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首页> 外文期刊>Journal of Clinical Microbiology >Development and Application of a Broadly Sensitive Dried-Blood-Spot-Based Genotyping Assay for Global Surveillance of HIV-1 Drug Resistance
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Development and Application of a Broadly Sensitive Dried-Blood-Spot-Based Genotyping Assay for Global Surveillance of HIV-1 Drug Resistance

机译:基于HIV-1耐药性全球监测的基于干血点的广泛敏感性基因分型分析方法的开发和应用

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As antiretroviral therapy (ART) is scaled up in resource-limited countries, surveillance for HIV drug resistance (DR) is vital to ensure sustained effectiveness of first-line ART. We have developed and applied a broadly sensitive dried-blood-spot (DBS)-based genotyping assay for surveillance of HIV-1 DR in international settings. In 2005 and 2006, 171 DBS samples were collected under field conditions from newly diagnosed HIV-1-infected individuals from Malawi (n = 58), Tanzania (n = 60), and China (n =53). In addition, 30 DBS and 40 plasma specimens collected from ART patients in China and Cameroon, respectively, were also tested. Of the 171 DBS analyzed at the protease and RT regions, 149 (87.1%) could be genotyped, including 49 (81.7%) from Tanzania, 47 (88.7%) from China, and 53 (91.4%) from Malawi. Among the 70 ART patient samples analyzed, 100% (30/30) of the Chinese DBS and 90% (36/40) of the Cameroonian plasma specimens were genotyped, including 8 samples with a viral load of <400 copies/ml. The results of phylogenetic analyses indicated that the subtype, circulating recombinant form (CRF), and unique recombinant form (URF) distribution was as follows: 73 strains were subtype C (34%), 37 were subtype B (17.2%), 24 each were CRF01_AE or CRF02_AG (11.2% each), 22 were subtype A1 (10.2%), and 9 were unclassifiable (UC) (4.2%). The remaining samples were minor strains comprised of 6 that were CRF07_BC (2.8%), 5 that were CRF10_CD (2.3%), 3 each that were URF_A1C and CRF08_BC (1.4%), 2 each that were G, URF_BC, and URF_D/UC (0.9%), and 1 each that were subtype F1, subtype F2, and URF_A1D (0.5%). Our results indicate that this broadly sensitive genotyping assay can be used to genotype DBS collected from areas with diverse HIV-1 group M subtypes and CRFs. Thus, the assay is likely to become a useful screening tool in the global resistance surveillance and monitoring of HIV-1 where multiple subtypes and CRFs are found.
机译:随着在资源有限的国家扩大抗逆转录病毒疗法(ART)的规模,对HIV耐药性(DR)的监视对于确保一线抗病毒治疗的持续有效性至关重要。我们已经开发并应用了一种基于广泛敏感的干血斑(DBS)的基因型分析方法,用于在国际环境中监测HIV-1 DR。在2005年和2006年,在野外条件下,从马拉维( n = 58),坦桑尼亚( n = 60)的新诊断出HIV-1感染者中采集了171个DBS样本。 ,以及中国( n = 53)。此外,还对分别从中国和喀麦隆的ART患者收集的30个DBS和40个血浆标本进行了测试。在蛋白酶和RT区域分析的171个DBS中,有149个(87.1%)可以进行基因分型,包括来自坦桑尼亚的49个(81.7%),来自中国的47个(88.7%)和来自马拉维的53个(91.4%)。在分析的70例ART患者样本中,对100%(30/30)的中国DBS和90%(36/40)的喀麦隆血浆样本进行了基因分型,包括8个病毒载量小于400拷贝/毫升的样本。系统发育分析结果表明,亚型,循环重组体(CRF)和独特重组体(URF)分布如下:C亚型73株(34%),B亚型37株(17.2%),各24株分别是CRF01_AE或CRF02_AG(各为11.2%),22个为A1亚型(10.2%)和9个为无法分类(UC)(4.2%)。其余样本为次要菌株,其中包括CRF07_BC(2.8%)6个,CRF10_CD(2.3%)5个,URF_A1C和CRF08_BC 3个(1.4%),G,URF_BC和URF_D / UC 2个(0.9%),以及分别为F1,F2和URF_A1D(0.5%)的1个。我们的结果表明,这种广泛敏感的基因分型测定法可用于对从具有多种HIV-1 M组亚型和CRF区域的DBS进行基因分型。因此,该测定法可能会成为在发现多种亚型和CRF的HIV-1的全球耐药性监测和监测中的有用筛选工具。

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