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水貂阿留申病病毒体内外感染分析:感染水貂组织中阿留申病病毒DNA的证明

Analysis of Aleutian disease virus infection in vitro and in vivo: demonstration of Aleutian disease virus DNA in tissues of infected mink.

作者信息

Bloom M E, Race R E, Aasted B, Wolfinbarger J B

出版信息

J Virol. 1985 Sep;55(3):696-703. doi: 10.1128/JVI.55.3.696-703.1985.

Abstract

Aleutian disease virus (ADV) infection was analyzed in vivo and in vitro to compare virus replication in cell culture and in mink. Initial experiments compared cultures of Crandell feline kidney (CRFK) cells infected with the avirulent ADV-G strain or the highly virulent Utah I ADV. The number of ADV-infected cells was estimated by calculating the percentage of cells displaying ADV antigen by immunofluorescence (IFA), and several parameters of infection were determined. Infected cells contained large quantities of viral DNA (more than 10(5) genomes per infected cell) as estimated by dot-blot DNA-DNA hybridization, and much of the viral DNA, when analyzed by Southern blot hybridization, was found to be of a 4.8-kilobase-pair duplex monomeric replicative form (DM DNA). Furthermore, the cultures contained 7 to 67 fluorescence-forming units (FFU) per infected cell, and the ADV genome per FFU ratio ranged between 2 X 10(3) and 164 X 10(3). Finally, the pattern of viral antigen detected by IFA was characteristically nuclear, although cytoplasmic fluorescence was often found in the same cells. Because no difference was noted between the two virus strains when cultures containing similar numbers of infected cells were compared, it seemed that both viruses behaved similarly in infected cell culture. These data were used as a basis for the analysis of infection of mink by virulent Utah I ADV. Ten days after infection, the highest levels of viral DNA were detected in spleen (373 genomes per cell), mesenteric lymph node (MLN; 750 genomes per cell), and liver (373 genomes per cell). In marked contrast to infected CRFK cells, the predominant species of ADV DNA in all tissues was single-stranded virion DNA; however, 4.8-kilobase-pair DM DNA was found in MLN and spleen. This observation suggested that MLN and spleen were sites of virus replication, but that the DNA found in liver reflected sequestration of virus produced elsewhere. A final set of experiments examined MLN taken from nine mink 10 days after Utah I ADV infection. All of the nodes contained ADV DNA (46 to 750 genomes per cell), and although single-stranded virion DNA was always the most abundant species, DM DNA was observed. All of the lymph nodes contained virus infectious for CRFK cells, but when the genome per FFU ratio was calculated, virus from the lymph nodes required almost 1,000 times more genomes to produce an FFU than did virus prepared from infected cell cultures.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

对水貂阿留申病病毒(ADV)感染进行了体内和体外分析,以比较该病毒在细胞培养物和水貂体内的复制情况。最初的实验比较了用无毒力的ADV-G株或高毒力的犹他I型ADV感染的克兰德尔猫肾(CRFK)细胞培养物。通过免疫荧光法(IFA)计算显示ADV抗原的细胞百分比来估计被ADV感染的细胞数量,并确定了几个感染参数。通过斑点印迹DNA-DNA杂交估计,感染细胞含有大量病毒DNA(每个感染细胞超过10⁵个基因组),并且通过Southern印迹杂交分析发现,大部分病毒DNA是4.8千碱基对的双链单体复制形式(DM DNA)。此外,培养物中每个感染细胞含有7至67个荧光形成单位(FFU),每个FFU的ADV基因组比率在2×10³至164×10³之间。最后,IFA检测到的病毒抗原模式典型地为核内,尽管在同一细胞中经常发现胞质荧光。当比较含有相似数量感染细胞的培养物时,未发现两种病毒株之间有差异,似乎两种病毒在感染的细胞培养物中的行为相似。这些数据被用作分析高毒力的犹他I型ADV感染水貂的基础。感染后10天,在脾脏(每个细胞373个基因组)、肠系膜淋巴结(MLN;每个细胞750个基因组)和肝脏(每个细胞373个基因组)中检测到最高水平的病毒DNA。与感染的CRFK细胞形成鲜明对比的是,所有组织中ADV DNA的主要种类是单链病毒粒子DNA;然而,在MLN和脾脏中发现了4.8千碱基对的DM DNA。这一观察结果表明,MLN和脾脏是病毒复制的部位,但在肝脏中发现的DNA反映了在其他地方产生的病毒的隔离。最后一组实验检查了犹他I型ADV感染10天后取自9只水貂的MLN。所有淋巴结都含有ADV DNA(每个细胞46至750个基因组),尽管单链病毒粒子DNA总是最丰富的种类,但也观察到了DM DNA。所有淋巴结都含有对CRFK细胞有感染性的病毒,但是当计算每个FFU的基因组比率时,来自淋巴结的病毒产生一个FFU所需的基因组几乎是从感染细胞培养物中制备的病毒的1000倍。(摘要截短至400字)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3099/255047/cd664cd84288/jvirol00120-0192-a.jpg

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