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寨卡病毒脑炎会导致功能性皮质连接暂时减少。

Zika virus encephalitis causes transient reduction of functional cortical connectivity.

作者信息

Agner Shannon C, Brier Lindsey M, Hill Jeremy D, Liu Ethan Y, Bice Annie, Rahn Rachel M, Chen Shengxuan, Culver Joseph P, Klein Robyn S

机构信息

Washington University School of Medicine, Center for Neuroimmunology and Neuroinfectious Diseases, St. Louis, Missouri, United States.

Washington University School of Medicine, Department of Neurology, St. Louis, Missouri, United States.

出版信息

Neurophotonics. 2025 Jan;12(Suppl 1):S14603. doi: 10.1117/1.NPh.12.S1.S14603. Epub 2024 Nov 28.

Abstract

SIGNIFICANCE

Determining the long-term cognitive impact of infections is clinically challenging. Using functional cortical connectivity, we demonstrate that interhemispheric cortical connectivity is decreased in individuals with acute Zika virus (ZIKV) encephalitis. This correlates with decreased presynaptic terminals in the somatosensory cortex. During recovery from ZIKV infection, presynaptic terminals recover, which is associated with recovered interhemispheric connectivity. This supports the contribution of synapses in the cortex to functional networks in the brain, which can be detected by widefield optical imaging. Although myeloid cell and astrocyte numbers are still increased during recovery, RNA transcription of multiple proinflammatory cytokines that increase during acute infection decreases to levels comparable to mock-infected mice during recovery. These findings also suggest that the immune response and cytokine-mediated neuroinflammation play significant roles in the integrity of brain networks during and after viral encephalitis.

AIM

We hypothesized that widefield optical imaging would allow us to assess functional cortical network disruption by ZIKV, including hippocampal-cortical networks.

APPROACH

We use widefield optical imaging to measure cortical functional connectivity (FC) in mice during acute infection with, and recovery from, intracranial infection with a mouse-adapted strain of ZIKV.

RESULTS

Acute ZIKV infection leads to high levels of myeloid cell activation, with loss of neurons and presynaptic termini in the cerebral cortex and associated loss of FC primarily within the somatosensory cortex. During recovery, neuron numbers, synapses, and FC recover to levels near those of healthy mice. However, hippocampal injury and impaired spatial cognition persist. The magnitude of activated myeloid cells during acute infection predicted both recovery of synapses and the degree of FC recovery after recovery from ZIKV infection.

CONCLUSIONS

These findings suggest that a robust inflammatory response may contribute to the health of functional brain networks after recovery from infection.

摘要

意义

确定感染对长期认知的影响在临床上具有挑战性。利用功能性皮质连接性,我们证明急性寨卡病毒(ZIKV)脑炎患者的半球间皮质连接性降低。这与体感皮质中突触前终末的减少相关。在从ZIKV感染中恢复期间,突触前终末恢复,这与恢复的半球间连接性相关。这支持了皮质中的突触对大脑功能网络的贡献,这可以通过宽场光学成像检测到。尽管在恢复期间髓样细胞和星形胶质细胞数量仍增加,但急性感染期间增加的多种促炎细胞因子的RNA转录在恢复期间降至与模拟感染小鼠相当的水平。这些发现还表明,免疫反应和细胞因子介导的神经炎症在病毒性脑炎期间及之后的脑网络完整性中起重要作用。

目的

我们假设宽场光学成像将使我们能够评估ZIKV对功能性皮质网络的破坏,包括海马-皮质网络。

方法

我们使用宽场光学成像来测量小鼠在颅内感染适应小鼠的ZIKV毒株的急性感染期间及恢复过程中的皮质功能连接性(FC)。

结果

急性ZIKV感染导致高水平的髓样细胞激活,大脑皮质中神经元和突触前终末丧失,并且主要在体感皮质内相关的FC丧失。在恢复期间,神经元数量、突触和FC恢复到接近健康小鼠的水平。然而,海马损伤和空间认知受损仍然存在。急性感染期间活化髓样细胞的程度预测了从ZIKV感染恢复后突触的恢复和FC恢复的程度。

结论

这些发现表明,强烈的炎症反应可能有助于感染恢复后功能性脑网络的健康。

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