Vaginal <i>Prevotella timonensis</i> Bacteria Enhance HIV‐1 Uptake and Differentially Affect Transmission by Distinct Primary Dendritic Cell Subsets

Young females are at high risk of acquiring HIV-1 infections and an imbalance in the vaginal microbiome enhances susceptibility to HIV-1 infection. More insights into the underlying mechanisms could open up new strategies to prevent HIV-1 acquisition and dissemination. Here, we investigated the effect of anaerobic bacteria associated with bacterial vaginosis (BV) on HIV-1 transmission by two distinct dendritic cell (DC) subsets, that is, inflammatory monocyte-derived DCs (moDCs) and primary CD1c<sup>+</sup> DCs. Notably, in contrast to other BV-associated microbiota, Prevotella timonensis enhanced uptake of HIV-1 by both moDCs and CD1c<sup>+</sup> DCs and the increased uptake was independent of cellular HIV-1 (co-)receptors. Imaging flow cytometry analyses showed that HIV-1 did not co-localise with P. timonensis but was internalized into tetraspanin-positive compartments known to be involved in HIV-1 transmission. P. timonensis bacteria enhanced HIV-1 transmission by CD1c<sup>+</sup> DCs, but not by moDCs, and the enhanced transmission was independent of viral infection. Our study strongly suggests that mucosal DC subsets have distinct functions in BV-associated HIV-1 susceptibility, and underscores the importance of early diagnosis and targeted treatment of vaginal dysbiosis to reduce the risk of HIV-1 acquisition.

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Publication Details

Journal
European Journal of Immunology
Published
2025-03-01
DOI
https://doi.org/10.1002/eji.202451192
Citations
4
Primary Topic
Reproductive tract infections research
Type
article
Field-Weighted Citation Impact
4.73

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article

Vaginal Prevotella timonensis Bacteria Enhance HIV‐1 Uptake and Differentially Affect Transmission by Distinct Primary Dendritic Cell Subsets

Teunis B. H. Geijtenbeek, Celia Segui‐Perez, Ester B. M. Remmerswaal, Marleen Y. van Smoorenburg et al.
4 citations
European Journal of Immunology
Reproductive tract infections research
4.73
article

Vaginal Prevotella timonensis Bacteria Enhance HIV‐1 Uptake and Differentially Affect Transmission by Distinct Primary Dendritic Cell Subsets

Teunis B. H. Geijtenbeek, Celia Segui‐Perez, Ester B. M. Remmerswaal, Marleen Y. van Smoorenburg, Karin Strijbis, John L. van Hamme
article en
4 citations

Abstract

Young females are at high risk of acquiring HIV-1 infections and an imbalance in the vaginal microbiome enhances susceptibility to HIV-1 infection. More insights into the underlying mechanisms could open up new strategies to prevent HIV-1 acquisition and dissemination. Here, we investigated the effect of anaerobic bacteria associated with bacterial vaginosis (BV) on HIV-1 transmission by two distinct dendritic cell (DC) subsets, that is, inflammatory monocyte-derived DCs (moDCs) and primary CD1c<sup>+</sup> DCs. Notably, in contrast to other BV-associated microbiota, Prevotella timonensis enhanced uptake of HIV-1 by both moDCs and CD1c<sup>+</sup> DCs and the increased uptake was independent of cellular HIV-1 (co-)receptors. Imaging flow cytometry analyses showed that HIV-1 did not co-localise with P. timonensis but was internalized into tetraspanin-positive compartments known to be involved in HIV-1 transmission. P. timonensis bacteria enhanced HIV-1 transmission by CD1c<sup>+</sup> DCs, but not by moDCs, and the enhanced transmission was independent of viral infection. Our study strongly suggests that mucosal DC subsets have distinct functions in BV-associated HIV-1 susceptibility, and underscores the importance of early diagnosis and targeted treatment of vaginal dysbiosis to reduce the risk of HIV-1 acquisition.

European Journal of ImmunologyVol. 55(3)
University of Applied Sciences Utrecht (NL), Utrecht University (NL), Netherlands Center for Occupational Diseases (NL), Amsterdam University Medical Centers (NL), University of Amsterdam (NL)
ZonMw, Nederlandse Organisatie voor Wetenschappelijk Onderzoek
Good health and well-being
Openalex Percentile: Top 6%
Reproductive tract infections research
4.73
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