Bradford Russell D, Yoo Young-Gun, Golemac Mijo, Pugel Ester Pernjak, Jonjic Stipan, Britt William J
Department of Pediatrics, University of Alabama School of Medicine, Birmingham, Alabama, United States of America.
Department of Histology and Embryology, Faculty of Medicine, University of Rijeka, Rijeka, Croatia.
PLoS Pathog. 2015 Apr 13;11(4):e1004774. doi: 10.1371/journal.ppat.1004774. eCollection 2015 Apr.
Congenital human cytomegalovirus (HCMV) occurs in 0.5-1% of live births and approximately 10% of infected infants develop hearing loss. The mechanism(s) of hearing loss remain unknown. We developed a murine model of CMV induced hearing loss in which murine cytomegalovirus (MCMV) infection of newborn mice leads to hematogenous spread of virus to the inner ear, induction of inflammatory responses, and hearing loss. Characteristics of the hearing loss described in infants with congenital HCMV infection were observed including, delayed onset, progressive hearing loss, and unilateral hearing loss in this model and, these characteristics were viral inoculum dependent. Viral antigens were present in the inner ear as were CD(3+) mononuclear cells in the spiral ganglion and stria vascularis. Spiral ganglion neuron density was decreased after infection, thus providing a mechanism for hearing loss. The lack of significant inner ear histopathology and persistence of inflammation in cochlea of mice with hearing loss raised the possibility that inflammation was a major component of the mechanism(s) of hearing loss in MCMV infected mice.
先天性人类巨细胞病毒(HCMV)感染发生于0.5% - 1%的活产婴儿中,约10%的受感染婴儿会出现听力损失。听力损失的机制尚不清楚。我们建立了一种巨细胞病毒诱导的听力损失小鼠模型,其中新生小鼠感染鼠巨细胞病毒(MCMV)会导致病毒经血行扩散至内耳,引发炎症反应并导致听力损失。在该模型中观察到了先天性HCMV感染婴儿所描述的听力损失特征,包括发病延迟、进行性听力损失和单侧听力损失,并且这些特征依赖于病毒接种量。内耳中存在病毒抗原,螺旋神经节和血管纹中也存在CD(3+)单核细胞。感染后螺旋神经节神经元密度降低,从而为听力损失提供了一种机制。听力损失小鼠的内耳组织病理学无明显变化且耳蜗炎症持续存在,这增加了炎症是MCMV感染小鼠听力损失机制主要组成部分的可能性。