Utah Veterinary Diagnostic Laboratory, School of Veterinary Medicine, Department of Animal, Dairy, and Veterinary Sciences, Utah State University, Logan, Utah; Institute for Antiviral Research, Department of Animal, Dairy, and Veterinary Sciences, Utah State University, Logan, Utah.
Utah Veterinary Diagnostic Laboratory, School of Veterinary Medicine, Department of Animal, Dairy, and Veterinary Sciences, Utah State University, Logan, Utah.
Am J Pathol. 2018 Apr;188(4):904-915. doi: 10.1016/j.ajpath.2017.12.019. Epub 2018 Jan 31.
An understanding of the pathogenesis of infection with the Zika virus in the male reproductive tract is vital for the development of vaccines and antivirals that will limit or prevent sexual transmission. Two common immunocompromised mouse strains used in transmission studies-male with genes encoding interferon types I and II receptor gene knockout (IFNAR/IFNGR; AG129) and with interferon type 1 receptor knockout (Ifnar) were infected with a Puerto Rican Zika virus isolate (PRVABC59), and pathology was assessed 5 to 11 days after infection. Virus was detected by immunohistochemistry and quantitative RT-PCR in the testicle and epididymis of AG129 and Ifnar mice, and by immunohistochemistry in the prostate and seminal vesicle of infected AG129 mice. Severe disease manifestations initiating as epididymitis and progressing to orchitis were observed in both models, with more severe inflammation noted in the AG129 mouse strain. Significant inflammation was not observed in any evaluated accessory sex gland at any point during infection. Time-course analysis of infection revealed an increase in the severity of disease within the epididymis of both strains, indicating a potential route of sexual transmission. Male mice with Ifnar may better recapitulate Zika virus in humans and provide insight into the mechanism of sexual transmission, due to milder histopathologic lesions, the presence of histologically normal sperm in epididymal tubules, and an ability to survive the acute phase of disease.
了解寨卡病毒在男性生殖道感染的发病机制对于开发疫苗和抗病毒药物至关重要,这些药物将限制或预防性传播。在传播研究中常用的两种免疫功能低下的小鼠品系——干扰素 I 和 II 受体基因敲除(IFNAR/IFNGR;AG129)和干扰素 1 受体敲除(Ifnar)的雄性小鼠感染了波多黎各寨卡病毒分离株(PRVABC59),并在感染后 5 至 11 天评估病理学。通过免疫组织化学和定量 RT-PCR 在 AG129 和 Ifnar 小鼠的睾丸和附睾中以及在感染的 AG129 小鼠的前列腺和精囊中检测到病毒。在这两种模型中均观察到以附睾炎开始并进展为睾丸炎的严重疾病表现,AG129 小鼠的炎症更严重。在感染过程中的任何时间点,在任何评估的附属性生殖腺中均未观察到明显的炎症。感染的时间过程分析显示,两种品系的附睾疾病严重程度均增加,表明存在性传播的潜在途径。由于组织病理学病变较轻、附睾管中存在组织学正常的精子以及能够在疾病急性期存活,因此具有 Ifnar 的雄性小鼠可能更好地模拟人类寨卡病毒,并深入了解性传播的机制。