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口蹄疫病毒O/JPN/2000弱毒株在实验感染猪中的致病机制

Pathogenesis of the attenuated foot-and-mouth disease virus O/JPN/2000 in experimentally infected pigs.

作者信息

Yamada Manabu, Fukai Katsuhiko, Morioka Kazuki, Nishi Tatsuya, Yamazoe Reiko, Kitano Rie, Shimada Nobuaki, Yoshida Kazuo, Kanno Toru, Sakamoto Kenichi, Yamakawa Makoto

机构信息

Exotic Disease Research Station, National Institute of Animal Health, National Agriculture and Food Research Organization, Kodaira, Tokyo 187-0022, Japan.

Hokkaido Research Station, National Institute of Animal Health, National Agriculture and Food Research Organization, Sapporo, Hokkaido 062-0045, Japan.

出版信息

J Vet Med Sci. 2018 Nov 9;80(11):1669-1675. doi: 10.1292/jvms.18-0377. Epub 2018 Sep 14.

DOI:10.1292/jvms.18-0377
PMID:30224577
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6261817/
Abstract

We examined the pathogenesis of the attenuated foot-and-mouth disease virus (FMDV) O/JPN/2000 in pigs. The virus used in this study was passaged three times in primary bovine kidney (BK) cells and once in baby hamster kidney-21 (BHK-21) cells after isolation. A plaque assay demonstrated that this virus exhibited the small plaque (SP) phenotype. There was no clinical or histological evidence of vesicular lesions in pigs intraorally inoculated with 10 50% tissue culture infectious dose (TCID)/ml of the SP virus (SPV) of FMDV O/JPN/2000. Although fever was detected from 2 or 3 days post inoculation (dpi), there was no other prominent clinical sign up to 6 dpi. Virus shedding from saliva and nasal swab samples was not observed in any pigs inoculated with the SPV of FMDV O/JPN/2000. In the foot, mild lamellar degeneration of prickle cells in the upper layer of the stratum spinosum was histologically observed without development into vesicular or necrotic lesions. Immunohistochemical virus antigen- and terminal deoxynucleotidyl transferase-mediated dUTP-nick end labeling (TUNEL)-positive reactions observed in the foot at 1 dpi seemed to disappear after 3 and 6 dpi. Our findings suggest that the SPV of FMDV O/JPN/2000 had low pathogenicity against pigs by intraoral inoculation.

摘要

我们研究了口蹄疫病毒(FMDV)O/JPN/2000弱毒株在猪体内的致病机制。本研究中使用的病毒在分离后,先在原代牛肾(BK)细胞中传代3次,再在幼仓鼠肾-21(BHK-21)细胞中传代1次。空斑试验表明,该病毒呈现小空斑(SP)表型。用1050%组织培养感染剂量(TCID)/ml的FMDV O/JPN/2000的SP病毒(SPV)经口接种猪后,没有出现水疱性病变的临床或组织学证据。虽然在接种后2或3天(dpi)检测到发热,但直到6 dpi都没有其他明显的临床症状。在任何接种FMDV O/JPN/2000的SPV的猪中,均未观察到唾液和鼻拭子样本中有病毒排出。在足部,组织学观察到棘层上层的棘细胞有轻度板层变性,但未发展成水疱或坏死性病变。在1 dpi时足部观察到的免疫组化病毒抗原和末端脱氧核苷酸转移酶介导的dUTP缺口末端标记(TUNEL)阳性反应在3和6 dpi后似乎消失。我们的研究结果表明,FMDV O/JPN/2000的SPV经口接种对猪的致病性较低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5844/6261817/52c97689bcf6/jvms-80-1669-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5844/6261817/e1a64035b4de/jvms-80-1669-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5844/6261817/52c97689bcf6/jvms-80-1669-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5844/6261817/e1a64035b4de/jvms-80-1669-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5844/6261817/52c97689bcf6/jvms-80-1669-g002.jpg

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本文引用的文献

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J Vet Med Sci. 2018 Apr 27;80(4):689-700. doi: 10.1292/jvms.17-0683. Epub 2018 Mar 6.
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Pathogenesis of virulent and attenuated foot-and-mouth disease virus in cattle.牛中强毒和弱毒口蹄疫病毒的发病机制
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Experimental infections using the foot-and-mouth disease virus O/JPN/2010 in animals administered a vaccine preserved for emergency use in Japan.
使用口蹄疫病毒O/JPN/2010对在日本保存用于紧急情况的疫苗接种的动物进行实验性感染。
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The Pathogenesis of Foot-and-Mouth Disease in Pigs.猪口蹄疫的发病机制。
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Dose-dependent responses of pigs infected with foot-and-mouth disease virus O/JPN/2010 by the intranasal and intraoral routes.经鼻内和口腔途径感染口蹄疫病毒O/JPN/2010的猪的剂量依赖性反应。
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