quantifying hepatitis b virus (hbv) dna in human serum samples using real-time pcr

Detection and Quantification of Hepatitis B Virus DNA in Human Serum

Hepatitis B virus (HBV) is a partially double-stranded DNA virus from the genus Orthohepadnavirus and the Hepadnaviridae family1. It can trigger a chronic infection that persists throughout one&#39;s life, potentially leading to liver cirrhosis and hepatocellular carcinoma2,3,4. According to the World Health Organization (WHO), an estimated population of 296 million people were living with chronic hepatitis B infection in 2019, and 1.5 million people were newly infected each year5.
The identification and measurement of HBV DNA in serum or plasma samples serve as a valuable method for detecting individuals with an ongoing hepatitis B infection, assessing the efficacy of antiviral treatment, and predicting the probability of treatment success6,7,8,9,10,11. High viral load is associated with an increased risk of liver disease progression, including cirrhosis and liver cancer12,13. Hence, precise measurement of viral load is crucial for tracking the progression of HBV infection and informing decisions regarding treatment.
Quantitative real-time PCR assays have higher sensitivity, broader dynamic range, and more accurate quantification of HBV DNA than conventional PCR techniques14,15,16,17. Several commercial real-time PCR-based molecular diagnostic kits for the quantitation of HBV DNA in serum or plasma samples are available in the market. Here, we describe a detailed workflow for the detection and quantification of HBV DNA in human serum or plasma using a commercially available, IVD-marked real-time PCR-based kit. The kit is a widely used18,19, low-cost, yet highly sensitive assay, and its performance characteristics are comparable with other commercially available CE-marked kit(s)18. Apart from the HBV target region amplification, an endogenous internal control gene is also included in the kit to verify the quality of samples, quality of extracted DNA, PCR amplification, and possible PCR inhibition.

Author Spotlight: Advancements and Challenges in Hepatitis B Virus Detection 

Real-Time Polymerase Chain Reaction-Based Detection and Quantification of Hepatitis B Virus DNA

In this video, we will show you a step-by-step protocol to detect HBV DNA and quantify its viral load using our IVD approved real-time PCR waste, through PCR HBV viral load kit. HBV diagnosis research uses, real time PCR, digital PCR, NGS and serological tests. Realtime PCR is the gold standard for HBV DNA detection and viral load quantification.Digital PCR quantifies absolute viral load. NGS identifies new mutations and serological tests detect antigens or antibodies. There are several experimental challenges with detecting low viral load cases and occult HBV infections.Some assays may not fall from well across all HBV genotypes and emerging new mutations may lead to false negative results. Compared to other techniques the realtime PCR based protocol is the most sensitive, specific and quantitative method available for HBV detection. It is also a relatively fast technique, which makes it ideal for clinical use.

Watch this Scientific Journal Video about Quantifying Hepatitis B Virus HBV DNA in Human Serum Samples Using Real-Time PCR at JoVE.com

Quantifying Hepatitis B Virus (HBV) DNA in Human Serum Samples Using Real-Time PCR  

To begin, thaw all reagents provided in the real-time PCR kit at room temperature. Once thawed, pulse vortex the components for 10 seconds at a moderate speed to mix them. Then, centrifuge at 8, 000G for 10 seconds at room temperature.Keep the thawed components on a cooling block. Next, prepare a PCR mix for an HBV positive sample, five HBV standards, and no template control. Thoroughly mix the added reagents by gently pipetting seven to 10 times, followed by pulse vortexing, and centrifuge at 8, 000G for 10 seconds at room temperature.Then, pipette 15 microliters of the PCR mix into each PCR tube. Add 15 microliters of extracted DNA sample, five HBV standards, and nuclease free water as a no template control. Close the PCR tubes and briefly spin in the centrifuge.Load the PCR tubes in a real-time PCR machine. Now, initiate the thermal cycler software. Choose fluorescent dyes and program the thermal cycler for real-time PCR.Post run, analyze the amplification plot using a linear scale. Set the PCR reaction threshold within the exponential phase. Maintain consistency in threshold settings for accuracy and reproducibility.Use the same threshold for all samples on a specific PCR machine. Consider samples with amplification before CD value 38 as HBV positive based on the assay's cutoff. Use five quantification standards for HBV-specific DNA, calibrated against the Fourth WHO international standard for HBV DNA.Generate a standard curve with these standards to quantify HBV DNA in unknown samples. Interpret values for unknown samples only if the standard curve slope is between minus 3.1 and minus 3.6, the R square value is between 0.99 and 1.0, PCR efficiency is within 90%to 110%and there is no amplification in the negative control.

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293 Views.  3B BlackBio Biotech India Limited. To begin, thaw all reagents provided in the real-time PCR kit at room temperature. Once thawed, pulse vortex the components for 10 seconds at a moderate speed to mix them. Then, centrifuge at 8, 000G for 10 seconds at room temperature.Keep the thawed components on a cooling block. Next, prepare a PCR mix for an HBV positive sample, five HBV standards, and no template control. Thoroughly mix the added reagents by gently pipetting seven to 10 times, followed by pulse vortexing, and centr...

Video: Quantifying Hepatitis B Virus (HBV) DNA in Human Serum Samples Using Real-Time PCR  

Hepatitis B virus (HBV) is a significant cause of liver disease worldwide. It can lead to acute or chronic infections, making individuals highly susceptible to fatal cirrhosis and liver cancer. Accurate detection and quantification of HBV DNA in the blood are essential for diagnosing and monitoring HBV infection. The most common method for detecting HBV DNA is real-time PCR, which can be used to detect the virus and assess the viral load to monitor the response to antiviral therapy. Here, we describe a detailed protocol for the detection and quantification of HBV DNA in human serum or plasma using an IVD-marked real-time PCR-based kit. The kit uses primers and probes that target the highly conserved core region of the HBV genome and can accurately quantify all HBV genotypes (A, B, C, D, E, F, G, H, I, and J). The kit also includes an endogenous internal control to monitor possible PCR inhibition. This assay runs for 40 cycles, and its cutoff is 38 Ct. For the quantification of HBV DNA in clinical samples, a set of 5 quantification standards is provided with the kit. The standards contain known concentrations of HBV-specific DNA that are calibrated against the 4th WHO International Standard for HBV DNA for the nucleic acid test (NIBSC code 10/266). The standards are used to validate the functionality of the HBV-specific DNA amplification and to generate a standard curve, allowing the quantification of HBV DNA in a sample. HBV DNA as low as 2.5 IU/mL was detected using the PCR kit. The high sensitivity and reproducibility of the kit make it a powerful tool in clinical laboratories, aiding healthcare professionals in effectively diagnosing and managing HBV infections.

Real-time polymerase chain reaction (PCR)-based detection and quantification of hepatitis B virus (HBV) DNA is a sensitive and accurate method for diagnosing and monitoring HBV infection. Here, we present a protocol for HBV DNA detection and the viral load measurement of a sample.