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解析基孔肯雅热病毒感染的复杂性:急性和慢性患者的免疫和遗传见解。

Unraveling the Complexity of Chikungunya Virus Infection Immunological and Genetic Insights in Acute and Chronic Patients.

机构信息

Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte 31270-901, Brazil.

Institut National de la Santé et de la Recherche Médicale, U1259-MAVIVHe, Université de Tours, 37032 Tours, France.

出版信息

Genes (Basel). 2024 Oct 24;15(11):1365. doi: 10.3390/genes15111365.

DOI:10.3390/genes15111365
PMID:39596565
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11593632/
Abstract

: The chikungunya virus (CHIKV), transmitted by infected Aedes mosquitoes, has caused a significant number of infections worldwide. In Brazil, the emergence of the CHIKV-ECSA genotype in 2014 posed a major public health challenge due to its association with more severe symptoms. : This study aimed to shed new light on the host immune response by examining the whole-blood transcriptomic profile of both CHIKV-acute and chronically infected individuals from Feira de Santana, Bahia, Brazil, a region heavily affected by CHIKV, Dengue, and Zika virus epidemics. : Our data reveal complex symptomatology characterized by arthralgia and post-chikungunya neuropathy in individuals with chronic sequelae, particularly affecting women living in socially vulnerable situations. Analysis of gene modules suggests heightened metabolic processes, represented by an increase in NADH, COX5A, COA3, CYC1, and cap methylation in patients with acute disease. In contrast, individuals with chronic manifestations exhibit a distinct pattern of histone methylation, probably mediated by NCOA3 in the coactivation of different nuclear receptors, KMT2 genes, KDM3B and TET2, and with alterations in the immunological response, majorly led by IL-17RA, IL-6R, and STAT3 Th17 genes. : Our results emphasize the complexity of CHIKV disease progression, demonstrating the heterogeneous gene expression and symptomatologic scenario across both acute and chronic phases. Moreover, the identification of specific gene modules associated with viral pathogenesis provides critical insights into the molecular mechanisms underlying these distinct clinical manifestations.

摘要

基孔肯雅病毒(CHIKV)通过受感染的伊蚊传播,已在全球范围内导致大量感染。在巴西,2014 年出现的 ECSA 基因型 CHIKV 由于与更严重的症状相关,构成了重大的公共卫生挑战。

本研究旨在通过检测来自巴西巴伊亚州费拉迪圣安娜的 CHIKV 急性和慢性感染个体的全血转录组谱,深入了解宿主免疫反应,该地区深受 CHIKV、登革热和寨卡病毒流行的影响。

我们的数据揭示了复杂的症状学特征,表现为慢性后遗症个体的关节痛和 post-chikungunya 神经病,特别是生活在社会弱势环境中的女性。基因模块分析表明,代谢过程增强,急性疾病患者的 NADH、COX5A、COA3、CYC1 和帽甲基化增加。相比之下,慢性表现个体表现出明显的组蛋白甲基化模式,可能由 NCOA3 介导,从而激活不同的核受体、KMT2 基因、KDM3B 和 TET2,并改变免疫反应,主要由 IL-17RA、IL-6R 和 STAT3 Th17 基因主导。

我们的研究结果强调了 CHIKV 疾病进展的复杂性,表明急性和慢性阶段均存在基因表达和症状学的异质性。此外,确定与病毒发病机制相关的特定基因模块为理解这些不同临床表现的分子机制提供了关键见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cae7/11593632/e7833da0e874/genes-15-01365-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cae7/11593632/bcebb43e5172/genes-15-01365-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cae7/11593632/e7833da0e874/genes-15-01365-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cae7/11593632/bcebb43e5172/genes-15-01365-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cae7/11593632/e7833da0e874/genes-15-01365-g002.jpg

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