Department of Comparative, Diagnostic, and Population Medicine, College of Veterinary Medicine, University of Florida, Gainesville, FL 32608, USA.
Department of Infectious Diseases and Immunology, College of Veterinary Medicine, University of Florida, Gainesville, FL 32608, USA.
Viruses. 2020 Mar 7;12(3):291. doi: 10.3390/v12030291.
Zika virus (ZIKV) is an arbovirus that causes birth defects, persistent male infection, and sexual transmission in humans. The purpose of this study was to continue the development of an ovine ZIKV infection model; thus, two experiments were undertaken. In the first experiment, we built on previous pregnant sheep experiments by developing a mid-gestation model of ZIKV infection. Four pregnant sheep were challenged with ZIKV at 57-64 days gestation; two animals served as controls. After 13-15 days (corresponding with 70-79 days of gestation), one control and two infected animals were euthanized; the remaining animals were euthanized at 20-22 days post-infection (corresponding with 77-86 days of gestation). In the second experiment, six sexually mature, intact, male sheep were challenged with ZIKV and two animals served as controls. Infected animals were serially euthanized on days 2-6 and day 9 post-infection with the goal of isolating ZIKV from the male reproductive tract. In the mid-gestation study, virus was detected in maternal placenta and spleen, and in fetal organs, including the brains, spleens/liver, and umbilicus of infected fetuses. Fetuses from infected animals had visibly misshapen heads and morphometrics revealed significantly smaller head sizes in infected fetuses when compared to controls. Placental pathology was evident in infected dams. In the male experiment, ZIKV was detected in the spleen, liver, testes/epididymides, and accessory sex glands of infected animals. Results from both experiments indicate that mid-gestation ewes can be infected with ZIKV with subsequent disruption of fetal development and that intact male sheep are susceptible to ZIKV infection and viral dissemination and replication occurs in highly vascular tissues (including those of the male reproductive tract).
寨卡病毒(ZIKV)是一种虫媒病毒,可导致人类出生缺陷、持续性男性感染和性传播。本研究的目的是继续开发绵羊寨卡病毒感染模型;因此,进行了两项实验。在第一项实验中,我们在前一个妊娠绵羊实验的基础上,建立了寨卡病毒感染的中期妊娠模型。四只妊娠绵羊在妊娠 57-64 天接受寨卡病毒挑战;两只动物作为对照。在 13-15 天后(相当于妊娠 70-79 天),一只对照动物和两只感染动物被安乐死;其余动物在感染后 20-22 天(相当于妊娠 77-86 天)被安乐死。在第二项实验中,六只性成熟、完整、雄性绵羊接受寨卡病毒挑战,两只动物作为对照。感染动物在感染后第 2-6 天和第 9 天连续安乐死,目的是从雄性生殖道中分离寨卡病毒。在中期妊娠研究中,病毒在母体胎盘和脾脏以及感染胎儿的胎儿器官中被检测到,包括感染胎儿的大脑、脾脏/肝脏和脐带。感染动物的胎儿头部明显变形,形态测量学显示感染胎儿的头部尺寸明显小于对照。感染母羊的胎盘病理学明显。在雄性实验中,ZIKV 在感染动物的脾脏、肝脏、睾丸/附睾和附属生殖腺中被检测到。两项实验的结果均表明,妊娠中期母羊可以感染寨卡病毒,随后破坏胎儿发育,完整的雄性绵羊易感染寨卡病毒,病毒在高度血管组织(包括雄性生殖道组织)中传播和复制。