Department of Neurology, and Chronobiology and Sleep Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104.
Department of Biology, University of Nevada, Reno, Nevada 89557.
J Neurosci. 2024 Aug 28;44(35):e1700222024. doi: 10.1523/JNEUROSCI.1700-22.2024.
Infection causes reduced activity, anorexia, and sleep, which are components of the phylogenetically conserved but poorly understood sickness behavior. We developed a model to study quiescence during chronic infection, using infection with the Orsay virus. The Orsay virus infects intestinal cells yet strongly affects behavior, indicating gut-to-nervous system communication. Infection quiescence has the sleep properties of reduced responsiveness and rapid reversibility. Both the ALA and RIS neurons regulate virus-induced quiescence though ALA plays a more prominent role. Quiescence-defective animals have decreased survival when infected, indicating a benefit of quiescence during chronic infectious disease. The survival benefit of quiescence is not explained by a difference in viral load, indicating that it improves resilience rather than resistance to infection. Orsay infection is associated with a decrease in ATP levels, and this decrease is more severe in quiescence-defective animals. We propose that quiescence preserves energetic resources by reducing energy expenditures and/or by increasing extraction of energy from nutrients. This model presents an opportunity to explore the role of sleep and fatigue in chronic infectious illness.
感染会导致活动减少、食欲不振和睡眠不足,这些都是从进化上保守但知之甚少的疾病行为的组成部分。我们开发了一种模型来研究慢性感染期间的静止状态,使用 Orsay 病毒感染。Orsay 病毒感染肠道细胞,但强烈影响行为,表明肠道与神经系统的通讯。感染静止具有反应迟钝和快速可逆性的睡眠特性。ALA 和 RIS 神经元都调节病毒诱导的静止,但 ALA 发挥更突出的作用。静止缺陷动物在感染时的存活率降低,表明在慢性传染病中静止具有益处。静止的生存益处不能用病毒载量的差异来解释,这表明它提高了恢复力而不是对感染的抵抗力。Orsay 感染与 ATP 水平降低有关,而在静止缺陷动物中这种降低更为严重。我们提出,静止通过减少能量消耗和/或增加从营养物质中提取能量来保存能量资源。这种模型为探索睡眠和疲劳在慢性传染病中的作用提供了机会。