Mori C M C, Mori E, Favaro L L, Santos C R, Lara M C C S H, Villalobos E M C, Cunha E M S, Brandao P E, Richtzenhain L J, Maiorka P C
Department of Pathology, School of Veterinary Medicine and Animal Science, University of Sao Paulo, Sao Paulo, Brazil.
J Comp Pathol. 2012 Feb-Apr;146(2-3):202-10. doi: 10.1016/j.jcpa.2011.04.003.
Intranasal inoculation of equid herpesvirus type-1 (EHV-1) Brazilian strains A4/72 and A9/92 induced an acute and lethal infection in four different inbred mouse strains. Clinical and neurological signs appeared between the 2nd and 3rd day post inoculation (dpi) and included weight loss, ruffled fur, a hunched posture, crouching in corners, nasal and ocular discharges, dyspnoea, dehydration and increased salivation. These signs were followed by increased reactivity to external stimulation, seizures, recumbency and death. The virus was recovered consistently from the brain and viscera of all mice with neurological signs. Histopathological changes consisted of leptomeningitis, focal haemorrhage, ventriculitis, neuronal degeneration and necrosis, neuronophagia, non-suppurative inflammation, multifocal gliosis and perivascular infiltration of polymorphonuclear and mononuclear cells. Immunohistochemical examination demonstrated that EHV-1 strains A4/72 and A9/92 replicated in neurons of the olfactory bulb, the cortex and the hippocampus. In contrast, mice inoculated with the EHV-1 Brazilian strain A3/97 showed neither weight loss nor apparent clinical or neurological signs; however, the virus was recovered consistently from their lungs at 3 dpi. These three EHV-1 strains showed distinct degrees of virulence and tissue tropism in mice. EHV-1 strains A4/72 and A9/92 exhibited a high degree of central nervous system tropism with neuroinvasion and neurovirulence. EHV-1 strain A3/97 was not neurovirulent despite being detected in the brains of infected BALB/c nude mice. These findings indicate that several inbred mouse strains are susceptible to neuropathogenic EHV-1 strains and should be useful models for studying the pathogenesis and mechanisms contributing to EHV-induced myeloencephalopathy in horses.
鼻内接种1型马疱疹病毒(EHV-1)巴西毒株A4/72和A9/92可在四种不同的近交系小鼠品系中引发急性致死性感染。接种后第2天至第3天出现临床和神经症状,包括体重减轻、被毛蓬松、弓背姿势、蜷缩在角落、鼻眼分泌物、呼吸困难、脱水和流涎增加。随后出现对外界刺激反应性增强、惊厥、侧卧和死亡。在所有出现神经症状的小鼠的脑和内脏中均持续检测到病毒。组织病理学变化包括软脑膜炎、局灶性出血、脑室炎、神经元变性和坏死、噬神经元现象、非化脓性炎症、多灶性胶质细胞增生以及多形核细胞和单核细胞的血管周围浸润。免疫组织化学检查表明,EHV-1毒株A4/72和A9/92在嗅球、皮质和海马体的神经元中复制。相比之下,接种EHV-1巴西毒株A3/97的小鼠既没有体重减轻,也没有明显的临床或神经症状;然而,在接种后3天,在它们的肺中持续检测到病毒。这三种EHV-1毒株在小鼠中表现出不同程度的毒力和组织嗜性。EHV-1毒株A4/72和A9/92表现出高度的中枢神经系统嗜性,具有神经侵袭性和神经毒力。尽管在感染的BALB/c裸鼠的脑中检测到EHV-1毒株A3/97,但它没有神经毒力。这些发现表明,几种近交系小鼠品系对神经致病性EHV-1毒株易感,应成为研究EHV诱导马脊髓脑脊髓炎的发病机制和机制的有用模型。