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在感染阿留申水貂病细小病毒的细胞中同时鉴定病毒蛋白和核酸。

Simultaneous identification of viral proteins and nucleic acids in cells infected with Aleutian mink disease parvovirus.

作者信息

Mori S, Wolfinbarger J B, Dowling N, Wei W, Bloom M E

机构信息

Laboratory of Persistent Viral Diseases, Rocky Mountain Laboratories, National Institutes of Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana 59840.

出版信息

Microb Pathog. 1990 Oct;9(4):243-53. doi: 10.1016/0882-4010(90)90013-g.

DOI:10.1016/0882-4010(90)90013-g
PMID:1965846
Abstract

A method combining in situ hybridization and immunohistochemistry was used to characterize cells infected with Aleutian mink disease parvovirus (ADV). Single-stranded RNA hybridization probes specific for obligate replicative intermediates and antisera specific for virion or non-structural proteins were employed. Crandell feline kidney cells in which the ADV-G strain of ADV was permissively replicating contained virion and non-structural proteins, large amounts of single stranded virion DNA, duplex replicative form (RF) DNA, and mRNA. Late in the infectious cycle, however, cells containing non-structural proteins but little nucleic acid were observed, probably representing cells in the end stage of viral cytopathology. Sections of lung prepared from mink kits infected with the ADV-Utah 1 strain were then examined. Alveolar type II cells permissively replicating ADV contained viral nucleic acids and proteins in patterns nearly identical to CRFK cells, suggesting that permissive ADV replication was similar in vitro and in vivo. Another population of ADV containing cells that had cytoplasmic virion antigen, but undetectable levels of non-structural protein was found in vivo. Furthermore, although virion DNA was present in the cytoplasm of these cells, RF DNA or mRNA could not be detected. These cells may have been alveolar macrophages sequestering viral particles.

摘要

采用原位杂交和免疫组织化学相结合的方法对感染阿留申水貂病细小病毒(ADV)的细胞进行特征分析。使用了针对专性复制中间体的单链RNA杂交探针以及针对病毒粒子或非结构蛋白的抗血清。允许ADV-G株ADV进行复制的克兰德尔猫肾细胞含有病毒粒子和非结构蛋白、大量单链病毒粒子DNA、双链复制型(RF)DNA和mRNA。然而,在感染周期后期,观察到含有非结构蛋白但核酸含量很少的细胞,可能代表处于病毒细胞病理学终末期的细胞。然后对感染ADV-犹他1株的水貂幼崽的肺组织切片进行检查。允许ADV复制的II型肺泡细胞所含病毒核酸和蛋白的模式与克兰德尔猫肾细胞几乎相同,这表明ADV在体外和体内的允许性复制相似。在体内发现了另一群含有ADV的细胞,这些细胞具有细胞质病毒粒子抗原,但非结构蛋白水平检测不到。此外,尽管这些细胞的细胞质中存在病毒粒子DNA,但未检测到RF DNA或mRNA。这些细胞可能是隔离病毒颗粒的肺泡巨噬细胞。

相似文献

1
Simultaneous identification of viral proteins and nucleic acids in cells infected with Aleutian mink disease parvovirus.在感染阿留申水貂病细小病毒的细胞中同时鉴定病毒蛋白和核酸。
Microb Pathog. 1990 Oct;9(4):243-53. doi: 10.1016/0882-4010(90)90013-g.
2
In situ molecular hybridization for detection of Aleutian mink disease parvovirus DNA by using strand-specific probes: identification of target cells for viral replication in cell cultures and in mink kits with virus-induced interstitial pneumonia.利用链特异性探针通过原位分子杂交检测阿留申水貂病细小病毒DNA:确定细胞培养物及患病毒诱导间质性肺炎的水貂幼崽中病毒复制的靶细胞
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APMIS Suppl. 1990;14:1-32.

引用本文的文献

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Replication of Aleutian mink disease parvovirus in vivo is influenced by residues in the VP2 protein.阿留申水貂病细小病毒在体内的复制受VP2蛋白中氨基酸残基的影响。
J Virol. 1999 Oct;73(10):8713-9. doi: 10.1128/JVI.73.10.8713-8719.1999.
2
Identification of a cell surface protein from Crandell feline kidney cells that specifically binds Aleutian mink disease parvovirus.从克兰德尔猫肾细胞中鉴定出一种特异性结合阿留申水貂病细小病毒的细胞表面蛋白。
J Virol. 1999 May;73(5):3835-42. doi: 10.1128/JVI.73.5.3835-3842.1999.
3
Subcellular localization of Aleutian mink disease parvovirus proteins and DNA during permissive infection of Crandell feline kidney cells.
阿留申水貂病细小病毒蛋白和DNA在克兰德尔猫肾细胞允许性感染过程中的亚细胞定位
J Virol. 1996 May;70(5):3242-7. doi: 10.1128/JVI.70.5.3242-3247.1996.
4
Characterization of chimeric full-length molecular clones of Aleutian mink disease parvovirus (ADV): identification of a determinant governing replication of ADV in cell culture.阿留申水貂病细小病毒(ADV)嵌合全长分子克隆的特性分析:确定细胞培养中ADV复制的决定因素。
J Virol. 1993 Oct;67(10):5976-88. doi: 10.1128/JVI.67.10.5976-5988.1993.
5
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Am J Pathol. 1994 Jun;144(6):1326-33.
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J Virol. 1995 Jun;69(6):3915-9. doi: 10.1128/JVI.69.6.3915-3919.1995.
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