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Rotavirus Viremia and Extraintestinal Viral Infection in the Neonatal Rat Model

机译:新生大鼠模型中的轮状病毒病毒血症和肠外病毒感染

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摘要

Rotaviruses infect mature, differentiated enterocytes of the small intestine and, by an unknown mechanism, escape the gastrointestinal tract and cause viremia. The neonatal rat model of rotavirus infection was used to determine the kinetics of viremia, spread, and pathology of rotavirus in extraintestinal organs. Five-day-old rat pups were inoculated intragastrically with an animal (RRV) or human (HAL1166) rotavirus or phosphate-buffered saline. Blood was collected from a subset of rat pups, and following perfusion to remove residual blood, organs were removed and homogenized to analyze rotavirus-specific antigen by enzyme-linked immunosorbent assay and infectious rotavirus by fluorescent focus assay or fixed in formalin for histology and immunohistochemistry. Viremia was detected following rotavirus infection with RRV and HAL1166. The RRV 50% antigenemia dose was 1.8 × 103 PFU, and the 50% diarrhea dose was 7.7 × 105 PFU, indicating that infection and viremia occurred in the absence of diarrhea and that detecting rotavirus antigen in the blood was a more sensitive measure of infection than diarrhea. Rotavirus antigens and infectious virus were detected in multiple organs (stomach, intestines, liver, lungs, spleen, kidneys, pancreas, thymus, and bladder). Histopathological changes due to rotavirus infection included acute inflammation of the portal tract and bile duct, microsteatosis, necrosis, and inflammatory cell infiltrates in the parenchymas of the liver and lungs. Colocalization of structural and nonstructural proteins with histopathology in the liver and lungs indicated that the histological changes observed were due to rotavirus infection and replication. Replicating rotavirus was also detected in macrophages in the lungs and blood vessels, indicating a possible mechanism of rotavirus dissemination. Extraintestinal infectious rotavirus, but not diarrhea, was observed in the presence of passively or actively acquired rotavirus-specific antibody. These findings alter the previously accepted concept of rotavirus pathogenesis to include not only gastroenteritis but also viremia, and they indicate that rotavirus could cause a broad array of systemic diseases in a number of different organs.
机译:轮状病毒感染小肠成熟,分化的肠细胞,并以未知的机制逃逸到胃肠道并引起病毒血症。轮状病毒感染的新生大鼠模型用于确定肠外器官中轮状病毒的病毒血症,传播和病理学动力学。给五日龄的幼鼠在胃内接种动物(RRV)或人(HAL1166)轮状病毒或磷酸盐缓冲液。从一部分大鼠幼仔中收集血液,灌注去除残留血液后,取出器官并匀浆以通过酶联免疫吸附测定法分析轮状病毒特异性抗原,并通过荧光聚焦测定法分析感染性轮状病毒或固定在福尔马林中以进行组织学和免疫组化。轮状病毒感染RRV和HAL1166后检测到病毒血症。 RRV的50%抗原血症剂量为1.8×10 3 PFU,而50%的腹泻剂量为7.7×10 5 PFU,表明感染和病毒血症是在无乙型肝炎的情况下发生的腹泻和检测血液中的轮状病毒抗原是一种比腹泻更为敏感的感染措施。在多个器官(胃,肠,肝,肺,脾,肾,胰腺,胸腺和膀胱)中检测到轮状病毒抗原和感染性病毒。由轮状病毒感染引起的组织病理学变化包括门静脉和胆管的急性炎症,微脂肪变性,坏死以及肝和肺实质中的炎性细胞浸润。结构和非结构蛋白与肝脏和肺组织病理学的共定位表明,观察到的组织学变化是由于轮状病毒感染和复制所致。在肺和血管中的巨噬细胞中也检测到轮状病毒复制,这表明轮状病毒传播的可能机制。在被动或主动获得轮状病毒特异性抗体的情况下,观察到肠外感染性轮状病毒,但未观察到腹泻。这些发现改变了以前公认的轮状病毒发病机理的概念,不仅包括胃肠炎,还包括病毒血症,并且它们表明轮状病毒可以在许多不同器官中引起广泛的系统性疾病。

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