[小鼠实验朱宁病毒感染:疾病的原型]。

O A Giovanniello, M C Boxaca, N R Nota, M R Nejamkis
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引用次数: 0

摘要

如前所述,1 ~ 4日龄小鼠脑内接种1 ~ 1000 DL50 Junín病毒原型株(XJ)后出现的病理改变为小鼠EHFm实验性出血热。本文介绍了病毒分布、血液学变化、干扰素和循环抗体反应。93.45%的死亡率发生在感染后9至20天,81.6%的死亡率发生在感染后11至18天。这一最后时期可被认为是疾病的关键期。对病毒分布的研究表明,接种病毒的大脑是唯一能检测到病毒的地方,48小时后,4天后,大脑滴度显著增加,血液中检测到病毒。在相同值范围内的病毒可以被隔离到10号。的一天。10日出现肝脾侵犯。和15。(图1)临床症状的出现与病毒的广泛传播相吻合。仅在术后15天发现CF抗体,滴度为1/64。在整个实验过程中,中和抗体始终低于检测水平(图1)。存活小鼠(6.3%)40天后的循环抗体滴度较高。这一结果表明EHFm的发病率约为100%(表1)。在所有检查的器官中,干扰素反应较差,表明Junin病毒产生干扰素的能力较低6。总白细胞和淋巴细胞计数有轻微下降的趋势,尽管在前十天的数值在正常范围内(表2,图1)。在第14天,发现有统计学意义的下降(p < 0.001)。这种白细胞淋巴肿大一直持续到动物死亡。预计本文提供的数据将有助于更好地了解用于实验动物的新生小鼠中的Junin病毒感染。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Experimental Junin virus infection in the mouse: rototype of the disease].

As previously postulated, the pathological changes which develop in 1-4 day old mice after intracerebral inoculation of 1-1000 DL50 of Junín virus prototype strain (XJ), was designated as experimental hemorrhagic fever of the mouse EHFm. In this paper, virus distribution, hematological alterations, interferon and circulating antibody responses are described. A mortality of 93.45% occurred between 9 and 20 days post-infection (p.i.), with 81.6% of death occurring between 11 and 18 days p.i. This last period can be considered to be the critical period of the disease. The study of virus distribution shows that the brain, where the virus was inoculated, was the only place where virus could be detected 48 hs, p.i. Four days p.i., the titer in the brain increased remarkably and virus was detected in the blood. Virus, within the same values, could be isolated up to the 10th. day. Invasion of liver and spleen occurred on the 10th. and 15th. days p.i., respectively (Fig. 1). The onset of clinical symptoms coincided with widespread disemination of the virus. CF antibodies were found only 15 days p.i., with a titer of 1/64. Neutralizing antibodies remained below detection levels during the whole experiment (Fig. 1). Surviving mice (6.3%) had high circulating antibody titers 40 days p.i. This result would indicate that the morobidity of EHFm is aproximately 100% (Table 1). Poor interferon response was registered in all the organs examined, indicating a low intereron producing ability for Junin virus6. Total leukocytes and lymphocyte counts showed a slight tendecy to drop, although the values were within normal range during the first ten days (Table 2, Fig 1). On day 14 p.i., a statistically significant decrease (p less than 0.001) was found. This leuko-lymphopaenia continued until death of the animals. It is expected that the data presente here would contribute to a better understanding of the Junin virus infection in the newborn mouse, the experimental animal used.

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