Department of Microbiology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Laboratory Animal Center, Capital Medical University, Beijing, China.
PLoS Negl Trop Dis. 2021 Mar 5;15(3):e0009211. doi: 10.1371/journal.pntd.0009211. eCollection 2021 Mar.
Several studies have demonstrated that Zika virus (ZIKV) damages testis and leads to infertility in mice; however, the infection in the epididymis, another important organ of male reproductive health, has gained less attention. Previously, we detected lesions in the epididymis in interferon type I and II receptor knockout male mice during ZIKV infection. Herein, the pathogenesis of ZIKV in the epididymis was further assessed in the infected mice after footpad inoculation. ZIKV efficiently replicated in the epididymis, and principal cells were susceptible to ZIKV. ZIKV infection disrupted the histomorphology of the epididymis, and the effects were characterized by a decrease in the thickness of the epithelial layer and an increase in the luminal diameter, especially at the proximal end. Significant inflammatory cell infiltration was observed in the epididymis accompanied by an increase in the levels of interleukin (IL)-6 and IL-28. The expression of tight junction proteins was downregulated and associated with disordered arrangement of the junctions. Importantly, the expression levels of aquaporin 1 and lipocalin 8, indicators of the absorption and secretion functions of the epididymis, were markedly reduced, and the proteins were redistributed. These events synergistically altered the microenvironment for sperm maturation, disturbed sperm transport downstream, and may impact male reproductive health. Overall, these results provide new insights into the pathogenesis of the male reproductive damage caused by ZIKV infection and the possible contribution of epididymal injury into this process. Therefore, male fertility of the population in areas of ZIKV epidemic requires additional attention.
几项研究表明,寨卡病毒(ZIKV)会损害睾丸,导致小鼠不育;然而,另一个重要的男性生殖健康器官——附睾的感染却较少受到关注。此前,我们在 ZIKV 感染的 I 型和 II 型干扰素受体敲除雄性小鼠中检测到附睾损伤。在此,我们通过足垫接种感染的小鼠进一步评估了 ZIKV 在附睾中的发病机制。ZIKV 在附睾中高效复制,主细胞易受 ZIKV 感染。ZIKV 感染破坏了附睾的组织形态学,其影响特征是上皮层厚度减少和管腔直径增加,特别是在近端。附睾中观察到明显的炎症细胞浸润,同时白细胞介素 (IL)-6 和 IL-28 水平升高。紧密连接蛋白的表达下调,并与连接的排列紊乱有关。重要的是,水通道蛋白 1 和脂联素 8 的表达明显降低,这两种蛋白是附睾吸收和分泌功能的标志物,并且其蛋白发生了再分布。这些事件协同改变了精子成熟的微环境,扰乱了精子向下游的运输,可能影响男性生殖健康。总的来说,这些结果为 ZIKV 感染引起的男性生殖损伤的发病机制提供了新的见解,也提示附睾损伤可能在这一过程中发挥作用。因此,寨卡病毒流行地区人群的男性生育能力需要引起额外关注。