Department of Pathology, UTMB, Galveston, TX, 77555, USA.
Sealy Institute for Vaccine Sciences, UTMB, Galveston, TX, 77555, USA.
Sci Rep. 2018 Mar 20;8(1):4900. doi: 10.1038/s41598-018-22618-w.
The mosquito-borne disease dengue is caused by four serologically- and genetically-related viruses, termed DENV-1 to DENV-4. Historical setbacks due to lack of human-like mouse models of dengue were partially remedied with characterization of lethal DENV-2 infection in immunocompromised AG129 mice (deficient in IFN-α/β/γ receptors). Recently, our group established lethal AG129 mouse infection models of DENV-1, DENV-3, and DENV-4 using human isolates. Here we compare a non-lethal, disseminated model of DENV-3 infection using strain D83-144 to that of the lethal outcome following infection by strain C0360/94. Both strains belong to DENV-3 genotype II and differ by only 13 amino acids. Intraperitoneal inoculation of AG129 mice with strain D83-144 led to clinical signs of dengue infection, such as cytokine induction, thrombocytopenia, and systemic infection. However, C0360/94 infection led to features of severe human dengue, including coagulopathy and lethal outcome, whereas D83-144 infection does not. This study is the first to investigate a low passage, non-mouse lethal strain in AG129 mice and demonstrates that D83-144 infection induces milder features of human dengue than those induced by lethal C0360/94 infection. The results suggest that the AG129 mouse model has applications to investigate factors associated with mild or severe disease.
登革热是由四种血清学和遗传学上相关的病毒引起的,分别称为 DENV-1 至 DENV-4。由于缺乏类似于人类的登革热小鼠模型,历史上曾出现过挫折,后来通过对免疫功能低下的 AG129 小鼠(缺乏 IFN-α/β/γ 受体)中致死性 DENV-2 感染的特征进行研究,部分得到了补救。最近,我们小组使用人分离株建立了 DENV-1、DENV-3 和 DENV-4 的致死性 AG129 小鼠感染模型。在这里,我们将使用 D83-144 株建立的非致死性、弥散性 DENV-3 感染模型与 C0360/94 株感染引起的致死结果进行比较。这两种株均属于 DENV-3 基因型 II,仅相差 13 个氨基酸。腹腔接种 D83-144 株可导致 AG129 小鼠出现登革热感染的临床症状,如细胞因子诱导、血小板减少和全身感染。然而,C0360/94 株感染可导致严重人类登革热的特征,包括凝血功能障碍和致死结局,而 D83-144 株感染则不会。这项研究首次在 AG129 小鼠中研究了低传代、非致死性株,表明 D83-144 株感染比致死性 C0360/94 株感染诱导的人类登革热特征更温和。结果表明,AG129 小鼠模型可用于研究与轻症或重症疾病相关的因素。