发病机制
基孔肯雅
病毒学
病毒
体内
病毒载量
病毒病机
病毒释放
免疫学
医学
病态的
病毒复制
病毒性疾病
疾病
生物
临床疾病
α病毒
甲病毒感染
抗病毒药物
动物模型
实验病理学
病毒性心肌炎
组织病理学
病毒感染
作者
Marília Mazzi Moraes,Natália de Godoy,Eduardo Maffud Cilli,Paulo Ricardo da Silva Sanches
出处
期刊:Pathogens
[Multidisciplinary Digital Publishing Institute]
日期:2026-04-22
卷期号:15 (5): 454-454
标识
DOI:10.3390/pathogens15050454
摘要
Chikungunya virus (CHIKV) infection presents a wide spectrum of clinical outcomes, ranging from mild self-limiting disease to severe and fatal manifestations, which are influenced by both host and viral factors. Animal models are essential for elucidating CHIKV pathogenesis and for preclinical evaluation of antiviral strategies; however, a well-characterized model evaluating the effect of different viral doses in AG129 mice remains limited. In this study, we investigated the clinical, virological, and pathological outcomes of CHIKV infection in male AG129 mice inoculated intraperitoneally with different viral doses (10, 100, and 1000 PFU/mL) of a Brazilian strain belonging to the East/Central/South African (ECSA) lineage. Lower-dose inoculation (10 PFU/mL) resulted in a milder disease course, characterized by transient viremia, limited tissue viral dissemination, minimal histopathological alterations, partial survival, and viral clearance. In contrast, higher doses (≥100 PFU/mL) led to rapid systemic viral dissemination, severe histopathological damage in the spleen, liver, and kidneys, and uniform lethality. Viral RNA was detected in serum and multiple organs in a time-dependent manner, with limited differences among inoculum doses in most tissues. Notably, dose-related differences were observed in specific compartments and time points, particularly in hind-limb muscles at early time points and in serum at later stages.
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