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[严重发热伴血小板减少综合征病毒在Balb/C小鼠和仓鼠中的感染]

[Infection of the Severe Fever with Thrombocytopenia Syndrome Virus in Balb/C Mice and Hamsters].

作者信息

Jin Cong, Han Ying, Li Chuan, Gu Wen, Jiang Hong, Chen Ting, Zhu Hua, Wei Qiang, Qiu Peihong, Liang Mifang, Li Dexin

出版信息

Bing Du Xue Bao. 2015 Jul;31(4):379-87.

PMID:26524910
Abstract

The severe fever with thrombocytopenia syndrome virus (SFTSV) is the causative pathogen of an emerging infectious disease severe fever with thrombocytopenia syndrome and a new member in the genus Phlebovirus of family Bunyaviridae. Immune responses and pathological lesions in SFTSV-infected Balb/C mice and hamsters were evaluated by inoculation of SFTSV at 105 TCID50 or 103 TCID50 per animal through four different routes of infection, including intravenous, intramuscular, intraperitoneal, and intracerebral injections. The vehicle control groups were also included. At different time points after the inoculation blood and plasma samples were collected. Blood cell counts, blood viral RNA copies, and plasma antibodies were detected by automatic blood cell counters, real-time PCR, and luminex assays, respectively. At two weeks post inoculation, the animals were sacrificed. Tissues including heart, liver, spleen, lung, kidney, intestine, muscle, and brain, were collected for pathological analyses. Results showed that the SFTSV could infect Balb/C mice and hamsters with SFTSV-specific immunoglobulin (Ig) M and IgG antibodies detected in plasma samples on day 7 post inoculation. The SFTSV-specific IgM levels peaked on day 7 post inoculation and then decreased, whereas the SFTSV-specific IgG levels started to increase on day 7 and then peaked on day 14 post inoculation. Pathological analyses indicated significant pathological lesions in liver and kidney tissues. In conclusion, SFTSV could can infect different strains of rodent animals and cause similar immunological and pathological responses.

摘要

发热伴血小板减少综合征病毒(SFTSV)是新发传染病发热伴血小板减少综合征的致病病原体,属于布尼亚病毒科白蛉病毒属的一个新成员。通过对Balb/C小鼠和仓鼠分别经静脉、肌肉、腹腔和脑内注射四种不同途径接种105 TCID50或103 TCID50的SFTSV,评估其在感染SFTSV后的免疫反应和病理损伤。同时设置了载体对照组。在接种后的不同时间点采集血液和血浆样本。分别通过自动血细胞计数器、实时PCR和Luminex检测法检测血细胞计数、血液病毒RNA拷贝数和血浆抗体。接种后两周,处死动物。采集心脏、肝脏、脾脏、肺、肾脏、肠道、肌肉和脑等组织进行病理分析。结果显示,SFTSV可感染Balb/C小鼠和仓鼠,接种后第7天在血浆样本中检测到SFTSV特异性免疫球蛋白(Ig)M和IgG抗体。SFTSV特异性IgM水平在接种后第7天达到峰值,随后下降,而SFTSV特异性IgG水平在第7天开始升高,并在接种后第14天达到峰值。病理分析表明肝脏和肾脏组织出现明显病理损伤。总之,SFTSV可感染不同品系的啮齿动物,并引起相似的免疫和病理反应。

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引用本文的文献

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Animal Model of Severe Fever With Thrombocytopenia Syndrome Virus Infection.严重发热伴血小板减少综合征病毒感染的动物模型
Front Microbiol. 2022 Jan 11;12:797189. doi: 10.3389/fmicb.2021.797189. eCollection 2021.