Hepatitis B virus is a stealth virus that minimizes proteomic and secretomic changes in primary human hepatocytes
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F25%3A00641862" target="_blank" >RIV/61388963:_____/25:00641862 - isvavai.cz</a>
Result on the web
<a href="https://doi.org/10.1099/jgv.0.002170" target="_blank" >https://doi.org/10.1099/jgv.0.002170</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1099/jgv.0.002170" target="_blank" >10.1099/jgv.0.002170</a>
Alternative languages
Result language
angličtina
Original language name
Hepatitis B virus is a stealth virus that minimizes proteomic and secretomic changes in primary human hepatocytes
Original language description
Hepatitis B virus (HBV) is a hepatotropic DNA virus that infects over 250 million people worldwide and causes serious liver diseases. HBV infection can modulate host cellular processes, potentially inducing proteomic changes in hepatocytes. In this study, we investigated how acute HBV infection alters the proteome and secretome of primary human hepatocytes, a physiologically relevant in vitro model that retains essential liver-specific functions. Protein-level changes in cell lysates and culture supernatants were quantified 8 days post-infection using data-independent acquisition MS. We used HBV infection in the presence of the entry inhibitor bulevirtide as a control to separate the effects of productive infection from those caused by inoculum-associated components. Despite robust infection, active HBV replication induced only subtle changes in host protein levels. Orthogonal validation of MS-identified candidates confirmed reticulocalbin-2 as a novel host factor downregulated during productive HBV infection. The functional role of candidate proteins identified by MS was assessed in vitro by siRNA-mediated knockdown and measurement of viral replication markers. Knockdown had no impact on viral RNA or antigen levels, suggesting that the observed proteomic changes may reflect stress responses or broader modulation of the hepatic microenvironment. Our findings support the concept of HBV as a stealth virus and underscore the importance of carefully controlled experimental systems for studying host responses to infection in vitro.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10607 - Virology
Result continuities
Project
<a href="/en/project/LX22NPO5103" target="_blank" >LX22NPO5103: National Institute of Virology and Bacteriology</a><br>
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2025
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Journal of General Virology
ISSN
0022-1317
e-ISSN
1465-2099
Volume of the periodical
106
Issue of the periodical within the volume
11
Country of publishing house
GB - UNITED KINGDOM
Number of pages
18
Pages from-to
002170
UT code for WoS article
001622006800004
EID of the result in the Scopus database
2-s2.0-105021075849