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中国HIV-1基因多样性对病毒载量检测的影响

Impact of HIV-1 genetic diversity in China on the measurement of viral load.

作者信息

Wang Youchun, Song Aijing, Xu Sihong, Li Xiuhua, Chong Huihui, Zhao Chenyan, Nie Jianhui, Zhang Chuntao

机构信息

Department of Cell Biology, National Institute for the Control of Pharmaceutical and Biological Products, Beijing, PR China.

出版信息

J Med Virol. 2008 Jan;80(1):1-8. doi: 10.1002/jmv.21048.

Abstract

In this study, 190 HIV-positive samples were collected from different regions of China. The HIV clades of 153 samples were determined successfully based on env sequencing. Specifically, 48, 5, 87, and 13 isolates belonged to clades B', B, BC, and AE, respectively. The viral loads in all samples were measured using three commercial assays, Amplicor HIV-1 monitor v1.5, Nuclisens HIV-1 QT and NucliSens EasyQ HIV-1 assays. The differences and linear correlations for individual assays were compared, with expected 1:1 relationships. Significant differences were found for the following viral loads: clade BC measured by any two assays (P < 0.001); clade AE between Amplicor 1.5 and Easy Q (P = 0.005); clade B' between Amplicor 1.5 and Nuclisens QT (P = 0.002); clade AE between Amplicor 1.5 and Nuclisens QT (P = 0.025); and clade B' between Amplicor 1.5 and EasyQ (P = 0.04). The largest mean difference in the log(10) values was 0.9518, which was found between Amplicor 1.5 and Nuclisens QT. However, the viral loads for clades AE and B' measured by EasyQ and Nuclisens QT, and those for clade B measured by any two assays did not differ significantly. The degrees of correlation for clades B and B' between any two assays (R > 0.8) were higher that those for clades AE and BC between any two assays (R < 0.7), except for clade AE between Amplicor 1.5 and Easy Q. Thus, the clade types, especially clades BC and AE, are most likely to impact on the quantitation of viral load using differentassays.

摘要

在本研究中,从中国不同地区收集了190份HIV阳性样本。基于env测序成功确定了153份样本的HIV进化枝。具体而言,分别有48、5、87和13株分离株属于B'、B、BC和AE进化枝。使用三种商业检测方法,即Amplicor HIV-1 monitor v1.5、Nuclisens HIV-1 QT和NucliSens EasyQ HIV-1检测方法,对所有样本的病毒载量进行了测量。比较了各检测方法之间的差异和线性相关性,预期为1:1关系。发现以下病毒载量存在显著差异:任何两种检测方法测量的BC进化枝(P < 0.001);Amplicor 1.5和Easy Q之间的AE进化枝(P = 0.005);Amplicor 1.5和Nuclisens QT之间的B'进化枝(P = 0.002);Amplicor 1.5和Nuclisens QT之间的AE进化枝(P = 0.025);以及Amplicor 1.5和EasyQ之间的B'进化枝(P = 0.04)。log(10)值的最大平均差异为0.9518,出现在Amplicor 1.5和Nuclisens QT之间。然而,EasyQ和Nuclisens QT测量的AE和B'进化枝的病毒载量,以及任何两种检测方法测量的B进化枝的病毒载量之间没有显著差异。除了Amplicor 1.5和Easy Q之间的AE进化枝外,任何两种检测方法之间B和B'进化枝的相关性程度(R > 0.8)高于AE和BC进化枝之间的相关性程度(R < 0.7)。因此,进化枝类型,尤其是BC和AE进化枝,最有可能影响使用不同检测方法对病毒载量的定量。

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