Development of a two-step HCV quantification assay based on third generation evagreen dye for real-time PCR : a pilot study /
HCV exhibits extreme genome heterogeneity, additionally it is usually present in blood at a low copy number. Thus, high specificity and sensitivity represent a major challenge during development of any HCV detection and quantification assay. The aim of the present study was to establish a highly spe...
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| Main Author: | |
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| Format: | Thesis |
| Language: | English |
| Published: |
Kuantan, Pahang :
Kulliyyah of Medicine, International Islamic University Malaysia,
2016
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| Subjects: | |
| Online Access: | Click here to view 1st 24 pages of the thesis. Members can view fulltext at the specified PCs in the library. |
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| LEADER | 032790000a22002770004500 | ||
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| 008 | 160211t2016 my a g m 000 0 eng d | ||
| 040 | |a UIAM |b eng | ||
| 041 | |a eng | ||
| 043 | |a a-my--- | ||
| 050 | 0 | 0 | |a RC848.H425 |
| 100 | 1 | |a Habil, Akrahm M. Saleh | |
| 245 | 1 | |a Development of a two-step HCV quantification assay based on third generation evagreen dye for real-time PCR : |b a pilot study / |c by Akrahm M. Saleh Habil | |
| 260 | |a Kuantan, Pahang : |b Kulliyyah of Medicine, International Islamic University Malaysia, |c 2016 | ||
| 300 | |a xii, 68 leaves : |b ill. ; |c 30cm. | ||
| 502 | |a Thesis (MMDS)--International Islamic University Malaysia, 2016. | ||
| 504 | |a Includes bibliographical references (leaves 55-67). | ||
| 520 | |a HCV exhibits extreme genome heterogeneity, additionally it is usually present in blood at a low copy number. Thus, high specificity and sensitivity represent a major challenge during development of any HCV detection and quantification assay. The aim of the present study was to establish a highly specific and sensitive semi-nested real time PCR using EvaGreen dye for detecting and quantifying HCV RNA. A total of 50 serum samples, comprising 40 HCV- positive and 10 HCV-negative, were included in our study. RNA was extracted, reverse transcribed, and then subjected to two rounds of PCR amplification. In the first round, conventional PCR was performed using a pair of primers targeting the 5'UTR. In the second round, real time PCR using EvaGreen dye and primers targeting a region within the previously amplified product was carried out for sensitive detection and quantification. Reference samplesnumber 15 and 39with known viral load were treated similarly to the unknown samples and used to create the standard curves.Our method showed a high level of analytical specificity and accuracy, with a low limit of detection (~2 IU/ml). It yielded repeatable results with less than 4% of intra- assay variation. The assay covered a broad dynamic range of quantification, ranging from 0.34 to 6 log IU/ml. The diagnostic sensitivity, specificity, and accuracy were all 100%, indicating neither false positive nor false negative results were obtained. The newly developed semi-nested real time PCR using EvaGreen has demonstrated a high analytical and diagnostic performance, suggesting its potential to have wide applications in clinical diagnosis, therapeutic management, and epidemiological studies of HCV. | ||
| 596 | |a 1 6 | ||
| 655 | 7 | |a Theses, IIUM local | |
| 690 | |a Dissertations, Academic |x Department of Basic Medical Sciences |z IIUM | ||
| 710 | 2 | |a International Islamic University Malaysia. |b Department of Basic Medical Sciences | |
| 856 | 4 | |u https://lib.iium.edu.my/mom/services/mom/document/getFile/5AfhxAsRue9bAiAbR74a0YZqdUB12Dnc20160530123047366 |z Click here to view 1st 24 pages of the thesis. Members can view fulltext at the specified PCs in the library. | |
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| 952 | |0 0 |6 TS CDF RC 848 H425 H116D 2016 |7 0 |8 THESES |9 854229 |a IIUM |b IIUM |c MULTIMEDIA |g 0.00 |o ts cdf RC 848 H425 H116D 2016 |p 11100344086 |r 2017-10-26 |t 1 |v 0.00 |y THESISDIG | ||