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Mechanism of selection of class II recombinant murine leukemia viruses in the highly leukemic strain CWD.

机译:高白血病株CWD中II类重组鼠白血病病毒的选择机制。

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摘要

The development of spontaneous lymphomas in CWD mice is associated with the expression of endogenous ecotropic murine leukemia viruses (MuLV) and the formation of recombinant viruses. However, the pattern of substitution of nonecotropic sequences within the envelope genes of the CWD class II recombinant viruses differs from that seen in class I recombinant MuLVs of AKR, C58, and HRS mice. To determine how CWD host genes might influence the envelope gene structure of the recombinant viruses, we characterized the responses of these mice to two different types of exogenous MuLVs. Neonatal mice injected the HRS class I recombinant PTV-1 became infected and developed T-cell lymphomas more rapidly than controls did. The inoculation of CWD mice with the leukemogenic AKR ecotropic virus SL3-3 led to the formation of recombinant MuLVs with a novel genetic structure and class II-like envelope genes, although SL3-3 generates class I recombinants in other strains. These results suggest that the absence of class I recombinant MuLVs in CWD mice is not related to the restriction of the replication or oncogenicity of class I viruses or to the absence of an appropriate ecotropic virus that can generate class I recombinants. More likely, the genes of CWD mice that direct the formation or selection of class II recombinant viruses affect the process of recombination between the ecotropic and nonecotropic envelope gene sequences.
机译:CWD小鼠中自发性淋巴瘤的发生与内源性嗜性鼠白血病病毒(MuLV)的表达和重组病毒的形成有关。但是,CWD II类重组病毒的包膜基因内非嗜性序列的替换模式不同于AKR,C58和HRS小鼠的I类重组MuLV。为了确定CWD宿主基因如何影响重组病毒的包膜基因结构,我们表征了这些小鼠对两种不同类型的外源MuLV的反应。注射HRS I类重组PTV-1的新生小鼠被感染并比对照组更快地发展为T细胞淋巴瘤。向CWD小鼠接种致白血病的AKR亲嗜性病毒SL3-3导致形成具有新型遗传结构和II类样包膜基因的重组MuLV,尽管SL3-3在其他菌株中产生I类重组体。这些结果表明在CWD小鼠中不存在I类重组MuLV与对I类病毒的复制或致癌性的限制或与可以产生I类重组体的合适的亲嗜性病毒的存在无关。指导II类重组病毒形成或选择的CWD小鼠基因更可能影响亲热和非亲热包膜基因序列之间的重组过程。

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