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活动性结核病的HIV感染者中HIV-1准种的多样性更高。

Greater diversity of HIV-1 quasispecies in HIV-infected individuals with active tuberculosis.

作者信息

Collins K R, Mayanja-Kizza H, Sullivan B A, Quiñones-Mateu M E, Toossi Z, Arts E J

机构信息

Division of Infectious Diseases, Department of Medicine, and Molecular Virology Training Program, Case Western Reserve University, Cleveland, Ohio 44106, USA.

出版信息

J Acquir Immune Defic Syndr. 2000 Aug 15;24(5):408-17. doi: 10.1097/00126334-200008150-00002.

Abstract

OBJECTIVE

A continual increase in intrapatient HIV-1 heterogeneity is thought to contribute to evasion of host immune response and eventual progression to AIDS. Tuberculosis (TB) is diagnosed both early and late during the course of HIV-1 disease and may increase diversity of HIV-1 quasispecies by activating the HIV-1 immune response and increasing HIV-1 replication. We examined whether HIV-1 heterogeneity is altered in HIV-1-infected individuals with TB.

METHODS

Blood samples were obtained from 7 HIV-1-infected patients with active TB (HIV/TB patients) and 9 HIV-1-infected patients (HIV patients) in Kampala, Uganda (CD4 counts of 0-650 cells/microl and HIV loads of 700-750,000 RNA copies/ml). The C2-C3 region of the HIV-1 envelope gene (env) was amplified by nested polymerase chain reaction (PCR) from lysed peripheral blood mononuclear cells (PBMCs) of each patient, and then subject to sequencing, clonal-quasispecies analysis and heteroduplex tracking analysis (HTA).

RESULTS

HTA of env DNA fragments showed increased heterogeneity in the HIV/TB individuals compared with the HIV group. Further sequence and HTA analysis on ten individual env clones for each patient showed significantly greater HIV mutation frequencies in HIV/TB patients than in HIV patients.

CONCLUSION

An increase in HIV-1 heterogeneity may be associated with a TB-mediated increase in HIV-1 replication. However, a diverse HIV-1 quasispecies population in HIV/TB patients as opposed to tight quasispecies clusters in HIV patients suggests a possible dissemination of lung-derived HIV-1 isolates from the TB-affected organ.

摘要

目的

患者体内HIV-1异质性的持续增加被认为有助于逃避免疫反应并最终发展为艾滋病。结核病(TB)在HIV-1疾病过程的早期和晚期均可被诊断出来,并且可能通过激活HIV-1免疫反应和增加HIV-1复制来增加HIV-1准种的多样性。我们研究了合并结核病的HIV-1感染者体内的HIV-1异质性是否发生改变。

方法

从乌干达坎帕拉的7例合并活动性结核病的HIV-1感染者(HIV/TB患者)和9例HIV-1感染者(HIV患者)中采集血样(CD4细胞计数为0 - 650个/微升,HIV载量为700 - 750,000个RNA拷贝/毫升)。通过巢式聚合酶链反应(PCR)从每位患者裂解的外周血单个核细胞(PBMC)中扩增HIV-1包膜基因(env)的C2 - C3区域,然后进行测序、克隆准种分析和异源双链跟踪分析(HTA)。

结果

与HIV组相比,HIV/TB个体的env DNA片段的HTA显示异质性增加。对每位患者的10个单个env克隆进行进一步的序列和HTA分析表明,HIV/TB患者的HIV突变频率显著高于HIV患者。

结论

HIV-1异质性增加可能与结核病介导的HIV-1复制增加有关。然而,HIV/TB患者中存在多样的HIV-1准种群体,而HIV患者中则为准种紧密聚类,这表明可能存在从受结核病影响的器官播散而来的源自肺部的HIV-1毒株。

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