Key result
The recombinant non-structural protein 3C Pro exhibited 96.9% sensitivity and 93.2% specificity for detecting anti-HAV IgM antibodies, outperforming capsid proteins for diagnostic use.
Why the study?
With an epidemiological transition in India leading to hepatitis A outbreaks in adolescents and young adults, timely diagnosis is needed, prompting exploration of HAV recombinant structural and non-structural proteins as diagnostic antigens.
Observational
The non-structural protein 3C Pro shows high sensitivity and specificity for detecting anti-HAV IgM and IgG antibodies, indicating its potential usefulness for developing hepatitis A diagnostic assays.
Hepatitis A virus (HAV) is a major causative agent of self-limiting liver infections. India was highly endemic for HAV in the past; children were exposed to the virus at an early age without any disease symptoms and developed lifelong immunity. With improvements in living conditions, an epidemiological transition is occurring. There is a significant increase in hepatitis A outbreaks involving adolescents and young adults. The gold standard for hepatitis A diagnosis is anti-HAV IgM antibodies. Although antibody responses are primarily targeted against HAV structural proteins (capsid proteins), non-structural proteins are also immunogenic. In the present study, we expressed HAV capsid proteins VP1-2A, VP0 (VP4 + VP2), VP3, and non-structural protein 3C Pro in the bacterial system and explored the possible use of these as antigens to detect anti-HAV IgM and IgG antibodies using a well-defined serum sample panel. The capsid protein-based assays showed overall less sensitivity for detection of both anti-HAV IgM and IgG antibodies as compared to whole virus antigen-based commercial assays. Among capsid proteins, rVP1-2A showed the highest sensitivity (86.3%) and specificity (84.2%) in detecting anti-HAV IgG, while rVP0 (VP2 + VP4) exhibited the highest sensitivity (79.5%) and specificity (80.2%) for IgM antibodies. Interestingly, r3C Pro exhibited higher sensitivity (96.9%) and specificity (93.2%) in IgM detection and 93.94% sensitivity and 88% specificity for IgG, indicating its usefulness in detecting both anti-HAV IgM and IgG antibodies during the acute phase of the disease. Though 3C Pro appeared to be useful in differentiating antibody responses due to infection and vaccination, our analysis revealed that the anti-3C Pro antibody response is short-lived after natural infection, and hence, it cannot be used as a marker to differentiate between infection and vaccination. However, 3C Pro would be useful for developing a hepatitis A diagnostic assay. IMPORTANCE Hepatitis A was highly endemic in India earlier. With recent developments, there is a shift in the endemicity to intermediate levels. This has resulted in the occurrence of hepatitis outbreaks with symptomatic infections in adolescents and adults. Occasionally, the disease manifestations are serious, leading to acute liver failure. In such a situation, there is a need for a timely diagnosis of the infection.
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Hunderkar et al. (2025) conducted an observational in Hepatitis A virus infection. Recombinant HAV proteins (VP1-2A, VP0, VP3, 3C Pro) vs. Whole virus antigen-based commercial assays was evaluated on Sensitivity and specificity for detecting anti-HAV IgM and IgG antibodies. The recombinant non-structural protein 3C Pro exhibited 96.9% sensitivity and 93.2% specificity for detecting anti-HAV IgM antibodies, outperforming capsid proteins for diagnostic use.
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