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两种尼日利亚虫媒病毒的感染性及补体结合抗原的器官分布

Organ distribution of infectivity and complement-fixing antigen with two Nigerian arboviruses.

作者信息

David-West T S

出版信息

Br J Exp Pathol. 1970 Jun;51(3):332-9.

PMID:5429077
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2072280/
Abstract

Time course studies intended to throw some light on the pathogenesis of some recently isolated Nigerian arboviruses were conducted by following the production of infective virus and complement-fixing (CF) antigen and correlating these with pathological changes in the brain and in the liver of suckling white Swiss mice. Two prototypes of the Nigerian arboviruses were employed: IB.AR.1792 (Dugbe) a hitherto undescribed arbovirus, isolated from and IB.AR.2012 (Thogoto) isolated from Following infection with virus 1792, titres of both infective virus and CF antigen increased rapidly in the brain. Infective virus was also produced in the liver but CF antigen was virtually negative. With virus 2012 infection, infective virus and CF antigen titres rose rapidly in the liver. But in the brain although infective virus was produced to a high titre, CF antigen was not demonstrated. Histopathological examination showed a positive correlation between the presence of CF antigen (and not infective virus ) and pathologic changes. There was encephalitis and cell degeneration in brain infected with virus 1792. The striking pathological changes in liver infected with virus 2012 were proliferation of the bile ducts, congested vessels and dilation of the sinusoids.

摘要

通过追踪感染性病毒和补体结合(CF)抗原的产生,并将这些与乳鼠瑞士小白鼠大脑和肝脏的病理变化相关联,进行了时间进程研究,旨在阐明一些最近分离出的尼日利亚虫媒病毒的发病机制。使用了两种尼日利亚虫媒病毒的原型:IB.AR.1792(杜贝病毒),一种迄今未描述的虫媒病毒,从……分离得到;以及IB.AR.2012(托戈托病毒),从……分离得到。用病毒1792感染后,大脑中感染性病毒和CF抗原的滴度迅速升高。肝脏中也产生了感染性病毒,但CF抗原实际上呈阴性。用病毒2012感染后,肝脏中感染性病毒和CF抗原滴度迅速上升。但在大脑中,尽管产生了高滴度的感染性病毒,但未检测到CF抗原。组织病理学检查显示CF抗原(而非感染性病毒)的存在与病理变化之间存在正相关。感染病毒1792的大脑出现脑炎和细胞变性。感染病毒2012的肝脏中显著的病理变化是胆管增生、血管充血和肝血窦扩张。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5495/2072280/a368e032ab0f/brjexppathol00429-0123-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5495/2072280/a2f516acaf66/brjexppathol00429-0124-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5495/2072280/a368e032ab0f/brjexppathol00429-0123-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5495/2072280/a2f516acaf66/brjexppathol00429-0124-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5495/2072280/a368e032ab0f/brjexppathol00429-0123-a.jpg

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Effect of route of inoculation on histopathological changes induced in mice by dugbe virus (a Nigerian tick-borne virus).接种途径对杜格贝病毒(一种尼日利亚蜱传病毒)诱导的小鼠组织病理学变化的影响。

本文引用的文献

1
THOGOTO VIRUS: A HITHERTO UNDERSCRIBED AGENT ISOLATED FROM TICKS IN KENYA.托高托病毒:一种从肯尼亚蜱虫中分离出的此前未被充分描述的病原体。
J Gen Microbiol. 1965 Mar;38:389-94. doi: 10.1099/00221287-38-3-389.
2
Group C, a new serological group of hitherto undescribed arthropod-borne viruses. Immunological studies.C组,一个迄今为止尚未描述的节肢动物传播病毒的新血清学组。免疫学研究。
Am J Trop Med Hyg. 1961 Mar;10:250-8. doi: 10.4269/ajtmh.1961.10.250.
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The course of Semliki Forest virus infection in mice.小鼠感染Semliki森林病毒的病程。
Br J Exp Pathol. 1974 Aug;55(4):421-6.
Br J Exp Pathol. 1967 Aug;48(4):395-402.
4
On the pathogenesis of Semliki forest virus (SFV) infection in the hamster.关于仓鼠感染Semliki森林病毒(SFV)的发病机制
Br J Exp Pathol. 1967 Apr;48(2):228-34.
5
The use of adjuvant and sarcoma 180 cells in the production of mouse hyperimmune ascitic fluids to arboviruses.佐剂和肉瘤180细胞在制备抗虫媒病毒小鼠超免疫腹水液中的应用。
Am J Trop Med Hyg. 1966 Mar;15(2):219-26. doi: 10.4269/ajtmh.1966.15.219.