The impact of storage time on HCV RNA quantitative detection in serum samples by TaqMan real-time PCR
نویسندگان
چکیده
Information on the concentration of hepatitis C virus (HCV) RNA is useful for patient management, including assessing treatment initiation and treatment response, and monitoring follow-up. Previous studies have reported that poor sample processing and storage conditions might influence the stability of HCV RNA, and hence its detectability. We analyzed 30 patients known to be positive with high/intermediate/low HCV RNA load, and kept their serum samples in storage at 4°C for 0, 1, 2, 3, 7, 14, 21 and 28 days. Quantitative detection of HCV RNA was performed by TaqMan real-time PCR. The results showed that no decrease in the concentration of HCV RNA was detected over the 14 days period at 4°C (P > 0.05) for the high and intermediate HCV RNA load groups. However, after 21 and 28 days of storage, the mean viral loads in both groups differed significantly from those at Day 0 (P > 0.005). For the low HCV RNA load group, an important loss of HCV RNA concentration was observed when the serums were stored at 4°C after 14 days, 21 days and 28 days (P < 0.001). These data demonstrated that serum samples with HCV RNA levels up to 104 IU/ml can be stored at 4°C for 14 days, and that lower than 104 IU/ml can be performed for up to only 7 days when the samples are stored at 4°C.
منابع مشابه
Development of an In-House TaqMan Real Time RT-PCR Assay to Quantify Hepatitis C Virus RNA in Serum and Peripheral Blood Mononuclear Cells in Patients With Chronic Hepatitis C Virus Infection
BACKGROUND Viral load measurements are commonly used to monitor HCV infection in patients with chronic diseases or determining the number of HCV-genomes in serum samples of patients after sustained virological response. However, in some patients, HCV viral load in serum samples is too low to be detected by PCR, especially after treatment. OBJECTIVES The aim of this study was to develop a high...
متن کاملتعیین کمی بار ویروسی هپاتیت C با استفاده از روش Real-Time PCR In-House در بیماران آلوده به هپاتیت C در شهرستان خرم آباد
Background : Molecular diagnostic methods are among major tools in management of hepatitis C virus (HCV) in infected patients. Many studies have shown that viral load is associated with stage of infection and response to treatment. Therefore, the evaluation and quantification of viral load is very important. The goal of this study is implementation of inexpensive, yet accurate method for quanti...
متن کاملEvaluation of a new set of Real-Time PCR for Brucella detection within human and animal samples
A quantitative TaqMn Real-Time PCR assay was developed and its diagnostic value on human serum and livestock samples were evaluated. Brucella species could be distributed through communities as a biological agent. Rapid detection of biological threat agents is critical for timely therapeutic administration. Quantitative real-time PCR provides a rapid, sensitive and specific tool for molecular i...
متن کاملDevelopment and Evaluation of Real-Time Reverse Transcription Polymerase Chain Reaction Test for Quantitative and Qualitative Recognition of H5 Subtype of Avian Influenza Viruses
Avian influenza viruses (AIV) affect a wide range of birds and mammals, cause severe economic damage to the poultry industry, and pose a serious threat to humans. Highly pathogenic avian influenza viruses (HPAI) H5N1 were first identified in Southeast Asia in 1996 and spread to four continents over the following years. The viruses have caused high mortality in chickens and various bird species ...
متن کاملTaqMan real-time PCR: a reliable method to detect meat species
The aim of this study was to detect and identify meat species (beef, lamb, pork, chicken, donkey, and horse) in Kebab as a Halal meat-based food sold in on-road-restaurants of North Khorasan province (Iran) using TaqMan real-time polymerase chain reaction (PCR). Raw Kebab samples (150 samples) were obtained from on-road restaurants. The samples were prepared, DNA was extracted and TaqMan real-t...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره شماره
صفحات -
تاریخ انتشار 2016