Literature DB >> 10555293

Recombination of hepatitis D virus RNA sequences and its implications.

J C Wu1, T Y Chiang, W K Shiue, S Y Wang, I J Sheen, Y H Huang, W J Syu.   

Abstract

Recombination between RNA sequences plays a role in the fast evolution of a few viruses. There has been no report on hepatitis D virus (HDV) recombination. In this study, we analyzed genetic recombination of HDV and its possible impact on evolution and clinical course. The aligned HDV sequences allowed us to construct a phylogenetic tree which supported the notion of distinct lineages of HDV. The tree was also used in the analysis of recombination using partial likelihoods assessed through optimization. Nine segments of the HDV genome with significant levels of genetic recombination were detected. Five segments were in the hypervariable region, and four were in the delta-antigen- coding region. None could be found in the well-conserved autocleavage region that is essential for replication. Recombination occurred both between and within types. The results of this study indicated that the remarkable variation in HDV genomic sequences, particularly in the hypervariable region, among different genotypes may at least partly result from multiple episodes of genetic recombination during evolution. Genetic recombination may play a significant role in increasing genetic diversity. Importantly, a genetic recombination (nt 1082-1093) occurred in one of the immunogenic domains of hepatitis delta virus antigen recognized by human and woodchuck antibodies (amino acids 174-195). Genetic recombination also occurred at another segment between nt 1517 and 1535, which was close to one of the predicted T-cell epitopes (amino acids 26-41). In longitudinal analysis of HDV genomes at different time points during chronic infection, novel dominant HDV strains with amino acid changes at these epitopes usually emerged after severe hepatitis attacks. In the comparison of HDV clones during or shortly after flare-up of liver disease, Ka/Ks ratios of > 1 were frequently found, suggesting Darwinian positive selection. Therefore, recombination in these two segments may play an important role for HDV in the evasion of immunity.

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Year:  1999        PMID: 10555293     DOI: 10.1093/oxfordjournals.molbev.a026075

Source DB:  PubMed          Journal:  Mol Biol Evol        ISSN: 0737-4038            Impact factor:   16.240


  20 in total

1.  Effect of recombination on the accuracy of the likelihood method for detecting positive selection at amino acid sites.

Authors:  Maria Anisimova; Rasmus Nielsen; Ziheng Yang
Journal:  Genetics       Date:  2003-07       Impact factor: 4.562

2.  Reconstitution in cultured cells of replicating HDV RNA from pairs of less than full-length RNAs.

Authors:  Severin O Gudima; Jinhong Chang; John M Taylor
Journal:  RNA       Date:  2004-12-01       Impact factor: 4.942

3.  Evolution of hepatitis delta virus RNA genome following long-term replication in cell culture.

Authors:  Jinhong Chang; Severin O Gudima; John M Taylor
Journal:  J Virol       Date:  2005-11       Impact factor: 5.103

4.  Molecular evolution of the hepatitis delta virus antigen gene: recombination or positive selection?

Authors:  Maria Anisimova; Ziheng Yang
Journal:  J Mol Evol       Date:  2004-12       Impact factor: 2.395

5.  Phylogeography and conservation genetics of Hygrophila pogonocalyx (Acanthaceae) based on atpB-rbcL noncoding spacer cpDNA.

Authors:  Jao-Ching Huang; Wei-Kuang Wang; Ching-I Peng; Tzen-Yuh Chiang
Journal:  J Plant Res       Date:  2005-01-13       Impact factor: 2.629

6.  Efficient in vitro system of homologous recombination in brome mosaic bromovirus.

Authors:  Rafal Wierzchoslawski; Jozef J Bujarski
Journal:  J Virol       Date:  2006-06       Impact factor: 5.103

7.  RNA recombination of hepatitis delta virus in natural mixed-genotype infection and transfected cultured cells.

Authors:  Tzu-Chi Wang; Mei Chao
Journal:  J Virol       Date:  2005-02       Impact factor: 5.103

8.  "Defective" mutations of hepatitis D viruses in chronic hepatitis D patients.

Authors:  Jaw-Ching Wu; Sheng-Chieh Hsu; Shen-Yung Wang; Yi-Hsiang Huang; I-Jane Sheen; Hsuan-Hui Shih; Wan-Jr Syu
Journal:  World J Gastroenterol       Date:  2005-03-21       Impact factor: 5.742

9.  Evolution and diversity of the human hepatitis d virus genome.

Authors:  Chi-Ruei Huang; Szecheng J Lo
Journal:  Adv Bioinformatics       Date:  2010-02-24

Review 10.  Hepatitis D Virus Replication.

Authors:  John M Taylor
Journal:  Cold Spring Harb Perspect Med       Date:  2015-11-02       Impact factor: 6.915

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