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Novel Postentry Resistance to AKV Ecotropic Mouse Gammaretroviruses in the African Pygmy Mouse Mus minutoides

机译:在非洲侏儒小鼠Mus minutoides中对AKV嗜性小鼠γ-逆转录病毒的新型进入后抗性

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摘要

Cells of Mus minutoides, an African pygmy mouse of the subgenus Nannomys, are susceptible to ecotropic Moloney and Friend mouse leukemia viruses (MLVs) but not to AKV-type MLVs. Transfected MA139 ferret cells expressing the mCAT-1 cell surface receptor, with the minCAT-1 substitutions K222Q and V233L, did not restrict AKV MLV. The resistance of M. minutoides cells to AKV MLV was not relieved by inhibitors of glycosylation or by the introduction of NIH 3T3 mCAT-1. Resistance is thus not mediated by receptor sequence variation, expression level, or glycosylation. M. minutoides cells are also infectible with LacZ pseudotypes having AKV Env and Moloney MLV (MoMLV) Gag proteins, further indicating that AKV Env sequence variations do not contribute to the observed block. The pattern of virus resistance in M. minutoides differs from that of the known variants of the Fv1 postentry resistance gene; M. minutoides is equally resistant to N-, B-, and NR-tropic AKV viruses and is equally susceptible to NR- and NB-tropic Friend MLVs. This novel resistance blocks replication before reverse transcription, whereas Fv1 generally restricts replication after reverse transcription; M. minutoides cells produce 2-long-terminal-repeat viral DNA circles and linear viral DNA after infection with MoMLV but not with AKV MLV. Analysis of MoMLV-AKV MLV chimeras determined that the target of resistance is in the virus capsid gene. Mutagenesis demonstrated that restriction is mediated by two amino acid substitutions, H117L and A110R; substitutions at these sites can also be targeted by the resistance genes Fv1 and TRIM5α. M. minutoides cells thus have a novel postentry resistance to AKV MLVs.
机译:细小家鼠(Mus minutoides)的细胞是Nannomys属的非洲侏儒鼠,对易嗜性Moloney和Friend小鼠白血病病毒(MLV)敏感,但对AKV型MLV则不敏感。表达了mCAT-1细胞表面受体的min139-1替代K222Q和V233L的转染MA139雪貂细胞不限制AKV MLV。糖基化抑制剂或NIH 3T3 mCAT-1的引入不能减轻小分枝杆菌对AKV MLV的抗性。因此,抗性不是由受体序列变化,表达水平或糖基化介导的。微小支原体细胞也可被具有AKV Env和Moloney MLV(MoMLV)Gag蛋白的LacZ假型感染,进一步表明AKV Env序列变异对观察到的阻滞没有贡献。 Minutoides中的病毒抗性模式与Fv1进入后抗性基因的已知变体不同。 minutoide分枝杆菌对N,B和NR嗜性AKV病毒具有同等抵抗力,并且对NR和NB嗜性Friend MLV同样易感。这种新颖的抗性可以阻止逆转录之前的复制,而Fv1通常会限制逆转录之后的复制。用MoMLV感染但不用AKV MLV感染后,微小支原体细胞会产生2个长末端重复的病毒DNA圈和线性病毒DNA。 MoMLV-AKV MLV嵌合体的分析确定抗性的靶标位于病毒衣壳基因中。诱变表明限制是由两个氨基酸取代介导的,即H117L和A110R。这些位点的取代也可以被抗性基因Fv1和TRIM5α靶向。因此,小分枝杆菌细胞对AKV MLV具有新的进入后抗性。

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