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Group A Rotavirus Infection and Age-Dependent Diarrheal Disease in Rats: a New Animal Model To Study the Pathophysiology of Rotavirus Infection

机译:A组轮状病毒感染和大鼠年龄依赖性腹泻疾病:研究轮状病毒感染病理生理的新动物模型

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摘要

Group A rotaviruses are major pathogens causing acute gastroenteritis in children and animals. To determine if group A rotavirus replicates and induces disease in rats, antibody-negative Lewis neonatal or adult rats were inoculated orally with tissue culture-adapted human (Wa, WI61, and HAL1166), simian (rhesus rotavirus [RRV] and SA11), bovine (WC3), lapine (ALA), or porcine (OSU) rotavirus strains, wild-type murine (ECwt) rotavirus strain, or phosphate-buffered saline (PBS). Rotavirus infection in rats was evaluated by (i) clinical findings, (ii) virus antigen shedding or infectious virus titers in the feces or intestinal contents measured by enzyme-linked immunosorbent assay or fluorescent-focus assay, (iii) histopathological changes in the small intestine, (iv) distribution of rotavirus antigen in small-intestine sections by immunofluorescence, and (v) growth rate. Rotavirus infection of 5-day-old but not ≥21-day-old rats resulted in diarrhea that lasted from 1 to 10 days postinoculation. The severity of disease and spread of infection to naÏve littermates differed depending on the virus strain used for inoculation. The duration of virus antigen shedding following infection was considerably prolonged (up to 10 days) in neonatal rats compared to that in 21-day-old rats (1 or 2 days). Based on lack of virus antigen shedding and disease induction, the murine ECwt rotavirus was the only strain tested that did not infect rats. Histopathological changes in the small-intestine mucosa of 5-day-old RRV-inoculated rats but not of PBS-inoculated rats was limited to extensive enterocyte vacuolation in the ileum. In RRV-inoculated neonatal rats, rotavirus antigen was detected in the epithelial cells on the upper half of the intestinal villi of the jejunum and ileum. In addition, infection of neonatal rats with RRV but not with PBS resulted in reduced weight gain. Rats infected with group A rotaviruses provide a new animal model with unique features amenable to investigate rotavirus pathogenesis and the molecular mechanisms of intestinal development, including physiological factors that may regulate age-dependent rotavirus-induced diarrhea.
机译:A组轮状病毒是引起儿童和动物急性胃肠炎的主要病原体。为了确定A组轮状病毒是否在大鼠中复制并诱发了疾病,将抗体阴性的Lewis新生或成年大鼠口服适应组织培养的人(Wa,WI61和HAL1166),猿猴(猴轮状病毒[RRV]和SA11),牛(WC3),拉丁美洲(ALA)或猪(OSU)轮状病毒株,野生型鼠(ECwt)轮状病毒株或磷酸盐缓冲液(PBS)。通过以下方法评估大鼠轮状病毒感染:(i)临床发现,(ii)粪便中的病毒抗原脱落或感染性病毒滴度或肠道内容物,通过酶联免疫吸附法或荧光聚焦法测定,(iii)小组织病理学改变(iv)轮状病毒抗原在小肠切片中的免疫荧光分布,以及(v)生长速率。轮状病毒感染5日龄但不≥21日龄的大鼠导致的腹泻持续到接种后1到10天。疾病的严重程度和感染传播到幼稚的同窝仔猪取决于用于接种的病毒株。与21天大的大鼠(1或2天)相比,新生大鼠的病毒抗原脱落后的持续时间大大延长(长达10天)。基于缺乏病毒抗原脱落和疾病诱导的原因,鼠ECwt轮状病毒是唯一未感染大鼠的测试菌株。 5天大的RRV接种大鼠的小肠粘膜的组织病理学变化仅限于回肠中广泛的肠细胞空泡化,而PBS接种的大鼠则没有。在接种RRV的新生大鼠中,在空肠和回肠小肠绒毛上半部的上皮细胞中检测到轮状病毒抗原。另外,RRV感染新生大鼠,但PBS感染并未导致体重增加减少。被A组轮状病毒感染的大鼠提供了一种新的动物模型,具有独特的特征,可以研究轮状病毒的发病机理和肠道发育的分子机制,包括可能调节年龄依赖性轮状病毒引起的腹泻的生理因素。

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