scholarly journals Evaluation of Accumulation of Hepatitis C Virus Mutations in a Chronically Infected Chimpanzee: Comparison of the Core, E1, HVR1, and NS5b Regions

2001 ◽  
Vol 75 (6) ◽  
pp. 3004-3009 ◽  
Author(s):  
Ling Lu ◽  
Tatsunori Nakano ◽  
Etsuro Orito ◽  
Masashi Mizokami ◽  
Betty H. Robertson

ABSTRACT Four hepatitis C virus genome regions (the core, E1, HVR1, and NS5b) were amplified and sequenced from yearly samples obtained from a chronically infected chimpanzee over a 12-year span. Nucleotide substitutions were found to accumulate in the core, E1, and HVR1 regions during the course of chronic infection; substitutions within the NS5b region were not detected for the first 8 years and were found to be minimal during the last 4 years. The rate of accumulation of mutations in the core and E1 regions, based on a direct comparison between the first 1979 sequence and the last 1990 sequence, was 1.120 × 10−3, while phylogenetic ancestral comparison using the 12 yearly sequences showed a rate of 0.816 × 10−3bases per site per year. Temporal evaluation of the sequences revealed that there appeared to be periods in which substitutions accumulated and became fixed, followed by periods with relative stasis or random substitutions that did not persist. Synonymous and nonsynonymous substitutions within the core, E1, and HVR1 regions were also analyzed. In the core and E1 regions, synonymous substitutions predominated and gradually increased over time. However, within the HVR1 region, nonsynonymous substitutions predominated but gradually decreased over time.

2012 ◽  
Vol 8 (3) ◽  
pp. e1002561 ◽  
Author(s):  
Tomomi Ando ◽  
Hiromi Imamura ◽  
Ryosuke Suzuki ◽  
Hideki Aizaki ◽  
Toshiki Watanabe ◽  
...  

1994 ◽  
Vol 106 (6) ◽  
pp. 1603-1610 ◽  
Author(s):  
Kojiro Michitaka ◽  
Marilena Durazzo ◽  
Hans L. Tillmann ◽  
Diana Walker ◽  
Thomas Philipp ◽  
...  

2018 ◽  
Vol 34 (2) ◽  
pp. 197-210 ◽  
Author(s):  
Catherine Sodroski ◽  
Brianna Lowey ◽  
Laura Hertz ◽  
T. Jake Liang ◽  
Qisheng Li

PLoS ONE ◽  
2011 ◽  
Vol 6 (5) ◽  
pp. e19562 ◽  
Author(s):  
Hui Li ◽  
Austin L. Hughes ◽  
Nazneen Bano ◽  
Susan McArdle ◽  
Stephen Livingston ◽  
...  

1996 ◽  
Vol 9 (2) ◽  
pp. 89-96 ◽  
Author(s):  
FLOR H. PUJOL ◽  
YURY E. KHUDYAKOV ◽  
MARISOL DEVESA ◽  
GRACIELA LEÓN ◽  
LINDA BLITZ-DORFMAN ◽  
...  

1993 ◽  
Vol 4 (6) ◽  
pp. 1288-1293
Author(s):  
D M Burstein ◽  
R A Rodby

The hepatitis C virus genome has been recently sequenced and cloned, allowing the identification of patients exposed to this virus, which is now felt to be the principal cause of "non-A, non-B" hepatitis. The hepatitis B virus has long been implicated in the pathogenesis of several glomerulopathies including membranoproliferative glomerulonephritis, mixed cryoglobulinemia, and membranous glomerulonephritis. Several authors have recently reported an association between hepatitis C virus infection and glomerular disease. The case of a patient with chronic hepatitis C virus infection who developed the nephrotic syndrome 3 months after liver transplantation is described. Serologic testing was significant for an elevated rheumatoid factor, circulating cryoglobulins, and a mildly depressed C4 level. Hepatitis C virus antibody and viral RNA (by polymerase chain reaction) were present in both the serum and cryoglobulin fraction. A renal biopsy demonstrated membranoproliferative glomerulonephritis. It is believed that persistent infection with the hepatitis C virus is responsible for an immune complex-mediated glomerulonephritis in this patient. Because hepatitis C has now been pathogenetically linked to several glomerulopathies, testing for this virus should be considered in the serologic work-up of the patient with glomerulonephritis.


2015 ◽  
Vol 36 (3) ◽  
pp. 159-167 ◽  
Author(s):  
Mohammod Johirul ISLAM ◽  
Keisuke HIKOSAKA ◽  
Hidenao NORITAKE ◽  
Mohammad Khaja Mafij UDDIN ◽  
Mohammed Badrul AMIN ◽  
...  

1998 ◽  
Vol 36 (5) ◽  
pp. 1461-1463 ◽  
Author(s):  
S. Le Pogam ◽  
F. Dubois ◽  
R. Christen ◽  
C. Raby ◽  
A. Cavicchini ◽  
...  

Two methods for genotyping hepatitis C virus (DNA enzyme immunoassay [DEIA] and line probe assay [Inno-LiPA HCV I and II]) were compared on 120 samples and of these 87% were assigned to the same subtype by both assays. There were 15 subtyping discrepancies which involved 5% of type 1 isolates and 90% of type 2 isolates. Amplified products from the core and 5′ untranslated regions (UTR) were sequenced to resolve conflicts. Type 1 discordant samples had a guanosine at position −99 in the 5′ UTR, a characteristic of genotype 1b, and a core region typical of subtype 1a. The eight isolates classified as 2a/2c by LiPA and as subtype 2c by DEIA belonged to type 2.


Gene ◽  
1997 ◽  
Vol 200 (1-2) ◽  
pp. 157-162 ◽  
Author(s):  
Masashi Urabe ◽  
Yoko Hasumi ◽  
Yoji Ogasawara ◽  
Takashi Matsushita ◽  
Nobuhiko Kamoshita ◽  
...  

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