alexa Developing Strategies for Early Detection of Hepatitis B Infection
ISSN: 2327-5073

Clinical Microbiology: Open Access
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Research Article

Developing Strategies for Early Detection of Hepatitis B Infection

Saurabh Bandhavkar*

Department of Biochemistry, G. S. Medical College and KEM Hospital, Mumbai, Maharashtra, India

*Corresponding Author:
Saurabh Bandhavkar
Department of Biochemistry
G. S. Medical College and KEM Hospital
Mumbai, Maharashtra, India
Tel: +91-8879879008
E-mail: [email protected]

Received Date: January 20, 2016 Accepted Date: February 12, 2016 Published Date: February 19, 2016

Citation: Bandhavkar S (2016) Developing Strategies for Early Detection of Hepatitis B Infection. Clin Microbiol 5:234. doi: 10.4172/2327-5073.1000234

Copyright: © 2016 Bandhavkar S. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.



Hepatitis B caused by hepatitis B virus (HBV) is regarded as the most common form of chronic hepatitis worldwide. Around 15%-40% of people infected with HBV develop HBV-related complications and approximately 25% die as a result of these complications. Since HBV is infectious and spreads through blood, semen and other body fluids, it will be easy to detect the presence of this virus in these body fluids. Polymerase chain reactions (PCR) assays are often employed to detect these viruses in blood. While most of these assays generally rely on detection of HBV Surface Antigen (HBsAg) or hepatitis b core IgM Antibody (anti-HBc IgM), recent developments have made possible the detection of HBV DNA in blood. These assays, however, necessitate the requirement of adequate controls to distinguish true from false negative results. To address this issue, we have developed positive controls for Hepatitis B virus using molecular biology techniques. These controls can be used in PCR assays for detection of HBV by competitive amplification, thereby allowing detection of false negatives. The controls developed in this study were successfully tested with virus-seeded blood sample concentrates.


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