scholarly journals Male-to-Female Sexual Transmission of Zika Virus—United States, January–April 2016

2016 ◽  
Vol 64 (2) ◽  
pp. 211-213 ◽  
Author(s):  
Kate Russell ◽  
Susan L. Hills ◽  
Alexandra M. Oster ◽  
Charsey Cole Porse ◽  
Gregory Danyluk ◽  
...  
Author(s):  
Alexandra M. Oster ◽  
Kate Russell ◽  
Jo Ellen Stryker ◽  
Allison Friedman ◽  
Rachel E. Kachur ◽  
...  

Viruses ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 2244
Author(s):  
Elizabeth Balint ◽  
Amelia Montemarano ◽  
Emily Feng ◽  
Ali A. Ashkar

Following the recent outbreak of Zika virus (ZIKV) infections in Latin America, ZIKV has emerged as a global health threat due to its ability to induce neurological disease in both adults and the developing fetus. ZIKV is largely mosquito-borne and is now endemic in many parts of Africa, Asia, and South America. However, several reports have demonstrated persistent ZIKV infection of the male reproductive tract and evidence of male-to-female sexual transmission of ZIKV. Sexual transmission may broaden the reach of ZIKV infections beyond its current geographical limits, presenting a significant threat worldwide. Several mouse models of ZIKV infection have been developed to investigate ZIKV pathogenesis and develop effective vaccines and therapeutics. However, the majority of these models focus on mosquito-borne infection, while few have considered the impact of sexual transmission on immunity and pathogenesis. This review will examine the advantages and disadvantages of current models of mosquito-borne and sexually transmitted ZIKV and provide recommendations for the effective use of ZIKV mouse models.


2016 ◽  
Vol 65 (12) ◽  
pp. 323-325 ◽  
Author(s):  
Alexandra M. Oster ◽  
Kate Russell ◽  
Jo Ellen Stryker ◽  
Allison Friedman ◽  
Rachel E. Kachur ◽  
...  

2016 ◽  
Vol 65 (5) ◽  
pp. 1-2 ◽  
Author(s):  
Alexandra M. Oster ◽  
John T. Brooks ◽  
Jo Ellen Stryker ◽  
Rachel E. Kachur ◽  
Paul Mead ◽  
...  

Author(s):  
Chelsea G Major ◽  
Gabriela Paz-Bailey ◽  
Susan L Hills ◽  
Dania M Rodriguez ◽  
Brad J Biggerstaff ◽  
...  

Abstract Background Zika virus (ZIKV) can be transmitted sexually, but the risk of sexual transmission remains unknown. Most evidence of sexual transmission is from partners of infected travelers returning from areas with ZIKV circulation. Methods We used data from the U.S. national arboviral disease surveillance system (ArboNET) on travel- and sexually-acquired ZIKV disease cases during 2016–2017 to develop individual-level simulations for estimating risk of male-to-female, male-to-male, and female-to-male sexual transmission of ZIKV via vaginal and/or anal intercourse. We specified parametric distributions to characterize individual-level variability of parameters for ZIKV persistence and sexual behaviors. Results Using ZIKV RNA persistence in semen/vaginal fluids to approximate infectiousness duration, male-to-male transmission had the highest estimated probability [1.3% (95% CI: 0.4–6.0) per anal sex act], followed by male-to-female and female-to-male transmission [0.4% (95% CI: 0.3–0.6) per vaginal/anal sex act and 0.1% (95% CI:0–0.8) per vaginal sex act, respectively]. Models using viral isolation in semen vs. RNA detection to approximate infectiousness duration predicted greater risk of sexual transmission. Conclusions While likely insufficient to maintain sustained transmission, the estimated risk of ZIKV transmission through unprotected sex is not trivial and is especially important for pregnant women, as ZIKV infection can cause severe congenital disorders.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Alexander G. Pletnev ◽  
Olga A. Maximova ◽  
Guangping Liu ◽  
Heather Kenney ◽  
Bianca M. Nagata ◽  
...  

AbstractRecognition of Zika virus (ZIKV) sexual transmission (ST) among humans challenges our understanding of the maintenance of mosquito-borne viruses in nature. Here we dissected the relative contributions of the components of male reproductive system (MRS) during early male-to-female ZIKV transmission by utilizing mice with altered antiviral responses, in which ZIKV is provided an equal opportunity to be seeded in the MRS tissues. Using microRNA-targeted ZIKV clones engineered to abolish viral infectivity to different parts of the MRS or a library of ZIKV genomes with unique molecular identifiers, we pinpoint epithelial cells of the epididymis (rather than cells of the testis, vas deferens, prostate, or seminal vesicles) as a most likely source of the sexually transmitted ZIKV genomes during the early (most productive) phase of ZIKV shedding into the semen. Incorporation of this mechanistic knowledge into the development of a live-attenuated ZIKV vaccine restricts its ST potential.


2016 ◽  
Vol 65 (5) ◽  
pp. 120-121 ◽  
Author(s):  
Alexandra M. Oster ◽  
John T. Brooks ◽  
Jo Ellen Stryker ◽  
Rachel E. Kachur ◽  
Paul Mead ◽  
...  

2016 ◽  
Vol 65 (29) ◽  
pp. 745-747 ◽  
Author(s):  
John T. Brooks ◽  
Allison Friedman ◽  
Rachel E. Kachur ◽  
Michael LaFlam ◽  
Philip J. Peters ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document