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肠道菌群失调与肠道感染 Theiler 氏鼠脑脊髓炎病毒后的神经免疫反应。

Gut dysbiosis and neuroimmune responses to brain infection with Theiler's murine encephalomyelitis virus.

机构信息

Grupo de Neuroinmunología, Departamento de Neurobiología Funcional y de Sistemas, Instituto Cajal, CSIC, Madrid, Spain.

Red Española de Esclerosis Múltiple (REEM), Spain.

出版信息

Sci Rep. 2017 Mar 14;7:44377. doi: 10.1038/srep44377.

Abstract

Recent studies have begun to point out the contribution of microbiota to multiple sclerosis (MS) pathogenesis. Theiler's murine encephalomyelitis virus induced demyelinating disease (TMEV-IDD) is a model of progressive MS. Here, we first analyze the effect of intracerebral infection with TMEV on commensal microbiota and secondly, whether the early microbiota depletion influences the immune responses to TMEV on the acute phase (14 dpi) and its impact on the chronic phase (85 dpi). The intracranial inoculation of TMEV was associated with a moderate dysbiosis. The oral administration of antibiotics (ABX) of broad spectrum modified neuroimmune responses to TMEV dampening brain CD4 and CD8 T infiltration during the acute phase. The expression of cytokines, chemokines and VP2 capsid protein was enhanced and accompanied by clusters of activated microglia disseminated throughout the brain. Furthermore, ABX treated mice displayed lower levels of CD4 and CD8T cells in cervical and mesenteric lymph nodes. Increased mortality to TMEV was observed after ABX cessation at day 28pi. On the chronic phase, mice that survived after ABX withdrawal and recovered microbiota diversity showed subtle changes in brain cell infiltrates, microglia and gene expression of cytokines. Accordingly, the surviving mice of the group ABX-TMEV displayed similar disease severity than TMEV mice.

摘要

最近的研究开始指出微生物群对多发性硬化症(MS)发病机制的贡献。Theiler 鼠脑炎病毒诱导的脱髓鞘疾病(TMEV-IDD)是进行性 MS 的模型。在这里,我们首先分析 TMEV 脑内感染对共生微生物群的影响,其次,早期微生物群耗竭是否会影响 TMEV 在急性期(14dpi)的免疫反应及其对慢性期(85dpi)的影响。TMEV 的颅内接种与中度菌群失调有关。广谱抗生素(ABX)的口服给药改变了 TMEV 的神经免疫反应,在急性期减轻了大脑 CD4 和 CD8 T 细胞的浸润。细胞因子、趋化因子和 VP2 衣壳蛋白的表达增强,并伴有散在大脑各处的活化小胶质细胞簇。此外,ABX 治疗的小鼠在颈和肠系膜淋巴结中的 CD4 和 CD8T 细胞水平较低。在 28dpi 时停止 ABX 治疗后,观察到 TMEV 死亡率增加。在慢性期,停止 ABX 治疗并恢复微生物多样性后存活的小鼠,其大脑细胞浸润、小胶质细胞和细胞因子的基因表达仅出现细微变化。因此,ABX-TMEV 组存活的小鼠与 TMEV 小鼠的疾病严重程度相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b6d/5349526/91cded03eb8a/srep44377-f1.jpg

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