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TruGene 1型人类免疫缺陷病毒基因分型试剂盒及OpenGene DNA测序系统在稀释至每毫升约100拷贝的临床样本上的性能。

Performance of the TruGene human immunodeficiency virus type 1 genotyping kit and OpenGene DNA sequencing system on clinical samples diluted to approximately 100 copies per milliliter.

作者信息

Gale Howard B, Kan Virginia L, Shinol Rebecca C

机构信息

Infectious Diseases Section (151B), Veterans Affairs Medical Center, 50 Irving Street N.W., Washington, DC 20422, USA.

出版信息

Clin Vaccine Immunol. 2006 Feb;13(2):235-8. doi: 10.1128/CVI.13.2.235-238.2006.

Abstract

The TruGene human immunodeficiency virus type 1 (HIV-1) genotyping kit/OpenGene DNA sequencing system (Bayer HealthCare, Tarrytown, NY) reliably produced clinically acceptable resistance profiles for reverse transcriptase and protease inhibitors on patient samples diluted to approximately 100 copies/ml following extraction with the QIAamp viral RNA minikit (QIAGEN Inc., Valencia, CA). One modification of the standard protocol was made to guarantee PCR amplification: a centrifugation step to concentrate virus was added before RNA extraction. For genotypic antiretroviral resistance testing, no significant differences in the identification and sensitivity of detection for codon mutations, base mutations, and multibase sites were found between the original and diluted samples.

摘要

TruGene 1型人类免疫缺陷病毒(HIV-1)基因分型试剂盒/OpenGene DNA测序系统(拜耳医疗保健公司,纽约塔里敦)在用QIAamp病毒RNA微量提取试剂盒(QIAGEN公司,加利福尼亚瓦伦西亚)提取后,对稀释至约100拷贝/毫升的患者样本,能可靠地生成针对逆转录酶和蛋白酶抑制剂的临床可接受的耐药性图谱。为确保PCR扩增,对标准方案做了一处修改:在RNA提取前增加了一个浓缩病毒的离心步骤。对于基因型抗逆转录病毒耐药性检测,在原始样本和稀释样本之间,密码子突变、碱基突变和多位点的识别及检测灵敏度方面未发现显著差异。

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