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在缺乏α/β干扰素受体的小鼠中建立蓝舌病毒感染模型。

Establishment of a bluetongue virus infection model in mice that are deficient in the alpha/beta interferon receptor.

作者信息

Calvo-Pinilla Eva, Rodríguez-Calvo Teresa, Anguita Juan, Sevilla Noemí, Ortego Javier

机构信息

Centro de Investigación en Sanidad Animal, CISA-INIA, Madrid, Spain.

出版信息

PLoS One. 2009;4(4):e5171. doi: 10.1371/journal.pone.0005171. Epub 2009 Apr 9.

DOI:10.1371/journal.pone.0005171
PMID:19357779
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2663843/
Abstract

Bluetongue (BT) is a noncontagious, insect-transmitted disease of ruminants caused by the bluetongue virus (BTV). A laboratory animal model would greatly facilitate the studies of pathogenesis, immune response and vaccination against BTV. Herein, we show that adult mice deficient in type I IFN receptor (IFNAR((-/-))) are highly susceptible to BTV-4 and BTV-8 infection when the virus is administered intravenously. Disease was characterized by ocular discharges and apathy, starting at 48 hours post-infection and quickly leading to animal death within 60 hours of inoculation. Infectious virus was recovered from the spleen, lung, thymus, and lymph nodes indicating a systemic infection. In addition, a lymphoid depletion in spleen, and severe pneumonia were observed in the infected mice. Furthermore, IFNAR((-/-)) adult mice immunized with a BTV-4 inactivated vaccine showed the induction of neutralizing antibodies against BTV-4 and complete protection against challenge with a lethal dose of this virus. The data indicate that this mouse model may facilitate the study of BTV pathogenesis, and the development of new effective vaccines for BTV.

摘要

蓝舌病(BT)是一种由蓝舌病病毒(BTV)引起的反刍动物非传染性昆虫传播疾病。实验动物模型将极大地促进对BTV发病机制、免疫反应和疫苗接种的研究。在此,我们表明,当通过静脉注射病毒时,缺乏I型干扰素受体(IFNAR(-/-))的成年小鼠对BTV-4和BTV-8感染高度敏感。疾病表现为眼部分泌物和冷漠,在感染后48小时开始,在接种后60小时内迅速导致动物死亡。从脾脏、肺、胸腺和淋巴结中回收了传染性病毒,表明发生了全身感染。此外,在感染小鼠中观察到脾脏淋巴细胞耗竭和严重肺炎。此外,用BTV-4灭活疫苗免疫的IFNAR(-/-)成年小鼠显示出针对BTV-4的中和抗体诱导,并对致死剂量的该病毒攻击具有完全保护作用。数据表明,该小鼠模型可能有助于研究BTV发病机制以及开发针对BTV的新型有效疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c35/2663843/9b9bacd89885/pone.0005171.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c35/2663843/2c84ced2ec6d/pone.0005171.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c35/2663843/3b7dd0d09670/pone.0005171.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c35/2663843/a34d6c2da86d/pone.0005171.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c35/2663843/7d5f408cce56/pone.0005171.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c35/2663843/9b9bacd89885/pone.0005171.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c35/2663843/2c84ced2ec6d/pone.0005171.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c35/2663843/3b7dd0d09670/pone.0005171.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c35/2663843/a34d6c2da86d/pone.0005171.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c35/2663843/7d5f408cce56/pone.0005171.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c35/2663843/9b9bacd89885/pone.0005171.g005.jpg

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