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Sequence conservation in field and experimental isolates of Borna disease virus.博尔纳病病毒野外分离株和实验分离株中的序列保守性。
J Virol. 1994 Jan;68(1):63-8. doi: 10.1128/JVI.68.1.63-68.1994.
2
Sequence analyses of the p24 gene of Borna disease virus in naturally infected horse, donkey and sheep.自然感染的马、驴和绵羊中博尔纳病病毒p24基因的序列分析
Virus Res. 1994 Dec;34(3):281-9. doi: 10.1016/0168-1702(94)90128-7.
3
A borna virus cDNA encoding a protein recognized by antibodies in humans with behavioral diseases.一种博尔纳病毒cDNA,其编码一种可被患有行为疾病的人类体内抗体识别的蛋白质。
Science. 1990 Nov 30;250(4985):1278-81. doi: 10.1126/science.2244211.
4
Conservation of coding potential and terminal sequences in four different isolates of Borna disease virus.博尔纳病病毒四种不同分离株编码潜能和末端序列的保守性
J Gen Virol. 2001 Nov;82(Pt 11):2681-2690. doi: 10.1099/0022-1317-82-11-2681.
5
Detection of Borna disease virus RNA in naturally infected animals by a nested polymerase chain reaction.通过巢式聚合酶链反应检测自然感染动物中的博尔纳病病毒RNA
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Molecular biology of borna disease virus: prototype of a new group of animal viruses.博尔纳病病毒的分子生物学:一类新型动物病毒的原型
J Virol. 1994 Dec;68(12):7669-75. doi: 10.1128/JVI.68.12.7669-7675.1994.
7
Full-length genomic sequencing and characterization of Borna disease virus 1 isolates: Lessons in epidemiology.博尔纳病病毒1分离株的全长基因组测序与特征分析:流行病学经验教训
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8
Sequence variability of Borna disease virus open reading frame II found in human peripheral blood mononuclear cells.在人类外周血单核细胞中发现的博尔纳病病毒开放阅读框II的序列变异性。
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Detection of Borna disease virus (BDV) antibodies and BDV RNA in psychiatric patients: evidence for high sequence conservation of human blood-derived BDV RNA.精神疾病患者中博尔纳病病毒(BDV)抗体和BDV RNA的检测:人血源性BDV RNA高度序列保守性的证据
J Virol. 1996 Nov;70(11):7713-24. doi: 10.1128/JVI.70.11.7713-7724.1996.
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Varied prevalence of Borna disease virus infection in Arabic, thoroughbred and their cross-bred horses in Iran.伊朗阿拉伯马、纯种马及其杂交马中博尔纳病病毒感染的不同流行率。
Virus Res. 1996 Nov;45(1):1-13. doi: 10.1016/0168-1702(96)01355-x.

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Int J Mol Sci. 2024 Mar 20;25(6):3523. doi: 10.3390/ijms25063523.
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Contact-number-driven virus evolution: A multi-level modeling framework for the evolution of acute or persistent RNA virus infection.联系人数量驱动的病毒进化:急性或持续性 RNA 病毒感染进化的多层次建模框架。
PLoS Comput Biol. 2023 May 30;19(5):e1011173. doi: 10.1371/journal.pcbi.1011173. eCollection 2023 May.
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The bicolored white-toothed shrew Crocidura leucodon (HERMANN 1780) is an indigenous host of mammalian Borna disease virus.双色白齿鼩鼱(Crocidura leucodon)(赫尔曼,1780年)是哺乳动物博尔纳病病毒的本土宿主。
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Evolutionarily conserved interaction between the phosphoproteins and X proteins of bornaviruses from different vertebrate species.不同脊椎动物来源的博尔纳病毒的磷酸蛋白和 X 蛋白之间进化上保守的相互作用。
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Identification of host factors involved in borna disease virus cell entry through a small interfering RNA functional genetic screen.通过小干扰 RNA 功能遗传筛选鉴定参与博尔纳病病毒细胞进入的宿主因子。
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7
Cell entry of Borna disease virus follows a clathrin-mediated endocytosis pathway that requires Rab5 and microtubules.博尔纳病病毒的细胞进入遵循网格蛋白介导的内吞途径,该途径需要Rab5和微管。
J Virol. 2009 Oct;83(20):10406-16. doi: 10.1128/JVI.00990-09. Epub 2009 Aug 5.
8
Borna disease virus requires cholesterol in both cellular membrane and viral envelope for efficient cell entry.博尔纳病病毒在细胞膜和病毒包膜中都需要胆固醇才能有效地进入细胞。
J Virol. 2009 Mar;83(6):2655-62. doi: 10.1128/JVI.02206-08. Epub 2009 Jan 7.
9
Generation and characterization of a recombinant vesicular stomatitis virus expressing the glycoprotein of Borna disease virus.表达博尔纳病病毒糖蛋白的重组水疱性口炎病毒的产生及特性分析
J Virol. 2007 Jun;81(11):5527-36. doi: 10.1128/JVI.02586-06. Epub 2007 Mar 21.
10
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本文引用的文献

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Detection of antibodies against Borna disease virus in sera and cerebrospinal fluid of horses in the USA.美国马匹血清和脑脊液中博尔纳病病毒抗体的检测
Vet Rec. 1993 Mar 6;132(10):241-4. doi: 10.1136/vr.132.10.241.
2
Detection of Borna disease virus-reactive antibodies from patients with affective disorders by western immunoblot technique.采用蛋白质免疫印迹技术检测情感障碍患者中博尔纳病病毒反应性抗体。
J Affect Disord. 1993 Jan;27(1):61-8. doi: 10.1016/0165-0327(93)90098-5.
3
Precise missense and silent point mutations are fixed in the genomes of poliovirus mutants from persistently infected cells.精确的错义突变和沉默点突变在持续感染细胞来源的脊髓灰质炎病毒突变体基因组中固定下来。
J Virol. 1993 May;67(5):2914-7. doi: 10.1128/JVI.67.5.2914-2917.1993.
4
Clinically diseased cats with non-suppurative meningoencephalomyelitis have Borna disease virus-specific antibodies.患有非化脓性脑膜脑脊髓炎的临床患病猫具有博尔纳病病毒特异性抗体。
Acta Vet Scand. 1993;34(1):101-3. doi: 10.1186/BF03548230.
5
Genomic organization of the structural proteins of borna disease virus revealed by a cDNA clone encoding the 38-kDa protein.通过编码38 kDa蛋白的cDNA克隆揭示的博尔纳病病毒结构蛋白的基因组组织。
Virology. 1993 Jul;195(1):229-38. doi: 10.1006/viro.1993.1364.
6
Rapid evolution of RNA genomes.RNA基因组的快速进化。
Science. 1982 Mar 26;215(4540):1577-85. doi: 10.1126/science.7041255.
7
Replication of Borna disease virus in cell cultures.博尔纳病病毒在细胞培养物中的复制
Med Microbiol Immunol. 1980;168(3):153-8. doi: 10.1007/BF02122849.
8
Pathogenesis of Borna disease in rats: immune-mediated viral ophthalmoencephalopathy causing blindness and behavioral abnormalities.大鼠博尔纳病的发病机制:免疫介导的病毒性眼脑病变导致失明和行为异常。
J Infect Dis. 1983 Aug;148(2):305-15. doi: 10.1093/infdis/148.2.305.
9
Persistent, tolerant or subacute infection in Borna disease virus-infected rats.博尔纳病病毒感染大鼠中的持续性、耐受性或亚急性感染。
J Gen Virol. 1983 Jul;64 (Pt 7):1521-30. doi: 10.1099/0022-1317-64-7-1521.
10
Isolation and characterization of a 14500 molecular weight protein from brains and tissue cultures persistently infected with borna disease virus.从持续感染博尔纳病病毒的大脑和组织培养物中分离并鉴定一种分子量为14500的蛋白质。
J Gen Virol. 1985 Nov;66 ( Pt 11):2479-84. doi: 10.1099/0022-1317-66-11-2479.

博尔纳病病毒野外分离株和实验分离株中的序列保守性。

Sequence conservation in field and experimental isolates of Borna disease virus.

作者信息

Schneider P A, Briese T, Zimmermann W, Ludwig H, Lipkin W I

机构信息

Department of Microbiology and Molecular Genetics, University of California, Irvine 92717.

出版信息

J Virol. 1994 Jan;68(1):63-8. doi: 10.1128/JVI.68.1.63-68.1994.

DOI:10.1128/JVI.68.1.63-68.1994
PMID:8254777
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC236264/
Abstract

Coding and noncoding sequences were analyzed from field and experimental isolates of Borna disease virus. For a 24-kDa protein, maximum divergence was 1.5% at the predicted amino acid level and 3.1% at the nucleotide level. For a 40-kDa protein, maximum divergence was 1.1% at the predicted amino acid level and 4.1% at the nucleotide level. The highest variability in sequence (10%) was found in a 40-nucleotide stretch of genomic RNA between coding sequences for the 40- and 24-kDa proteins. The degree of sequence conservation in these isolates, passaged in various host species in vivo and in vitro over a period of 64 years, is unusual for negative-strand RNA viruses.

摘要

对博尔纳病病毒的野外分离株和实验分离株的编码及非编码序列进行了分析。对于一种24 kDa的蛋白质,预测氨基酸水平的最大差异为1.5%,核苷酸水平为3.1%。对于一种40 kDa的蛋白质,预测氨基酸水平的最大差异为1.1%,核苷酸水平为4.1%。在40 kDa和24 kDa蛋白质编码序列之间的一段40个核苷酸的基因组RNA中发现了最高的序列变异性(10%)。这些在64年的时间里在各种宿主物种体内和体外传代的分离株中的序列保守程度,对于负链RNA病毒来说是不寻常的。