首页> 外文期刊>Cardiovascular pathology: the official journal of the Society for Cardiovascular Pathology >Initial weight and virus dose: Two factors affecting the onset of acute coxsackievirus B3 myocarditis in C57BL/6 mouse - A histopathology-based study
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Initial weight and virus dose: Two factors affecting the onset of acute coxsackievirus B3 myocarditis in C57BL/6 mouse - A histopathology-based study

机译:初始重量和病毒剂量:影响C57BL / 6小鼠急性柯萨奇B3心肌炎发作的两个因素-基于组织病理学的研究

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Background: C57BL/6 mice have been considered resistant to cardiotropic coxsackievirus B3 (CVB3)-induced myocarditis. However, establishment of viral myocarditis model in C57BL/6 mouse is still a necessity. Here, we discuss the effects of mouse initial body weight and different virus inoculation doses on the onset of acute viral myocarditis in C57BL/6 mouse. Methods: According to initial body weight, mice were grouped into group A (3-4 weeks, 11-15 g) and group B (5-6 weeks, 18-20 g). Then, each group was divided into three subgroups inoculated with different virus doses: 1000 50% tissue culture infectious dose (TCID50)/ml, 10,000 TCID50/ml, and 100,000 TCID 50/ml. Virus existence and myocardium inflammatory infiltration conditions were observed and evaluated 7 days postinfection. Results: Immunohistochemistry staining showed that virus capsid protein VP1 appeared in the myocardia of virus-infected mice. Three subgroups in the lower-body-weight group (group A) came out with a higher mortality (40%-100%), while the higher-body-weight group (group B) showed a tendency for body weight decline. Histopathologically, myocardia of the survival cases in the lower-initial-body- weight group got inflammatory infiltration, while almost no inflammation appeared in the dead cases. In the higher-body-weight group, myocardium inflammatory infiltration deteriorated with the increase of virus doses and bared a relatively sound survival rate. Conclusions: This study indicated that the initial body weight and virus infection dose are two factors affecting the onset of viral myocarditis in C57BL/6 mice. Accordingly, initial body weight of 18-20 g and an inoculation dose of 100,000 TCID50/ml×0.3 ml CVB3 might be an optimal choice to induce acute viral myocarditis in C57BL/6 mice.
机译:背景:C57BL / 6小鼠被认为具有抗心肌病性柯萨奇病毒B3(CVB3)诱导的心肌炎的能力。但是,仍需要在C57BL / 6小鼠中建立病毒性心肌炎模型。在这里,我们讨论了小鼠初始体重和不同病毒接种剂量对C57BL / 6小鼠急性病毒性心肌炎发作的影响。方法:根据初始体重,将小鼠分为A组(3-4周,11-15 g)和B组(5-6周,18-20 g)。然后,将每组分为三个亚组,分别接种不同的病毒剂量:1000 50%组织培养物感染剂量(TCID50)/ ml,10,000 TCID50 / ml和100,000 TCID 50 / ml。感染后7天观察并评估病毒的存在和心肌炎性浸润条件。结果:免疫组织化学染色显示病毒衣壳蛋白VP1出现在病毒感染小鼠的心肌中。低体重组(A组)的三个亚组死亡率较高(40%-100%),而高体重组(B组)则表现出体重下降的趋势。在组织病理学上,低体重组存活病例的心肌有炎症浸润,而死亡病例几乎没有炎症出现。在高体重组中,心肌炎性浸润随着病毒剂量的增加而恶化,并且生存率相对较高。结论:这项研究表明,初始体重和病毒感染剂量是影响C57BL / 6小鼠病毒性心肌炎发作的两个因素。因此,初始体重为18-20 g,接种剂量为100,000 TCID50 / ml×0.3 ml CVB3可能是诱导C57BL / 6小鼠急性病毒性心肌炎的最佳选择。

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