Screening of different species reveals cat hepatocytes support HBV infection

Hepatitis B virus (HBV) remains a major public health challenge, with nearly 300 million chronic infections, yet research is hindered by the lack of suitable animal models. This study aimed to identify HBV-susceptible species and establish a novel infection model. Primary hepatocytes from humans, cats, rabbits, Syrian hamsters, Siberian hamsters, guinea pigs, bulls, goats, pigs, cynomolgus macaques, and dogs were assessed for HBV entry using hepatitis D virus (HDV) infection. HBV relaxed circular DNA (rcDNA) transfection was performed to evaluate its repair into covalently closed circular DNA (cccDNA). HBV infection assays were conducted in vitro. Results showed that primary hepatocytes from humans and cats were susceptible to HDV, suggesting their potential to support HBV entry. All tested hepatocytes converted rcDNA into cccDNA, confirming their ability to complete early HBV replication steps. Notably, cat hepatocytes uniquely supported HBV infection, displaying time-dependent viral replication marker expression. Cat hepatocytes also responded to antiviral treatments, underscoring their relevance for drug evaluation. This study provides the first evidence that cats can support HBV infection in vitro, offering a promising new platform for HBV research and antiviral development.

Authors

Institutions

Publication Details

Journal
PLoS Pathogens
Published
2025-08-04
DOI
https://doi.org/10.1371/journal.ppat.1013390
Citations
1
Primary Topic
Hepatitis B Virus Studies
Type
article
Field-Weighted Citation Impact
1.35

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Screening of different species reveals cat hepatocytes support HBV infection

Yuchen Xia, N.C. Chen, Zaichao Xu, Mengfei Wang et al.
1 citations
PLoS Pathogens
Hepatitis B Virus Studies
1.35
article

Screening of different species reveals cat hepatocytes support HBV infection

Yuchen Xia, N.C. Chen, Zaichao Xu, Mengfei Wang, Kaitao Zhao, Gaihong Zhao, Tianchi Xin, Lu Zhang, Sijia Chen, Jingjing Wang, Chengliang Zhu, Jiatong Yin, Xiaoming Cheng
article en
1 citations

Abstract

Hepatitis B virus (HBV) remains a major public health challenge, with nearly 300 million chronic infections, yet research is hindered by the lack of suitable animal models. This study aimed to identify HBV-susceptible species and establish a novel infection model. Primary hepatocytes from humans, cats, rabbits, Syrian hamsters, Siberian hamsters, guinea pigs, bulls, goats, pigs, cynomolgus macaques, and dogs were assessed for HBV entry using hepatitis D virus (HDV) infection. HBV relaxed circular DNA (rcDNA) transfection was performed to evaluate its repair into covalently closed circular DNA (cccDNA). HBV infection assays were conducted in vitro. Results showed that primary hepatocytes from humans and cats were susceptible to HDV, suggesting their potential to support HBV entry. All tested hepatocytes converted rcDNA into cccDNA, confirming their ability to complete early HBV replication steps. Notably, cat hepatocytes uniquely supported HBV infection, displaying time-dependent viral replication marker expression. Cat hepatocytes also responded to antiviral treatments, underscoring their relevance for drug evaluation. This study provides the first evidence that cats can support HBV infection in vitro, offering a promising new platform for HBV research and antiviral development.

PLoS PathogensVol. 21(8)
Wuhan University (CN), Wuhan Institute of Virology (CN), Zhongnan Hospital of Wuhan University (CN), Renmin Hospital of Wuhan University (CN)
National Natural Science Foundation of China, Postdoctoral Research Foundation of China, Key Technologies Research and Development Program, Fundamental Research Funds for the Central Universities
Good health and well-being
Openalex Percentile: Top 17%
Hepatitis B Virus Studies
1.35
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.