Vaginal microbiota associated with oncogenic HPV in a cohort of HPV-vaccinated women living with HIV

Author:

McClymont Elisabeth12ORCID,Albert Arianne Y3,Wang Christine4,Dos Santos Scott J5ORCID,Coutlée François6,Lee Marette1,Walmsley Sharon78,Lipsky Nancy3,Loutfy Mona9ORCID,Trottier Sylvie10,Smaill Fiona11ORCID,Klein Marina B12,Yudin Mark H913,Harris Marianne414,Wobeser Wendy15,Hill Janet E5,Money Deborah M13,

Affiliation:

1. Department of Obstetrics and Gynecology, University of British Columbia, Vancouver, BC, Canada

2. Canadian HIV Trials Network, Vancouver, BC, Canada

3. Women’s Health Research Institute, Vancouver, BC, Canada

4. Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada

5. Department of Veterinary Microbiology, University of Saskatchewan, Saskatoon, SK, Canada

6. Département de Microbiologie Médicale et Infectiologie, l’Université de Montréal, Montréal, QC, Canada

7. Toronto General Hospital Research Institute, University of Toronto, University Health Network, Toronto, ON, Canada

8. Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada

9. Women’s College Research Institute, University of Toronto, Toronto, ON, Canada

10. Infectious Diseases Research Centre, Université Laval, Québec City, QC, Canada

11. Department of Pathology and Molecular Medicine, McMaster University, Hamilton, ON, Canada

12. McGill University Health Centre, Montreal, QC, Canada

13. Department of Obstetrics and Gynecology, University of Toronto, St. Michael’s Hospital, Toronto, ON, Canada

14. British Columbia Centre for Excellence in HIV/AIDS, Vancouver, BC, Canada

15. Departments of Public Health and Molecular & Biomedical Sciences, Queen’s University, Kingston, ON, Canada

Abstract

Background Women living with HIV (WLWH) experience higher rates of human papillomavirus (HPV) infection and cervical cancer than women without HIV. Changes in the vaginal microbiome have been implicated in HPV-related disease processes such as persistence of high-risk HPV infection but this has not been well defined in a population living with HIV. Methods Four hundred and 20 girls and WLWH, age ≥9, across 14 clinical sites in Canada were enrolled to receive three doses of quadrivalent HPV vaccine for assessment of vaccine immunogenicity. Blood, cervical cytology, and cervico-vaginal swabs were collected. Cervico-vaginal samples were tested for HPV DNA and underwent microbiota sequencing. Results Principal component analysis (PCA) and hierarchical clustering generated community state types (CSTs). Relationships between taxa and CSTs with HPV infection were examined using mixed-effects logistic regressions, Poisson regressions, or generalized linear mixed-effects models, as appropriate. Three hundred and fifty-six cervico-vaginal microbiota samples from 172 women were sequenced. Human papillomavirus DNA was detected in 211 (59%) samples; 110 (31%) contained oncogenic HPV. Sixty-five samples (18%) were taken concurrently with incident oncogenic HPV infection and 56 (16%) were collected from women with concurrent persistent oncogenic HPV infection. Conclusions No significant associations between taxa, CST, or microbial diversity and HPV-related outcomes were found. However, we observed weak associations between a dysbiotic microbiome and specific species, including Gardnerella, Porphyromonas, and Prevotella species, with incident HPV infection.

Funder

Merck

Canadian Institutes of Health Research

Canadian HIV Trials Network, Canadian Institutes of Health Research

Publisher

SAGE Publications

Subject

Infectious Diseases,Pharmacology (medical),Public Health, Environmental and Occupational Health,Dermatology

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