Mina Hannan - Department of Microbiology, Karaj Branch, Islamic Azad University, Karaj, Iran
Leila Jabalameli - Department of Microbiology, Karaj Branch, Islamic Azad University, Karaj, Iran
Mohammad Reza Aghasadeghi - Department of Hepatitis and AIDS and Blood Borne Diseases, Pasteur Institute of Iran, Tehran, Iran
Naser Harzandi - Department of Microbiology, Karaj Branch, Islamic Azad University, Karaj, Iran
Seyed Mehdi Sadat - Department of Hepatitis and AIDS and Blood Borne Diseases, Pasteur Institute of Iran, Tehran, Iran

Introduction: Hepatitis A virus (HAV) is a causative agent of acute hepatitis in humans, infecting more than one million individuals every year, including both symptomatic and asymptomatic infections. The currently available preventive vaccines for HAV are based on either wild-type or live-attenuated virus strains, which can contribute to the costliness of the vaccination process. Therefore, it may be worthwhile to explore the potential of subunit vaccines that utilize immunogenic viral products. Methods: This study presents the results of a novel recombinant protein production study that employed the native structures of HAV-VP۱ and HBs-Ag. The fusion protein underwent comprehensive characterization to evaluate its potential applications in diagnostics and immunization. The truncated recombinant protein, HAV-VP۱ (position ۹۹-۲۵۹ aa) -HBs-Ag, was successfully expressed in the Escherichia coli BL۲۱-DE۳ system. Results: The recombinant protein, with a molecular weight of ۴۶ kDa, was evaluated using SDS-PAGE gel electrophoresis and confirmed by western blotting. The fusion protein was successfully detected in serum samples positive for HBV or HAV using anti-HBs and anti-VP۱ antibodies. Additionally, it elicited a potent humoral response in BALB/c mice. Conclusion: The novel recombinant protein described in this study has the potential to serve as a bivalent vaccine against HAV and HBV infections. The next step involves evaluating the immunogenicity and safety profile of the protein.

Hepatitis A, Hepatitis B, Recombinant protein, Purification, Immunization, Diagnosis