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E亚组重组病毒快速诱导骨硬化症

Rapid induction of osteopetrosis by subgroup E recombinant viruses.

作者信息

Morgan J H, Smith R E

出版信息

Virology. 1983 Sep;129(2):493-500. doi: 10.1016/0042-6822(83)90189-7.

Abstract

Avian osteopetrosis is a proliferative bone disorder initiated at high frequency by MAV-2(O), a subgroup B avian myeloblastosis-associated virus. To examine the role of the MAV-2(O) genome in osteopetrosis induction, a series of recombinant viruses between MAV-2(O) and RAV-O was constructed. Recombinant viruses were selected for rapid growth and subgroup E envelopes. The T1 oligonucleotide fingerprint patterns of viruses selected in this manner demonstrated that they were recombinants and were clonally pure because they had oligonucleotides from each parent, and each oligonucleotide was present in single molar yield. When injected into 10-day-old chicken embryos, approximately 50% of the recombinant viruses induced osteopetrosis within 3 weeks after hatch. Therefore, subgroup E envelope did not inhibit osteopetrosis induction. The osteopetrosis that was induced varied from slight to severe, but none of the recombinant viruses induced osteopetrosis as severe as the MAV-2(O) parent.

摘要

禽骨质石化症是一种增殖性骨病,由B亚群禽成髓细胞瘤相关病毒MAV-2(O)高频引发。为研究MAV-2(O)基因组在骨质石化症诱导中的作用,构建了一系列MAV-2(O)与RAV-O之间的重组病毒。选择重组病毒以实现快速生长并具有E亚群包膜。以这种方式选择的病毒的T1寡核苷酸指纹图谱表明它们是重组体且克隆纯,因为它们具有来自每个亲本的寡核苷酸,并且每个寡核苷酸以单摩尔产量存在。当注射到10日龄鸡胚中时,约50%的重组病毒在孵化后3周内诱导出骨质石化症。因此,E亚群包膜并不抑制骨质石化症的诱导。所诱导的骨质石化症从轻微到严重不等,但没有一种重组病毒诱导出与MAV-2(O)亲本一样严重的骨质石化症。

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