Fei Li1,2,3, Chen Chen2,3, Weixia Wei4,5, Zirong Wang2, Juanjuan Dai4,5, Lilan Hao2,3, Liju Song2,3, Xiaowei Zhang2,3, Liping Zeng4,5, Hui Du4,5, Huiru Tang4,5, Na Liu6, Huanming Yang2,7, Jian Wang2,7, Lise Madsen2,8,9, Susanne Brix10, Karsten Kristiansen2,8, Xun Xu2,3, Junhua Li2,3,11,12, Ruifang Wu4,5, Huijue Jia2,3,11,13. 1. BGI Education Center, University of Chinese Academy of Sciences, Shenzhen 518083, China. 2. BGI-Shenzhen, Shenzhen 518083, China. 3. China National GeneBank, BGI-Shenzhen, Shenzhen 518120, China. 4. Peking University Shenzhen Hospital, Shenzhen 518036, China. 5. Shenzhen Key Laboratory on Technology for Early Diagnosis of Major Gynecological diseases, Shenzhen, PR China. 6. BGI genomics, BGI-Shenzhen, Shenzhen 518083, China. 7. James D. Watson Institute of Genome Sciences, Hangzhou310000, China. 8. Laboratory of Genomics and Molecular Biomedicine, Department of Biology, University of Copenhagen, Universitetsparken 13, 2100 Copenhagen, Denmark. 9. Institute of Marine Research (IMR), Postboks 1870, Nordnes, N-5817, Bergen, Norway. 10. Department of Biotechnology and Biomedicine, Technical University of Denmark, Soltofts Plads, 2800 Kongens. Lyngby, Denmark. 11. Shenzhen Key Laboratory of Human Commensal Microorganisms and Health Research, BGI-Shenzhen, Shenzhen 518083, China. 12. School of Bioscience and Biotechnology, South China University of Technology, Guangzhou 510006, China. 13. Macau University of Science and Technology, Taipa, Macau 999078, China.
Abstract
Background: The human uterus is traditionally believed to be sterile, while the vaginal microbiota plays an important role in fending off pathogens. Emerging evidence demonstrates the presence of bacteria beyond the vagina. However, a microbiome-wide metagenomic analysis characterizing the diverse microbial communities has been lacking. Results: We performed shotgun-sequencing of 52 samples from the cervical canal and the peritoneal fluid of Chinese women of reproductive age using the Illumina platform. Direct annotation of sequencing reads identified the taxonomy of bacteria, archaea, fungi and viruses, confirming and extending the results from our previous study. We replicated our previous findings in another 24 samples from the vagina, the cervical canal, the uterus and the peritoneal fluid using the BGISEQ-500 platform revealing that microorganisms in the samples from the same individuals were largely shared in the entire reproductive tract. Human sequences made up more than 99% of the 20GB raw data. After filtering, vaginal microorganisms were well covered in the generated reproductive tract gene catalogue, while the more diverse upper reproductive tract microbiota would require greater depth of sequencing and more samples to meet the full coverage scale. Conclusions: We provide novel detailed data on the microbial composition of a largely unchartered body site, the female reproductive tract. Our results indicated the presence of an intra-individual continuum of microorganisms that gradually changed from the vagina to the peritoneal fluid. This study also provides a framework for understanding the implications of the composition and functional potential of the distinct microbial ecosystems of the female reproductive tract in relation to health and disease.
Background: The human uterus is traditionally believed to be sterile, while the vaginal microbiota plays an important role in fending off pathogens. Emerging evidence demonstrates the presence of bacteria beyond the vagina. However, a microbiome-wide metagenomic analysis characterizing the diverse microbial communities has been lacking. Results: We performed shotgun-sequencing of 52 samples from the cervical canal and the peritoneal fluid of Chinese women of reproductive age using the Illumina platform. Direct annotation of sequencing reads identified the taxonomy of bacteria, archaea, fungi and viruses, confirming and extending the results from our previous study. We replicated our previous findings in another 24 samples from the vagina, the cervical canal, the uterus and the peritoneal fluid using the BGISEQ-500 platform revealing that microorganisms in the samples from the same individuals were largely shared in the entire reproductive tract. Human sequences made up more than 99% of the 20GB raw data. After filtering, vaginal microorganisms were well covered in the generated reproductive tract gene catalogue, while the more diverse upper reproductive tract microbiota would require greater depth of sequencing and more samples to meet the full coverage scale. Conclusions: We provide novel detailed data on the microbial composition of a largely unchartered body site, the female reproductive tract. Our results indicated the presence of an intra-individual continuum of microorganisms that gradually changed from the vagina to the peritoneal fluid. This study also provides a framework for understanding the implications of the composition and functional potential of the distinct microbial ecosystems of the female reproductive tract in relation to health and disease.
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