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Bacterial microbiome and host inflammatory gene expression in foreskin tissue

The penile epithelial microbiome remains underexplored. We sequenced human RNA and a segment of the bacterial 16S rRNA gene from the foreskin tissue of 144 adolescents from South Africa and Uganda collected during penile circumcision after receipt of 1–2 doses of placebo, emtricitabine + tenofovir d...

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Bibliographic Details
Published in:Heliyon 2023-11, Vol.9 (11), p.e22145-e22145, Article e22145
Main Authors: Maust, Brandon S., Petkov, Stefan, Herrera, Carolina, Feng, Colin, Brown, Bryan P., Lebina, Limakatso, Opoka, Daniel, Ssemata, Andrew, Pillay, Natasha, Serwanga, Jennifer, Seatlholo, Portia, Namubiru, Patricia, Odoch, Geoffrey, Mugaba, Susan, Seiphetlo, Thabiso, Gray, Clive M., Kaleebu, Pontiano, Webb, Emily L., Martinson, Neil, Chiodi, Francesca, Fox, Julie, Jaspan, Heather B.
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Language:English
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Summary:The penile epithelial microbiome remains underexplored. We sequenced human RNA and a segment of the bacterial 16S rRNA gene from the foreskin tissue of 144 adolescents from South Africa and Uganda collected during penile circumcision after receipt of 1–2 doses of placebo, emtricitabine + tenofovir disoproxil fumarate, or emtricitabine + tenofovir alafenamide to investigate the microbiome of foreskin tissue and its potential changes with antiretroviral use. We identified a large number of anaerobic species, including Corynebacterium acnes, which was detected more frequently in participants from South Africa than Uganda. Bacterial populations did not differ by treatment received, and no differentially abundant taxa were identified between placebo versus active drug recipients. The relative abundance of specific bacterial taxa was negatively correlated with expression of genes downstream of the innate immune response to bacteria and regulation of inflammation. Our results show no difference in the tissue microbiome of the foreskin with short-course antiretroviral use but that bacterial taxa were largely inversely correlated with inflammatory gene expression, consistent with commensal colonization.
ISSN:2405-8440
2405-8440
DOI:10.1016/j.heliyon.2023.e22145