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Routes of Zika virus dissemination in the testis and epididymis of immunodeficient mice

Author

Listed:
  • Konstantin A. Tsetsarkin

    (National Institutes of Health (NIH))

  • Olga A. Maximova

    (National Institutes of Health (NIH))

  • Guangping Liu

    (National Institutes of Health (NIH))

  • Heather Kenney

    (National Institutes of Health (NIH))

  • Natalia Teterina

    (National Institutes of Health (NIH))

  • Marshall E. Bloom

    (Laboratory of Virology, Rocky Mountain Laboratories, NIAID, NIH)

  • Jeffrey M. Grabowski

    (Laboratory of Virology, Rocky Mountain Laboratories, NIAID, NIH)

  • Luwanika Mlera

    (Laboratory of Virology, Rocky Mountain Laboratories, NIAID, NIH)

  • Bianca M. Nagata

    (Comparative Medicine Branch, NIAID, NIH)

  • Ian Moore

    (Comparative Medicine Branch, NIAID, NIH)

  • Craig Martens

    (RT Branch, Rocky Mountain Laboratories, NIAID, NIH)

  • Emerito Amaro-Carambot

    (Laboratory of Viral Diseases, NIAID, NIH)

  • Elaine W. Lamirande

    (Laboratory of Viral Diseases, NIAID, NIH)

  • Stephen S. Whitehead

    (Laboratory of Viral Diseases, NIAID, NIH)

  • Alexander G. Pletnev

    (National Institutes of Health (NIH))

Abstract

Sexual transmission and persistence of Zika virus (ZIKV) in the male reproductive tract (MRT) poses new challenges for controlling virus outbreaks and developing live-attenuated vaccines. To elucidate routes of ZIKV dissemination in the MRT, we here generate microRNA-targeted ZIKV clones that lose the infectivity for (1) the cells inside seminiferous tubules of the testis, or (2) epithelial cells of the epididymis. We trace ZIKV dissemination in the MRT using an established mouse model of ZIKV pathogenesis. Our results support a model in which ZIKV infects the testis via a hematogenous route, while infection of the epididymis can occur via two routes: (1) hematogenous/lymphogenous and (2) excurrent testicular. Co-targeting of the ZIKV genome with brain-, testis-, and epididymis-specific microRNAs restricts virus infection of these organs, but does not affect virus-induced protective immunity in mice and monkeys. These defined alterations of ZIKV tropism represent a rational design of a safe live-attenuated ZIKV vaccine.

Suggested Citation

  • Konstantin A. Tsetsarkin & Olga A. Maximova & Guangping Liu & Heather Kenney & Natalia Teterina & Marshall E. Bloom & Jeffrey M. Grabowski & Luwanika Mlera & Bianca M. Nagata & Ian Moore & Craig Marte, 2018. "Routes of Zika virus dissemination in the testis and epididymis of immunodeficient mice," Nature Communications, Nature, vol. 9(1), pages 1-13, December.
    • Handle: RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-07782-x
    DOI: 10.1038/s41467-018-07782-x
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    Cited by:

    1. Shuo Li & Nianchao Qian & Chao Jiang & Wenhong Zu & Anthony Liang & Mamie Li & Stephen J. Elledge & Xu Tan, 2022. "Gain-of-function genetic screening identifies the antiviral function of TMEM120A via STING activation," Nature Communications, Nature, vol. 13(1), pages 1-12, December.

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