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猪肾细胞中猪腮腺炎病毒(LPMV)持续感染的建立与特性研究

Establishment and characterisation of a porcine rubulavirus (LPMV) persistent infection in porcine kidney cells.

作者信息

Hjertner B, Linné T, Moreno-López J

机构信息

Department of Veterinary Microbiology, Swedish University of Agricultural Sciences, Uppsala, Sweden.

出版信息

Acta Vet Scand. 1997;38(3):213-24. doi: 10.1186/BF03548484.

Abstract

Porcine rubulavirus (LPMV) can establish persistent infections in porcine kidney cells. Cell cultures characterised at passages 25 and 65 demonstrated haemadsorption, formation of syncytia, and a slower growth rate. The nucleoprotein (NP) and haemagglutinin-neuraminidase (HN) protein were present in all cells, although not to the same extent as in wild type infected cells. Incubation of the cell cultures with virus neutralising antibodies could not cure them from the infection. The cells were resistant to LPMV high multiplicity superinfection, but lysed rapidly upon infection with VSV. These cells thus fulfilled the criteria of a true persistent infection. Viral particles were released into the medium from the persistently infected cells as measured by HA and infection of PK-15 cells with medium from the persistently infected cells. The infectious titer of the virus released from the persistently infected cells was 3 logs lower compared to wild type virus, the HN titer still being comparable. Virus released from the persistently infected cells was unable to cause a lytic infection in PK-15 cells, and showed a reduced ability to spread when compared to a LPMV lytic infection.

摘要

猪副流感病毒(LPMV)可在猪肾细胞中建立持续性感染。在第25代和第65代传代时对细胞培养物进行的特征分析显示有血细胞吸附、多核巨细胞形成以及较慢的生长速率。核蛋白(NP)和血凝素神经氨酸酶(HN)蛋白在所有细胞中均有存在,尽管其程度与野生型感染细胞中的不同。用病毒中和抗体孵育细胞培养物并不能使其从感染中治愈。这些细胞对LPMV高复数重复感染具有抗性,但感染水疱性口炎病毒(VSV)后会迅速裂解。因此,这些细胞符合真正持续性感染的标准。通过血凝试验(HA)以及用来自持续性感染细胞的培养基感染PK - 15细胞检测发现,病毒颗粒从持续性感染细胞释放到培养基中。与野生型病毒相比,从持续性感染细胞释放的病毒的感染滴度低3个对数级,HN滴度仍具有可比性。从持续性感染细胞释放的病毒在PK - 15细胞中无法引起溶细胞性感染,并且与LPMV溶细胞性感染相比,其传播能力有所降低。

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Uptake of porcine rubulavirus (LPMV) by PK-15 cells.猪副流感病毒(LPMV)被PK - 15细胞摄取。
Arch Med Res. 2001 Sep-Oct;32(5):400-9. doi: 10.1016/s0188-4409(01)00314-9.

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