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Genetic mapping of reovirus virulence and organ tropism in severe combined immunodeficient mice: organ-specific virulence genes.

机译:严重的联合免疫缺陷小鼠中呼肠孤病毒毒力和器官嗜性的遗传作图:器官特异性毒力基因。

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摘要

We used reovirus reassortant genetics and severe combined immunodeficient (SCID) mice to define viral genes important for organ tropism and virulence in the absence of antigen-specific immunity. Adult SCID mice infected with reovirus serotype 1 strain Lang (T1L) died after 20 +/- 6 days, while infection with serotype 3 strain Dearing (T3D) was lethal after 77 +/- 22 days. One hundred forty-five adult SCID mice were infected with T1L, T3D, and 25 different T1L x T3D reassortant reoviruses, and gene segments associated with the increased virulence of T1L were identified. Gene segments S1, L2, M1, and L1 accounted for > 90% of the genetically determined increase in T1L virulence. Gene segment M1 was independently important for virulence, with S1, L2, and L1 alone or in combination also playing a role. T1L grew to higher titers in multiple organs and caused more severe hepatitis than T3D. Seventy adult SCID mice, T1L, T3D, and 15 T1L x T3D reassortant viruses were used to map genetic determinants of viral titers in the brain, intestines, and liver, as well as the severity of hepatitis. Different sets of gene segments were important for determining viral titers in different organs. Gene segments L1 (encoding a core protein) and L2 (encoding the core spike of the virion) were important in all of the organs analyzed. The M1 gene segment (encoding a core protein), but not the S1 gene segment, was a critical determinant of reovirus titer in the liver and severity of hepatitis. The S1 gene segment (encoding the viral cell attachment protein and a nonstructural protein), but not the M1 gene segment, was a critical determinant of titers in intestines and brains. These studies demonstrate that viral growth in different organs is dependent on different subsets of the genes important for virulence. The virion-associated protein products of the four gene segments (L1, L2, M1, and S1) important for virulence and organ tropism in SCID mice likely form a structural unit, the reovirus vertex. Organs (the brain and intestines versus the liver) differ in properties that determine which virulence genes, and thus which parts of this structural unit, are important.
机译:我们使用呼肠孤病毒重配基因和严重的联合免疫缺陷(SCID)小鼠定义了在缺乏抗原特异性免疫的情况下对器官嗜性和毒力重要的病毒基因。感染呼肠孤病毒血清型1血清Lang(T1L)的成年SCID小鼠在20 +/- 6天后死亡,而感染血清型3菌株Dearing(T3D)在77 +/- 22天后致死。 145只成年SCID小鼠感染了T1L,T3D和25种不同的T1L x T3D重配呼肠孤病毒,并鉴定了与T1L毒力增加相关的基因片段。基因区段S1,L2,M1和L1占遗传确定的T1L毒力增加的90%以上。 M1基因片段对于毒力是独立重要的,单独或联合使用S1,L2和L1也起作用。 T1L在多个器官中的滴度更高,并导致比T3D更严重的肝炎。使用70只成年SCID小鼠,T1L,T3D和15种T1L x T3D重配病毒来绘制大脑,肠道和肝脏中病毒滴度的遗传决定因素,以及肝炎的严重程度。不同组的基因片段对于确定不同器官中的病毒滴度很重要。基因片段L1(编码核心蛋白)和L2(编码病毒体的核心刺突)在所有分析的器官中都很重要。 M1基因片段(编码核心蛋白)而不是S1基因片段,是决定呼肠孤病毒在肝脏中滴度和肝炎严重程度的关键因素。 S1基因片段(编码病毒细胞附着蛋白和非结构蛋白)而不是M1基因片段,是决定肠道和大脑效价的关键因素。这些研究表明,不同器官中的病毒生长取决于对毒力重要的基因的不同子集。对SCID小鼠的毒力和器官嗜性很重要的四个基因片段(L1,L2,M1和S1)与病毒体相关的蛋白质产物可能形成了呼肠孤病毒的顶点,即一个结构单元。器官(大脑和肠道相对于肝脏)的属性不同,这决定了哪些毒力基因以及该结构单元的哪些部分很重要。

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