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与弗瑞德相关的致麻痹性PVC - 441小鼠白血病病毒(MuLV)的完整核苷酸序列及其与PVC - 211 MuLV和弗瑞德MuLV的比较。

The entire nucleotide sequence of friend-related and paralysis-inducing PVC-441 murine leukemia virus (MuLV) and its comparison with those of PVC-211 MuLV and Friend MuLV.

作者信息

Tanaka A, Oka K, Tanaka K, Jinno A, Ruscetti S K, Kai K

机构信息

Department of Veterinary Microbiology, Faculty of Agriculture, Yamaguchi University, Yamaguchi City, Japan.

出版信息

J Virol. 1998 Apr;72(4):3423-6. doi: 10.1128/JVI.72.4.3423-3426.1998.

Abstract

PVC-441 murine leukemia virus (MuLV) is a member of the PVC group of Friend MuLV (F-MuLV)-derived neuropathogenic retroviruses. In order to determine the molecular basis for the difference in neuropathogenicity between PVC-441 and the previously characterized PVC-211 MuLVs, the entire nucleotide sequence of PVC-441 MuLV was determined and compared with those of PVC-211 and F-MuLV. The results suggest that PVC-441 and PVC-211 MuLVs were formed as a result of random mutations of F-MuLV and developed differently. The distinct pathogenicities of PVC-441 and PVC-211 MuLVs were maintained in the viruses regenerated from their molecular clones, and the sequences responsible for the pathological differences observed can be localized to the env gene. The amino acid sequence of PVC-441 deduced from its nucleotide sequence revealed a number of differences from PVC-211, the most striking of which was a difference at position 129 of the SU proteins in the two viruses. Host range studies with a brain capillary endothelial cell line (RTEC-6) and Chinese hamster ovary cells (CHO-K1) revealed that PVC-441, like PVC-211, could infect these cells but its efficiency of infection was lower than that of PVC-211. These results may account for the difference in neuropathogenicity between PVC-441 and PVC-211.

摘要

PVC - 441鼠白血病病毒(MuLV)是源自弗瑞德鼠白血病病毒(F - MuLV)的神经致病性逆转录病毒PVC组的成员。为了确定PVC - 441与先前已鉴定的PVC - 211 MuLV在神经致病性方面存在差异的分子基础,测定了PVC - 441 MuLV的完整核苷酸序列,并与PVC - 211和F - MuLV的核苷酸序列进行了比较。结果表明,PVC - 441和PVC - 211 MuLV是F - MuLV随机突变的结果,且发展方式不同。PVC - 441和PVC - 211 MuLV的独特致病性在从其分子克隆再生的病毒中得以保留,并且观察到的导致病理差异的序列可定位到env基因。从其核苷酸序列推导的PVC - 441氨基酸序列显示出与PVC - 211存在许多差异,其中最显著的是两种病毒的SU蛋白在第129位存在差异。对脑毛细血管内皮细胞系(RTEC - 6)和中国仓鼠卵巢细胞(CHO - K1)进行的宿主范围研究表明,PVC - 441与PVC - 211一样,可以感染这些细胞,但其感染效率低于PVC - 211。这些结果可能解释了PVC - 441和PVC - 211在神经致病性方面的差异。

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