Association of Female Genital Schistosomiasis With the Cervicovaginal Microbiota and Sexually Transmitted Infections in Zambian Women

Author:

Sturt Amy S1ORCID,Webb Emily L2ORCID,Himschoot Lisa3,Phiri Comfort R4,Mapani Joyce5,Mudenda Maina5,Kjetland Eyrun F67,Mweene Tobias4,Levecke Bruno8,van Dam Govert J9,Corstjens Paul L A M10,Ayles Helen14,Hayes Richard J2,van Lieshout Lisette9,Hansingo Isaiah5,Francis Suzanna C2,Cools Piet38,Bustinduy Amaya L1

Affiliation:

1. Department of Clinical Research, London School of Hygiene and Tropical Medicine, London, UK

2. MRC International Statistics and Epidemiology Group, London School of Hygiene and Tropical Medicine, London, UK

3. Department of Diagnostic Sciences, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium

4. Zambart, Lusaka, Zambia

5. Department of Obstetrics and Gynecology, Livingstone Central Hospital, Livingstone, Zambia

6. Department of Infectious Diseases, Oslo University Hospital, Oslo, Norway

7. University of KwaZulu-Natal, Durban, South Africa

8. Department of Virology, Parasitology, and Immunology, Ghent University, Merelbeke, Belgium

9. Department of Parasitology, Leiden University Medical Center, Leiden, the Netherlands

10. Department of Cell and Chemical Biology, Leiden University Medical Center, Leiden, the Netherlands

Abstract

Abstract Background The cervicovaginal microbiota, including sexually transmitted infections (STIs), have not been well described in female genital schistosomiasis (FGS). Methods Women (aged 18–31, sexually active, nonpregnant) were invited to participate at the final follow-up of the HPTN 071 (PopART) Population Cohort in January–August 2018. We measured key species of the cervicovaginal microbiota (Lactobacillus crispatus, L. iners, Gardnerella vaginalis, Atopobium vaginae, and Candida) and STIs (Chlamydia trachomatis, Neisseria gonorrhoeae, Trichomonas vaginalis, and Mycoplasma genitalium) using quantitative PCR (qPCR). We evaluated associations of the microbiota and STI presence and concentration with FGS (qPCR-detected Schistosoma DNA in any of 3 genital specimens). Results The presence and concentration of key cervicovaginal species did not differ between participants with (n = 30) or without FGS (n = 158). A higher proportion of participants with FGS had T. vaginalis compared with FGS-negative women (P = .08), with further analysis showing that T. vaginalis was more prevalent among women with ≥2 Schistosoma qPCR-positive genital specimens (50.0%, 8/16) than among FGS-negative women (21.5%, 34/158; P = .01). Conclusions We found weak evidence of an association between the presence of T. vaginalis and FGS, with a stronger association in women with a higher-burden FGS infection. Additional research is needed on potential between-parasite interactions, especially regarding HIV-1 vulnerability.

Funder

Wellcome Trust

Research Foundation–Flanders

Bill and Melinda Gates Foundation

Medical Research Council

UK Department for International Development

National Institute of Allergy and Infectious Diseases

National Institute on Drug Abuse

National Institute of Mental Health

National Institutes of Health

South-Eastern Regional Health Authority, Norway

Fund for Scientific Research–Flanders

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Oncology

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