Metronidazole Treatment Failure and Persistent BV Lead to Increased Frequencies of Activated T- and Dendritic-Cell Subsets

Author:

Qulu Wenkosi Perez12,Mzobe Gugulethu12,Mtshali Andile12,Letsoalo Marothi Peter1,Osman Farzana1,San James Emmanuel3ORCID,Kama Asavela Olona1,Garrett Nigel14,Mindel Adrian1,Rompalo Anne5,Liebenberg Lenine J. P.126,Archary Derseree12,Sivro Aida1278,Ngcapu Sinaye12ORCID

Affiliation:

1. Centre for the AIDS Programme of Research in South Africa (CAPRISA), Durban 4001, South Africa

2. Department of Medical Microbiology, University of KwaZulu-Natal, Durban 4001, South Africa

3. KwaZulu-Natal Research Innovation and Sequencing Platform, Nelson R Mandela School of Medicine, University of KwaZulu-Natal, Durban 4001, South Africa

4. Discipline of Public Health Medicine, University of KwaZulu-Natal, Durban 4001, South Africa

5. Department of Gynecology and Obstetrics, Johns Hopkins University, Baltimore, MD 21287, USA

6. Centre for Epidemic Response and Innovation (CERI), Stellenbosch 7600, South Africa

7. JC Wilt Infectious Disease Research Centre, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, MB R3E 3L5, Canada

8. Department of Medical Microbiology and Infectious Diseases, University of Manitoba, Winnipeg, MB R3E 3L5, Canada

Abstract

Metronidazole (MDZ) treatment failure and bacterial vaginosis (BV) recurrence rates are high among African women. This cohort study identified genital immune parameters associated with treatment response by comparing vaginal microbiota and immune cell frequencies in endocervical cytobrushes obtained from 32 South African women with symptomatic BV pre- and post-metronidazole treatment. Cervical T- and dendritic-cell subsets were phenotyped using multiparameter flow cytometry and the composition of vaginal microbial communities was characterized using 16S rRNA gene sequencing. MDZ treatment led to a modest decrease in the relative abundance of BV-associated bacteria, but colonization with Lactobacillus species (other than L. iners) was rare. At 6 and 12 weeks, MDZ-treated women had a significant increase in the frequencies of CCR5+ CD4+ T cells and plasmacytoid dendritic cells compared to the pre-treatment timepoint. In addition, MDZ non-responders had significantly higher frequencies of activated CD4 T cells and monocytes compared to MDZ responders. We conclude that MDZ treatment failure was characterized by an increased expression of activated T- and dendritic-cell subsets that may enhance HIV susceptibility. These data suggest the need to further assess the long-term impact of MDZ treatment on mucosal immune response and the vaginal microbiota.

Funder

Poliomyelitis Research Foundation

Department of Science and Innovation, and the National Research Foundation

South African Medical Research Council and the National Institute of Health

CAPRISA Research Administration and Management Training Program

DST-NRF CoE in HIV Prevention

DST/NRF Innovation Postdoctoral Fellowship

Publisher

MDPI AG

Subject

Virology,Microbiology (medical),Microbiology

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