Replication of Zika virus in human prostate cells: a potential source of sexually transmitted virus

JL Spencer, A Lahon, LL Tran, RP Arya… - The Journal of …, 2018 - academic.oup.com
JL Spencer, A Lahon, LL Tran, RP Arya, AR Kneubehl, MB Vogt, D Xavier, DR Rowley…
The Journal of infectious diseases, 2018academic.oup.com
Abstract Background While Zika virus (ZIKV) is mainly transmitted by mosquitoes, numerous
cases of sexual transmission have been reported during recent outbreaks. Little is known
about which host cell types or entry factors aid in mediating this sexual transmission.
Methods In this study, we investigated ZIKV cell tropism by infecting 2 types of human
prostate cells with 3 contemporary ZIKV isolates from persons infected in the Americas. We
used real-time quantitative polymerase chain reaction and immunofluorescence analyses to …
Background
While Zika virus (ZIKV) is mainly transmitted by mosquitoes, numerous cases of sexual transmission have been reported during recent outbreaks. Little is known about which host cell types or entry factors aid in mediating this sexual transmission.
Methods
In this study, we investigated ZIKV cell tropism by infecting 2 types of human prostate cells with 3 contemporary ZIKV isolates from persons infected in the Americas. We used real-time quantitative polymerase chain reaction and immunofluorescence analyses to measure infection and flow cytometry to detect entry factor expression.
Results
Here we show that ZIKV infects, replicates, and produces infectious virus in prostate stromal mesenchymal stem cells, epithelial cells, and organoids made with a combination of these cells. We also show that prostate cells express several well-characterized flavivirus attachment factors. In contrast, dengue virus does not infect or does not replicate in these prostate cells, although it is known to use similar receptors.
Conclusions
Our results indicate that ZIKV favors infection of stromal cells more so than epithelial cells in organoids, possibly indicating a preference for stem cells in general. Overall, these results suggest that ZIKV replication occurs in the human prostate and can account for ZIKV secretion in semen, thus leading to sexual transmission.
Oxford University Press