Volume 15, Issue 4 (September 2012)
J Arak Uni Med Sci 2012, 15(4): 18-25 |
Back to browse issues page
Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
Paryan M, Mohammadi yeganeh S, Khansari nejad B, Mondanizadeh M, Paryan S. Rapid detection of HIV-1 viral RNA by real-time transcription mediated amplification assay. J Arak Uni Med Sci 2012; 15 (4) :18-25
URL: http://jams.arakmu.ac.ir/article-1-1220-en.html
URL: http://jams.arakmu.ac.ir/article-1-1220-en.html
Mahdi Paryan1 
, Samira Mohammadi yeganeh2 , Behzad Khansari nejad3 , Mahdieh Mondanizadeh4 , Saeed Paryan5
, Samira Mohammadi yeganeh2 , Behzad Khansari nejad3 , Mahdieh Mondanizadeh4 , Saeed Paryan5
1- pasteur institute , mparyan@gmail.com
2- pasteur institute
3- tarbiat modares university
4- medical university of hamedan
5- medical university of mashhad
2- pasteur institute
3- tarbiat modares university
4- medical university of hamedan
5- medical university of mashhad
Abstract: (17138 Views)
Background: Several different molecular methods have been developed that are capable of detecting HIV-1 in clinical specimens with different levels of sensitivity and specificity. This article describes the results of a reliability study on the development and application of a new real-time TMA method for isothermal detection of HIV-1. Materials and Methods: In this ex Primental study, the molecular beacon primer and probe set were designed for a 176-base-pair region of HIV-1 pol gene using a specialized software. Logarithmic serial dilutions from 10-107 copies of an in-vitro transcribed RNA were used for determination of the analytical sensitivity of the assay. Clinical specimens that had previously been evaluated positive or negative by a valid commercial assay were used for assessing the clinical sensitivity and specificity of the assay. Results: The analytical and clinical sensitivities of the assay were determined 500 copies/ml and 93.3%, respectively. The primers and the probe were HIV-1 specific and no cross-reaction was observed with other blood-borne viruses and human genome bioinformatically. The clinical specificity of the developed real-time TMA assay was examined experimentally using 20 negative samples and determined to be 100%. Conclusion: The developed real-time TMA assay can be used as an appropriate tool for the rapid and isothermal detection of HIV-1 in patients' blood and plasma samples.
Keywords: Human immunodeficiency virus-1, Molecular Beacon, Probe, Transcription mediated amplification
Send email to the article author
| Rights and permissions | |
 |
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. |
