Department of Obstetrics and Gynecology, Stanford, United States; Stanford Maternal & Child Health Research Institute, Stanford University School of Medicine, Stanford, United States
Congzhou Liu
Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, United States
Sean C Proll
Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, United States
Enna Manhardt
Department of Obstetrics and Gynecology, University of Washington, Seattle, United States
Shuying Liang
Department of Obstetrics and Gynecology, University of Washington, Seattle, United States
Sujatha Srinivasan
Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, United States
Elizabeth Swisher
Department of Obstetrics and Gynecology, University of Washington, Seattle, United States
David N Fredricks
Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, United States
Investigating the human fallopian tube (FT) microbiota has significant implications for understanding the pathogenesis of ovarian cancer (OC). In this large prospective study, we collected swabs intraoperatively from the FT and other surgical sites as controls to profile the microbiota in the FT and to assess its relationship with OC. Eighty-one OC and 106 non-cancer patients were enrolled and 1001 swabs were processed for 16S rRNA gene PCR and sequencing. We identified 84 bacterial species that may represent the FT microbiota and found a clear shift in the microbiota of the OC patients when compared to the non-cancer patients. Of the top 20 species that were most prevalent in the FT of OC patients, 60% were bacteria that predominantly reside in the gastrointestinal tract, while 30% normally reside in the mouth. Serous carcinoma had higher prevalence of almost all 84 FT bacterial species compared to the other OC subtypes. The clear shift in the FT microbiota in OC patients establishes the scientific foundation for future investigation into the role of these bacteria in the pathogenesis of OC.