Down-regulation of hepatitis delta virus super-infection in the woodchuck model

被引:3
|
作者
Lukash, Tetyana [1 ]
Freitas, Natalia [1 ]
Menne, Stephan [2 ]
Gudima, Severin O. [1 ]
机构
[1] Univ Kansas, Med Ctr, Dept Microbiol Mol Genet & Immunol, Room WHW 5031C,3901 Rainbow Blvd, Kansas City, KS 66160 USA
[2] Georgetown Univ, Med Ctr, Dept Microbiol & Immunol, Washington, DC 20007 USA
关键词
Hepatitis delta virus; HDV-host interactions; Regulation of HDV infection outcome; CIRCULATING IMMUNE-COMPLEXES; SURFACE-ANTIGEN HBSAG; B-VIRUS; HEPATOCELLULAR-CARCINOMA; ENVELOPE PROTEINS; HUMAN HEPATOCYTES; RNA; REPLICATION; GLYCOSYLATION; DETERMINANTS;
D O I
10.1016/j.virol.2019.03.002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Mechanisms mediating clearance of hepatitis delta virus (HDV) are poorly understood. This study analyzed in detail profound down-regulation of HDV infection in the woodchuck model. Super-infection with HDV of woodchucks chronically infected with HBV-related woodchuck hepatitis virus produced two patterns. In the first, HDV viremia had a sharp peak followed by a considerable decline, and initial rise of HDV virions' infectivity followed by abrupt infectivity loss. In the second, HDV titer rose and later displayed plateau-like profile with high HDV levels; and HDV infectivity became persistently high when HDV titer reached the plateau. The infectivity loss was not due to defects in the virions' envelope, binding to anti-envelope antibodies, or mutations in HDV genome, but it correlated with profound reduction of the replication capacity of virion-associated HDV genomes. Subsequent finding that in virions with reduced infectivity most HDV RNAs were not full-length genomes suggests possible HDV clearance via RNA fragmentation.
引用
收藏
页码:100 / 113
页数:14
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