Sequence-Specific Detection Method for Reverse Transcription, Loop-Mediated Isothermal Amplification of HIV-1

被引:59
作者
Curtis, Kelly A. [1 ]
Rudolph, Donna L. [1 ]
Owen, Michele [1 ]
机构
[1] Ctr Dis Control & Prevent, Branch Lab, Div HIV AIDS Prevent, Natl Ctr HIV AIDS Hepatitis STD & TB Prevent, Atlanta, GA 30333 USA
关键词
loop-mediated isothermal amplification; HIV-1; nucleic acid amplification; RAPID DETECTION; DNA AMPLIFICATION; VISUAL DETECTION; LAMP; INFECTION; DIAGNOSIS; VIRUS; HYBRIDIZATION; TUBERCULOSIS; STATE;
D O I
10.1002/jmv.21490
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
HIV diagnosis at the point-of-care or in resource-limited settings poses considerable challenges due to time and cost limitations. Currently, nucleic acid-based tests are the only reliable method for diagnosing recent infections during the window period post-infection and pre-sero-conversion, but these tests are only suitable for well-equipped laboratory settings. The reverse transcription loop-mediated isothermal amplification (RT-LAMP) technology exhibits characteristics that are ideal for the development of a rapid, cost-effective nucleic acid-based test for detection of HIV DNA and RNA. In this study, a sequence-specific detection method was developed for immediate, naked-eye visualization of RT-LAMP products with high sensitivity and specificity. The rapid detection method was incorporated into the HIV-1-specific RT-LAMP assay and validated using minute volumes of whole blood from HIV-1-infected individuals. Together with the minimal sample preparation time and one-step, isothermal amplification reaction, the sequence-specific detection method adds to the overall versatility of the RT-LAMP assay and enhances the applicability for use at point-of-care or resource-limited sites. J. Med. Virol. 81:966-972, 2009. Publislied 2009 Wiley-Liss, Inc.dagger
引用
收藏
页码:966 / 972
页数:7
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