Hsu C C, Piotrowski S L, Meeker S M, Smith K D, Maggio-Price L, Treuting P M
Department of Comparative Medicine, University of Washington, Seattle, WA, USA
Department of Comparative Medicine, University of Washington, Seattle, WA, USA The University of Texas Health Science Center at Houston, Center for Laboratory Animal Medicine and Care, Houston, TX, USA.
Vet Pathol. 2016 Jul;53(4):754-63. doi: 10.1177/0300985815618439. Epub 2016 Jan 20.
Murine noroviruses (MNVs) are highly prevalent in laboratory mice, can cause persistent infections, and have been shown to infect macrophages, dendritic cells, and B cells. To address the potential impact of MNV infection on research outcomes, numerous studies have been conducted with various mouse models of human disease and have generated mixed results, ranging from no impact to significant disease. Many of these studies included histologic evaluations after MNV infection, and these results have similarly been variable in terms of whether MNV induces lesions, despite the fact that localization of MNV by viral culture and molecular techniques have demonstrated systemic distribution regardless of mouse immune status. The aim of this review is to summarize the histologic findings that have been reported with MNV infection in several mouse models. The studies demonstrate that experimental infection of MNV in wild-type mice results in minimal to no histologic changes. In contrast, immunodeficient mice consistently have detectable MNV-induced lesions that are typically inflammatory and, in the most severe cases, accompanied by necrosis. In these, the liver is commonly affected, with more variable lesions reported in the lung, gastrointestinal tract, mesenteric lymph nodes, brain, and spleen. In specific disease models including atherosclerosis, MNV infection had a variable impact that was dependent on the mouse model, viral strain, timing of infection, or other experimental variables. It is important to recognize the reported MNV lesions to help discern the possible influence of MNV infection on data generated in mouse models.
小鼠诺如病毒(MNVs)在实验小鼠中高度流行,可引起持续性感染,并且已被证明能感染巨噬细胞、树突状细胞和B细胞。为了探究MNV感染对研究结果的潜在影响,人们使用各种人类疾病的小鼠模型进行了大量研究,结果不一,从无影响到严重疾病都有。这些研究中有许多包括了MNV感染后的组织学评估,尽管通过病毒培养和分子技术对MNV的定位显示,无论小鼠免疫状态如何,MNV都呈全身分布,但关于MNV是否会诱导病变,这些结果同样存在差异。本综述的目的是总结在几种小鼠模型中报道的MNV感染的组织学发现。研究表明,野生型小鼠实验性感染MNV后,组织学变化极小或无变化。相比之下,免疫缺陷小鼠始终存在可检测到的MNV诱导的病变,这些病变通常是炎症性的,在最严重的情况下伴有坏死。在这些病变中,肝脏通常会受到影响,而在肺、胃肠道、肠系膜淋巴结、脑和脾脏中报道的病变则更具多样性。在包括动脉粥样硬化在内的特定疾病模型中,MNV感染的影响各不相同,这取决于小鼠模型、病毒株、感染时间或其他实验变量。认识到已报道的MNV病变,有助于辨别MNV感染对小鼠模型中产生的数据可能产生的影响,这一点很重要。