Abstract

We previously demonstrated, using the Piry virus model, that environmental enrichment promotes higher T-cell infiltration, fewer microglial changes, and faster central nervous system (CNS) virus clearance in adult mice. However, little is known about disease progression, behavioral changes, CNS cytokine concentration, and neuropathology in limbic encephalitis in experimental models. Using Cocal virus, we infected C57Bl6 adult mice and studied the neuroanatomical distribution of viral antigens in correlation with the microglial morphological response, measured the CNS cytokine concentration, and assessed behavioral changes. C57Bl6 adult mice were maintained in an impoverished environment (IE) or enriched environment (EE) for four months and then subjected to the open field test. Afterwards, an equal volume of normal or virus-infected brain homogenate was nasally instilled. The brains were processed to detect viral antigens and microglial morphological changes using selective immunolabeling. We demonstrated earlier significant weight loss and higher mortality in IE mice. Additionally, behavioral analysis revealed a significant influence of the environment on locomotor and exploratory activity that was associated with less neuroinvasion and a reduced microglial response. Thus, environmental enrichment was associated with a more effective immune response in a mouse model of limbic encephalitis, allowing faster viral clearance/decreased viral dissemination, reduced disease progression, and less CNS damage.

Highlights

  • Viral encephalitis is considered a medical emergency characterized by inflammatory processes in the cerebral parenchyma associated with clinical signs of loss of brain function and significant morbidity and mortality [1]

  • vesicular stomatitis virus (VSV) encephalitis can be experimentally induced by intranasal inoculation in mice [12,13,14,15], causing an initial infection of olfactory receptor neurons [16] and olfactory bulb neurons followed by acute infection of other central nervous system (CNS) regions [17,18]

  • We investigated the influence of the enriched environment on the progression of limbic encephalitis induced with the Cocal virus, using the adult female mouse model C57BL/6

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Summary

Introduction

Viral encephalitis is considered a medical emergency characterized by inflammatory processes in the cerebral parenchyma associated with clinical signs of loss of brain function and significant morbidity and mortality [1]. Some neurotropic viruses, such as human herpesvirus (HHV)-1, HHV-6, and HHV-7, may cause limbic encephalitis in immunocompetent and immunocompromised patients [2,3,4,5]. It is considered one of the serotypes of vesicular stomatitis virus (VSV) [8]. VSV reaches its highest CNS concentration around the 7th/8th day after infection and is directly related to animal mortality. In mice that survive until day 12 post-inoculation, the virus is completely eliminated without apparent CNS damage [18,19]

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