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从澳大利亚原住民中分离出一株I型人类嗜T细胞病毒。

Isolation of a human T-lymphotropic virus type I strain from Australian aboriginals.

作者信息

Bastian I, Gardner J, Webb D, Gardner I

机构信息

Menzies School of Health Research, Casuarina, Darwin, Northern Territory, Australia.

出版信息

J Virol. 1993 Feb;67(2):843-51. doi: 10.1128/JVI.67.2.843-851.1993.

Abstract

A human T-lymphotropic virus type I (HTLV-I) strain was isolated in a CD4+ T-lymphocyte culture established from a healthy seropositive Australian Aboriginal. This isolate, identified as HTLV-IMSHR-1, was detected by immunofluorescence with monoclonal antibodies, by the presence of gag-encoded protein p24 in the culture supernatant, and by cocultivation leading to infection and transformation of lymphocytes from an HTLV-I-negative donor. By using the polymerase chain reaction technique, the env gene and segments of the pol and pX regions of the proviral genome of HTLV-I(MSHR-1) were amplified and sequenced. Comparison with the envelope sequences of prototype strains revealed up to 7% divergence at the nucleotide level and 3.1 to 4.3% divergence in the predicted amino acid sequence. Phylogenetic analysis showed that the Australian and Melanesian isolates are related. Differential reactivity with monoclonal antibodies suggests that gag protein p19 of HTLV-I(MSHR-1) is also divergent. The potential for antigenic divergence between the prototype HTLV-I isolates and the Austro-Melanesian variants requires further investigation, because it would have implications for serodiagnosis and vaccine development.

摘要

从一名血清反应阳性的健康澳大利亚原住民建立的CD4 + T淋巴细胞培养物中分离出一株I型人类嗜T淋巴细胞病毒(HTLV-I)。该分离株被鉴定为HTLV-IMSHR-1,通过用单克隆抗体进行免疫荧光检测、培养上清液中gag编码蛋白p24的存在以及共培养导致来自HTLV-I阴性供体的淋巴细胞感染和转化来检测。通过使用聚合酶链反应技术,扩增并测序了HTLV-I(MSHR-1)前病毒基因组的env基因以及pol和pX区域的片段。与原型株包膜序列的比较显示,核苷酸水平上的差异高达7%,预测氨基酸序列中的差异为3.1%至4.3%。系统发育分析表明,澳大利亚和美拉尼西亚分离株相关。与单克隆抗体的不同反应性表明HTLV-I(MSHR-1)的gag蛋白p19也存在差异。原型HTLV-I分离株与澳大拉西亚-美拉尼西亚变体之间抗原差异的可能性需要进一步研究,因为这将对血清学诊断和疫苗开发产生影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39dd/237438/53b14cbedad0/jvirol00023-0231-a.jpg

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