pregnant women had a Lactobacillus-dominant vaginal microbiota profile. Our findings show that the main cervicotypes (“CTs”) were CT1 which was predominantly non-iners Lactobacillus (6%, 11/179), CT2 which was dominated by L. iners (13%, 24/179), CT3 that was Gardnerella dominant (49%, 87/179) and CT4, a mixed CT co-dominated by L. iners, Gardnerella and Atopobium. Cervical lavage of women with non-Lactobacillus CT had significantly higher levels of inflammatory cytokines IL-1beta, TNF-alpha, and chemokines IL-6 and IL-8.

Highly diverse cervicotype (CT4) was associated with inflammation, a known catalyst of HIV acquisition and transmission, within pregnant women regardless of HIV sero-status.

Abstract Image

在乌干达孕妇中,不同的阴道微生物群与促炎阴道环境有关
阴道微生物群被认为是女性感染艾滋病毒风险过高的关键因素。阴道内的共生菌群与HIV发病机制有关,加德纳菌和普雷沃菌等严格的厌氧菌引起炎症并增加HIV靶细胞的频率。非洲年轻妇女感染艾滋病毒的可能性是同龄男性的六倍。对艾滋病毒感染易感性增加的潜在生物学机制尚不完全清楚,特别是在孕妇中,她们也有将感染传染给未出生婴儿的风险。我们描述了接受产前护理的孕妇阴道微生物组。利用16S rRNA测序,我们分析了女性生殖道内共生菌群落的丰富度和丰度。使用qiime2 2018版、Dada2插件和Naive-Bayes分类器对数据进行分类分析。我们报告19%(35/179)的孕妇阴道微生物群以乳酸杆菌为主。结果表明,主要宫颈型为CT1型(6%,11/179)、CT2型(13%,24/179)、CT3型(49%,87/179)和CT4型(L. iners、Gardnerella和Atopobium混合型)。宫颈灌洗非乳杆菌CT的女性炎症因子il -1 β、tnf - α和趋化因子IL-6和IL-8水平明显升高。无论HIV血清状态如何,高度多样化的宫颈型(CT4)与炎症有关,炎症是已知的HIV获取和传播的催化剂。
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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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