Zika virus shedding in the stool and infection through the anorectal mucosa in mice
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Updated: Feb 3, 2026

Evaluation of Zika Virus-specific T-cell Responses in Immunoprivileged Organs of Infected Ifnar1-/- Mice
Published on: October 17, 2018
Chunfeng Li1,2,3, Yong-Qiang Deng2,4, Shulong Zu5,6
1Center for Systems Medicine, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100005, China.
Abstract:
Zika virus (ZIKV) has elicited global concern due to its unique biological features, unusual transmission routes, and unexpected clinical outcomes. Although ZIKV transmission through anal intercourse has been reported in humans, it remains unclear if ZIKV is detectable in the stool, if it can infect the host through the anal canal mucosa, and what the pathogenesis of such a route of infection might be in the mouse model. Herein, we demonstrate that ZIKV RNA can be recovered from stools in multiple mouse models, as well as from the stool of a ZIKV patient. Remarkably, intra-anal (i.a.) inoculation with ZIKV leads to efficient infection in both Ifnar1-/- and immunocompetent mice, characterized by extensive viral replication in the blood and multiple organs, including the brain, small intestine, testes, and rectum, as well as robust humoral and innate immune responses. Moreover, i.a. inoculation of ZIKV in pregnant mice resulted in transplacental infection and delayed fetal development. Overall, our results identify the anorectal mucosa as a potential site of ZIKV infection in mice, reveal the associated pathogenesis of i.a. infection, and highlight the complexity of ZIKV transmission through anal intercourse.
Insights
Zika virus (ZIKV) RNA is found in stool and can infect mice via the anus. Intra-anal inoculation causes widespread infection, immune responses, and affects fetal development, revealing a new transmission route.
Area of Science:
- Virology
- Immunology
- Pathogenesis
Background:
- Zika virus (ZIKV) poses global health concerns due to its unique biology and transmission.
- Human anal intercourse transmission of ZIKV is reported, but the anal route's infectivity and pathogenesis are unclear.
Purpose of the Study:
- To investigate ZIKV detectability in stool.
- To determine if ZIKV can infect hosts via the anal canal mucosa.
- To elucidate the pathogenesis of intra-anal ZIKV infection in a mouse model.
Main Methods:
- ZIKV RNA detection in stool from mouse models and a human patient.
- Intra-anal (i.a.) inoculation of ZIKV in Ifnar1-/- and immunocompetent mice, including pregnant models.
- Analysis of viral replication, organ distribution, and immune responses.
Main Results:
- ZIKV RNA was recovered from stools in multiple mouse models and a ZIKV patient.
- i.a. ZIKV inoculation resulted in efficient infection, viremia, and replication in organs (brain, intestine, testes, rectum).
- Infection triggered robust immune responses and, in pregnant mice, transplacental infection and fetal developmental issues.
Conclusions:
- The anorectal mucosa is a potential site for ZIKV infection.
- Intra-anal ZIKV infection leads to systemic disease and impacts fetal development.
- These findings underscore the complexity of ZIKV transmission, particularly through anal intercourse.
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