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Evolution of different antiviral strategies in wild mouse populations exposed to different gammaretroviruses

机译:暴露于不同γ逆转录病毒的野生小鼠种群中不同抗病毒策略的演变

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摘要

Laboratory mice carry 3 host range groups of gammaretroviruses all of which are linked to leukemia induction. Although polytropic mouse leukemia viruses (P-MLVs) are generally recognized as the proximate cause of MLV-induced leukemias in laboratory mice, wild mice that carry only endogenous P-MLVs do not produce infectious virus and are not prone to disease; these mice carry the permissive XPR1 retroviral receptor and an attenuated variant of the retroviral restriction factor, APOBEC3. In contrast, Eurasian mice carrying ecotropic and xenotropic MLVs have evolved multiple restrictive XPR1 variants, other factors that interfere with MLV entry, and more effectively antiviral variants of APOBEC3. These different antiviral restrictions in Mus musculus subspecies suggest that the different virus types found in these natural populations may pose different but largely uncharacterized survival risks in their host subspecies.
机译:实验小鼠携带3个宿主范围的γ逆转录病毒,所有这些都与白血病的诱导有关。尽管多变性小鼠白血病病毒(P-MLV)通常被认为是实验室小鼠MLV诱发的白血病的近因,但仅携带内源性P-MLV的野生小鼠不会产生传染性病毒,也不容易患病;这些小鼠携带许可的XPR1逆转录病毒受体和逆转录病毒限制因子APOBEC3的减毒变体。相比之下,携带亲和异种MLV的欧亚小鼠已经进化出多个限制性XPR1变体,其他干扰MLV进入的因素以及更有效的APOBEC3抗病毒变体。小家鼠亚种中的这些不同的抗病毒限制表明,在这些自然种群中发现的不同病毒类型可能在其寄主亚种中构成不同但基本上没有特征的生存风险。

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