Genomic landscape in the human vaginal microbiome links to host geographics and genetics

Author:

Chen Chen1ORCID,Jie Zhuye2,Liang Weiting1,Ding Qiuxia1,Tong XinORCID,Zhang Yunhong3,Chen Na4,Li Shenghui5ORCID,Liu Xiaomin6ORCID,Gao Hongqin7,Huang Xincheng8,Zhang Zhe1,Liu Na1ORCID,Xie Zhangwei9,Wang Xiaman10,Qi Le10,Li Yumei10,Xiao Liang6ORCID,Zhang Shaoqiao11,Jin Xin11ORCID,Xu Xun6ORCID,Yang Huanming1ORCID,Wang Jian8,Zhao Fangqing12ORCID,Jia HuijueORCID,Zhang Tao6ORCID,Hao Lilan11ORCID,Zhu Lan13

Affiliation:

1. Beijing Genomics Institute

2. BGI-Shenzhen, Shenzhen 518083, China

3. Social Affairs Bureau of Suzhou National New and Hi-tech Industrial Development Zone

4. Peking Union Medical College Hospital

5. China Agricultural University

6. BGI-Shenzhen

7. Suzhou National New and Hi-tech Industrial Development Zone Center for Maternal and Child Health and Family Planning Service

8. China National GeneBank

9. Clin Lab, BGI Genomics

10. BGI Genomics

11. BGI Research

12. Beijing Institutes of Life Science, Chinese Academy of Sciences

13. Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing

Abstract

Abstract The vaginal microbiota is essential for women’s health, yet its genomic diversity and host relevance remains incompletely characterized. Here we established a Chinese cohort with 10,281 vaginal metagenomes. We developed an extensive catalog of vaginal microbial genomes (VMG) by integrating 6,979 in-house metagenomes with 1,817 publicly available metagenomes and over 1,000 bacterial isolates. This catalog comprised 46,906 genomes from 913 prokaryotic species and 3,763 viral populations, with 23.8% of prokaryotes and 75.1% of viruses being not found in public reference databases. Leveraging VMG, we identified substantial intraspecies genomic and functional variations within the vaginal microbiome that display geographic specificity. Notably, this included the novel bacterium CAISGS01(ID u199), unique to Chinese samples with marked biosynthetic capabilities, as well as BVAB1, which exhibited distinct regional genomic variations in pathogenic potential. Moreover, by utilizing genome-resolved microbial profiles from the VMG, we conducted a metagenome-genome-wide association study involving 6,893 individuals, and identified 7 vaginal microbial taxa whose abundances were significantly associated with 31 host genomic loci, including a notable correlation between novel bacterium Prevotella (ID u35) and loci on 22p11.2 (beta = 1.51, p = 6.826 × 10− 38). These associations were consistently and robustly replicated across three independent cohorts. In summary, our research provides a vital reference for future studies on the genotype-phenotype interplay within the human vaginal microbiome.

Publisher

Research Square Platform LLC

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