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斑马鱼中病毒神经侵袭的成像显示,辛德毕斯病毒和基孔肯雅病毒倾向于不同的进入途径。

Imaging of viral neuroinvasion in the zebrafish reveals that Sindbis and chikungunya viruses favour different entry routes.

作者信息

Passoni Gabriella, Langevin Christelle, Palha Nuno, Mounce Bryan C, Briolat Valérie, Affaticati Pierre, De Job Elodie, Joly Jean-Stéphane, Vignuzzi Marco, Saleh Maria-Carla, Herbomel Philippe, Boudinot Pierre, Levraud Jean-Pierre

机构信息

Virology and Molecular Immunology, INRA, Université Paris-Saclay, Domaine de Vilvert, Jouy-en-Josas F-78352, France.

Macrophages and Development of Immunity, Institut Pasteur, CNRS UMR 3738, 25 rue du docteur Roux, Paris F-75015, France.

出版信息

Dis Model Mech. 2017 Jul 1;10(7):847-857. doi: 10.1242/dmm.029231. Epub 2017 May 8.

DOI:10.1242/dmm.029231
PMID:28483796
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5536907/
Abstract

Alphaviruses, such as chikungunya virus (CHIKV) and Sindbis virus (SINV), are vector-borne pathogens that cause acute illnesses in humans and are sometimes associated with neuropathies, especially in infants and elderly patients. Little is known about their mechanism of entry into the central nervous system (CNS), even for SINV, which has been used extensively as a model for viral encephalopathies. We previously established a CHIKV infection model in the optically transparent zebrafish larva; here we describe a new SINV infection model in this host. We imaged the onset and progression of the infection caused by intravenous SINV inoculation. Similar to that described for CHIKV, infection in the periphery was detected early and was transient, whereas CNS infection started at later time points and was persistent or progressive. We then tested the possible mechanisms of neuroinvasion by CHIKV and SINV. Neither virus relied on macrophage-mediated transport to access the CNS. CHIKV, but not SINV, always infects endothelial cells of the brain vasculature. By contrast, axonal transport was much more efficient with SINV than CHIKV, both from the periphery to the CNS and between neural tissues. Thus, the preferred mechanisms of neuroinvasion by these two related viruses are distinct, providing a powerful imaging-friendly system to compare mechanisms and prevention methods of encephalopathies.

摘要

甲病毒,如基孔肯雅病毒(CHIKV)和辛德毕斯病毒(SINV),是媒介传播的病原体,可导致人类急性疾病,有时还与神经病变有关,尤其是在婴儿和老年患者中。关于它们进入中枢神经系统(CNS)的机制,人们知之甚少,即使是对于被广泛用作病毒性脑病模型的SINV也是如此。我们之前在光学透明的斑马鱼幼虫中建立了CHIKV感染模型;在此我们描述了该宿主中的一种新的SINV感染模型。我们对静脉注射SINV引起的感染的起始和进展进行了成像。与CHIKV的情况类似,外周感染早期即可检测到且是短暂的,而CNS感染在较晚时间点开始且是持续的或进行性的。然后我们测试了CHIKV和SINV可能的神经侵袭机制。两种病毒都不依赖巨噬细胞介导的转运来进入CNS。CHIKV总是感染脑血管的内皮细胞,而SINV则不然。相比之下,无论是从外周到CNS还是在神经组织之间,SINV的轴突运输都比CHIKV更有效。因此,这两种相关病毒的首选神经侵袭机制是不同的,这为比较脑病的机制和预防方法提供了一个强大的、对成像友好的系统。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b77/5536907/392653c2b23e/dmm-10-029231-g6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b77/5536907/8d99cf39a137/dmm-10-029231-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b77/5536907/2d5bc0563797/dmm-10-029231-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b77/5536907/8d250eedd7eb/dmm-10-029231-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b77/5536907/e9a28146c62b/dmm-10-029231-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b77/5536907/06d6cc13ecf0/dmm-10-029231-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b77/5536907/392653c2b23e/dmm-10-029231-g6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b77/5536907/8d99cf39a137/dmm-10-029231-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b77/5536907/2d5bc0563797/dmm-10-029231-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b77/5536907/8d250eedd7eb/dmm-10-029231-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b77/5536907/e9a28146c62b/dmm-10-029231-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b77/5536907/06d6cc13ecf0/dmm-10-029231-g5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b77/5536907/392653c2b23e/dmm-10-029231-g6.jpg

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