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Evaluation of Dried Blood Spots Collected on Filter Papers from Three Manufacturers Stored at Ambient Temperature for Application in HIV-1 Drug Resistance Monitoring

机译:评价在室温下储存的三个制造商的滤纸上收集的干血斑,用于HIV-1耐药性监测

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摘要

As more HIV-infected people gain access to antiretroviral therapy (ART), monitoring HIV drug resistance (HIVDR) becomes essential to combat both acquired and transmitted HIVDR. Studies have demonstrated dried blood spots (DBS) are a suitable alternative in HIVDR monitoring using DBS collected on Whatman 903 (W-903). In this study, we sought to evaluate two other commercially available filter papers, Ahlstrom 226 (A-226) and Munktell TFN (M-TFN), for HIVDR genotyping following ambient temperature storage. DBS were prepared from remnant blood specimens collected from 334 ART patients and stored at ambient temperature for a median time of 30 days. HIV-1 viral load was determined using NucliSENS EasyQ® HIV-1 v2.0 RUO test kits prior to genotyping of the protease and reverse transcriptase regions of the HIV-1 pol gene using an in-house assay. Among the DBS tested, 26 specimens had a viral load ≥1000 copies/mL in all three types of filter paper and were included in the genotyping analysis. Genotyping efficiencies were similar between DBS collected on W-903 (92.3%), A-226 (88.5%), and M-TFN (92.3%) filter papers (P = 1.00). We identified 50 DR-associated mutations in DBS collected on W-903, 33 in DBS collected on A-226, and 48 in DBS collected on M-TFN, resulting in mutation detection sensitivities of 66.0% for A-226 and 88.0% for M-TFN when compared to W-903. Our data indicate that differences among filter papers may exist at this storage condition and warrant further studies evaluating filter paper type for HIVDR monitoring.
机译:随着越来越多的HIV感染者获得抗逆转录病毒疗法(ART),监视HIV耐药性(HIVDR)对于对抗获得性和传播性HIVDR至关重要。研究表明,使用Whatman 903(W-903)上收集的DBS,干血斑(DBS)是HIVDR监测的合适替代方法。在这项研究中,我们试图评估其他两种市售滤纸,Ahlstrom 226(A-226)和Munktell TFN(M-TFN),用于在环境温度存储后进行HIVDR基因分型。 DBS是从334名ART患者的残余血液样本中制备的,并在环境温度下保存30天。使用NucliSENSEasyQ®HIV-1 v2.0 RUO测试试剂盒确定HIV-1病毒载量,然后使用内部分析对HIV-1 pol基因的蛋白酶和逆转录酶区域进行基因分型。在所测试的DBS中,在所有三种类型的滤纸中,有26个样本的病毒载量≥1000拷贝/ mL,并包括在基因分型分析中。在W-903(92.3%),A-226(88.5%)和M-TFN(92.3%)滤纸上收集的DBS之间的基因分型效率相似(P = 1.00)。我们在W-903收集的DBS中鉴定了50个与DR相关的突变,在A-226收集的DBS中鉴定了33个,在M-TFN收集的DBS中鉴定了48个,导致A-226的突变检测敏感性为66.0%,对于A-226的突变检测敏感性为88.0%。与W-903相比,M-TFN。我们的数据表明,在这种储存条件下,滤纸之间可能存在差异,因此有必要进行进一步的研究,评估用于HIVDR监测的滤纸类型。

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