Conserved use of the sodium/bile acid cotransporter (NTCP) as an entry receptor by hepatitis B virus and domestic cat hepadnavirus

被引:8
|
作者
Shofa, Maya [1 ,2 ]
Ohkawa, Akiho [1 ]
Kaneko, Yasuyuki [1 ,3 ]
Saito, Akatsuki [1 ,2 ,4 ]
机构
[1] Univ Miyazaki, Dept Vet Sci, Miyazaki, Miyazaki 8892192, Japan
[2] Univ Miyazaki, Grad Sch Med & Vet Med, Miyazaki, Miyazaki 8891692, Japan
[3] Univ Miyazaki, Vet Teaching Hosp, Miyazaki, Miyazaki 8892192, Japan
[4] Univ Miyazaki, Ctr Anim Dis Control, Miyazaki, Miyazaki 8892192, Japan
关键词
Hepadnavirus; Hepatitis B virus (HBV); Domestic cat hepadnavirus; Sodium/bile acid cotransporter (NTCP); DELTA VIRUS; IN-VIVO; INFECTION; DNA; HEPATOCYTES; RECOVERY; SEQUENCE;
D O I
10.1016/j.antiviral.2023.105695
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The Orthohepadnavirus genus includes hepatitis B virus (HBV) that can cause chronic hepatitis and hepatocarcinoma in humans. Recently, a novel hepadnavirus in cats, domestic cat hepadnavirus (DCH), was identified that is genetically close to HBV. DCH infection is associated with chronic hepatitis in cats, suggesting a similarity with HBV pathogenesis and the potential to use DCH as a novel animal model for HBV research. HBV is shown to use the sodium/bile acid cotransporter (NTCP) as a major cell entry receptor, but the equivalent receptor for DCH remains unknown. Here we sought to identify the entry receptor for DCH. HBV- and DCH-derived preS1 peptides efficiently bound to both human and cat NTCPs, and residue 158 of NTCP proteins determined the species-specific binding of the DCH preS1 peptide. Myrcludex B, an HBV entry inhibitor, blocked the binding of the DCH preS1 peptide. Thus, DCH and HBV may share cell entry molecules, suggesting a possibility of interspecies transmission. Furthermore, our study suggests that DCH can be useful as a novel model for HBV research.
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页数:13
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